Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79905 |
| ensemblid | ENSG00000170537.13 |
| hgncid | 23000 |
| symbol | TMC7 |
| name | transmembrane channel like 7 |
| refseq_nuc | NM_024847.4 |
| refseq_prot | NP_079123.3 |
| ensembl_nuc | ENST00000304381.10 |
| ensembl_prot | ENSP00000304710.5 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 18983934 |
| end | 19063942 |
| strand | + |
| ver | v1.2 |
| region | chr16:18983934-19063942 |
| region5000 | chr16:18978934-19068942 |
| regionname0 | TMC7_chr16_18983934_19063942 |
| regionname5000 | TMC7_chr16_18978934_19068942 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 723 | 140 | 59 | 28 | 30 | 4 | 17 | 17 | TMC7_chr16_18978934_19068942 | TMC7 | MSESS others(718): Show |
chr16 | 18978934 | 19068942 |
| a0002 | 0/0 | 723 | 126 | 13 | 28 | 61 | 5 | 19 | 41 | TMC7_chr16_18978934_19068942 | TMC7 | MSESS others(718): Show |
chr16 | 18978934 | 19068942 |
| a0003 | 0/0 | 723 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | MSESS others(718): Show |
chr16 | 18978934 | 19068942 |
| a0004 | 0/0 | 723 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | MSESS others(718): Show |
chr16 | 18978934 | 19068942 |
| a0005 | 0/0 | 723 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | MSESS others(718): Show |
chr16 | 18978934 | 19068942 |
| a0006 | 0/0 | 723 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | MSESS others(718): Show |
chr16 | 18978934 | 19068942 |
| a0007 | 0/0 | 723 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | MSESS others(718): Show |
chr16 | 18978934 | 19068942 |
| a0008 | 0/0 | 723 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | MSESS others(718): Show |
chr16 | 18978934 | 19068942 |
| a0009 | 0/0 | 723 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | MSESS others(718): Show |
chr16 | 18978934 | 19068942 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2169 | 128 | 57 | 23 | 26 | 4 | 16 | TMC7_chr16_18978934_19068942 | TMC7 | ATGAG others(2164): Show |
chr16 | 18978934 | 19068942 | ||
| a0001c0005 | 0/0 | 2169 | 5 | 0 | 1 | 4 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ATGAG others(2164): Show |
chr16 | 18978934 | 19068942 | ||
| a0001c0006 | 0/0 | 2169 | 4 | 2 | 2 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ATGAG others(2164): Show |
chr16 | 18978934 | 19068942 | ||
| a0001c0009 | 0/0 | 2169 | 2 | 0 | 2 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ATGAG others(2164): Show |
chr16 | 18978934 | 19068942 | ||
| a0001c0017 | 0/0 | 2169 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | ATGAG others(2164): Show |
chr16 | 18978934 | 19068942 | ||
| a0002c0002 | 0/0 | 2169 | 96 | 7 | 23 | 46 | 4 | 16 | TMC7_chr16_18978934_19068942 | TMC7 | ATGAG others(2164): Show |
chr16 | 18978934 | 19068942 | ||
| a0002c0003 | 0/0 | 2169 | 28 | 6 | 5 | 14 | 0 | 3 | TMC7_chr16_18978934_19068942 | TMC7 | ATGAG others(2164): Show |
chr16 | 18978934 | 19068942 | ||
| a0002c0013 | 0/0 | 2169 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ATGAG others(2164): Show |
chr16 | 18978934 | 19068942 | ||
| a0002c0015 | 0/0 | 2169 | 1 | 0 | 0 | 0 | 1 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ATGAG others(2164): Show |
chr16 | 18978934 | 19068942 | ||
| a0003c0004 | 0/0 | 2169 | 5 | 5 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ATGAG others(2164): Show |
chr16 | 18978934 | 19068942 | ||
| a0004c0008 | 0/0 | 2169 | 2 | 2 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ATGAG others(2164): Show |
chr16 | 18978934 | 19068942 | ||
| a0004c0011 | 0/0 | 2169 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ATGAG others(2164): Show |
chr16 | 18978934 | 19068942 | ||
| a0004c0012 | 0/0 | 2169 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ATGAG others(2164): Show |
chr16 | 18978934 | 19068942 | ||
| a0005c0007 | 0/0 | 2169 | 3 | 3 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ATGAG others(2164): Show |
chr16 | 18978934 | 19068942 | ||
| a0006c0016 | 0/0 | 2169 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ATGAG others(2164): Show |
chr16 | 18978934 | 19068942 | ||
| a0007c0018 | 0/0 | 2169 | 1 | 0 | 0 | 0 | 1 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ATGAG others(2164): Show |
chr16 | 18978934 | 19068942 | ||
| a0008c0010 | 0/0 | 2169 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ATGAG others(2164): Show |
chr16 | 18978934 | 19068942 | ||
| a0009c0014 | 0/0 | 2169 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ATGAG others(2164): Show |
chr16 | 18978934 | 19068942 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4401 | 77 | 24 | 18 | 18 | 4 | 12 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4396): Show |
chr16 | 18978934 | 19068942 |
| a0001c0001t0003 | 1/0 | 4401 | 32 | 19 | 2 | 7 | 0 | 3 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4396): Show |
chr16 | 18978934 | 19068942 |
| a0001c0001t0005 | 0/0 | 4399 | 2 | 0 | 2 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4394): Show |
chr16 | 18978934 | 19068942 |
| a0001c0001t0006 | 0/0 | 4403 | 2 | 2 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4398): Show |
chr16 | 18978934 | 19068942 |
| a0001c0001t0007 | 0/0 | 4406 | 4 | 4 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4401): Show |
chr16 | 18978934 | 19068942 |
| a0001c0001t0008 | 0/0 | 4401 | 4 | 4 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4396): Show |
chr16 | 18978934 | 19068942 |
| a0001c0001t0009 | 0/0 | 4405 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4400): Show |
chr16 | 18978934 | 19068942 |
| a0001c0001t0010 | 0/0 | 4410 | 3 | 3 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4405): Show |
chr16 | 18978934 | 19068942 |
| a0001c0001t0026 | 0/0 | 4404 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4399): Show |
chr16 | 18978934 | 19068942 |
| a0001c0001t0028 | 0/0 | 4401 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4396): Show |
chr16 | 18978934 | 19068942 |
| a0001c0001t0030 | 0/0 | 4401 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4396): Show |
chr16 | 18978934 | 19068942 |
| a0001c0005t0002 | 0/0 | 4403 | 5 | 0 | 1 | 4 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4398): Show |
chr16 | 18978934 | 19068942 |
| a0001c0006t0006 | 0/0 | 4403 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4398): Show |
chr16 | 18978934 | 19068942 |
| a0001c0006t0018 | 0/0 | 4409 | 2 | 1 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4404): Show |
chr16 | 18978934 | 19068942 |
| a0001c0006t0034 | 0/0 | 4407 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4402): Show |
chr16 | 18978934 | 19068942 |
| a0001c0009t0001 | 0/0 | 4401 | 2 | 0 | 2 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4396): Show |
chr16 | 18978934 | 19068942 |
| a0001c0017t0033 | 0/0 | 4401 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4396): Show |
chr16 | 18978934 | 19068942 |
| a0002c0002t0001 | 0/0 | 4401 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4396): Show |
chr16 | 18978934 | 19068942 |
| a0002c0002t0002 | 0/0 | 4403 | 75 | 2 | 18 | 37 | 4 | 14 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4398): Show |
chr16 | 18978934 | 19068942 |
| a0002c0002t0005 | 0/0 | 4399 | 4 | 0 | 3 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4394): Show |
chr16 | 18978934 | 19068942 |
| a0002c0002t0011 | 0/0 | 4405 | 3 | 1 | 0 | 1 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4400): Show |
chr16 | 18978934 | 19068942 |
| a0002c0002t0012 | 0/0 | 4403 | 3 | 0 | 0 | 3 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4398): Show |
chr16 | 18978934 | 19068942 |
| a0002c0002t0017 | 0/0 | 4407 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4402): Show |
chr16 | 18978934 | 19068942 |
| a0002c0002t0019 | 0/0 | 4403 | 2 | 2 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4398): Show |
chr16 | 18978934 | 19068942 |
| a0002c0002t0020 | 0/0 | 4403 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4398): Show |
chr16 | 18978934 | 19068942 |
| a0002c0002t0024 | 0/0 | 4412 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4407): Show |
chr16 | 18978934 | 19068942 |
| a0002c0002t0027 | 0/0 | 4405 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4400): Show |
chr16 | 18978934 | 19068942 |
| a0002c0002t0029 | 0/0 | 4403 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4398): Show |
chr16 | 18978934 | 19068942 |
| a0002c0002t0031 | 0/0 | 4403 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4398): Show |
chr16 | 18978934 | 19068942 |
| a0002c0002t0035 | 0/0 | 4403 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4398): Show |
chr16 | 18978934 | 19068942 |
| a0002c0002t0036 | 0/0 | 4403 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4398): Show |
chr16 | 18978934 | 19068942 |
| a0002c0003t0001 | 0/0 | 4401 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4396): Show |
chr16 | 18978934 | 19068942 |
| a0002c0003t0004 | 0/0 | 4405 | 18 | 0 | 4 | 12 | 0 | 2 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4400): Show |
chr16 | 18978934 | 19068942 |
| a0002c0003t0009 | 0/0 | 4405 | 3 | 2 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4400): Show |
chr16 | 18978934 | 19068942 |
| a0002c0003t0014 | 0/0 | 4407 | 2 | 0 | 0 | 2 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4402): Show |
chr16 | 18978934 | 19068942 |
| a0002c0003t0015 | 0/0 | 4403 | 2 | 2 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4398): Show |
chr16 | 18978934 | 19068942 |
| a0002c0003t0016 | 0/0 | 4409 | 2 | 2 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4404): Show |
chr16 | 18978934 | 19068942 |
| a0002c0013t0037 | 0/0 | 4403 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4398): Show |
chr16 | 18978934 | 19068942 |
| a0002c0015t0002 | 0/0 | 4403 | 1 | 0 | 0 | 0 | 1 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4398): Show |
chr16 | 18978934 | 19068942 |
| a0003c0004t0003 | 0/0 | 4401 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4396): Show |
chr16 | 18978934 | 19068942 |
| a0003c0004t0006 | 0/0 | 4403 | 3 | 3 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4398): Show |
chr16 | 18978934 | 19068942 |
| a0003c0004t0023 | 0/0 | 4412 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4407): Show |
chr16 | 18978934 | 19068942 |
| a0004c0008t0022 | 0/0 | 4410 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4405): Show |
chr16 | 18978934 | 19068942 |
| a0004c0008t0025 | 0/0 | 4410 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4405): Show |
chr16 | 18978934 | 19068942 |
| a0004c0011t0017 | 0/0 | 4407 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4402): Show |
chr16 | 18978934 | 19068942 |
| a0004c0012t0032 | 0/0 | 4401 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4396): Show |
chr16 | 18978934 | 19068942 |
| a0005c0007t0013 | 0/0 | 4410 | 2 | 2 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4405): Show |
chr16 | 18978934 | 19068942 |
| a0005c0007t0021 | 0/0 | 4413 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4408): Show |
chr16 | 18978934 | 19068942 |
| a0006c0016t0001 | 0/0 | 4401 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4396): Show |
chr16 | 18978934 | 19068942 |
| a0007c0018t0002 | 0/0 | 4403 | 1 | 0 | 0 | 0 | 1 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4398): Show |
chr16 | 18978934 | 19068942 |
| a0008c0010t0001 | 0/0 | 4401 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4396): Show |
chr16 | 18978934 | 19068942 |
| a0009c0014t0002 | 0/0 | 4403 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | ACTCC others(4398): Show |
chr16 | 18978934 | 19068942 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0212 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0172 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0005g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0005g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0006g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0006g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0007g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0007g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0007g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0007g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0008g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0008g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0008g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0008g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0009g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0010g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0010g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0010g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0026g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0028g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0001t0030g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0005t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0005t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0005t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0005t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0005t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0006t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0006t0018g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0006t0018g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0006t0034g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0009t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0009t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0001c0017t0033g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0005g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0005g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0005g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0005g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0011g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0011g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0011g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0012g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0012g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0012g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0017g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0019g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0019g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0020g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0024g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0027g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0029g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0031g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0035g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0002t0036g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0003t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0003t0004g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0003t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0003t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0003t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0003t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0003t0004g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0003t0004g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0003t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0003t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0003t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0003t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0003t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0003t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0003t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0003t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0003t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0003t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0003t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0003t0009g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0003t0009g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0003t0009g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0003t0014g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0003t0014g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0003t0015g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0003t0015g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0003t0016g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0003t0016g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0013t0037g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0002c0015t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0003c0004t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0003c0004t0006g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0003c0004t0006g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0003c0004t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0003c0004t0023g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0004c0008t0022g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0004c0008t0025g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0004c0011t0017g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0004c0012t0032g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0005c0007t0013g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0005c0007t0013g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0005c0007t0021g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0006c0016t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0007c0018t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0008c0010t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| a0009c0014t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0216 | EUR | FIN | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0102 | EUR | FIN | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0096 | EAS | CHS | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG00408 | hp2 | a0002 | c0013 | t0037 | g0081 | EAS | CHS | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG00423 | hp1 | a0006 | c0016 | t0001 | g0257 | EAS | CHS | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0044 | EAS | CHS | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0041 | EAS | CHS | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0100 | EAS | CHS | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG00609 | hp1 | a0002 | c0003 | t0004 | g0124 | EAS | CHS | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG00609 | hp2 | a0001 | c0005 | t0002 | g0175 | EAS | CHS | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0071 | AMR | PUR | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG00642 | hp1 | a0002 | c0002 | t0005 | g0060 | AMR | PUR | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0037 | EAS | CHS | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0174 | AMR | PUR | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0046 | AMR | PUR | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0028 | AMR | PUR | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG00738 | hp2 | a0001 | c0006 | t0034 | g0154 | AMR | PUR | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG00741 | hp1 | a0001 | c0005 | t0002 | g0248 | AMR | PUR | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0226 | AMR | PUR | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01069 | hp2 | a0002 | c0002 | t0005 | g0068 | AMR | PUR | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0094 | AMR | PUR | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01074 | hp2 | a0001 | c0006 | t0018 | g0155 | AMR | PUR | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0026 | AMR | PUR | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01081 | hp2 | a0001 | c0001 | t0026 | g0208 | AMR | PUR | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0093 | AMR | PUR | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0086 | AMR | PUR | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01167 | hp2 | a0001 | c0009 | t0001 | g0264 | AMR | PUR | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0104 | AMR | PUR | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01169 | hp2 | a0001 | c0009 | t0001 | g0261 | AMR | PUR | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01243 | hp2 | a0002 | c0002 | t0005 | g0066 | AMR | PUR | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01256 | hp1 | a0001 | c0001 | t0005 | g0258 | AMR | CLM | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01256 | hp2 | a0002 | c0002 | t0036 | g0176 | AMR | CLM | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0040 | AMR | CLM | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01433 | hp2 | a0002 | c0003 | t0001 | g0222 | AMR | CLM | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0085 | AMR | CLM | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0227 | EUR | IBS | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01515 | hp2 | a0007 | c0018 | t0002 | g0015 | EUR | IBS | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01516 | hp1 | a0002 | c0002 | t0002 | g0103 | EUR | IBS | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0076 | EUR | IBS | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01884 | hp2 | a0002 | c0003 | t0009 | g0113 | AFR | ACB | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0063 | AMR | PEL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0048 | AMR | PEL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0017 | AMR | PEL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01934 | hp2 | a0002 | c0003 | t0004 | g0144 | AMR | PEL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0088 | AMR | PEL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01975 | hp1 | a0008 | c0010 | t0001 | g0219 | AMR | PEL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01975 | hp2 | a0009 | c0014 | t0002 | g0032 | AMR | PEL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0089 | AMR | PEL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01981 | hp1 | a0002 | c0003 | t0004 | g0143 | AMR | PEL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01981 | hp2 | a0002 | c0002 | t0017 | g0078 | AMR | PEL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0091 | AMR | PEL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02015 | hp2 | a0002 | c0002 | t0002 | g0052 | EAS | KHV | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0043 | EAS | KHV | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0112 | EAS | KHV | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0153 | AFR | ACB | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0111 | EAS | KHV | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02056 | hp2 | a0002 | c0003 | t0004 | g0118 | EAS | KHV | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0016 | EAS | KHV | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0059 | EAS | KHV | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0105 | EAS | KHV | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0025 | EAS | KHV | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | KHV | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | KHV | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0023 | EAS | KHV | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0056 | EAS | KHV | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0163 | AFR | ACB | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0024 | EAS | CDX | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CDX | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02258 | hp1 | a0002 | c0003 | t0009 | g0116 | AFR | ACB | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02258 | hp2 | a0004 | c0012 | t0032 | g0189 | AFR | ACB | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0097 | AMR | PEL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02273 | hp2 | a0002 | c0003 | t0004 | g0145 | AMR | PEL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02300 | hp1 | a0002 | c0003 | t0004 | g0115 | AMR | PEL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02451 | hp1 | a0003 | c0004 | t0006 | g0252 | AFR | ACB | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0162 | AFR | GWD | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02572 | hp2 | a0005 | c0007 | t0021 | g0203 | AFR | GWD | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0218 | SAS | PJL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02615 | hp1 | a0004 | c0008 | t0025 | g0198 | AFR | GWD | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0204 | AFR | GWD | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02622 | hp2 | a0003 | c0004 | t0006 | g0255 | AFR | GWD | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02647 | hp1 | a0002 | c0003 | t0015 | g0127 | AFR | GWD | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02647 | hp2 | a0002 | c0002 | t0019 | g0191 | AFR | GWD | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02683 | hp1 | a0002 | c0002 | t0011 | g0073 | SAS | PJL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02698 | hp1 | a0002 | c0003 | t0009 | g0130 | SAS | PJL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0125 | SAS | PJL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0207 | AFR | GWD | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0020 | SAS | PJL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0158 | AFR | GWD | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02809 | hp2 | a0002 | c0002 | t0019 | g0190 | AFR | GWD | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02818 | hp1 | a0002 | c0003 | t0016 | g0129 | AFR | GWD | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02886 | hp1 | a0002 | c0002 | t0024 | g0199 | AFR | GWD | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02886 | hp2 | a0001 | c0001 | t0010 | g0211 | AFR | GWD | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0195 | AFR | GWD | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02896 | hp1 | a0004 | c0011 | t0017 | g0186 | AFR | GWD | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0169 | AFR | ESN | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ESN | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02965 | hp1 | a0004 | c0008 | t0022 | g0197 | AFR | ESN | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02965 | hp2 | a0002 | c0002 | t0011 | g0194 | AFR | ESN | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | ESN | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0012 | AFR | ESN | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0008 | AFR | ESN | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0051 | SAS | PJL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0009 | AFR | GWD | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03098 | hp2 | a0003 | c0004 | t0023 | g0201 | AFR | MSL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03130 | hp2 | a0005 | c0007 | t0013 | g0200 | AFR | ESN | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0254 | AFR | ESN | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03195 | hp1 | a0001 | c0001 | t0008 | g0187 | AFR | ESN | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03195 | hp2 | a0002 | c0003 | t0015 | g0128 | AFR | ESN | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0205 | AFR | MSL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0166 | SAS | PJL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0031 | SAS | PJL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03453 | hp1 | a0005 | c0007 | t0013 | g0202 | AFR | MSL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03490 | hp1 | a0002 | c0003 | t0004 | g0122 | SAS | PJL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03492 | hp1 | a0002 | c0003 | t0004 | g0123 | SAS | PJL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03516 | hp1 | a0001 | c0001 | t0028 | g0245 | AFR | ESN | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0011 | AFR | ESN | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | MSL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03579 | hp2 | a0001 | c0001 | t0010 | g0210 | AFR | MSL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0033 | SAS | PJL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0108 | SAS | PJL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0021 | SAS | BEB | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0064 | SAS | BEB | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | BEB | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0087 | SAS | BEB | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0072 | SAS | BEB | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | BEB | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0038 | SAS | BEB | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG04184 | hp2 | a0001 | c0017 | t0033 | g0247 | SAS | BEB | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | STU | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG04204 | hp2 | a0002 | c0002 | t0005 | g0065 | SAS | STU | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG04228 | hp1 | a0001 | c0001 | t0009 | g0236 | SAS | STU | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0018 | SAS | STU | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | YRI | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | YRI | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | CHB | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18612 | hp2 | a0001 | c0001 | t0030 | g0271 | EAS | CHB | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0160 | AFR | YRI | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | YRI | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18940 | hp2 | a0002 | c0002 | t0012 | g0107 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18946 | hp1 | a0002 | c0003 | t0004 | g0117 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0058 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18947 | hp2 | a0001 | c0005 | t0002 | g0168 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18948 | hp1 | a0002 | c0003 | t0004 | g0149 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18948 | hp2 | a0002 | c0002 | t0035 | g0030 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18950 | hp1 | a0002 | c0003 | t0004 | g0148 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0054 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18959 | hp2 | a0002 | c0003 | t0004 | g0142 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18966 | hp1 | a0002 | c0002 | t0029 | g0036 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18966 | hp2 | a0002 | c0003 | t0004 | g0140 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18967 | hp1 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18968 | hp2 | a0002 | c0002 | t0027 | g0099 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18971 | hp2 | a0002 | c0002 | t0011 | g0090 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18973 | hp1 | a0001 | c0005 | t0002 | g0164 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18973 | hp2 | a0002 | c0003 | t0004 | g0119 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18975 | hp1 | a0002 | c0002 | t0012 | g0035 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18977 | hp2 | a0002 | c0003 | t0004 | g0120 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18989 | hp2 | a0002 | c0002 | t0002 | g0192 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18990 | hp2 | a0001 | c0005 | t0002 | g0165 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA19002 | hp2 | a0002 | c0003 | t0004 | g0147 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA19005 | hp1 | a0002 | c0002 | t0012 | g0034 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA19030 | hp1 | a0001 | c0001 | t0008 | g0188 | AFR | LWK | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA19043 | hp1 | a0003 | c0004 | t0006 | g0253 | AFR | LWK | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0159 | AFR | LWK | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA19057 | hp1 | a0002 | c0003 | t0014 | g0150 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA19057 | hp2 | a0002 | c0002 | t0020 | g0077 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA19079 | hp1 | a0002 | c0003 | t0004 | g0146 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA19085 | hp2 | a0002 | c0003 | t0004 | g0126 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA19087 | hp1 | a0002 | c0003 | t0014 | g0121 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA19089 | hp1 | a0002 | c0002 | t0002 | g0050 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA19240 | hp1 | a0002 | c0003 | t0016 | g0151 | AFR | YRI | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA19240 | hp2 | a0003 | c0004 | t0003 | g0251 | AFR | YRI | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0092 | AFR | ASW | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA20129 | hp2 | a0001 | c0006 | t0006 | g0180 | AFR | ASW | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0079 | EUR | TSI | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0084 | EUR | TSI | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0220 | EUR | TSI | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA20805 | hp2 | a0002 | c0015 | t0002 | g0027 | EUR | TSI | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0171 | SAS | GIH | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0067 | SAS | GIH | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0070 | AMR | CLM | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02109 | hp2 | a0001 | c0001 | t0010 | g0209 | AFR | ACB | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0152 | AFR | ACB | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | MSL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0206 | AFR | MSL | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG06807 | hp1 | a0002 | c0002 | t0031 | g0110 | AFR | USA | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | USA | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | USA | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | USA | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0223 | AFR | LWK | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| NA21309 | hp2 | a0001 | c0006 | t0018 | g0156 | AFR | LWK | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0212 | REF | REF | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0172 | REF | REF | TMC7_chr16_18978934_19068942 | TMC7 | chr16 | 18978934 | 19068942 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:19009198 | T | C | 1 | a0008 | 1 | HG01975.hp1 | missense_variant | MODERATE | c.94T>C | p.Phe32Leu | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/16 | 224/4401 | 94/2172 | 32/723 | chr16 | 19009198 | |||
| chr16:19009312 | A | G | 1 | a0007 | 1 | HG01515.hp2 | missense_variant | MODERATE | c.208A>G | p.Thr70Ala | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/16 | 338/4401 | 208/2172 | 70/723 | chr16 | 19009312 | |||
| chr16:19016512 | G | A | 1 | a0004 | 4 | HG02258.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
missense_variant | MODERATE | c.374G>A | p.Ser125Asn | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/16 | 504/4401 | 374/2172 | 125/723 | chr16 | 19016512 | |||
| chr16:19030273 | G | A | 3 | a0002 a0007 a0009 |
128 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
missense_variant | MODERATE | c.761G>A | p.Gly254Glu | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/16 | 891/4401 | 761/2172 | 254/723 | chr16 | 19030273 | |||
| chr16:19040419 | G | A | 1 | a0003 | 5 | HG02451.hp1 HG02622.hp2 HG03098.hp2 others(2): Show |
missense_variant | MODERATE | c.1310G>A | p.Gly437Asp | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/16 | 1440/4401 | 1310/2172 | 437/723 | chr16 | 19040419 | |||
| chr16:19044978 | G | A | 1 | a0009 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.1432G>A | p.Gly478Ser | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 10/16 | 1562/4401 | 1432/2172 | 478/723 | chr16 | 19044978 | |||
| chr16:19056553 | C | T | 1 | a0006 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.1883C>T | p.Ser628Leu | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/16 | 2013/4401 | 1883/2172 | 628/723 | chr16 | 19056553 | |||
| chr16:19056574 | C | T | 1 | a0005 | 3 | HG02572.hp2 HG03130.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.1904C>T | p.Thr635Ile | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/16 | 2034/4401 | 1904/2172 | 635/723 | chr16 | 19056574 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:19009224 | C | T | 1 | a0001c0009 | 2 | HG01167.hp2 HG01169.hp2 |
synonymous_variant | LOW | c.120C>T | p.Leu40Leu | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/16 | 250/4401 | 120/2172 | 40/723 | chr16 | 19009224 | |||
| chr16:19009236 | A | G | 1 | a0004c0008 | 2 | HG02615.hp1 HG02965.hp1 |
synonymous_variant | LOW | c.132A>G | p.Pro44Pro | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/16 | 262/4401 | 132/2172 | 44/723 | chr16 | 19009236 | |||
| chr16:19009341 | C | T | 1 | a0001c0006 | 4 | HG00738.hp2 HG01074.hp2 NA20129.hp2 others(1): Show |
synonymous_variant | LOW | c.237C>T | p.Asp79Asp | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/16 | 367/4401 | 237/2172 | 79/723 | chr16 | 19009341 | |||
| chr16:19035751 | C | T | 1 | a0002c0015 | 1 | NA20805.hp2 | synonymous_variant | LOW | c.933C>T | p.Ala311Ala | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 7/16 | 1063/4401 | 933/2172 | 311/723 | chr16 | 19035751 | |||
| chr16:19038029 | G | A | 1 | a0002c0013 | 1 | HG00408.hp2 | synonymous_variant | LOW | c.1161G>A | p.Ser387Ser | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 8/16 | 1291/4401 | 1161/2172 | 387/723 | chr16 | 19038029 | |||
| chr16:19047156 | C | T | 1 | a0001c0017 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.1647C>T | p.Tyr549Tyr | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/16 | 1777/4401 | 1647/2172 | 549/723 | chr16 | 19047156 | |||
| chr16:19056611 | G | A | 7 | a0001c0005 a0002c0002 a0002c0013 others(4): Show |
106 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
synonymous_variant | LOW | c.1941G>A | p.Thr647Thr | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/16 | 2071/4401 | 1941/2172 | 647/723 | chr16 | 19056611 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:18983998 | A | AGGC | 2 | a0001c0001t0007 a0001c0001t0026 |
5 | HG01081.hp2 HG02615.hp2 HG02723.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-47_-45dupGGC | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/16 | 44 | INFO_REALIGN_3_PRIME | chr16 | 18983998 | |||||
| chr16:18983998 | A | AGGCGGCG others(2): Show |
6 | a0001c0001t0010 a0002c0002t0024 a0003c0004t0023 others(3): Show |
9 | HG02109.hp2 HG02615.hp1 HG02886.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-53_-45dupGGCGGCGG others(1): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/16 | 44 | INFO_REALIGN_3_PRIME | chr16 | 18983998 | |||||
| chr16:18983998 | A | AGGCGGCG others(5): Show |
1 | a0005c0007t0021 | 1 | HG02572.hp2 | 5_prime_UTR_variant | MODIFIER | c.-56_-45dupGGCGGCGG others(4): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/16 | 44 | INFO_REALIGN_3_PRIME | chr16 | 18983998 | |||||
| chr16:18984005 | G | A | 1 | a0002c0002t0020 | 1 | NA19057.hp2 | 5_prime_UTR_variant | MODIFIER | c.-59G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/16 | 59 | chr16 | 18984005 | ||||||
| chr16:18984047 | G | C | 1 | a0002c0002t0027 | 1 | NA18968.hp2 | 5_prime_UTR_variant | MODIFIER | c.-17G>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/16 | 17 | chr16 | 18984047 | ||||||
| chr16:19062112 | C | A | 2 | a0001c0001t0008 a0004c0008t0022 |
5 | HG02965.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*269C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 16/16 | 269 | chr16 | 19062112 | ||||||
| chr16:19062138 | C | T | 1 | a0002c0002t0012 | 3 | NA18940.hp2 NA18975.hp1 NA19005.hp1 |
3_prime_UTR_variant | MODIFIER | c.*295C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 16/16 | 295 | chr16 | 19062138 | ||||||
| chr16:19062242 | A | C | 1 | a0002c0002t0019 | 2 | HG02647.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*399A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 16/16 | 399 | chr16 | 19062242 | ||||||
| chr16:19062359 | G | A | 2 | a0001c0001t0028 a0002c0002t0029 |
2 | HG03516.hp1 NA18966.hp1 |
3_prime_UTR_variant | MODIFIER | c.*516G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 16/16 | 516 | chr16 | 19062359 | ||||||
| chr16:19062393 | C | T | 1 | a0002c0013t0037 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*550C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 16/16 | 550 | chr16 | 19062393 | ||||||
| chr16:19062394 | G | A | 2 | a0001c0001t0030 a0002c0002t0031 |
2 | HG06807.hp1 NA18612.hp2 |
3_prime_UTR_variant | MODIFIER | c.*551G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 16/16 | 551 | chr16 | 19062394 | ||||||
| chr16:19062495 | A | G | 1 | a0002c0002t0036 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*652A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 16/16 | 652 | chr16 | 19062495 | ||||||
| chr16:19062895 | C | G | 2 | a0005c0007t0013 a0005c0007t0021 |
3 | HG02572.hp2 HG03130.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1052C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 16/16 | 1052 | chr16 | 19062895 | ||||||
| chr16:19063014 | A | G | 2 | a0005c0007t0013 a0005c0007t0021 |
3 | HG02572.hp2 HG03130.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1171A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 16/16 | 1171 | chr16 | 19063014 | ||||||
| chr16:19063065 | T | A | 2 | a0002c0003t0004 a0002c0003t0014 |
20 | HG00609.hp1 HG01934.hp2 HG01981.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1222T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 16/16 | 1222 | chr16 | 19063065 | ||||||
| chr16:19063145 | T | C | 1 | a0001c0001t0010 | 3 | HG02109.hp2 HG02886.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1302T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 16/16 | 1302 | chr16 | 19063145 | ||||||
| chr16:19063362 | G | C | 2 | a0001c0001t0008 a0004c0008t0022 |
5 | HG02965.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1519G>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 16/16 | 1519 | chr16 | 19063362 | ||||||
| chr16:19063389 | C | T | 3 | a0001c0006t0018 a0001c0006t0034 a0002c0002t0035 |
4 | HG00738.hp2 HG01074.hp2 NA18948.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1546C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 16/16 | 1546 | chr16 | 19063389 | ||||||
| chr16:19063399 | A | C | 1 | a0004c0008t0025 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1556A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 16/16 | 1556 | chr16 | 19063399 | ||||||
| chr16:19063498 | T | A | 8 | a0001c0001t0009 a0001c0006t0018 a0001c0006t0034 others(5): Show |
31 | HG00609.hp1 HG00738.hp2 HG01074.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1655T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 16/16 | 1655 | chr16 | 19063498 | ||||||
| chr16:19063620 | T | A | 2 | a0005c0007t0013 a0005c0007t0021 |
3 | HG02572.hp2 HG03130.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1777T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 16/16 | 1777 | chr16 | 19063620 | ||||||
| chr16:19063670 | A | G | 1 | a0001c0017t0033 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1827A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 16/16 | 1827 | chr16 | 19063670 | ||||||
| chr16:19063672 | T | G | 1 | a0004c0012t0032 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1829T>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 16/16 | 1829 | chr16 | 19063672 | ||||||
| chr16:19063672 | T | TTG | 20 | a0001c0001t0006 a0001c0001t0007 a0001c0005t0002 others(17): Show |
108 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*1854_*1855dupTG | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 16/16 | 1856 | INFO_REALIGN_3_PRIME | chr16 | 19063672 | |||||
| chr16:19063672 | T | TTGTG | 5 | a0001c0001t0009 a0002c0002t0011 a0002c0002t0027 others(2): Show |
26 | HG00609.hp1 HG01884.hp2 HG01934.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1852_*1855dupTGTG | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 16/16 | 1856 | INFO_REALIGN_3_PRIME | chr16 | 19063672 | |||||
| chr16:19063672 | T | TTGTGTG | 4 | a0001c0006t0034 a0002c0002t0017 a0002c0003t0014 others(1): Show |
5 | HG00738.hp2 HG01981.hp2 HG02896.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1850_*1855dupTGTG others(2): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 16/16 | 1856 | INFO_REALIGN_3_PRIME | chr16 | 19063672 | |||||
| chr16:19063672 | T | TTGTGTGT others(1): Show |
2 | a0001c0006t0018 a0002c0003t0016 |
4 | HG01074.hp2 HG02818.hp1 NA19240.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1848_*1855dupTGTG others(4): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 16/16 | 1856 | INFO_REALIGN_3_PRIME | chr16 | 19063672 | |||||
| chr16:19063672 | TTG | T | 2 | a0001c0001t0005 a0002c0002t0005 |
6 | HG00642.hp1 HG00741.hp2 HG01069.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1854_*1855delTG | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 16/16 | 1854 | INFO_REALIGN_3_PRIME | chr16 | 19063672 | |||||
| chr16:19063869 | C | T | 43 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0009 others(40): Show |
232 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*2026C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 16/16 | 2026 | chr16 | 19063869 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:18984220 | G | A | 4 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(1): Show |
4 | HG02451.hp2 HG02723.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+90G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18984220 | |||||||
| chr16:18984240 | A | G | 84 | a0001c0001t0001g0002 a0001c0001t0001g0213 a0001c0001t0001g0214 others(81): Show |
85 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.67+110A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18984240 | |||||||
| chr16:18984263 | G | A | 3 | a0001c0001t0003g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02896.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.67+133G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18984263 | |||||||
| chr16:18984317 | T | C | 15 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(12): Show |
15 | HG01081.hp2 HG02109.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.67+187T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18984317 | |||||||
| chr16:18984569 | T | C | 15 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(12): Show |
15 | HG01081.hp2 HG02109.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.67+439T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18984569 | |||||||
| chr16:18984570 | G | T | 3 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 |
3 | HG02109.hp2 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.67+440G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18984570 | |||||||
| chr16:18984585 | A | C | 1 | a0002c0002t0002g0196 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.67+455A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18984585 | |||||||
| chr16:18984599 | T | C | 1 | a0001c0001t0003g0010 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.67+469T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18984599 | |||||||
| chr16:18984863 | T | C | 3 | a0001c0001t0003g0013 a0001c0001t0006g0011 a0001c0001t0006g0012 |
3 | HG02622.hp1 HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.67+733T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18984863 | |||||||
| chr16:18985004 | G | C | 1 | a0001c0001t0003g0014 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.67+874G>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18985004 | |||||||
| chr16:18985016 | C | T | 25 | a0001c0001t0001g0002 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00423.hp1 HG00673.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.67+886C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18985016 | |||||||
| chr16:18985019 | T | A | 1 | a0001c0001t0001g0213 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.67+889T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18985019 | |||||||
| chr16:18985183 | C | T | 84 | a0001c0001t0001g0002 a0001c0001t0001g0213 a0001c0001t0001g0214 others(81): Show |
85 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.67+1053C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18985183 | |||||||
| chr16:18985190 | C | T | 2 | a0001c0001t0003g0195 a0002c0002t0011g0194 |
2 | HG02895.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.67+1060C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18985190 | |||||||
| chr16:18985256 | C | CA | 113 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0069 others(110): Show |
113 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.67+1139dupA | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 18985256 | ||||||
| chr16:18985270 | G | T | 15 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(12): Show |
15 | HG01081.hp2 HG02109.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.67+1140G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18985270 | |||||||
| chr16:18985463 | C | T | 69 | a0001c0001t0001g0002 a0001c0001t0001g0213 a0001c0001t0001g0214 others(66): Show |
70 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.67+1333C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18985463 | |||||||
| chr16:18985562 | T | C | 5 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(2): Show |
5 | HG01081.hp2 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+1432T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18985562 | |||||||
| chr16:18985578 | T | G | 1 | a0001c0001t0001g0214 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.67+1448T>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18985578 | |||||||
| chr16:18985677 | C | G | 1 | a0002c0002t0002g0112 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.67+1547C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18985677 | |||||||
| chr16:18985698 | G | GT | 12 | a0001c0001t0001g0106 a0001c0001t0001g0193 a0001c0001t0003g0006 others(9): Show |
12 | HG01884.hp1 HG02056.hp1 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.67+1586dupT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 18985698 | ||||||
| chr16:18985698 | GT | G | 114 | a0001c0001t0001g0002 a0001c0001t0001g0114 a0001c0001t0001g0131 others(111): Show |
115 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.67+1586delT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 18985698 | ||||||
| chr16:18985698 | GTT | G | 6 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(3): Show |
6 | HG01081.hp2 HG01884.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+1585_67+1586del others(2): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 18985698 | ||||||
| chr16:18985719 | T | C | 1 | a0002c0002t0002g0016 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.67+1589T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18985719 | |||||||
| chr16:18985941 | G | A | 1 | a0001c0001t0003g0152 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.67+1811G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18985941 | |||||||
| chr16:18986024 | C | T | 4 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(1): Show |
4 | HG02451.hp2 HG02723.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+1894C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18986024 | |||||||
| chr16:18986314 | G | A | 64 | a0001c0001t0001g0002 a0001c0001t0001g0213 a0001c0001t0001g0214 others(61): Show |
65 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.67+2184G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18986314 | |||||||
| chr16:18986390 | G | GA | 39 | a0001c0001t0001g0002 a0001c0001t0001g0106 a0001c0001t0001g0114 others(36): Show |
40 | HG00738.hp2 HG01074.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.67+2279dupA | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 18986390 | ||||||
| chr16:18986497 | A | G | 1 | a0002c0003t0009g0113 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.67+2367A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18986497 | |||||||
| chr16:18986621 | C | T | 2 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
2 | HG01433.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.67+2491C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18986621 | |||||||
| chr16:18986706 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.67+2576T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18986706 | |||||||
| chr16:18986808 | T | C | 1 | a0002c0003t0004g0118 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.67+2678T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18986808 | |||||||
| chr16:18986835 | T | C | 15 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(12): Show |
15 | HG01081.hp2 HG02109.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.67+2705T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18986835 | |||||||
| chr16:18986858 | G | GCAGTGGC others(214): Show |
1 | a0001c0001t0003g0014 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.67+2732_67+2952dup others(221): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 18986858 | ||||||
| chr16:18986867 | C | T | 2 | a0001c0005t0002g0248 a0002c0003t0016g0151 |
2 | HG00741.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.67+2737C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18986867 | |||||||
| chr16:18987051 | C | T | 6 | a0001c0001t0003g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 others(3): Show |
6 | HG02258.hp2 HG02896.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+2921C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18987051 | |||||||
| chr16:18987052 | G | A | 64 | a0001c0001t0001g0002 a0001c0001t0001g0213 a0001c0001t0001g0214 others(61): Show |
65 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.67+2922G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18987052 | |||||||
| chr16:18987080 | C | T | 2 | a0001c0005t0002g0248 a0001c0017t0033g0247 |
2 | HG00741.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.67+2950C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18987080 | |||||||
| chr16:18987173 | G | A | 1 | a0001c0001t0010g0209 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.67+3043G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18987173 | |||||||
| chr16:18987190 | C | G | 10 | a0002c0003t0004g0115 a0002c0003t0004g0142 a0002c0003t0004g0143 others(7): Show |
10 | HG01934.hp2 HG01981.hp1 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+3060C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18987190 | |||||||
| chr16:18987205 | A | C | 10 | a0002c0003t0004g0115 a0002c0003t0004g0142 a0002c0003t0004g0143 others(7): Show |
10 | HG01934.hp2 HG01981.hp1 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+3075A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18987205 | |||||||
| chr16:18987211 | T | C | 1 | a0001c0001t0003g0153 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.67+3081T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18987211 | |||||||
| chr16:18987338 | T | C | 1 | a0001c0001t0001g0278 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.67+3208T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18987338 | |||||||
| chr16:18987357 | C | T | 5 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(2): Show |
5 | HG01081.hp2 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+3227C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18987357 | |||||||
| chr16:18987373 | C | T | 4 | a0001c0001t0001g0246 a0002c0002t0002g0102 a0002c0002t0002g0103 others(1): Show |
4 | HG00323.hp2 HG01169.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+3243C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18987373 | |||||||
| chr16:18987390 | A | G | 1 | a0004c0011t0017g0186 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.67+3260A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18987390 | |||||||
| chr16:18987392 | C | T | 1 | a0001c0001t0003g0014 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.67+3262C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18987392 | |||||||
| chr16:18987458 | G | A | 5 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(2): Show |
5 | HG02109.hp2 HG02615.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+3328G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18987458 | |||||||
| chr16:18987502 | G | A | 38 | a0001c0001t0001g0114 a0001c0001t0001g0131 a0001c0001t0001g0132 others(35): Show |
38 | HG00609.hp1 HG01109.hp1 HG01496.hp2 others(35): Show |
intron_variant | MODIFIER | c.67+3372G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18987502 | |||||||
| chr16:18987546 | T | C | 1 | a0001c0001t0003g0158 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.67+3416T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18987546 | |||||||
| chr16:18987597 | C | T | 6 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(3): Show |
6 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+3467C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18987597 | |||||||
| chr16:18987718 | G | A | 5 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(2): Show |
5 | HG01081.hp2 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+3588G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18987718 | |||||||
| chr16:18987816 | C | T | 1 | a0002c0002t0002g0101 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.67+3686C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18987816 | |||||||
| chr16:18987828 | C | T | 1 | a0002c0002t0002g0111 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.67+3698C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18987828 | |||||||
| chr16:18987834 | C | T | 1 | a0001c0006t0006g0180 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.67+3704C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18987834 | |||||||
| chr16:18987939 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.67+3809A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18987939 | |||||||
| chr16:18988028 | G | A | 64 | a0001c0001t0001g0002 a0001c0001t0001g0213 a0001c0001t0001g0214 others(61): Show |
65 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.67+3898G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18988028 | |||||||
| chr16:18988042 | T | A | 1 | a0002c0003t0009g0116 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.67+3912T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18988042 | |||||||
| chr16:18988064 | C | G | 1 | a0002c0003t0004g0140 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.67+3934C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18988064 | |||||||
| chr16:18988156 | C | CT | 5 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0003g0177 others(2): Show |
5 | NA18946.hp2 NA18955.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+4044dupT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 18988156 | ||||||
| chr16:18988156 | C | CTTT | 15 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(12): Show |
15 | HG01081.hp2 HG02109.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.67+4042_67+4044dup others(3): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 18988156 | ||||||
| chr16:18988570 | C | T | 1 | a0003c0004t0006g0255 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.67+4440C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18988570 | |||||||
| chr16:18988694 | T | C | 1 | a0002c0002t0002g0021 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.67+4564T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18988694 | |||||||
| chr16:18988771 | C | T | 2 | a0001c0001t0001g0244 a0001c0001t0028g0245 |
2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.67+4641C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18988771 | |||||||
| chr16:18988974 | C | T | 1 | a0002c0002t0002g0100 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.67+4844C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18988974 | |||||||
| chr16:18988975 | G | T | 68 | a0001c0001t0001g0002 a0001c0001t0001g0213 a0001c0001t0001g0214 others(65): Show |
69 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.67+4845G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18988975 | |||||||
| chr16:18989052 | CA | C | 84 | a0001c0001t0001g0002 a0001c0001t0001g0213 a0001c0001t0001g0214 others(81): Show |
85 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.67+4938delA | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 18989052 | ||||||
| chr16:18989068 | A | T | 15 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(12): Show |
15 | HG01081.hp2 HG02109.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.67+4938A>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18989068 | |||||||
| chr16:18989093 | T | C | 24 | a0002c0002t0002g0125 a0002c0003t0004g0115 a0002c0003t0004g0117 others(21): Show |
24 | HG00609.hp1 HG01934.hp2 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.67+4963T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18989093 | |||||||
| chr16:18989165 | T | C | 15 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(12): Show |
15 | HG01081.hp2 HG02109.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.67+5035T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18989165 | |||||||
| chr16:18989195 | C | T | 108 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0069 others(105): Show |
108 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.67+5065C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18989195 | |||||||
| chr16:18989452 | C | T | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.67+5322C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18989452 | |||||||
| chr16:18989467 | G | A | 68 | a0001c0001t0001g0002 a0001c0001t0001g0213 a0001c0001t0001g0214 others(65): Show |
69 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.67+5337G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18989467 | |||||||
| chr16:18989478 | T | C | 15 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(12): Show |
15 | HG01081.hp2 HG02109.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.67+5348T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18989478 | |||||||
| chr16:18989485 | C | T | 1 | a0001c0005t0002g0175 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.67+5355C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18989485 | |||||||
| chr16:18989508 | G | A | 1 | a0002c0002t0002g0022 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.67+5378G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18989508 | |||||||
| chr16:18989520 | C | T | 83 | a0001c0001t0001g0002 a0001c0001t0001g0213 a0001c0001t0001g0214 others(80): Show |
84 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.67+5390C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18989520 | |||||||
| chr16:18989529 | A | G | 68 | a0001c0001t0001g0002 a0001c0001t0001g0213 a0001c0001t0001g0214 others(65): Show |
69 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.67+5399A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18989529 | |||||||
| chr16:18989530 | C | G | 1 | a0001c0001t0003g0013 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.67+5400C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18989530 | |||||||
| chr16:18989550 | G | T | 68 | a0001c0001t0001g0002 a0001c0001t0001g0213 a0001c0001t0001g0214 others(65): Show |
69 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.67+5420G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18989550 | |||||||
| chr16:18989575 | G | A | 68 | a0001c0001t0001g0002 a0001c0001t0001g0213 a0001c0001t0001g0214 others(65): Show |
69 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.67+5445G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18989575 | |||||||
| chr16:18989611 | A | G | 15 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(12): Show |
15 | HG01081.hp2 HG02109.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.67+5481A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18989611 | |||||||
| chr16:18989620 | G | A | 6 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0220 others(3): Show |
6 | HG00323.hp1 HG01975.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+5490G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18989620 | |||||||
| chr16:18989632 | G | A | 68 | a0001c0001t0001g0002 a0001c0001t0001g0213 a0001c0001t0001g0214 others(65): Show |
69 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.67+5502G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18989632 | |||||||
| chr16:18989652 | C | CT | 68 | a0001c0001t0001g0002 a0001c0001t0001g0213 a0001c0001t0001g0214 others(65): Show |
69 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.67+5523dupT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 18989652 | ||||||
| chr16:18989683 | C | T | 1 | a0001c0001t0003g0174 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.67+5553C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18989683 | |||||||
| chr16:18989684 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.67+5554G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18989684 | |||||||
| chr16:18989692 | C | T | 15 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(12): Show |
15 | HG01081.hp2 HG02109.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.67+5562C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18989692 | |||||||
| chr16:18990055 | A | C | 1 | a0002c0002t0002g0104 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.67+5925A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18990055 | |||||||
| chr16:18990132 | G | A | 5 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(2): Show |
5 | HG02109.hp2 HG02615.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+6002G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18990132 | |||||||
| chr16:18990323 | C | A | 1 | a0002c0002t0002g0023 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.67+6193C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18990323 | |||||||
| chr16:18990456 | G | A | 1 | a0002c0002t0002g0024 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.67+6326G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18990456 | |||||||
| chr16:18990552 | A | G | 15 | a0002c0002t0002g0016 a0002c0002t0002g0088 a0002c0002t0002g0089 others(12): Show |
15 | HG00408.hp1 HG01071.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.67+6422A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18990552 | |||||||
| chr16:18990702 | G | T | 6 | a0001c0001t0003g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 others(3): Show |
6 | HG02258.hp2 HG02896.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+6572G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18990702 | |||||||
| chr16:18990789 | C | A | 10 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(7): Show |
10 | HG02109.hp2 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.67+6659C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18990789 | |||||||
| chr16:18990876 | A | G | 4 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(1): Show |
4 | HG02615.hp2 HG02723.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+6746A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18990876 | |||||||
| chr16:18991061 | G | T | 1 | a0001c0001t0007g0207 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.67+6931G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18991061 | |||||||
| chr16:18991078 | G | A | 6 | a0001c0001t0003g0254 a0003c0004t0003g0251 a0003c0004t0006g0252 others(3): Show |
6 | HG02451.hp1 HG02622.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+6948G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18991078 | |||||||
| chr16:18991105 | G | A | 108 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0069 others(105): Show |
108 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.67+6975G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18991105 | |||||||
| chr16:18991154 | A | AT | 4 | a0001c0001t0001g0217 a0001c0001t0001g0220 a0002c0002t0002g0218 others(1): Show |
4 | HG01975.hp1 HG02602.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+7028dupT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 18991154 | ||||||
| chr16:18991242 | A | G | 3 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 |
3 | HG02300.hp2 HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.67+7112A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18991242 | |||||||
| chr16:18991302 | A | G | 1 | a0001c0001t0010g0211 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.67+7172A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18991302 | |||||||
| chr16:18991522 | C | T | 3 | a0001c0001t0003g0013 a0001c0001t0006g0011 a0001c0001t0006g0012 |
3 | HG02622.hp1 HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.67+7392C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18991522 | |||||||
| chr16:18991721 | G | C | 1 | a0003c0004t0006g0255 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.67+7591G>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18991721 | |||||||
| chr16:18991832 | G | A | 1 | a0001c0001t0007g0204 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.67+7702G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18991832 | |||||||
| chr16:18991977 | T | G | 2 | a0002c0002t0019g0190 a0002c0002t0019g0191 |
2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.67+7847T>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18991977 | |||||||
| chr16:18991988 | G | GTCTAT | 15 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(12): Show |
15 | HG01081.hp2 HG02109.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.67+7859_67+7863dup others(5): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 18991988 | ||||||
| chr16:18992019 | T | C | 145 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0069 others(142): Show |
145 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.67+7889T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18992019 | |||||||
| chr16:18992033 | C | T | 16 | a0001c0001t0003g0007 a0001c0001t0003g0014 a0001c0001t0003g0254 others(13): Show |
16 | HG00642.hp2 HG00738.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.67+7903C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18992033 | |||||||
| chr16:18992095 | C | A | 1 | a0002c0002t0002g0025 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.67+7965C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18992095 | |||||||
| chr16:18992100 | G | T | 15 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(12): Show |
15 | HG01081.hp2 HG02109.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.67+7970G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18992100 | |||||||
| chr16:18992109 | C | T | 1 | a0004c0011t0017g0186 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.67+7979C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18992109 | |||||||
| chr16:18992376 | T | C | 108 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0069 others(105): Show |
108 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.67+8246T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18992376 | |||||||
| chr16:18992382 | T | G | 130 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0069 others(127): Show |
130 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.67+8252T>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18992382 | |||||||
| chr16:18992483 | G | A | 1 | a0001c0001t0003g0014 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.67+8353G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18992483 | |||||||
| chr16:18992498 | C | G | 1 | a0002c0002t0002g0087 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.67+8368C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18992498 | |||||||
| chr16:18992501 | T | C | 1 | a0001c0001t0003g0010 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.67+8371T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18992501 | |||||||
| chr16:18992541 | G | A | 4 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
4 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+8411G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18992541 | |||||||
| chr16:18992670 | C | A | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.67+8540C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18992670 | |||||||
| chr16:18992690 | G | A | 3 | a0001c0006t0018g0155 a0001c0006t0018g0156 a0001c0006t0034g0154 |
3 | HG00738.hp2 HG01074.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.67+8560G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18992690 | |||||||
| chr16:18992697 | C | T | 130 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0069 others(127): Show |
130 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.67+8567C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18992697 | |||||||
| chr16:18992963 | T | G | 2 | a0002c0002t0002g0026 a0002c0015t0002g0027 |
2 | HG01081.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.67+8833T>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18992963 | |||||||
| chr16:18993306 | C | T | 1 | a0006c0016t0001g0257 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.67+9176C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18993306 | |||||||
| chr16:18993358 | A | G | 5 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(2): Show |
5 | HG01081.hp2 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+9228A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18993358 | |||||||
| chr16:18993536 | C | T | 2 | a0004c0008t0022g0197 a0004c0008t0025g0198 |
2 | HG02615.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.67+9406C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18993536 | |||||||
| chr16:18993720 | G | A | 2 | a0002c0002t0002g0016 a0002c0002t0002g0112 |
2 | HG02040.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.67+9590G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18993720 | |||||||
| chr16:18993849 | C | T | 183 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0069 others(180): Show |
183 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.67+9719C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18993849 | |||||||
| chr16:18993858 | A | G | 251 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(248): Show |
252 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.67+9728A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18993858 | |||||||
| chr16:18993868 | G | A | 6 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(3): Show |
6 | HG00609.hp2 HG01081.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+9738G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18993868 | |||||||
| chr16:18993889 | A | G | 4 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
4 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+9759A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18993889 | |||||||
| chr16:18993933 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.67+9803T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18993933 | |||||||
| chr16:18994067 | G | A | 1 | a0007c0018t0002g0015 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.67+9937G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18994067 | |||||||
| chr16:18994081 | A | G | 6 | a0001c0001t0003g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 others(3): Show |
6 | HG02258.hp2 HG02896.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+9951A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18994081 | |||||||
| chr16:18994093 | G | A | 3 | a0001c0006t0018g0155 a0001c0006t0018g0156 a0001c0006t0034g0154 |
3 | HG00738.hp2 HG01074.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.67+9963G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18994093 | |||||||
| chr16:18994155 | T | C | 10 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(7): Show |
10 | HG02109.hp2 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.67+10025T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18994155 | |||||||
| chr16:18994286 | A | AAGC | 60 | a0001c0001t0001g0114 a0001c0001t0001g0131 a0001c0001t0001g0132 others(57): Show |
60 | HG00609.hp1 HG00642.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.67+10169_67+10171d others(5): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 18994286 | ||||||
| chr16:18994408 | G | A | 111 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0069 others(108): Show |
111 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.67+10278G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18994408 | |||||||
| chr16:18994408 | G | T | 5 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(2): Show |
5 | HG01081.hp2 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+10278G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18994408 | |||||||
| chr16:18994412 | C | T | 2 | a0002c0002t0002g0085 a0002c0002t0002g0086 |
2 | HG01167.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.67+10282C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18994412 | |||||||
| chr16:18994451 | CA | C | 20 | a0001c0001t0001g0240 a0001c0001t0007g0204 a0001c0001t0007g0205 others(17): Show |
20 | HG01081.hp2 HG01167.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.67+10335delA | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 18994451 | ||||||
| chr16:18994460 | A | C | 1 | a0002c0002t0002g0084 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.67+10330A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18994460 | |||||||
| chr16:18994737 | A | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0213 a0001c0001t0001g0214 others(59): Show |
63 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.67+10607A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18994737 | |||||||
| chr16:18994754 | G | A | 74 | a0001c0001t0001g0114 a0001c0001t0001g0131 a0001c0001t0001g0132 others(71): Show |
74 | HG00609.hp1 HG00642.hp2 HG00738.hp2 others(71): Show |
intron_variant | MODIFIER | c.67+10624G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18994754 | |||||||
| chr16:18994795 | A | C | 1 | a0002c0013t0037g0081 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.67+10665A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18994795 | |||||||
| chr16:18994822 | G | C | 1 | a0002c0002t0002g0028 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.67+10692G>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18994822 | |||||||
| chr16:18994932 | G | T | 5 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(2): Show |
5 | HG01081.hp2 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+10802G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18994932 | |||||||
| chr16:18994985 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.67+10855G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18994985 | |||||||
| chr16:18994986 | T | TG | 184 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0069 others(181): Show |
184 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.67+10860dupG | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 18994986 | ||||||
| chr16:18995005 | G | A | 2 | a0004c0008t0022g0197 a0004c0008t0025g0198 |
2 | HG02615.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.67+10875G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18995005 | |||||||
| chr16:18995324 | T | G | 1 | a0001c0001t0003g0014 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.67+11194T>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18995324 | |||||||
| chr16:18995336 | C | A | 110 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0069 others(107): Show |
110 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.67+11206C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18995336 | |||||||
| chr16:18995343 | G | A | 106 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0069 others(103): Show |
106 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.67+11213G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18995343 | |||||||
| chr16:18995380 | C | T | 2 | a0001c0001t0001g0216 a0001c0001t0001g0256 |
2 | HG00323.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.67+11250C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18995380 | |||||||
| chr16:18995388 | G | A | 5 | a0001c0001t0003g0159 a0001c0001t0003g0160 a0001c0001t0003g0161 others(2): Show |
5 | HG02145.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+11258G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18995388 | |||||||
| chr16:18995420 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.67+11290A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18995420 | |||||||
| chr16:18995473 | G | A | 6 | a0001c0001t0003g0254 a0003c0004t0003g0251 a0003c0004t0006g0252 others(3): Show |
6 | HG02451.hp1 HG02622.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+11343G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18995473 | |||||||
| chr16:18995638 | G | A | 33 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(30): Show |
33 | HG00609.hp1 HG01884.hp2 HG01934.hp2 others(30): Show |
intron_variant | MODIFIER | c.67+11508G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18995638 | |||||||
| chr16:18995793 | T | C | 2 | a0001c0001t0008g0187 a0001c0001t0008g0188 |
2 | HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.67+11663T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18995793 | |||||||
| chr16:18995839 | C | T | 22 | a0001c0001t0003g0007 a0001c0001t0003g0014 a0001c0001t0003g0254 others(19): Show |
22 | HG00642.hp2 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.67+11709C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18995839 | |||||||
| chr16:18995871 | A | G | 9 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(6): Show |
9 | HG02109.hp2 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+11741A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18995871 | |||||||
| chr16:18995948 | C | T | 4 | a0001c0006t0006g0180 a0001c0006t0018g0155 a0001c0006t0018g0156 others(1): Show |
4 | HG00738.hp2 HG01074.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+11818C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18995948 | |||||||
| chr16:18996022 | C | G | 1 | a0004c0012t0032g0189 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.67+11892C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18996022 | |||||||
| chr16:18996276 | T | C | 1 | a0002c0002t0036g0176 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.67+12146T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18996276 | |||||||
| chr16:18996442 | T | A | 1 | a0001c0001t0001g0193 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.67+12312T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18996442 | |||||||
| chr16:18996611 | G | C | 1 | a0001c0001t0001g0131 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.67+12481G>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18996611 | |||||||
| chr16:18996656 | G | T | 33 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(30): Show |
33 | HG00609.hp1 HG01884.hp2 HG01934.hp2 others(30): Show |
intron_variant | MODIFIER | c.68-12516G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18996656 | |||||||
| chr16:18996800 | A | T | 4 | a0001c0001t0003g0173 a0001c0001t0003g0177 a0001c0001t0003g0178 others(1): Show |
4 | NA18946.hp2 NA18955.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-12372A>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18996800 | |||||||
| chr16:18996918 | C | T | 1 | a0002c0002t0002g0079 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.68-12254C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18996918 | |||||||
| chr16:18996967 | T | C | 13 | a0001c0001t0003g0007 a0001c0001t0003g0014 a0001c0001t0003g0254 others(10): Show |
13 | HG00642.hp2 HG02258.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.68-12205T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18996967 | |||||||
| chr16:18997031 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.68-12141A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18997031 | |||||||
| chr16:18997223 | A | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0080 a0001c0001t0001g0114 others(71): Show |
75 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.68-11949A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18997223 | |||||||
| chr16:18997617 | A | G | 250 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(247): Show |
251 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.68-11555A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18997617 | |||||||
| chr16:18997640 | G | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0080 a0001c0001t0001g0114 others(71): Show |
75 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.68-11532G>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18997640 | |||||||
| chr16:18997664 | C | T | 22 | a0001c0001t0003g0007 a0001c0001t0003g0014 a0001c0001t0003g0254 others(19): Show |
22 | HG00642.hp2 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.68-11508C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18997664 | |||||||
| chr16:18997671 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.68-11501G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18997671 | |||||||
| chr16:18997729 | CT | C | 162 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0069 others(159): Show |
162 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.68-11425delT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 18997729 | ||||||
| chr16:18997729 | CTT | C | 75 | a0001c0001t0001g0002 a0001c0001t0001g0080 a0001c0001t0001g0114 others(72): Show |
76 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.68-11426_68-11425d others(4): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 18997729 | ||||||
| chr16:18997732 | T | C | 73 | a0001c0001t0001g0002 a0001c0001t0001g0080 a0001c0001t0001g0114 others(70): Show |
74 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.68-11440T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18997732 | |||||||
| chr16:18997733 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.68-11439T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18997733 | |||||||
| chr16:18998078 | C | A | 1 | a0001c0001t0001g0193 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.68-11094C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18998078 | |||||||
| chr16:18998384 | C | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0075 others(74): Show |
78 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.68-10788C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18998384 | |||||||
| chr16:18998386 | T | A | 106 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0069 others(103): Show |
106 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.68-10786T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18998386 | |||||||
| chr16:18998395 | T | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0075 others(74): Show |
78 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.68-10777T>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18998395 | |||||||
| chr16:18998452 | G | A | 7 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(4): Show |
7 | HG01884.hp1 HG02055.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-10720G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18998452 | |||||||
| chr16:18998465 | AG | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 |
3 | HG01361.hp2 HG01516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.68-10703delG | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 18998465 | ||||||
| chr16:18998466 | G | A | 7 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(4): Show |
7 | HG01884.hp1 HG02055.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-10706G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18998466 | |||||||
| chr16:18998565 | C | T | 1 | a0004c0012t0032g0189 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.68-10607C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18998565 | |||||||
| chr16:18998582 | G | A | 62 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0002c0002t0001g0029 others(59): Show |
62 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.68-10590G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18998582 | |||||||
| chr16:18998611 | G | A | 1 | a0002c0003t0009g0116 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.68-10561G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18998611 | |||||||
| chr16:18998686 | G | A | 1 | a0001c0001t0003g0014 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.68-10486G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18998686 | |||||||
| chr16:18998737 | G | T | 2 | a0001c0006t0018g0155 a0001c0006t0018g0156 |
2 | HG01074.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.68-10435G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18998737 | |||||||
| chr16:18998738 | A | C | 2 | a0001c0006t0018g0155 a0001c0006t0018g0156 |
2 | HG01074.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.68-10434A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18998738 | |||||||
| chr16:18998747 | C | G | 1 | a0001c0001t0001g0106 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.68-10425C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18998747 | |||||||
| chr16:18998753 | CA | C | 171 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0069 others(168): Show |
171 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.68-10406delA | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 18998753 | ||||||
| chr16:18998753 | CAA | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0075 others(74): Show |
78 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.68-10407_68-10406d others(4): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 18998753 | ||||||
| chr16:18998850 | T | A | 8 | a0001c0001t0003g0157 a0001c0001t0003g0166 a0001c0001t0003g0167 others(5): Show |
8 | HG00609.hp2 HG00735.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.68-10322T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18998850 | |||||||
| chr16:18998974 | C | T | 1 | a0002c0003t0004g0115 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.68-10198C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18998974 | |||||||
| chr16:18999073 | C | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0075 others(74): Show |
78 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.68-10099C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18999073 | |||||||
| chr16:18999116 | G | A | 1 | a0002c0002t0002g0112 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.68-10056G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18999116 | |||||||
| chr16:18999131 | C | T | 6 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(3): Show |
6 | HG02615.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-10041C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18999131 | |||||||
| chr16:18999364 | A | G | 1 | a0007c0018t0002g0015 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.68-9808A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18999364 | |||||||
| chr16:18999416 | C | T | 1 | a0001c0005t0002g0168 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.68-9756C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18999416 | |||||||
| chr16:18999418 | C | G | 250 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(247): Show |
251 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.68-9754C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18999418 | |||||||
| chr16:18999423 | C | A | 6 | a0001c0001t0003g0159 a0001c0001t0003g0160 a0001c0001t0003g0161 others(3): Show |
6 | HG02145.hp1 HG02572.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-9749C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18999423 | |||||||
| chr16:18999515 | C | T | 2 | a0002c0002t0002g0223 a0002c0003t0001g0222 |
2 | HG01433.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.68-9657C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18999515 | |||||||
| chr16:18999516 | G | A | 77 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0075 others(74): Show |
78 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.68-9656G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18999516 | |||||||
| chr16:18999618 | C | G | 78 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0075 others(75): Show |
79 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.68-9554C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18999618 | |||||||
| chr16:18999676 | A | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0075 others(74): Show |
78 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.68-9496A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18999676 | |||||||
| chr16:18999708 | C | A | 77 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0075 others(74): Show |
78 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.68-9464C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18999708 | |||||||
| chr16:18999737 | A | C | 1 | a0002c0002t0002g0020 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.68-9435A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18999737 | |||||||
| chr16:18999749 | G | A | 77 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0075 others(74): Show |
78 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.68-9423G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18999749 | |||||||
| chr16:18999753 | GT | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0075 others(74): Show |
78 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.68-9412delT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 18999753 | ||||||
| chr16:18999766 | T | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0075 others(74): Show |
78 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.68-9406T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18999766 | |||||||
| chr16:18999766 | T | G | 1 | a0002c0002t0020g0077 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.68-9406T>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18999766 | |||||||
| chr16:18999787 | A | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0075 others(74): Show |
78 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.68-9385A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18999787 | |||||||
| chr16:18999827 | G | A | 1 | a0002c0003t0009g0130 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.68-9345G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18999827 | |||||||
| chr16:18999856 | C | T | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.68-9316C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18999856 | |||||||
| chr16:18999864 | C | T | 3 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 |
3 | HG02109.hp2 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.68-9308C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18999864 | |||||||
| chr16:18999888 | A | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0075 others(74): Show |
78 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.68-9284A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18999888 | |||||||
| chr16:18999953 | C | G | 9 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(6): Show |
9 | HG02109.hp2 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-9219C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18999953 | |||||||
| chr16:18999953 | C | T | 6 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(3): Show |
6 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-9219C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18999953 | |||||||
| chr16:18999984 | C | T | 6 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(3): Show |
6 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-9188C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 18999984 | |||||||
| chr16:19000075 | G | A | 106 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0069 others(103): Show |
106 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.68-9097G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19000075 | |||||||
| chr16:19000145 | C | A | 107 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0069 others(104): Show |
107 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.68-9027C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19000145 | |||||||
| chr16:19000204 | G | A | 6 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(3): Show |
6 | HG02615.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-8968G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19000204 | |||||||
| chr16:19000242 | G | C | 1 | a0002c0003t0009g0113 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.68-8930G>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19000242 | |||||||
| chr16:19000254 | C | T | 103 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0069 others(100): Show |
103 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.68-8918C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19000254 | |||||||
| chr16:19000263 | C | T | 6 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(3): Show |
6 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-8909C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19000263 | |||||||
| chr16:19000498 | A | G | 1 | a0002c0002t0011g0073 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.68-8674A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19000498 | |||||||
| chr16:19000588 | A | G | 3 | a0002c0003t0015g0127 a0002c0003t0015g0128 a0002c0003t0016g0129 |
3 | HG02647.hp1 HG02818.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.68-8584A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19000588 | |||||||
| chr16:19000821 | C | A | 5 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(2): Show |
5 | HG02109.hp2 HG02615.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-8351C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19000821 | |||||||
| chr16:19000927 | A | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0075 others(74): Show |
78 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.68-8245A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19000927 | |||||||
| chr16:19000937 | T | C | 48 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0075 others(45): Show |
49 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.68-8235T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19000937 | |||||||
| chr16:19001018 | T | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0075 others(74): Show |
78 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.68-8154T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19001018 | |||||||
| chr16:19001019 | A | G | 1 | a0002c0002t0002g0109 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.68-8153A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19001019 | |||||||
| chr16:19001173 | G | A | 1 | a0002c0003t0004g0118 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.68-7999G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19001173 | |||||||
| chr16:19001450 | G | A | 4 | a0001c0001t0001g0193 a0001c0001t0003g0195 a0002c0002t0011g0194 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-7722G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19001450 | |||||||
| chr16:19001501 | C | A | 1 | a0002c0013t0037g0081 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.68-7671C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19001501 | |||||||
| chr16:19001502 | G | A | 2 | a0001c0001t0001g0244 a0001c0001t0028g0245 |
2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.68-7670G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19001502 | |||||||
| chr16:19001678 | G | T | 1 | a0001c0001t0001g0263 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.68-7494G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19001678 | |||||||
| chr16:19001710 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.68-7462A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19001710 | |||||||
| chr16:19001809 | A | C | 6 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(3): Show |
6 | HG02615.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-7363A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19001809 | |||||||
| chr16:19002060 | G | A | 15 | a0002c0002t0002g0016 a0002c0002t0002g0088 a0002c0002t0002g0089 others(12): Show |
15 | HG00408.hp1 HG01071.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.68-7112G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19002060 | |||||||
| chr16:19002234 | CT | C | 18 | a0001c0001t0001g0217 a0001c0001t0001g0246 a0001c0001t0003g0159 others(15): Show |
18 | HG00323.hp2 HG00738.hp2 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.68-6919delT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 19002234 | ||||||
| chr16:19002259 | G | A | 4 | a0001c0006t0006g0180 a0001c0006t0018g0155 a0001c0006t0018g0156 others(1): Show |
4 | HG00738.hp2 HG01074.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-6913G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19002259 | |||||||
| chr16:19002306 | G | A | 4 | a0001c0006t0006g0180 a0001c0006t0018g0155 a0001c0006t0018g0156 others(1): Show |
4 | HG00738.hp2 HG01074.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-6866G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19002306 | |||||||
| chr16:19002392 | C | T | 1 | a0005c0007t0021g0203 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.68-6780C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19002392 | |||||||
| chr16:19002426 | A | G | 184 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(181): Show |
185 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.68-6746A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19002426 | |||||||
| chr16:19002525 | C | G | 2 | a0004c0008t0022g0197 a0004c0008t0025g0198 |
2 | HG02615.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.68-6647C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19002525 | |||||||
| chr16:19002537 | C | G | 1 | a0002c0002t0002g0111 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.68-6635C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19002537 | |||||||
| chr16:19002986 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.68-6186C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19002986 | |||||||
| chr16:19003038 | A | G | 5 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(2): Show |
5 | HG02109.hp2 HG02615.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-6134A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19003038 | |||||||
| chr16:19003100 | G | A | 107 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0069 others(104): Show |
107 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.68-6072G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19003100 | |||||||
| chr16:19003109 | T | A | 107 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0069 others(104): Show |
107 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.68-6063T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19003109 | |||||||
| chr16:19003131 | G | A | 1 | a0001c0001t0003g0157 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.68-6041G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19003131 | |||||||
| chr16:19003371 | TCTGCCCG others(44): Show |
T | 3 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 |
3 | HG02109.hp2 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.68-5771_68-5721del others(51): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 19003371 | ||||||
| chr16:19003406 | G | C | 3 | a0001c0001t0001g0272 a0001c0001t0001g0274 a0001c0001t0001g0277 |
3 | NA18975.hp2 NA18989.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.68-5766G>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19003406 | |||||||
| chr16:19003441 | C | T | 6 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(3): Show |
6 | HG02615.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-5731C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19003441 | |||||||
| chr16:19003487 | A | G | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.68-5685A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19003487 | |||||||
| chr16:19003519 | G | T | 29 | a0001c0001t0001g0114 a0001c0001t0001g0131 a0001c0001t0001g0132 others(26): Show |
29 | HG00741.hp1 HG01074.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.68-5653G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19003519 | |||||||
| chr16:19003668 | T | A | 1 | a0001c0001t0003g0003 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.68-5504T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19003668 | |||||||
| chr16:19003814 | A | G | 1 | a0004c0012t0032g0189 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.68-5358A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19003814 | |||||||
| chr16:19003841 | G | C | 36 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(33): Show |
36 | HG00609.hp1 HG01884.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.68-5331G>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19003841 | |||||||
| chr16:19003895 | G | A | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.68-5277G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19003895 | |||||||
| chr16:19004041 | TTA | T | 99 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0069 others(96): Show |
99 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.68-5130_68-5129del others(2): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19004041 | |||||||
| chr16:19004041 | TTAA | T | 59 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(56): Show |
59 | HG00609.hp1 HG00642.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.68-5130_68-5128del others(3): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19004041 | |||||||
| chr16:19004041 | TTAAA | T | 13 | a0001c0001t0003g0007 a0001c0001t0006g0011 a0001c0001t0006g0012 others(10): Show |
13 | HG02258.hp2 HG02615.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.68-5130_68-5127del others(4): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19004041 | |||||||
| chr16:19004042 | TAA | T | 74 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0076 others(71): Show |
75 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.68-5114_68-5113del others(2): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 19004042 | ||||||
| chr16:19004062 | C | G | 1 | a0001c0001t0001g0280 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.68-5110C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19004062 | |||||||
| chr16:19004112 | A | G | 107 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0069 others(104): Show |
107 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.68-5060A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19004112 | |||||||
| chr16:19004460 | C | G | 250 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(247): Show |
251 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.68-4712C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19004460 | |||||||
| chr16:19004513 | T | C | 250 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(247): Show |
251 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.68-4659T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19004513 | |||||||
| chr16:19004772 | A | G | 1 | a0001c0001t0003g0010 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.68-4400A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19004772 | |||||||
| chr16:19004984 | G | A | 4 | a0001c0006t0006g0180 a0001c0006t0018g0155 a0001c0006t0018g0156 others(1): Show |
4 | HG00738.hp2 HG01074.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-4188G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19004984 | |||||||
| chr16:19005003 | C | G | 1 | a0002c0002t0002g0071 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.68-4169C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19005003 | |||||||
| chr16:19005056 | T | TTTTA | 30 | a0001c0001t0001g0062 a0001c0001t0001g0132 a0001c0001t0001g0133 others(27): Show |
31 | HG01071.hp2 HG01109.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.68-4072_68-4069dup others(4): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 19005056 | ||||||
| chr16:19005056 | TTTTA | T | 74 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0075 others(71): Show |
75 | HG00323.hp1 HG00639.hp1 HG00673.hp2 others(72): Show |
intron_variant | MODIFIER | c.68-4072_68-4069del others(4): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 19005056 | ||||||
| chr16:19005056 | TTTTATTT others(1): Show |
T | 6 | a0002c0002t0002g0018 a0002c0002t0002g0052 a0002c0003t0015g0127 others(3): Show |
6 | HG00423.hp1 HG02015.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-4076_68-4069del others(8): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 19005056 | ||||||
| chr16:19005056 | TTTTATTT others(5): Show |
T | 25 | a0001c0001t0001g0274 a0001c0001t0001g0277 a0001c0001t0003g0005 others(22): Show |
25 | HG00642.hp2 HG00741.hp1 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.68-4080_68-4069del others(12): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 19005056 | ||||||
| chr16:19005124 | T | C | 1 | a0002c0002t0036g0176 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.68-4048T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19005124 | |||||||
| chr16:19005214 | A | G | 212 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(209): Show |
213 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.68-3958A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19005214 | |||||||
| chr16:19005238 | C | T | 1 | a0002c0002t0002g0125 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.68-3934C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19005238 | |||||||
| chr16:19005305 | G | T | 1 | a0001c0001t0003g0170 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.68-3867G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19005305 | |||||||
| chr16:19005335 | G | A | 1 | a0002c0003t0009g0116 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.68-3837G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19005335 | |||||||
| chr16:19005339 | C | T | 9 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(6): Show |
9 | HG02109.hp2 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-3833C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19005339 | |||||||
| chr16:19005343 | C | T | 1 | a0004c0011t0017g0186 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.68-3829C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19005343 | |||||||
| chr16:19005389 | G | A | 47 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0075 others(44): Show |
48 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.68-3783G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19005389 | |||||||
| chr16:19005530 | A | T | 9 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(6): Show |
9 | HG02109.hp2 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-3642A>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19005530 | |||||||
| chr16:19005562 | T | C | 2 | a0002c0002t0002g0085 a0002c0002t0002g0086 |
2 | HG01167.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.68-3610T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19005562 | |||||||
| chr16:19005644 | A | G | 134 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0069 others(131): Show |
134 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.68-3528A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19005644 | |||||||
| chr16:19005858 | C | G | 1 | a0001c0001t0001g0273 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.68-3314C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19005858 | |||||||
| chr16:19006031 | C | G | 1 | a0001c0006t0006g0180 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.68-3141C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19006031 | |||||||
| chr16:19006096 | C | T | 1 | a0004c0008t0022g0197 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.68-3076C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19006096 | |||||||
| chr16:19006097 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.68-3075G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19006097 | |||||||
| chr16:19006116 | C | A | 2 | a0002c0003t0004g0117 a0002c0003t0004g0119 |
2 | NA18946.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.68-3056C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19006116 | |||||||
| chr16:19006166 | C | T | 1 | a0002c0002t0002g0061 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.68-3006C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19006166 | |||||||
| chr16:19006203 | C | CT | 9 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(6): Show |
9 | HG02055.hp2 HG02602.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-2954dupT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 19006203 | ||||||
| chr16:19006269 | C | T | 1 | a0001c0001t0003g0163 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.68-2903C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19006269 | |||||||
| chr16:19006316 | C | T | 2 | a0002c0002t0002g0093 a0002c0002t0002g0094 |
2 | HG01071.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.68-2856C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19006316 | |||||||
| chr16:19006515 | C | T | 1 | a0001c0001t0010g0211 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.68-2657C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19006515 | |||||||
| chr16:19006780 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.68-2392T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19006780 | |||||||
| chr16:19006983 | G | GT | 7 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(4): Show |
7 | HG01167.hp1 HG02055.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-2176dupT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 19006983 | ||||||
| chr16:19007260 | C | T | 1 | a0002c0002t0024g0199 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.68-1912C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19007260 | |||||||
| chr16:19007421 | A | G | 3 | a0001c0001t0003g0001 a0001c0001t0003g0152 a0001c0001t0003g0158 |
4 | HG02486.hp2 HG02809.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-1751A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19007421 | |||||||
| chr16:19007422 | T | C | 11 | a0001c0001t0001g0114 a0001c0001t0001g0131 a0001c0001t0001g0132 others(8): Show |
11 | HG01109.hp1 HG01496.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.68-1750T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19007422 | |||||||
| chr16:19007561 | G | T | 6 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(3): Show |
6 | HG02615.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-1611G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19007561 | |||||||
| chr16:19007616 | C | T | 2 | a0002c0003t0004g0149 a0002c0003t0014g0150 |
2 | NA18948.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.68-1556C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19007616 | |||||||
| chr16:19007669 | C | CA | 18 | a0001c0001t0003g0157 a0001c0001t0003g0159 a0001c0001t0003g0160 others(15): Show |
18 | HG00609.hp2 HG00735.hp1 HG02129.hp2 others(15): Show |
intron_variant | MODIFIER | c.68-1489dupA | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 19007669 | ||||||
| chr16:19007676 | A | C | 32 | a0001c0001t0001g0069 a0001c0001t0001g0106 a0001c0001t0003g0010 others(29): Show |
32 | HG00408.hp1 HG00558.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.68-1496A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19007676 | |||||||
| chr16:19007676 | A | T | 102 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0003g0195 others(99): Show |
102 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.68-1496A>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19007676 | |||||||
| chr16:19007680 | A | T | 136 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0069 others(133): Show |
136 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.68-1492A>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19007680 | |||||||
| chr16:19007683 | AT | A | 6 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(3): Show |
6 | HG02615.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-1488delT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19007683 | |||||||
| chr16:19007708 | A | T | 1 | a0001c0001t0003g0166 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.68-1464A>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19007708 | |||||||
| chr16:19007768 | A | T | 1 | a0001c0001t0001g0272 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.68-1404A>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19007768 | |||||||
| chr16:19007781 | CT | C | 11 | a0001c0001t0003g0254 a0001c0006t0006g0180 a0001c0006t0018g0155 others(8): Show |
11 | HG00738.hp2 HG01074.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.68-1377delT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 19007781 | ||||||
| chr16:19007894 | A | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0075 others(74): Show |
78 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.68-1278A>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19007894 | |||||||
| chr16:19008057 | C | T | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.68-1115C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19008057 | |||||||
| chr16:19008102 | C | A | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.68-1070C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19008102 | |||||||
| chr16:19008104 | T | C | 9 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(6): Show |
9 | HG02109.hp2 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-1068T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19008104 | |||||||
| chr16:19008324 | G | A | 4 | a0001c0001t0003g0159 a0001c0001t0003g0160 a0001c0001t0003g0161 others(1): Show |
4 | HG02572.hp1 HG02970.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-848G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19008324 | |||||||
| chr16:19008713 | A | G | 6 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(3): Show |
6 | HG02615.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-459A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19008713 | |||||||
| chr16:19008838 | GA | G | 3 | a0002c0003t0004g0117 a0002c0003t0004g0118 a0002c0003t0004g0119 |
3 | HG02056.hp2 NA18946.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.68-333delA | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19008838 | |||||||
| chr16:19008882 | C | G | 2 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.68-290C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 1/15 | chr16 | 19008882 | |||||||
| chr16:19009737 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.311+322C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19009737 | |||||||
| chr16:19009809 | C | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0075 others(74): Show |
78 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.311+394C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19009809 | |||||||
| chr16:19009846 | C | T | 4 | a0001c0006t0006g0180 a0001c0006t0018g0155 a0001c0006t0018g0156 others(1): Show |
4 | HG00738.hp2 HG01074.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.311+431C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19009846 | |||||||
| chr16:19009940 | C | CA | 88 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0075 others(85): Show |
90 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.311+542dupA | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 19009940 | ||||||
| chr16:19009940 | C | CAA | 7 | a0001c0001t0001g0263 a0001c0001t0001g0278 a0001c0001t0006g0011 others(4): Show |
7 | HG02074.hp1 HG02723.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.311+541_311+542dup others(2): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 19009940 | ||||||
| chr16:19009940 | CA | C | 6 | a0001c0001t0003g0157 a0001c0006t0034g0154 a0002c0002t0002g0018 others(3): Show |
6 | HG00738.hp2 HG02004.hp1 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.311+542delA | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 19009940 | ||||||
| chr16:19010124 | C | T | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.311+709C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19010124 | |||||||
| chr16:19010133 | T | TCTCCC | 60 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(57): Show |
60 | HG00609.hp1 HG00642.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.311+738_311+742dup others(5): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 19010133 | ||||||
| chr16:19010133 | T | TCTCCCCT others(3): Show |
107 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0069 others(104): Show |
107 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.311+733_311+742dup others(10): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 19010133 | ||||||
| chr16:19010140 | T | C | 1 | a0001c0005t0002g0164 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.311+725T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19010140 | |||||||
| chr16:19010230 | C | T | 107 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0069 others(104): Show |
107 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.311+815C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19010230 | |||||||
| chr16:19010257 | C | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0075 others(73): Show |
77 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.311+842C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19010257 | |||||||
| chr16:19010293 | T | C | 1 | a0002c0002t0002g0033 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.311+878T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19010293 | |||||||
| chr16:19010332 | G | T | 244 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(241): Show |
245 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.311+917G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19010332 | |||||||
| chr16:19010401 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.311+986G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19010401 | |||||||
| chr16:19010405 | T | A | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.311+990T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19010405 | |||||||
| chr16:19010443 | C | T | 4 | a0001c0006t0006g0180 a0001c0006t0018g0155 a0001c0006t0018g0156 others(1): Show |
4 | HG00738.hp2 HG01074.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.311+1028C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19010443 | |||||||
| chr16:19010444 | G | A | 9 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(6): Show |
9 | HG02109.hp2 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.311+1029G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19010444 | |||||||
| chr16:19010459 | T | TTATTTCT others(11): Show |
1 | a0001c0005t0002g0164 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.311+1045_311+1062d others(20): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 19010459 | ||||||
| chr16:19010588 | A | G | 1 | a0002c0003t0009g0116 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.311+1173A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19010588 | |||||||
| chr16:19010656 | A | G | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.311+1241A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19010656 | |||||||
| chr16:19010991 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.311+1576G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19010991 | |||||||
| chr16:19011020 | G | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0075 others(74): Show |
78 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.311+1605G>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19011020 | |||||||
| chr16:19011050 | C | A | 1 | a0001c0001t0003g0174 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.311+1635C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19011050 | |||||||
| chr16:19011053 | C | T | 4 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(1): Show |
4 | HG02451.hp2 HG02723.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.311+1638C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19011053 | |||||||
| chr16:19011126 | A | G | 134 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0069 others(131): Show |
134 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.311+1711A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19011126 | |||||||
| chr16:19011295 | G | A | 1 | a0002c0003t0001g0222 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.311+1880G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19011295 | |||||||
| chr16:19011347 | A | G | 1 | a0002c0002t0011g0090 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.311+1932A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19011347 | |||||||
| chr16:19011506 | A | AAAAT | 138 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(135): Show |
139 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.311+2131_311+2134d others(6): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 19011506 | ||||||
| chr16:19011506 | A | AAAATAAA others(1): Show |
61 | a0001c0001t0001g0069 a0001c0001t0001g0074 a0001c0001t0001g0075 others(58): Show |
61 | HG00408.hp1 HG00609.hp1 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.311+2127_311+2134d others(10): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 19011506 | ||||||
| chr16:19011506 | A | AAAATAAA others(5): Show |
4 | a0001c0001t0001g0138 a0001c0001t0009g0236 a0002c0002t0002g0100 others(1): Show |
4 | HG00558.hp2 HG02970.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.311+2123_311+2134d others(14): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 19011506 | ||||||
| chr16:19011506 | AAAATAAA others(9): Show |
A | 1 | a0004c0008t0022g0197 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.311+2119_311+2134d others(18): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 19011506 | ||||||
| chr16:19011621 | G | A | 97 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0075 others(94): Show |
98 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(95): Show |
intron_variant | MODIFIER | c.311+2206G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19011621 | |||||||
| chr16:19011625 | G | A | 2 | a0001c0001t0003g0163 a0001c0001t0003g0169 |
2 | HG02145.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.311+2210G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19011625 | |||||||
| chr16:19011637 | A | T | 1 | a0001c0006t0006g0180 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.311+2222A>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19011637 | |||||||
| chr16:19011682 | C | T | 1 | a0002c0002t0002g0223 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.311+2267C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19011682 | |||||||
| chr16:19011699 | CAG | C | 4 | a0001c0006t0006g0180 a0001c0006t0018g0155 a0001c0006t0018g0156 others(1): Show |
4 | HG00738.hp2 HG01074.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.311+2287_311+2288d others(4): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 19011699 | ||||||
| chr16:19011706 | A | G | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.311+2291A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19011706 | |||||||
| chr16:19012046 | C | A | 5 | a0001c0001t0003g0254 a0003c0004t0003g0251 a0003c0004t0006g0252 others(2): Show |
5 | HG02451.hp1 HG02622.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.311+2631C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19012046 | |||||||
| chr16:19012087 | A | G | 1 | a0004c0011t0017g0186 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.311+2672A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19012087 | |||||||
| chr16:19012129 | CA | C | 16 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(13): Show |
16 | HG00738.hp2 HG01074.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.311+2733delA | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 19012129 | ||||||
| chr16:19012129 | CAA | C | 13 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(10): Show |
13 | HG02055.hp2 HG02109.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.311+2732_311+2733d others(4): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 19012129 | ||||||
| chr16:19012129 | CAAA | C | 135 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0069 others(132): Show |
135 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.311+2731_311+2733d others(5): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 19012129 | ||||||
| chr16:19012129 | CAAAA | C | 78 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0075 others(75): Show |
79 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.311+2730_311+2733d others(6): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 19012129 | ||||||
| chr16:19012405 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.311+2990A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19012405 | |||||||
| chr16:19012582 | A | G | 1 | a0001c0006t0006g0180 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.311+3167A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19012582 | |||||||
| chr16:19012788 | CA | C | 22 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0005 others(19): Show |
23 | HG00609.hp2 HG00735.hp1 HG02129.hp2 others(20): Show |
intron_variant | MODIFIER | c.311+3403delA | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 19012788 | ||||||
| chr16:19012788 | CAA | C | 7 | a0001c0001t0001g0267 a0001c0001t0003g0014 a0002c0002t0002g0056 others(4): Show |
7 | HG00642.hp2 HG01981.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.311+3402_311+3403d others(4): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 19012788 | ||||||
| chr16:19012788 | CAAA | C | 62 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0106 others(59): Show |
62 | HG00423.hp1 HG00609.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.311+3401_311+3403d others(5): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 19012788 | ||||||
| chr16:19012788 | CAAAA | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(131): Show |
135 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.311+3400_311+3403d others(6): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 19012788 | ||||||
| chr16:19012788 | CAAAAA | C | 26 | a0001c0001t0001g0114 a0001c0001t0001g0182 a0001c0001t0001g0183 others(23): Show |
26 | HG01074.hp1 HG02055.hp1 HG02300.hp2 others(23): Show |
intron_variant | MODIFIER | c.311+3399_311+3403d others(7): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 19012788 | ||||||
| chr16:19012788 | CAAAAAA | C | 10 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(7): Show |
10 | HG01109.hp1 HG01496.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.311+3398_311+3403d others(8): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 19012788 | ||||||
| chr16:19012788 | CAAAAAAA others(14): Show |
C | 2 | a0001c0001t0001g0274 a0001c0001t0001g0277 |
2 | NA18975.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.311+3383_311+3403d others(23): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 19012788 | ||||||
| chr16:19012821 | A | G | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.311+3406A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19012821 | |||||||
| chr16:19012885 | C | T | 6 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(3): Show |
6 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.311+3470C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19012885 | |||||||
| chr16:19012972 | A | G | 3 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 |
3 | HG02109.hp2 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.312-3478A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19012972 | |||||||
| chr16:19013062 | C | T | 1 | a0001c0001t0001g0280 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.312-3388C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19013062 | |||||||
| chr16:19013155 | G | A | 27 | a0002c0002t0002g0125 a0002c0003t0004g0115 a0002c0003t0004g0117 others(24): Show |
27 | HG00609.hp1 HG01884.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.312-3295G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19013155 | |||||||
| chr16:19013263 | G | T | 6 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(3): Show |
6 | HG02615.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.312-3187G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19013263 | |||||||
| chr16:19013289 | G | T | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.312-3161G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19013289 | |||||||
| chr16:19013306 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.312-3144C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19013306 | |||||||
| chr16:19013610 | C | A | 17 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(14): Show |
17 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.312-2840C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19013610 | |||||||
| chr16:19013727 | T | A | 17 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(14): Show |
17 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.312-2723T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19013727 | |||||||
| chr16:19013811 | G | A | 1 | a0001c0001t0003g0170 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.312-2639G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19013811 | |||||||
| chr16:19013851 | C | CT | 5 | a0001c0001t0001g0039 a0001c0001t0003g0157 a0001c0005t0002g0164 others(2): Show |
5 | HG01515.hp2 NA18973.hp1 NA19087.hp1 others(2): Show |
intron_variant | MODIFIER | c.312-2579dupT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 19013851 | ||||||
| chr16:19013851 | C | CTT | 127 | a0001c0001t0001g0062 a0001c0001t0001g0069 a0001c0001t0001g0106 others(124): Show |
127 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.312-2580_312-2579d others(4): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 19013851 | ||||||
| chr16:19013851 | CT | C | 102 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0075 others(99): Show |
103 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.312-2579delT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 19013851 | ||||||
| chr16:19013884 | C | T | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG03225.hp2 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.312-2566C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19013884 | |||||||
| chr16:19014008 | C | T | 1 | a0004c0011t0017g0186 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.312-2442C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19014008 | |||||||
| chr16:19014028 | G | A | 2 | a0001c0001t0010g0209 a0001c0001t0010g0211 |
2 | HG02109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.312-2422G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19014028 | |||||||
| chr16:19014206 | G | C | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.312-2244G>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19014206 | |||||||
| chr16:19014228 | T | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0075 others(74): Show |
78 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.312-2222T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19014228 | |||||||
| chr16:19014249 | C | T | 1 | a0005c0007t0021g0203 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.312-2201C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19014249 | |||||||
| chr16:19014256 | C | T | 1 | a0002c0002t0024g0199 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.312-2194C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19014256 | |||||||
| chr16:19014270 | T | G | 3 | a0005c0007t0013g0200 a0005c0007t0013g0202 a0005c0007t0021g0203 |
3 | HG02572.hp2 HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.312-2180T>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19014270 | |||||||
| chr16:19014450 | C | T | 8 | a0001c0001t0003g0254 a0001c0001t0007g0206 a0001c0001t0007g0207 others(5): Show |
8 | HG02451.hp1 HG02622.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.312-2000C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19014450 | |||||||
| chr16:19014451 | G | A | 1 | a0002c0003t0016g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.312-1999G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19014451 | |||||||
| chr16:19014545 | C | T | 12 | a0001c0001t0003g0254 a0001c0001t0006g0011 a0001c0001t0006g0012 others(9): Show |
12 | HG02451.hp1 HG02615.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.312-1905C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19014545 | |||||||
| chr16:19014589 | G | A | 1 | a0002c0002t0036g0176 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.312-1861G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19014589 | |||||||
| chr16:19014610 | C | T | 1 | a0002c0002t0002g0052 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.312-1840C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19014610 | |||||||
| chr16:19014734 | T | C | 6 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(3): Show |
6 | HG02615.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.312-1716T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19014734 | |||||||
| chr16:19014791 | T | C | 131 | a0001c0001t0001g0069 a0001c0001t0001g0106 a0001c0001t0003g0195 others(128): Show |
131 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.312-1659T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19014791 | |||||||
| chr16:19014829 | T | C | 9 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(6): Show |
9 | HG02109.hp2 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.312-1621T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19014829 | |||||||
| chr16:19014889 | A | C | 104 | a0001c0001t0001g0069 a0001c0001t0001g0106 a0002c0002t0001g0029 others(101): Show |
104 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.312-1561A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19014889 | |||||||
| chr16:19014940 | T | C | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.312-1510T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19014940 | |||||||
| chr16:19015004 | C | A | 104 | a0001c0001t0001g0069 a0001c0001t0001g0106 a0002c0002t0001g0029 others(101): Show |
104 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.312-1446C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19015004 | |||||||
| chr16:19015122 | C | T | 1 | a0005c0007t0021g0203 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.312-1328C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19015122 | |||||||
| chr16:19015269 | G | GT | 8 | a0001c0001t0001g0243 a0001c0001t0003g0254 a0002c0003t0014g0150 others(5): Show |
8 | HG02451.hp1 HG02622.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.312-1170dupT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 19015269 | ||||||
| chr16:19015334 | C | T | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.312-1116C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19015334 | |||||||
| chr16:19015371 | C | T | 4 | a0004c0008t0022g0197 a0004c0008t0025g0198 a0004c0011t0017g0186 others(1): Show |
4 | HG02258.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.312-1079C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19015371 | |||||||
| chr16:19015375 | C | T | 6 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(3): Show |
6 | HG02109.hp2 HG02572.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.312-1075C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19015375 | |||||||
| chr16:19015570 | G | GT | 13 | a0001c0001t0001g0216 a0001c0001t0010g0209 a0001c0001t0010g0210 others(10): Show |
13 | HG00323.hp1 HG01167.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.312-863dupT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 19015570 | ||||||
| chr16:19015570 | GT | G | 15 | a0001c0001t0001g0132 a0001c0001t0001g0229 a0001c0001t0003g0254 others(12): Show |
15 | HG01069.hp1 HG02132.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.312-863delT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 19015570 | ||||||
| chr16:19015656 | C | A | 7 | a0002c0003t0004g0117 a0002c0003t0004g0118 a0002c0003t0004g0119 others(4): Show |
7 | HG02056.hp2 NA18946.hp1 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.312-794C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19015656 | |||||||
| chr16:19015663 | C | T | 1 | a0002c0003t0001g0222 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.312-787C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19015663 | |||||||
| chr16:19015669 | C | T | 28 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(25): Show |
29 | HG00423.hp1 HG00673.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.312-781C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19015669 | |||||||
| chr16:19015723 | G | A | 3 | a0002c0002t0002g0063 a0002c0002t0011g0073 a0002c0002t0017g0078 |
3 | HG01928.hp1 HG01981.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.312-727G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19015723 | |||||||
| chr16:19015778 | G | C | 97 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(94): Show |
98 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(95): Show |
intron_variant | MODIFIER | c.312-672G>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19015778 | |||||||
| chr16:19015795 | C | G | 2 | a0002c0002t0002g0063 a0002c0002t0017g0078 |
2 | HG01928.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.312-655C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19015795 | |||||||
| chr16:19015940 | A | G | 227 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(224): Show |
228 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.312-510A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19015940 | |||||||
| chr16:19016147 | A | C | 5 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(2): Show |
5 | HG02717.hp1 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.312-303A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19016147 | |||||||
| chr16:19016173 | C | T | 130 | a0001c0001t0001g0069 a0001c0001t0001g0106 a0002c0002t0001g0029 others(127): Show |
130 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.312-277C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19016173 | |||||||
| chr16:19016213 | G | A | 1 | a0002c0003t0009g0130 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.312-237G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19016213 | |||||||
| chr16:19016219 | T | A | 1 | a0002c0002t0002g0084 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.312-231T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19016219 | |||||||
| chr16:19016325 | G | C | 1 | a0008c0010t0001g0219 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.312-125G>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19016325 | |||||||
| chr16:19016342 | G | A | 1 | a0002c0003t0004g0144 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.312-108G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 2/15 | chr16 | 19016342 | |||||||
| chr16:19016621 | C | T | 1 | a0002c0002t0002g0082 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.460+23C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19016621 | |||||||
| chr16:19016808 | A | G | 1 | a0006c0016t0001g0257 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.460+210A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19016808 | |||||||
| chr16:19017120 | C | T | 5 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(2): Show |
5 | HG02717.hp1 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.460+522C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19017120 | |||||||
| chr16:19017227 | T | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(234): Show |
238 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.460+629T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19017227 | |||||||
| chr16:19017236 | A | G | 1 | a0001c0001t0003g0160 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.460+638A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19017236 | |||||||
| chr16:19017242 | A | G | 79 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(76): Show |
80 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.460+644A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19017242 | |||||||
| chr16:19017248 | A | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(234): Show |
238 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.460+650A>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19017248 | |||||||
| chr16:19017294 | G | T | 241 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(238): Show |
242 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.460+696G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19017294 | |||||||
| chr16:19017547 | T | C | 227 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(224): Show |
228 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.460+949T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19017547 | |||||||
| chr16:19017651 | G | C | 79 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(76): Show |
80 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.460+1053G>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19017651 | |||||||
| chr16:19017667 | G | GT | 103 | a0001c0001t0001g0069 a0001c0001t0001g0106 a0001c0001t0003g0014 others(100): Show |
103 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.460+1089dupT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 19017667 | ||||||
| chr16:19017667 | G | GTT | 5 | a0002c0002t0002g0055 a0002c0002t0002g0109 a0002c0002t0002g0125 others(2): Show |
5 | HG00642.hp1 HG02698.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.460+1088_460+1089d others(4): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 19017667 | ||||||
| chr16:19017667 | GT | G | 86 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(83): Show |
87 | HG00323.hp1 HG00423.hp1 HG00673.hp2 others(84): Show |
intron_variant | MODIFIER | c.460+1089delT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 19017667 | ||||||
| chr16:19017667 | GTT | G | 8 | a0001c0001t0001g0225 a0001c0001t0001g0231 a0001c0001t0001g0232 others(5): Show |
8 | HG00639.hp1 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.460+1088_460+1089d others(4): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 19017667 | ||||||
| chr16:19017667 | GTTT | G | 6 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(3): Show |
6 | HG02109.hp2 HG02572.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.460+1087_460+1089d others(5): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 19017667 | ||||||
| chr16:19017673 | T | G | 1 | a0001c0001t0001g0238 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.460+1075T>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19017673 | |||||||
| chr16:19017676 | T | G | 1 | a0001c0006t0006g0180 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.460+1078T>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19017676 | |||||||
| chr16:19017755 | C | T | 1 | a0004c0012t0032g0189 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.460+1157C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19017755 | |||||||
| chr16:19017872 | G | A | 1 | a0001c0001t0003g0013 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.460+1274G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19017872 | |||||||
| chr16:19017949 | C | A | 3 | a0002c0002t0002g0096 a0002c0002t0002g0098 a0002c0002t0011g0090 |
3 | HG00408.hp1 NA18969.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.460+1351C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19017949 | |||||||
| chr16:19017961 | C | T | 3 | a0002c0002t0002g0028 a0002c0002t0002g0046 a0002c0002t0002g0088 |
3 | HG00735.hp2 HG00738.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.460+1363C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19017961 | |||||||
| chr16:19017977 | A | C | 1 | a0001c0001t0001g0216 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.460+1379A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19017977 | |||||||
| chr16:19018519 | A | G | 1 | a0001c0001t0001g0267 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.460+1921A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19018519 | |||||||
| chr16:19018753 | T | C | 1 | a0001c0001t0003g0158 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.460+2155T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19018753 | |||||||
| chr16:19018872 | C | A | 6 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(3): Show |
6 | HG02615.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.460+2274C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19018872 | |||||||
| chr16:19018991 | C | T | 1 | a0001c0001t0003g0010 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.460+2393C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19018991 | |||||||
| chr16:19019006 | A | C | 1 | a0001c0001t0003g0157 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.460+2408A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19019006 | |||||||
| chr16:19019037 | A | G | 1 | a0001c0006t0006g0180 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.460+2439A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19019037 | |||||||
| chr16:19019039 | A | G | 97 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(94): Show |
98 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(95): Show |
intron_variant | MODIFIER | c.460+2441A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19019039 | |||||||
| chr16:19019098 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0106 |
2 | HG02071.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.460+2500C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19019098 | |||||||
| chr16:19019130 | G | A | 2 | a0001c0001t0001g0225 a0001c0001t0001g0249 |
2 | HG00639.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.461-2499G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19019130 | |||||||
| chr16:19019306 | A | G | 130 | a0001c0001t0001g0069 a0001c0001t0001g0106 a0002c0002t0001g0029 others(127): Show |
130 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.461-2323A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19019306 | |||||||
| chr16:19019322 | A | G | 2 | a0005c0007t0013g0200 a0005c0007t0013g0202 |
2 | HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.461-2307A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19019322 | |||||||
| chr16:19019331 | T | C | 5 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(2): Show |
5 | HG02717.hp1 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.461-2298T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19019331 | |||||||
| chr16:19019393 | T | A | 1 | a0001c0001t0003g0157 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.461-2236T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19019393 | |||||||
| chr16:19019754 | G | A | 4 | a0004c0008t0022g0197 a0004c0008t0025g0198 a0004c0011t0017g0186 others(1): Show |
4 | HG02258.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.461-1875G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19019754 | |||||||
| chr16:19019935 | G | A | 2 | a0001c0001t0001g0133 a0002c0002t0002g0061 |
2 | NA18906.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.461-1694G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19019935 | |||||||
| chr16:19020038 | G | T | 4 | a0001c0006t0006g0180 a0001c0006t0018g0155 a0001c0006t0018g0156 others(1): Show |
4 | HG00738.hp2 HG01074.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.461-1591G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19020038 | |||||||
| chr16:19020066 | T | C | 3 | a0004c0008t0022g0197 a0004c0008t0025g0198 a0004c0011t0017g0186 |
3 | HG02615.hp1 HG02896.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.461-1563T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19020066 | |||||||
| chr16:19020103 | A | G | 4 | a0004c0008t0022g0197 a0004c0008t0025g0198 a0004c0011t0017g0186 others(1): Show |
4 | HG02258.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.461-1526A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19020103 | |||||||
| chr16:19020532 | T | C | 4 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(1): Show |
4 | HG02615.hp2 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.461-1097T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19020532 | |||||||
| chr16:19020534 | GA | G | 11 | a0001c0001t0001g0114 a0001c0001t0001g0131 a0001c0001t0001g0132 others(8): Show |
11 | HG01109.hp1 HG01496.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.461-1092delA | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 19020534 | ||||||
| chr16:19020588 | C | T | 4 | a0004c0008t0022g0197 a0004c0008t0025g0198 a0004c0011t0017g0186 others(1): Show |
4 | HG02258.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.461-1041C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19020588 | |||||||
| chr16:19020600 | G | GCTCACGC others(9): Show |
1 | a0001c0001t0003g0157 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.461-1027_461-1012d others(18): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 19020600 | ||||||
| chr16:19020665 | C | T | 5 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(2): Show |
5 | HG02717.hp1 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.461-964C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19020665 | |||||||
| chr16:19020729 | G | A | 5 | a0001c0001t0003g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 others(2): Show |
5 | HG02896.hp2 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.461-900G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19020729 | |||||||
| chr16:19020787 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.461-842G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19020787 | |||||||
| chr16:19020853 | A | AAAAT | 141 | a0001c0001t0001g0069 a0001c0001t0001g0106 a0001c0001t0001g0114 others(138): Show |
141 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.461-740_461-737dup others(4): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 19020853 | ||||||
| chr16:19020853 | A | AAAATAAA others(1): Show |
24 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(21): Show |
24 | HG00323.hp2 HG00558.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.461-744_461-737dup others(8): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 19020853 | ||||||
| chr16:19020853 | A | AAAATAAA others(5): Show |
2 | a0001c0001t0001g0237 a0002c0002t0002g0104 |
2 | HG01169.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.461-748_461-737dup others(12): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 19020853 | ||||||
| chr16:19020853 | AAAAT | A | 3 | a0001c0001t0010g0209 a0001c0001t0010g0211 a0001c0001t0026g0208 |
3 | HG01081.hp2 HG02109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.461-740_461-737del others(4): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 19020853 | ||||||
| chr16:19020853 | AAAATAAA others(1): Show |
A | 14 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(11): Show |
14 | HG01361.hp2 HG01516.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.461-744_461-737del others(8): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 19020853 | ||||||
| chr16:19020893 | A | T | 1 | a0001c0001t0001g0243 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.461-736A>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19020893 | |||||||
| chr16:19020998 | G | A | 104 | a0001c0001t0001g0069 a0001c0001t0001g0106 a0002c0002t0001g0029 others(101): Show |
104 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.461-631G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19020998 | |||||||
| chr16:19021066 | G | T | 104 | a0001c0001t0001g0069 a0001c0001t0001g0106 a0002c0002t0001g0029 others(101): Show |
104 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.461-563G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19021066 | |||||||
| chr16:19021097 | C | T | 6 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(3): Show |
6 | HG02109.hp2 HG02572.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.461-532C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19021097 | |||||||
| chr16:19021148 | A | G | 1 | a0002c0002t0002g0111 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.461-481A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19021148 | |||||||
| chr16:19021240 | T | C | 1 | a0002c0002t0002g0223 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.461-389T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19021240 | |||||||
| chr16:19021458 | G | T | 227 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(224): Show |
228 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.461-171G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19021458 | |||||||
| chr16:19021501 | A | C | 16 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0157 others(13): Show |
16 | HG00609.hp2 HG00642.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.461-128A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19021501 | |||||||
| chr16:19021505 | T | C | 5 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(2): Show |
5 | HG02717.hp1 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.461-124T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 3/15 | chr16 | 19021505 | |||||||
| chr16:19021803 | G | T | 4 | a0001c0006t0006g0180 a0001c0006t0018g0155 a0001c0006t0018g0156 others(1): Show |
4 | HG00738.hp2 HG01074.hp2 NA20129.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.628+7G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 4/15 | chr16 | 19021803 | |||||||
| chr16:19021819 | T | C | 1 | a0002c0002t0002g0111 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.628+23T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 4/15 | chr16 | 19021819 | |||||||
| chr16:19021908 | G | A | 4 | a0001c0006t0006g0180 a0001c0006t0018g0155 a0001c0006t0018g0156 others(1): Show |
4 | HG00738.hp2 HG01074.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.628+112G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 4/15 | chr16 | 19021908 | |||||||
| chr16:19021988 | C | T | 6 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(3): Show |
6 | HG02109.hp2 HG02572.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.628+192C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 4/15 | chr16 | 19021988 | |||||||
| chr16:19022229 | G | C | 15 | a0002c0002t0002g0016 a0002c0002t0002g0088 a0002c0002t0002g0089 others(12): Show |
15 | HG00408.hp1 HG01071.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.628+433G>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 4/15 | chr16 | 19022229 | |||||||
| chr16:19022601 | C | T | 1 | a0002c0002t0011g0073 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.629-512C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 4/15 | chr16 | 19022601 | |||||||
| chr16:19022670 | A | C | 106 | a0001c0001t0001g0069 a0001c0001t0001g0106 a0002c0002t0001g0029 others(103): Show |
106 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.629-443A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 4/15 | chr16 | 19022670 | |||||||
| chr16:19022750 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.629-363C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 4/15 | chr16 | 19022750 | |||||||
| chr16:19022768 | C | T | 4 | a0004c0008t0022g0197 a0004c0008t0025g0198 a0004c0011t0017g0186 others(1): Show |
4 | HG02258.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.629-345C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 4/15 | chr16 | 19022768 | |||||||
| chr16:19022840 | C | T | 36 | a0001c0001t0001g0069 a0001c0001t0001g0106 a0002c0002t0002g0016 others(33): Show |
36 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.629-273C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 4/15 | chr16 | 19022840 | |||||||
| chr16:19022841 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.629-272G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 4/15 | chr16 | 19022841 | |||||||
| chr16:19022918 | G | A | 2 | a0002c0002t0002g0031 a0002c0002t0002g0108 |
2 | HG03239.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.629-195G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 4/15 | chr16 | 19022918 | |||||||
| chr16:19023247 | A | G | 8 | a0001c0006t0006g0180 a0001c0006t0018g0155 a0001c0006t0018g0156 others(5): Show |
8 | HG00738.hp2 HG01074.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.711+52A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19023247 | |||||||
| chr16:19023351 | C | T | 1 | a0001c0006t0006g0180 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.711+156C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19023351 | |||||||
| chr16:19023539 | T | C | 241 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(238): Show |
242 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.711+344T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19023539 | |||||||
| chr16:19023727 | G | A | 1 | a0002c0002t0002g0033 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.711+532G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19023727 | |||||||
| chr16:19023793 | C | T | 6 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(3): Show |
6 | HG02109.hp2 HG02572.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.711+598C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19023793 | |||||||
| chr16:19023803 | A | T | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.711+608A>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19023803 | |||||||
| chr16:19023827 | A | G | 6 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(3): Show |
6 | HG02615.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.711+632A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19023827 | |||||||
| chr16:19023877 | A | C | 1 | a0003c0004t0006g0253 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.711+682A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19023877 | |||||||
| chr16:19024260 | G | A | 241 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(238): Show |
242 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.711+1065G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19024260 | |||||||
| chr16:19024282 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.711+1087G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19024282 | |||||||
| chr16:19024289 | C | T | 1 | a0002c0002t0002g0045 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.711+1094C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19024289 | |||||||
| chr16:19024360 | G | A | 227 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(224): Show |
228 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.711+1165G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19024360 | |||||||
| chr16:19024530 | C | G | 85 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(82): Show |
86 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.711+1335C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19024530 | |||||||
| chr16:19024554 | T | A | 6 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(3): Show |
6 | HG02109.hp2 HG02572.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.711+1359T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19024554 | |||||||
| chr16:19024615 | G | A | 2 | a0004c0008t0022g0197 a0004c0008t0025g0198 |
2 | HG02615.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.711+1420G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19024615 | |||||||
| chr16:19024690 | C | T | 1 | a0002c0003t0001g0222 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.711+1495C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19024690 | |||||||
| chr16:19024772 | C | T | 1 | a0002c0002t0002g0059 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.711+1577C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19024772 | |||||||
| chr16:19024802 | C | T | 1 | a0002c0003t0009g0113 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.711+1607C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19024802 | |||||||
| chr16:19024822 | C | T | 5 | a0001c0001t0003g0170 a0001c0001t0003g0173 a0001c0001t0003g0177 others(2): Show |
5 | NA18612.hp1 NA18946.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.711+1627C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19024822 | |||||||
| chr16:19025248 | C | T | 6 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(3): Show |
6 | HG02109.hp2 HG02572.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.711+2053C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19025248 | |||||||
| chr16:19025253 | C | T | 1 | a0001c0001t0009g0236 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.711+2058C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19025253 | |||||||
| chr16:19025378 | A | G | 3 | a0004c0008t0022g0197 a0004c0008t0025g0198 a0004c0011t0017g0186 |
3 | HG02615.hp1 HG02896.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.711+2183A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19025378 | |||||||
| chr16:19025412 | A | G | 79 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(76): Show |
80 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.711+2217A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19025412 | |||||||
| chr16:19025436 | T | C | 4 | a0001c0006t0006g0180 a0001c0006t0018g0155 a0001c0006t0018g0156 others(1): Show |
4 | HG00738.hp2 HG01074.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.711+2241T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19025436 | |||||||
| chr16:19025489 | G | A | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.711+2294G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19025489 | |||||||
| chr16:19025615 | G | T | 8 | a0001c0006t0006g0180 a0001c0006t0018g0155 a0001c0006t0018g0156 others(5): Show |
8 | HG00738.hp2 HG01074.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.711+2420G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19025615 | |||||||
| chr16:19025617 | C | T | 6 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(3): Show |
6 | HG02615.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.711+2422C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19025617 | |||||||
| chr16:19025646 | C | CA | 4 | a0004c0008t0022g0197 a0004c0008t0025g0198 a0004c0011t0017g0186 others(1): Show |
4 | HG02258.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.711+2458dupA | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 19025646 | ||||||
| chr16:19025717 | A | T | 6 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(3): Show |
6 | HG01081.hp2 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.711+2522A>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19025717 | |||||||
| chr16:19025757 | CT | C | 6 | a0001c0001t0003g0254 a0003c0004t0003g0251 a0003c0004t0006g0252 others(3): Show |
6 | HG02451.hp1 HG02622.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.711+2574delT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 19025757 | ||||||
| chr16:19026101 | C | T | 28 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(25): Show |
29 | HG00423.hp1 HG00673.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.711+2906C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19026101 | |||||||
| chr16:19026180 | T | TA | 136 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(133): Show |
137 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(134): Show |
intron_variant | MODIFIER | c.711+2994dupA | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 19026180 | ||||||
| chr16:19026256 | C | T | 3 | a0004c0008t0022g0197 a0004c0008t0025g0198 a0004c0011t0017g0186 |
3 | HG02615.hp1 HG02896.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.711+3061C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19026256 | |||||||
| chr16:19026272 | C | T | 2 | a0002c0002t0002g0105 a0002c0013t0037g0081 |
2 | HG00408.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.711+3077C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19026272 | |||||||
| chr16:19026472 | G | A | 102 | a0001c0001t0001g0069 a0001c0001t0001g0106 a0002c0002t0001g0029 others(99): Show |
102 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.711+3277G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19026472 | |||||||
| chr16:19026476 | C | CA | 29 | a0002c0002t0002g0017 a0002c0002t0002g0040 a0002c0002t0002g0048 others(26): Show |
29 | HG00609.hp1 HG01257.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.711+3295dupA | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 19026476 | ||||||
| chr16:19026476 | CA | C | 6 | a0001c0001t0001g0227 a0001c0001t0001g0276 a0001c0006t0018g0155 others(3): Show |
6 | HG00738.hp2 HG01074.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.711+3295delA | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 19026476 | ||||||
| chr16:19026504 | G | A | 1 | a0002c0002t0002g0092 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.711+3309G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19026504 | |||||||
| chr16:19026584 | A | T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(76): Show |
80 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.711+3389A>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19026584 | |||||||
| chr16:19026617 | T | A | 1 | a0002c0002t0005g0065 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.711+3422T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19026617 | |||||||
| chr16:19026852 | C | T | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.712-3372C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19026852 | |||||||
| chr16:19026913 | C | G | 2 | a0001c0001t0003g0157 a0001c0001t0003g0167 |
2 | HG02129.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.712-3311C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19026913 | |||||||
| chr16:19026980 | T | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(76): Show |
80 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.712-3244T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19026980 | |||||||
| chr16:19027007 | C | G | 1 | a0001c0001t0008g0188 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.712-3217C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19027007 | |||||||
| chr16:19027023 | A | G | 79 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(76): Show |
80 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.712-3201A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19027023 | |||||||
| chr16:19027052 | A | G | 1 | a0001c0001t0007g0204 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.712-3172A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19027052 | |||||||
| chr16:19027061 | C | CT | 25 | a0001c0001t0001g0039 a0001c0001t0001g0250 a0001c0001t0003g0004 others(22): Show |
25 | HG01081.hp2 HG01169.hp1 HG02015.hp2 others(22): Show |
intron_variant | MODIFIER | c.712-3137dupT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 19027061 | ||||||
| chr16:19027061 | C | CTT | 158 | a0001c0001t0001g0002 a0001c0001t0001g0062 a0001c0001t0001g0076 others(155): Show |
159 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.712-3138_712-3137d others(4): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 19027061 | ||||||
| chr16:19027061 | C | CTTT | 43 | a0001c0001t0001g0069 a0001c0001t0001g0074 a0001c0001t0001g0075 others(40): Show |
43 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.712-3139_712-3137d others(5): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 19027061 | ||||||
| chr16:19027363 | G | A | 4 | a0001c0001t0003g0254 a0003c0004t0006g0252 a0003c0004t0006g0255 others(1): Show |
4 | HG02451.hp1 HG02622.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.712-2861G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19027363 | |||||||
| chr16:19027388 | A | G | 9 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(6): Show |
9 | HG01361.hp2 HG01516.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.712-2836A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19027388 | |||||||
| chr16:19027565 | A | G | 6 | a0001c0001t0003g0254 a0003c0004t0003g0251 a0003c0004t0006g0252 others(3): Show |
6 | HG02451.hp1 HG02622.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.712-2659A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19027565 | |||||||
| chr16:19027879 | A | G | 1 | a0002c0002t0002g0112 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.712-2345A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19027879 | |||||||
| chr16:19028113 | A | G | 1 | a0002c0002t0011g0194 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.712-2111A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19028113 | |||||||
| chr16:19028215 | T | C | 1 | a0002c0002t0002g0021 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.712-2009T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19028215 | |||||||
| chr16:19028355 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.712-1869C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19028355 | |||||||
| chr16:19028381 | TA | T | 80 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(77): Show |
81 | HG00323.hp1 HG00423.hp1 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.712-1834delA | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 19028381 | ||||||
| chr16:19028440 | T | G | 5 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(2): Show |
5 | HG02717.hp1 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.712-1784T>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19028440 | |||||||
| chr16:19028513 | C | G | 6 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(3): Show |
6 | HG02615.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.712-1711C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19028513 | |||||||
| chr16:19028647 | A | AATT | 5 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(2): Show |
5 | HG02717.hp1 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.712-1555_712-1553d others(5): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 19028647 | ||||||
| chr16:19028647 | AATTATT | A | 6 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(3): Show |
6 | HG02615.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.712-1558_712-1553d others(8): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 19028647 | ||||||
| chr16:19028872 | T | C | 2 | a0001c0001t0001g0244 a0001c0001t0028g0245 |
2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.712-1352T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19028872 | |||||||
| chr16:19028969 | TA | T | 81 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(78): Show |
82 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.712-1246delA | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 19028969 | ||||||
| chr16:19028970 | A | T | 22 | a0002c0002t0002g0016 a0002c0002t0002g0022 a0002c0002t0002g0057 others(19): Show |
22 | HG00408.hp1 HG00558.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.712-1254A>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19028970 | |||||||
| chr16:19028991 | T | A | 6 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(3): Show |
6 | HG02615.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.712-1233T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19028991 | |||||||
| chr16:19029058 | T | C | 1 | a0002c0002t0002g0052 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.712-1166T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19029058 | |||||||
| chr16:19029088 | A | C | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.712-1136A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19029088 | |||||||
| chr16:19029098 | C | T | 6 | a0001c0001t0003g0254 a0002c0003t0004g0118 a0003c0004t0003g0251 others(3): Show |
6 | HG02056.hp2 HG02451.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.712-1126C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19029098 | |||||||
| chr16:19029106 | C | T | 2 | a0002c0003t0004g0149 a0002c0003t0014g0150 |
2 | NA18948.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.712-1118C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19029106 | |||||||
| chr16:19029120 | T | C | 2 | a0002c0003t0004g0149 a0002c0003t0014g0150 |
2 | NA18948.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.712-1104T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19029120 | |||||||
| chr16:19029189 | T | C | 1 | a0001c0001t0006g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.712-1035T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19029189 | |||||||
| chr16:19029265 | A | G | 6 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(3): Show |
6 | HG02615.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.712-959A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19029265 | |||||||
| chr16:19029336 | C | T | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.712-888C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19029336 | |||||||
| chr16:19029473 | A | T | 227 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(224): Show |
228 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.712-751A>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19029473 | |||||||
| chr16:19029536 | A | AT | 4 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(1): Show |
4 | HG02615.hp2 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.712-681dupT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 19029536 | ||||||
| chr16:19029543 | T | A | 32 | a0001c0001t0003g0254 a0002c0003t0004g0115 a0002c0003t0004g0117 others(29): Show |
32 | HG00609.hp1 HG01884.hp2 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.712-681T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19029543 | |||||||
| chr16:19029647 | TTA | T | 5 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(2): Show |
5 | HG02717.hp1 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.712-576_712-575del others(2): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19029647 | |||||||
| chr16:19029666 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.712-558C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19029666 | |||||||
| chr16:19029717 | G | A | 6 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(3): Show |
6 | HG02109.hp2 HG02572.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.712-507G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19029717 | |||||||
| chr16:19029773 | C | G | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.712-451C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19029773 | |||||||
| chr16:19029774 | G | A | 1 | a0001c0001t0003g0166 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.712-450G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19029774 | |||||||
| chr16:19029779 | C | G | 1 | a0002c0003t0009g0130 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.712-445C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19029779 | |||||||
| chr16:19029783 | T | A | 1 | a0001c0001t0001g0275 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.712-441T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19029783 | |||||||
| chr16:19029806 | G | A | 1 | a0002c0002t0002g0051 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.712-418G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19029806 | |||||||
| chr16:19029859 | C | T | 128 | a0002c0002t0001g0029 a0002c0002t0002g0016 a0002c0002t0002g0017 others(125): Show |
128 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.712-365C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19029859 | |||||||
| chr16:19029876 | C | A | 1 | a0002c0002t0002g0097 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.712-348C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19029876 | |||||||
| chr16:19030008 | G | GC | 3 | a0004c0008t0025g0198 a0004c0011t0017g0186 a0004c0012t0032g0189 |
3 | HG02258.hp2 HG02615.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.712-213dupC | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 19030008 | ||||||
| chr16:19030168 | C | G | 1 | a0001c0001t0003g0162 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.712-56C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 5/15 | chr16 | 19030168 | |||||||
| chr16:19030545 | G | A | 1 | a0002c0002t0002g0111 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.857+176G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19030545 | |||||||
| chr16:19030578 | C | CT | 9 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(6): Show |
9 | HG01081.hp2 HG02135.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.857+226dupT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr16 | 19030578 | ||||||
| chr16:19030578 | CT | C | 8 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0003g0014 others(5): Show |
8 | HG00642.hp2 HG01074.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.857+226delT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr16 | 19030578 | ||||||
| chr16:19030581 | T | C | 1 | a0002c0002t0002g0020 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.857+212T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19030581 | |||||||
| chr16:19030640 | G | A | 4 | a0001c0006t0006g0180 a0001c0006t0018g0155 a0001c0006t0018g0156 others(1): Show |
4 | HG00738.hp2 HG01074.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.857+271G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19030640 | |||||||
| chr16:19030822 | C | A | 102 | a0002c0002t0001g0029 a0002c0002t0002g0016 a0002c0002t0002g0017 others(99): Show |
102 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.857+453C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19030822 | |||||||
| chr16:19030903 | C | A | 6 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(3): Show |
6 | HG01081.hp2 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.857+534C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19030903 | |||||||
| chr16:19030933 | A | G | 20 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0157 others(17): Show |
20 | HG00609.hp2 HG00642.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.857+564A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19030933 | |||||||
| chr16:19031091 | G | A | 6 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(3): Show |
6 | HG02615.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.857+722G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19031091 | |||||||
| chr16:19031141 | C | A | 2 | a0001c0001t0001g0244 a0001c0001t0028g0245 |
2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.857+772C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19031141 | |||||||
| chr16:19031186 | C | A | 1 | a0001c0001t0003g0174 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.857+817C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19031186 | |||||||
| chr16:19031196 | C | T | 2 | a0002c0002t0002g0061 a0002c0002t0002g0083 |
2 | NA18968.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.857+827C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19031196 | |||||||
| chr16:19031209 | G | A | 1 | a0002c0002t0002g0098 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.857+840G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19031209 | |||||||
| chr16:19031241 | G | A | 1 | a0004c0011t0017g0186 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.857+872G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19031241 | |||||||
| chr16:19031261 | C | T | 2 | a0004c0008t0025g0198 a0004c0012t0032g0189 |
2 | HG02258.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.857+892C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19031261 | |||||||
| chr16:19031262 | G | A | 2 | a0001c0001t0003g0010 a0007c0018t0002g0015 |
2 | HG01515.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.857+893G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19031262 | |||||||
| chr16:19031276 | G | A | 6 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(3): Show |
6 | HG01081.hp2 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.857+907G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19031276 | |||||||
| chr16:19031361 | G | A | 1 | a0001c0001t0003g0166 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.857+992G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19031361 | |||||||
| chr16:19031543 | C | A | 6 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(3): Show |
6 | HG02109.hp2 HG02572.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.857+1174C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19031543 | |||||||
| chr16:19031570 | A | C | 240 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(237): Show |
241 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.857+1201A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19031570 | |||||||
| chr16:19031649 | C | T | 6 | a0001c0001t0003g0254 a0003c0004t0003g0251 a0003c0004t0006g0252 others(3): Show |
6 | HG02451.hp1 HG02622.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.857+1280C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19031649 | |||||||
| chr16:19031753 | G | C | 2 | a0002c0002t0002g0016 a0002c0002t0002g0112 |
2 | HG02040.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.857+1384G>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19031753 | |||||||
| chr16:19031799 | G | A | 4 | a0001c0006t0006g0180 a0001c0006t0018g0155 a0001c0006t0018g0156 others(1): Show |
4 | HG00738.hp2 HG01074.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.857+1430G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19031799 | |||||||
| chr16:19031840 | G | A | 1 | a0002c0002t0012g0034 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.857+1471G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19031840 | |||||||
| chr16:19031861 | C | A | 3 | a0005c0007t0013g0200 a0005c0007t0013g0202 a0005c0007t0021g0203 |
3 | HG02572.hp2 HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.857+1492C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19031861 | |||||||
| chr16:19031861 | C | T | 228 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(225): Show |
229 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.857+1492C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19031861 | |||||||
| chr16:19031877 | G | A | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.857+1508G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19031877 | |||||||
| chr16:19031959 | C | T | 1 | a0004c0008t0025g0198 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.857+1590C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19031959 | |||||||
| chr16:19031962 | C | T | 81 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(78): Show |
82 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.857+1593C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19031962 | |||||||
| chr16:19032156 | A | C | 1 | a0001c0001t0001g0039 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.857+1787A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19032156 | |||||||
| chr16:19032219 | T | C | 240 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(237): Show |
241 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.857+1850T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19032219 | |||||||
| chr16:19032238 | A | G | 100 | a0002c0002t0001g0029 a0002c0002t0002g0016 a0002c0002t0002g0017 others(97): Show |
100 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.857+1869A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19032238 | |||||||
| chr16:19032437 | G | T | 1 | a0001c0001t0030g0271 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.857+2068G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19032437 | |||||||
| chr16:19032547 | TAA | T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(76): Show |
80 | HG00423.hp1 HG00639.hp1 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.857+2192_857+2193d others(4): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr16 | 19032547 | ||||||
| chr16:19032849 | G | A | 6 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(3): Show |
6 | HG02109.hp2 HG02572.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.857+2480G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19032849 | |||||||
| chr16:19032918 | C | T | 6 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(3): Show |
6 | HG02109.hp2 HG02572.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.857+2549C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19032918 | |||||||
| chr16:19033076 | G | A | 5 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(2): Show |
5 | HG02717.hp1 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.858-2600G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19033076 | |||||||
| chr16:19033090 | C | CAAAGAGT others(340): Show |
1 | a0002c0002t0002g0196 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.858-2569_858-2568i others(349): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr16 | 19033090 | ||||||
| chr16:19033278 | T | C | 1 | a0007c0018t0002g0015 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.858-2398T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19033278 | |||||||
| chr16:19033415 | C | T | 1 | a0001c0001t0008g0188 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.858-2261C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19033415 | |||||||
| chr16:19033537 | A | G | 2 | a0002c0002t0002g0028 a0002c0002t0002g0046 |
2 | HG00735.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.858-2139A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19033537 | |||||||
| chr16:19033574 | T | C | 81 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(78): Show |
82 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.858-2102T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19033574 | |||||||
| chr16:19033577 | G | A | 221 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(218): Show |
222 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.858-2099G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19033577 | |||||||
| chr16:19033880 | A | C | 240 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(237): Show |
241 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.858-1796A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19033880 | |||||||
| chr16:19033913 | A | C | 3 | a0001c0006t0018g0155 a0001c0006t0018g0156 a0001c0006t0034g0154 |
3 | HG00738.hp2 HG01074.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.858-1763A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19033913 | |||||||
| chr16:19034021 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.858-1655G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19034021 | |||||||
| chr16:19034331 | G | T | 33 | a0001c0001t0003g0254 a0002c0003t0004g0115 a0002c0003t0004g0117 others(30): Show |
33 | HG00609.hp1 HG01884.hp2 HG01934.hp2 others(30): Show |
intron_variant | MODIFIER | c.858-1345G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19034331 | |||||||
| chr16:19034426 | GTC | G | 27 | a0001c0001t0001g0114 a0001c0001t0001g0131 a0001c0001t0001g0132 others(24): Show |
27 | HG01074.hp1 HG01109.hp1 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.858-1246_858-1245d others(4): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr16 | 19034426 | ||||||
| chr16:19034434 | T | TAAAAATA others(278): Show |
1 | a0004c0008t0025g0198 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.858-1225_858-1224i others(287): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr16 | 19034434 | ||||||
| chr16:19034434 | T | TAAAAATA others(280): Show |
1 | a0004c0012t0032g0189 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.858-1225_858-1224i others(289): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr16 | 19034434 | ||||||
| chr16:19034517 | G | C | 6 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(3): Show |
6 | HG02109.hp2 HG02572.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.858-1159G>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19034517 | |||||||
| chr16:19034614 | G | GTAAA | 77 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(74): Show |
78 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.858-1041_858-1038d others(6): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr16 | 19034614 | ||||||
| chr16:19034614 | GTAAA | G | 12 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(9): Show |
12 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.858-1041_858-1038d others(6): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr16 | 19034614 | ||||||
| chr16:19034659 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.858-1017G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19034659 | |||||||
| chr16:19034791 | C | G | 2 | a0004c0008t0025g0198 a0004c0012t0032g0189 |
2 | HG02258.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.858-885C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19034791 | |||||||
| chr16:19034933 | T | C | 1 | a0001c0001t0003g0171 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.858-743T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19034933 | |||||||
| chr16:19034974 | C | T | 5 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(2): Show |
5 | HG02717.hp1 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.858-702C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19034974 | |||||||
| chr16:19035014 | G | A | 4 | a0001c0006t0006g0180 a0001c0006t0018g0155 a0001c0006t0018g0156 others(1): Show |
4 | HG00738.hp2 HG01074.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.858-662G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19035014 | |||||||
| chr16:19035190 | C | T | 6 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(3): Show |
6 | HG02109.hp2 HG02572.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.858-486C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19035190 | |||||||
| chr16:19035237 | A | G | 6 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(3): Show |
6 | HG01081.hp2 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.858-439A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19035237 | |||||||
| chr16:19035325 | G | A | 7 | a0001c0001t0003g0254 a0002c0003t0016g0151 a0003c0004t0003g0251 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.858-351G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19035325 | |||||||
| chr16:19035583 | A | G | 6 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(3): Show |
6 | HG02109.hp2 HG02572.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.858-93A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19035583 | |||||||
| chr16:19035628 | T | G | 6 | a0001c0006t0006g0180 a0001c0006t0018g0155 a0001c0006t0018g0156 others(3): Show |
6 | HG00738.hp2 HG01074.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.858-48T>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19035628 | |||||||
| chr16:19035638 | T | C | 81 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(78): Show |
82 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.858-38T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 6/15 | chr16 | 19035638 | |||||||
| chr16:19036129 | G | A | 1 | a0001c0001t0005g0226 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1005+306G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 7/15 | chr16 | 19036129 | |||||||
| chr16:19036305 | C | G | 1 | a0002c0002t0002g0108 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1005+482C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 7/15 | chr16 | 19036305 | |||||||
| chr16:19036571 | T | C | 231 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(228): Show |
232 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.1005+748T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 7/15 | chr16 | 19036571 | |||||||
| chr16:19036619 | G | A | 1 | a0001c0006t0006g0180 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1005+796G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 7/15 | chr16 | 19036619 | |||||||
| chr16:19036648 | G | T | 1 | a0001c0001t0001g0266 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1005+825G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 7/15 | chr16 | 19036648 | |||||||
| chr16:19036885 | C | T | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1006-989C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 7/15 | chr16 | 19036885 | |||||||
| chr16:19036886 | G | A | 1 | a0001c0001t0001g0267 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1006-988G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 7/15 | chr16 | 19036886 | |||||||
| chr16:19036900 | A | C | 240 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(237): Show |
241 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.1006-974A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 7/15 | chr16 | 19036900 | |||||||
| chr16:19036902 | C | T | 6 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(3): Show |
6 | HG02615.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1006-972C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 7/15 | chr16 | 19036902 | |||||||
| chr16:19037217 | G | A | 81 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(78): Show |
82 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.1006-657G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 7/15 | chr16 | 19037217 | |||||||
| chr16:19037253 | T | G | 10 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(7): Show |
10 | HG00738.hp2 HG01074.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1006-621T>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 7/15 | chr16 | 19037253 | |||||||
| chr16:19037346 | C | T | 1 | a0002c0002t0024g0199 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1006-528C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 7/15 | chr16 | 19037346 | |||||||
| chr16:19037386 | C | CA | 9 | a0001c0001t0003g0013 a0001c0001t0003g0173 a0001c0001t0010g0209 others(6): Show |
9 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1006-471dupA | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr16 | 19037386 | ||||||
| chr16:19037386 | C | T | 1 | a0002c0003t0004g0118 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1006-488C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 7/15 | chr16 | 19037386 | |||||||
| chr16:19037401 | AAAG | A | 95 | a0002c0002t0001g0029 a0002c0002t0002g0016 a0002c0002t0002g0017 others(92): Show |
95 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.1006-470_1006-468d others(5): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr16 | 19037401 | ||||||
| chr16:19037402 | AAG | A | 82 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(79): Show |
83 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.1006-470_1006-469d others(4): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr16 | 19037402 | ||||||
| chr16:19037403 | AG | A | 42 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(39): Show |
42 | HG00609.hp1 HG01081.hp2 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.1006-470delG | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 7/15 | chr16 | 19037403 | |||||||
| chr16:19037404 | G | A | 21 | a0001c0001t0003g0254 a0001c0001t0010g0209 a0001c0001t0010g0210 others(18): Show |
21 | HG00738.hp2 HG01074.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.1006-470G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 7/15 | chr16 | 19037404 | |||||||
| chr16:19037472 | C | CTT | 124 | a0001c0005t0002g0248 a0002c0002t0001g0029 a0002c0002t0002g0016 others(121): Show |
124 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1006-389_1006-388d others(4): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr16 | 19037472 | ||||||
| chr16:19037472 | C | CTTT | 5 | a0002c0002t0002g0023 a0002c0002t0002g0026 a0002c0002t0002g0196 others(2): Show |
5 | HG01081.hp1 HG02132.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1006-390_1006-388d others(5): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr16 | 19037472 | ||||||
| chr16:19037549 | C | G | 102 | a0001c0005t0002g0248 a0002c0002t0001g0029 a0002c0002t0002g0016 others(99): Show |
102 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.1006-325C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 7/15 | chr16 | 19037549 | |||||||
| chr16:19037620 | T | A | 6 | a0001c0001t0003g0254 a0003c0004t0003g0251 a0003c0004t0006g0252 others(3): Show |
6 | HG02451.hp1 HG02622.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1006-254T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 7/15 | chr16 | 19037620 | |||||||
| chr16:19037696 | C | A | 1 | a0002c0003t0016g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1006-178C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 7/15 | chr16 | 19037696 | |||||||
| chr16:19037830 | C | A | 1 | a0004c0011t0017g0186 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1006-44C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 7/15 | chr16 | 19037830 | |||||||
| chr16:19038056 | A | G | 151 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(148): Show |
151 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.1179+9A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 8/15 | chr16 | 19038056 | |||||||
| chr16:19038144 | C | G | 1 | a0001c0001t0009g0236 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1179+97C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 8/15 | chr16 | 19038144 | |||||||
| chr16:19038232 | C | G | 6 | a0001c0001t0003g0254 a0003c0004t0003g0251 a0003c0004t0006g0252 others(3): Show |
6 | HG02451.hp1 HG02622.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1179+185C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 8/15 | chr16 | 19038232 | |||||||
| chr16:19038356 | T | C | 240 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(237): Show |
241 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.1179+309T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 8/15 | chr16 | 19038356 | |||||||
| chr16:19038400 | G | A | 22 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(19): Show |
22 | HG00738.hp2 HG01074.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.1179+353G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 8/15 | chr16 | 19038400 | |||||||
| chr16:19038470 | C | T | 6 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(3): Show |
6 | HG02615.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1179+423C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 8/15 | chr16 | 19038470 | |||||||
| chr16:19038738 | G | A | 1 | a0001c0006t0006g0180 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1179+691G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 8/15 | chr16 | 19038738 | |||||||
| chr16:19038883 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1179+836A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 8/15 | chr16 | 19038883 | |||||||
| chr16:19039092 | C | CT | 107 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(104): Show |
108 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.1179+1061dupT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr16 | 19039092 | ||||||
| chr16:19039092 | C | T | 1 | a0001c0006t0006g0180 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1179+1045C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 8/15 | chr16 | 19039092 | |||||||
| chr16:19039183 | C | T | 6 | a0001c0001t0003g0254 a0003c0004t0003g0251 a0003c0004t0006g0252 others(3): Show |
6 | HG02451.hp1 HG02622.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1180-1106C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 8/15 | chr16 | 19039183 | |||||||
| chr16:19039296 | G | C | 129 | a0001c0005t0002g0248 a0002c0002t0001g0029 a0002c0002t0002g0016 others(126): Show |
129 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1180-993G>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 8/15 | chr16 | 19039296 | |||||||
| chr16:19039389 | C | G | 1 | a0002c0002t0024g0199 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1180-900C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 8/15 | chr16 | 19039389 | |||||||
| chr16:19039745 | T | A | 4 | a0001c0006t0018g0155 a0001c0006t0018g0156 a0001c0006t0034g0154 others(1): Show |
4 | HG00738.hp2 HG01074.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180-544T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 8/15 | chr16 | 19039745 | |||||||
| chr16:19039786 | T | A | 240 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(237): Show |
241 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.1180-503T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 8/15 | chr16 | 19039786 | |||||||
| chr16:19039829 | A | G | 151 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(148): Show |
151 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.1180-460A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 8/15 | chr16 | 19039829 | |||||||
| chr16:19040034 | T | C | 3 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 |
3 | HG02300.hp2 HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1180-255T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 8/15 | chr16 | 19040034 | |||||||
| chr16:19040047 | C | T | 80 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(77): Show |
81 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.1180-242C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 8/15 | chr16 | 19040047 | |||||||
| chr16:19040115 | C | CA | 106 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(103): Show |
106 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.1180-151dupA | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr16 | 19040115 | ||||||
| chr16:19040115 | C | CAA | 6 | a0002c0002t0002g0020 a0002c0002t0002g0059 a0002c0002t0002g0087 others(3): Show |
6 | HG00642.hp1 HG01243.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.1180-152_1180-151d others(4): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr16 | 19040115 | ||||||
| chr16:19040115 | CA | C | 60 | a0001c0001t0001g0134 a0001c0001t0001g0181 a0001c0001t0001g0182 others(57): Show |
60 | HG00609.hp1 HG00738.hp2 HG01074.hp2 others(57): Show |
intron_variant | MODIFIER | c.1180-151delA | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr16 | 19040115 | ||||||
| chr16:19040115 | CAA | C | 79 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(76): Show |
80 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.1180-152_1180-151d others(4): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr16 | 19040115 | ||||||
| chr16:19040198 | A | G | 150 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(147): Show |
150 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.1180-91A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 8/15 | chr16 | 19040198 | |||||||
| chr16:19040202 | C | T | 1 | a0001c0001t0003g0254 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1180-87C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 8/15 | chr16 | 19040202 | |||||||
| chr16:19040228 | A | T | 5 | a0003c0004t0003g0251 a0003c0004t0006g0252 a0003c0004t0006g0253 others(2): Show |
5 | HG02451.hp1 HG02622.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180-61A>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 8/15 | chr16 | 19040228 | |||||||
| chr16:19040499 | ACT | A | 3 | a0005c0007t0013g0200 a0005c0007t0013g0202 a0005c0007t0021g0203 |
3 | HG02572.hp2 HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1337+58_1337+59del others(2): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr16 | 19040499 | ||||||
| chr16:19040533 | TGTA | T | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG03225.hp2 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1337+90_1337+92del others(3): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr16 | 19040533 | ||||||
| chr16:19040539 | G | T | 1 | a0002c0002t0002g0064 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1337+93G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19040539 | |||||||
| chr16:19040841 | G | A | 4 | a0001c0001t0003g0159 a0001c0001t0003g0160 a0001c0001t0003g0161 others(1): Show |
4 | HG02572.hp1 HG02970.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1337+395G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19040841 | |||||||
| chr16:19040892 | C | CT | 6 | a0001c0001t0003g0157 a0002c0002t0002g0072 a0002c0002t0002g0109 others(3): Show |
6 | HG02258.hp2 HG02615.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1337+462dupT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr16 | 19040892 | ||||||
| chr16:19040892 | CT | C | 32 | a0001c0001t0001g0080 a0001c0001t0001g0139 a0001c0001t0001g0181 others(29): Show |
32 | HG00738.hp2 HG01069.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.1337+462delT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr16 | 19040892 | ||||||
| chr16:19040950 | A | C | 18 | a0001c0001t0001g0069 a0001c0001t0001g0074 a0001c0001t0001g0075 others(15): Show |
18 | HG00323.hp1 HG00639.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.1337+504A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19040950 | |||||||
| chr16:19041066 | A | T | 4 | a0003c0004t0006g0253 a0005c0007t0013g0200 a0005c0007t0013g0202 others(1): Show |
4 | HG02572.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1337+620A>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19041066 | |||||||
| chr16:19041067 | T | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0069 others(84): Show |
88 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1337+621T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19041067 | |||||||
| chr16:19041294 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1337+848A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19041294 | |||||||
| chr16:19041401 | C | T | 239 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(236): Show |
240 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1337+955C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19041401 | |||||||
| chr16:19041512 | C | T | 1 | a0004c0012t0032g0189 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1337+1066C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19041512 | |||||||
| chr16:19041578 | G | C | 6 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(3): Show |
6 | HG02615.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1337+1132G>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19041578 | |||||||
| chr16:19041579 | C | A | 6 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(3): Show |
6 | HG02615.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1337+1133C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19041579 | |||||||
| chr16:19041795 | T | C | 230 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(227): Show |
231 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.1337+1349T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19041795 | |||||||
| chr16:19041899 | G | A | 1 | a0001c0006t0006g0180 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1337+1453G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19041899 | |||||||
| chr16:19042168 | C | T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(76): Show |
80 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.1337+1722C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19042168 | |||||||
| chr16:19042285 | C | T | 1 | a0002c0002t0011g0090 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1337+1839C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19042285 | |||||||
| chr16:19042502 | CT | C | 104 | a0001c0001t0001g0229 a0001c0005t0002g0248 a0001c0009t0001g0261 others(101): Show |
104 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1337+2070delT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr16 | 19042502 | ||||||
| chr16:19042516 | T | C | 2 | a0002c0002t0002g0102 a0002c0002t0002g0103 |
2 | HG00323.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1337+2070T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19042516 | |||||||
| chr16:19042517 | C | T | 2 | a0002c0002t0002g0102 a0002c0002t0002g0103 |
2 | HG00323.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1337+2071C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19042517 | |||||||
| chr16:19042538 | C | T | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1337+2092C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19042538 | |||||||
| chr16:19042570 | C | T | 3 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 |
3 | HG02109.hp2 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1337+2124C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19042570 | |||||||
| chr16:19042666 | C | A | 226 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(223): Show |
227 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.1338-2218C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19042666 | |||||||
| chr16:19042701 | G | T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(76): Show |
80 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.1338-2183G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19042701 | |||||||
| chr16:19042772 | A | G | 11 | a0001c0001t0001g0114 a0001c0001t0001g0131 a0001c0001t0001g0132 others(8): Show |
11 | HG01109.hp1 HG01496.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1338-2112A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19042772 | |||||||
| chr16:19042809 | C | T | 2 | a0004c0008t0025g0198 a0004c0012t0032g0189 |
2 | HG02258.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1338-2075C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19042809 | |||||||
| chr16:19042832 | C | T | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0187 others(2): Show |
5 | HG02965.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1338-2052C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19042832 | |||||||
| chr16:19042907 | C | T | 4 | a0001c0001t0003g0001 a0001c0001t0003g0152 a0001c0001t0003g0158 others(1): Show |
5 | HG02486.hp2 HG02809.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1338-1977C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19042907 | |||||||
| chr16:19043041 | C | T | 1 | a0001c0001t0003g0014 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1338-1843C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19043041 | |||||||
| chr16:19043092 | TA | T | 10 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(7): Show |
10 | HG02615.hp2 HG02717.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1338-1781delA | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr16 | 19043092 | ||||||
| chr16:19043245 | C | T | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1338-1639C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19043245 | |||||||
| chr16:19043278 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1338-1606G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19043278 | |||||||
| chr16:19043343 | C | T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(76): Show |
80 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.1338-1541C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19043343 | |||||||
| chr16:19043426 | C | G | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1338-1458C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19043426 | |||||||
| chr16:19043460 | AT | A | 244 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(241): Show |
245 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.1338-1421delT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr16 | 19043460 | ||||||
| chr16:19043563 | A | ATTAT | 82 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(79): Show |
83 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.1338-1302_1338-129 others(8): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr16 | 19043563 | ||||||
| chr16:19044005 | G | T | 1 | a0001c0001t0001g0224 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1338-879G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19044005 | |||||||
| chr16:19044061 | T | C | 5 | a0001c0001t0001g0233 a0001c0001t0001g0238 a0001c0001t0001g0241 others(2): Show |
5 | HG01074.hp1 HG02300.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1338-823T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19044061 | |||||||
| chr16:19044068 | A | G | 32 | a0001c0001t0009g0236 a0001c0006t0018g0155 a0001c0006t0018g0156 others(29): Show |
32 | HG00609.hp1 HG00738.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.1338-816A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19044068 | |||||||
| chr16:19044174 | T | G | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1338-710T>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19044174 | |||||||
| chr16:19044249 | A | C | 31 | a0001c0001t0009g0236 a0001c0006t0018g0155 a0001c0006t0018g0156 others(28): Show |
31 | HG00609.hp1 HG00738.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1338-635A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19044249 | |||||||
| chr16:19044287 | A | C | 1 | a0004c0011t0017g0186 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1338-597A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19044287 | |||||||
| chr16:19044528 | C | G | 225 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(222): Show |
226 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.1338-356C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19044528 | |||||||
| chr16:19044747 | A | G | 244 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(241): Show |
245 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.1338-137A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19044747 | |||||||
| chr16:19044768 | C | CA | 16 | a0001c0001t0003g0013 a0001c0001t0003g0163 a0002c0002t0002g0017 others(13): Show |
16 | HG00558.hp1 HG00558.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1338-91dupA | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr16 | 19044768 | ||||||
| chr16:19044768 | CA | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(123): Show |
127 | HG00423.hp1 HG00609.hp1 HG00609.hp2 others(124): Show |
intron_variant | MODIFIER | c.1338-91delA | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr16 | 19044768 | ||||||
| chr16:19044864 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1338-20C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 9/15 | chr16 | 19044864 | |||||||
| chr16:19045011 | G | A | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1455+10G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 10/15 | chr16 | 19045011 | |||||||
| chr16:19045014 | G | C | 4 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(1): Show |
4 | HG02109.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1455+13G>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 10/15 | chr16 | 19045014 | |||||||
| chr16:19045015 | C | T | 4 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(1): Show |
4 | HG02109.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1455+14C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 10/15 | chr16 | 19045015 | |||||||
| chr16:19045022 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0062 |
2 | HG02132.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1455+21G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 10/15 | chr16 | 19045022 | |||||||
| chr16:19045022 | G | T | 1 | a0002c0002t0002g0092 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1455+21G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 10/15 | chr16 | 19045022 | |||||||
| chr16:19045027 | GCTGGGTG others(7): Show |
G | 1 | a0002c0003t0016g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1455+31_1455+44del others(14): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr16 | 19045027 | ||||||
| chr16:19045282 | C | G | 4 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(1): Show |
4 | HG02109.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1456-59C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 10/15 | chr16 | 19045282 | |||||||
| chr16:19045326 | T | C | 1 | a0002c0002t0002g0101 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1456-15T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 10/15 | chr16 | 19045326 | |||||||
| chr16:19045446 | C | T | 10 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(7): Show |
10 | HG02615.hp2 HG02717.hp1 HG02723.hp2 others(7): Show |
splice_region_variant&intron_variant | LOW | c.1553+8C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 11/15 | chr16 | 19045446 | |||||||
| chr16:19045447 | G | A | 103 | a0001c0005t0002g0248 a0002c0002t0001g0029 a0002c0002t0002g0016 others(100): Show |
103 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1553+9G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 11/15 | chr16 | 19045447 | |||||||
| chr16:19045591 | CT | C | 42 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0004 others(39): Show |
43 | HG00609.hp2 HG00642.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.1553+176delT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr16 | 19045591 | ||||||
| chr16:19045591 | CTT | C | 23 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(20): Show |
23 | HG00423.hp1 HG00735.hp2 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.1553+175_1553+176d others(4): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr16 | 19045591 | ||||||
| chr16:19045591 | CTTT | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(203): Show |
207 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.1553+174_1553+176d others(5): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr16 | 19045591 | ||||||
| chr16:19045807 | A | G | 31 | a0001c0001t0009g0236 a0001c0006t0018g0155 a0001c0006t0018g0156 others(28): Show |
31 | HG00609.hp1 HG00738.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1553+369A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 11/15 | chr16 | 19045807 | |||||||
| chr16:19045885 | C | T | 3 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 |
3 | HG02109.hp2 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1553+447C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 11/15 | chr16 | 19045885 | |||||||
| chr16:19045948 | C | G | 4 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(1): Show |
4 | HG02109.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1553+510C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 11/15 | chr16 | 19045948 | |||||||
| chr16:19046051 | T | G | 1 | a0001c0001t0007g0206 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1553+613T>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 11/15 | chr16 | 19046051 | |||||||
| chr16:19046198 | C | G | 1 | a0004c0008t0025g0198 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1553+760C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 11/15 | chr16 | 19046198 | |||||||
| chr16:19046237 | T | C | 3 | a0001c0001t0001g0217 a0001c0001t0001g0220 a0008c0010t0001g0219 |
3 | HG01975.hp1 HG03017.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1553+799T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 11/15 | chr16 | 19046237 | |||||||
| chr16:19046265 | A | G | 1 | a0001c0006t0006g0180 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1554-798A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 11/15 | chr16 | 19046265 | |||||||
| chr16:19046313 | A | T | 11 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(8): Show |
11 | HG01081.hp2 HG02615.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1554-750A>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 11/15 | chr16 | 19046313 | |||||||
| chr16:19046522 | G | C | 1 | a0002c0003t0016g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1554-541G>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 11/15 | chr16 | 19046522 | |||||||
| chr16:19046723 | C | G | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1554-340C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 11/15 | chr16 | 19046723 | |||||||
| chr16:19046832 | C | CA | 11 | a0001c0001t0003g0158 a0001c0001t0003g0173 a0001c0001t0006g0011 others(8): Show |
11 | HG00741.hp1 HG01884.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1554-215dupA | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr16 | 19046832 | ||||||
| chr16:19046832 | CA | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(61): Show |
65 | HG00423.hp1 HG00639.hp1 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.1554-215delA | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr16 | 19046832 | ||||||
| chr16:19046863 | G | C | 233 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(230): Show |
234 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.1554-200G>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 11/15 | chr16 | 19046863 | |||||||
| chr16:19046903 | G | A | 1 | a0002c0002t0002g0067 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1554-160G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 11/15 | chr16 | 19046903 | |||||||
| chr16:19046990 | T | A | 2 | a0002c0002t0002g0105 a0002c0013t0037g0081 |
2 | HG00408.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1554-73T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 11/15 | chr16 | 19046990 | |||||||
| chr16:19047400 | C | CT | 14 | a0001c0001t0001g0039 a0001c0001t0001g0074 a0001c0001t0001g0242 others(11): Show |
14 | HG01361.hp2 HG01934.hp1 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.1740+166dupT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr16 | 19047400 | ||||||
| chr16:19047626 | A | G | 1 | a0004c0008t0025g0198 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1740+377A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19047626 | |||||||
| chr16:19047631 | A | G | 225 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(222): Show |
226 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.1740+382A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19047631 | |||||||
| chr16:19047641 | C | T | 1 | a0001c0001t0003g0013 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1740+392C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19047641 | |||||||
| chr16:19047691 | G | A | 1 | a0002c0002t0002g0051 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1740+442G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19047691 | |||||||
| chr16:19047713 | AT | A | 126 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(123): Show |
127 | HG00323.hp1 HG00609.hp1 HG00639.hp1 others(124): Show |
intron_variant | MODIFIER | c.1740+481delT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr16 | 19047713 | ||||||
| chr16:19047713 | ATT | A | 96 | a0001c0005t0002g0248 a0002c0002t0001g0029 a0002c0002t0002g0016 others(93): Show |
96 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.1740+480_1740+481d others(4): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr16 | 19047713 | ||||||
| chr16:19047721 | T | G | 1 | a0002c0002t0002g0083 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1740+472T>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19047721 | |||||||
| chr16:19047781 | C | T | 1 | a0002c0003t0004g0147 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1740+532C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19047781 | |||||||
| chr16:19047804 | C | G | 1 | a0004c0008t0025g0198 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1740+555C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19047804 | |||||||
| chr16:19048055 | T | G | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0187 others(2): Show |
5 | HG02965.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1740+806T>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19048055 | |||||||
| chr16:19048137 | A | AT | 28 | a0001c0001t0001g0278 a0001c0001t0009g0236 a0002c0003t0004g0115 others(25): Show |
28 | HG00609.hp1 HG01884.hp2 HG01934.hp2 others(25): Show |
intron_variant | MODIFIER | c.1740+903dupT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr16 | 19048137 | ||||||
| chr16:19048137 | AT | A | 6 | a0001c0001t0001g0246 a0001c0001t0003g0179 a0001c0001t0003g0195 others(3): Show |
6 | HG01256.hp2 HG01975.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1740+903delT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr16 | 19048137 | ||||||
| chr16:19048234 | A | C | 239 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(236): Show |
240 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1740+985A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19048234 | |||||||
| chr16:19048267 | C | T | 2 | a0002c0002t0002g0085 a0002c0002t0002g0086 |
2 | HG01167.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1740+1018C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19048267 | |||||||
| chr16:19048333 | C | G | 5 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(2): Show |
5 | HG01081.hp2 HG02109.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1740+1084C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19048333 | |||||||
| chr16:19048846 | C | T | 1 | a0002c0002t0002g0223 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1740+1597C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19048846 | |||||||
| chr16:19049084 | C | T | 66 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(63): Show |
67 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.1740+1835C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19049084 | |||||||
| chr16:19049177 | C | A | 29 | a0001c0005t0002g0248 a0002c0002t0002g0016 a0002c0002t0002g0063 others(26): Show |
29 | HG00408.hp1 HG00558.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.1740+1928C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19049177 | |||||||
| chr16:19049215 | C | G | 229 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(226): Show |
230 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.1740+1966C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19049215 | |||||||
| chr16:19049238 | G | A | 5 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(2): Show |
5 | HG02615.hp2 HG02723.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1740+1989G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19049238 | |||||||
| chr16:19049243 | C | T | 1 | a0002c0002t0002g0045 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1740+1994C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19049243 | |||||||
| chr16:19049449 | C | T | 27 | a0001c0001t0009g0236 a0002c0003t0004g0115 a0002c0003t0004g0117 others(24): Show |
27 | HG00609.hp1 HG01884.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.1740+2200C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19049449 | |||||||
| chr16:19049540 | G | A | 229 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(226): Show |
230 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.1741-2146G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19049540 | |||||||
| chr16:19049626 | C | T | 229 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(226): Show |
230 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.1741-2060C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19049626 | |||||||
| chr16:19049707 | T | A | 1 | a0003c0004t0006g0252 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1741-1979T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19049707 | |||||||
| chr16:19049731 | C | T | 1 | a0002c0002t0002g0071 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1741-1955C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19049731 | |||||||
| chr16:19049797 | C | T | 20 | a0002c0003t0004g0115 a0002c0003t0004g0117 a0002c0003t0004g0118 others(17): Show |
20 | HG00609.hp1 HG01934.hp2 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.1741-1889C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19049797 | |||||||
| chr16:19049873 | C | G | 1 | a0002c0002t0002g0092 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1741-1813C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19049873 | |||||||
| chr16:19050093 | C | T | 12 | a0001c0001t0001g0213 a0001c0001t0001g0221 a0001c0001t0001g0224 others(9): Show |
12 | HG01074.hp1 HG02300.hp2 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.1741-1593C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19050093 | |||||||
| chr16:19050120 | C | G | 1 | a0004c0008t0025g0198 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1741-1566C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19050120 | |||||||
| chr16:19050144 | G | A | 1 | a0002c0002t0002g0218 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1741-1542G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19050144 | |||||||
| chr16:19050229 | G | A | 6 | a0001c0001t0007g0205 a0003c0004t0003g0251 a0003c0004t0006g0252 others(3): Show |
6 | HG02451.hp1 HG02622.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1741-1457G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19050229 | |||||||
| chr16:19050240 | G | A | 1 | a0002c0003t0016g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1741-1446G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19050240 | |||||||
| chr16:19050263 | C | T | 2 | a0005c0007t0013g0200 a0005c0007t0013g0202 |
2 | HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1741-1423C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19050263 | |||||||
| chr16:19050362 | G | A | 66 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(63): Show |
67 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.1741-1324G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19050362 | |||||||
| chr16:19050366 | C | CA | 19 | a0001c0001t0003g0006 a0001c0001t0003g0013 a0001c0001t0003g0152 others(16): Show |
19 | HG00609.hp2 HG02055.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.1741-1294dupA | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr16 | 19050366 | ||||||
| chr16:19050366 | CA | C | 61 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(58): Show |
61 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1741-1294delA | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr16 | 19050366 | ||||||
| chr16:19050366 | CAA | C | 106 | a0001c0001t0001g0069 a0001c0001t0001g0185 a0001c0001t0001g0220 others(103): Show |
106 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.1741-1295_1741-129 others(6): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr16 | 19050366 | ||||||
| chr16:19050366 | CAAA | C | 47 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(44): Show |
48 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.1741-1296_1741-129 others(7): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr16 | 19050366 | ||||||
| chr16:19050392 | A | C | 2 | a0002c0002t0002g0083 a0002c0003t0004g0143 |
2 | HG01981.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1741-1294A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19050392 | |||||||
| chr16:19050393 | C | A | 1 | a0001c0006t0006g0180 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1741-1293C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19050393 | |||||||
| chr16:19050394 | C | A | 2 | a0002c0002t0002g0083 a0002c0003t0004g0143 |
2 | HG01981.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1741-1292C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19050394 | |||||||
| chr16:19050402 | A | G | 4 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(1): Show |
4 | HG02109.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1741-1284A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19050402 | |||||||
| chr16:19050500 | T | A | 28 | a0001c0001t0001g0114 a0001c0001t0001g0131 a0001c0001t0001g0132 others(25): Show |
28 | HG01074.hp1 HG01109.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.1741-1186T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19050500 | |||||||
| chr16:19050567 | C | T | 2 | a0001c0001t0001g0274 a0001c0001t0001g0277 |
2 | NA18975.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1741-1119C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19050567 | |||||||
| chr16:19050680 | T | A | 1 | a0002c0002t0002g0061 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1741-1006T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19050680 | |||||||
| chr16:19050755 | C | A | 3 | a0001c0006t0018g0155 a0001c0006t0018g0156 a0001c0006t0034g0154 |
3 | HG00738.hp2 HG01074.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1741-931C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19050755 | |||||||
| chr16:19050833 | G | T | 229 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(226): Show |
230 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.1741-853G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19050833 | |||||||
| chr16:19051115 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1741-571C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19051115 | |||||||
| chr16:19051167 | A | C | 1 | a0002c0002t0002g0125 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1741-519A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19051167 | |||||||
| chr16:19051238 | CT | C | 226 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(223): Show |
227 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.1741-434delT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr16 | 19051238 | ||||||
| chr16:19051252 | T | A | 31 | a0001c0001t0009g0236 a0001c0006t0018g0155 a0001c0006t0018g0156 others(28): Show |
31 | HG00609.hp1 HG00738.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1741-434T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19051252 | |||||||
| chr16:19051254 | A | C | 1 | a0002c0002t0002g0087 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1741-432A>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19051254 | |||||||
| chr16:19051352 | T | C | 3 | a0005c0007t0013g0200 a0005c0007t0013g0202 a0005c0007t0021g0203 |
3 | HG02572.hp2 HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1741-334T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19051352 | |||||||
| chr16:19051526 | G | A | 1 | a0003c0004t0006g0253 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1741-160G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 12/15 | chr16 | 19051526 | |||||||
| chr16:19051883 | C | T | 3 | a0005c0007t0013g0200 a0005c0007t0013g0202 a0005c0007t0021g0203 |
3 | HG02572.hp2 HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1871+67C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19051883 | |||||||
| chr16:19051898 | AT | A | 28 | a0001c0001t0001g0234 a0001c0001t0009g0236 a0002c0002t0020g0077 others(25): Show |
28 | HG00609.hp1 HG01884.hp2 HG01934.hp2 others(25): Show |
intron_variant | MODIFIER | c.1871+96delT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr16 | 19051898 | ||||||
| chr16:19051947 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1871+131T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19051947 | |||||||
| chr16:19051961 | C | G | 56 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(53): Show |
57 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.1871+145C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19051961 | |||||||
| chr16:19052183 | T | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(234): Show |
238 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.1871+367T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19052183 | |||||||
| chr16:19052390 | G | A | 1 | a0002c0002t0002g0092 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1871+574G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19052390 | |||||||
| chr16:19052432 | A | G | 1 | a0002c0002t0002g0192 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1871+616A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19052432 | |||||||
| chr16:19052719 | CT | C | 28 | a0001c0001t0001g0114 a0001c0001t0001g0131 a0001c0001t0001g0132 others(25): Show |
28 | HG01074.hp1 HG01109.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.1871+912delT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr16 | 19052719 | ||||||
| chr16:19052880 | T | C | 1 | a0004c0008t0025g0198 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1871+1064T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19052880 | |||||||
| chr16:19052932 | C | T | 57 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(54): Show |
58 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.1871+1116C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19052932 | |||||||
| chr16:19053012 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1871+1196C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19053012 | |||||||
| chr16:19053058 | G | T | 1 | a0002c0002t0002g0043 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1871+1242G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19053058 | |||||||
| chr16:19053307 | C | CT | 230 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(227): Show |
231 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.1871+1501dupT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr16 | 19053307 | ||||||
| chr16:19053422 | A | G | 7 | a0002c0003t0004g0117 a0002c0003t0004g0118 a0002c0003t0004g0119 others(4): Show |
7 | HG02056.hp2 NA18946.hp1 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.1871+1606A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19053422 | |||||||
| chr16:19053543 | A | G | 135 | a0001c0001t0009g0236 a0001c0005t0002g0164 a0001c0005t0002g0165 others(132): Show |
135 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1871+1727A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19053543 | |||||||
| chr16:19053565 | G | A | 2 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1871+1749G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19053565 | |||||||
| chr16:19053810 | T | C | 5 | a0001c0001t0007g0205 a0003c0004t0006g0252 a0003c0004t0006g0253 others(2): Show |
5 | HG02451.hp1 HG02622.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1871+1994T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19053810 | |||||||
| chr16:19053843 | T | G | 4 | a0001c0006t0018g0155 a0001c0006t0018g0156 a0001c0006t0034g0154 others(1): Show |
4 | HG00738.hp2 HG01074.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1871+2027T>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19053843 | |||||||
| chr16:19053849 | CT | C | 109 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(106): Show |
110 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.1871+2049delT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr16 | 19053849 | ||||||
| chr16:19054119 | A | G | 27 | a0001c0001t0009g0236 a0002c0003t0004g0115 a0002c0003t0004g0117 others(24): Show |
27 | HG00609.hp1 HG01884.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.1871+2303A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19054119 | |||||||
| chr16:19054166 | C | T | 1 | a0002c0002t0002g0044 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1871+2350C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19054166 | |||||||
| chr16:19054285 | G | A | 1 | a0005c0007t0021g0203 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1872-2257G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19054285 | |||||||
| chr16:19054379 | C | G | 1 | a0001c0001t0001g0224 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1872-2163C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19054379 | |||||||
| chr16:19054386 | C | T | 28 | a0001c0001t0001g0114 a0001c0001t0001g0131 a0001c0001t0001g0132 others(25): Show |
28 | HG01074.hp1 HG01109.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.1872-2156C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19054386 | |||||||
| chr16:19054612 | G | A | 28 | a0001c0001t0001g0114 a0001c0001t0001g0131 a0001c0001t0001g0132 others(25): Show |
28 | HG01074.hp1 HG01109.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.1872-1930G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19054612 | |||||||
| chr16:19054740 | C | CT | 27 | a0001c0001t0001g0062 a0001c0001t0001g0106 a0001c0001t0001g0193 others(24): Show |
27 | HG00323.hp1 HG00423.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.1872-1780dupT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr16 | 19054740 | ||||||
| chr16:19054740 | CT | C | 115 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(112): Show |
115 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.1872-1780delT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr16 | 19054740 | ||||||
| chr16:19054815 | G | C | 4 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(1): Show |
4 | HG02109.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1872-1727G>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19054815 | |||||||
| chr16:19054819 | A | G | 1 | a0002c0002t0027g0099 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1872-1723A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19054819 | |||||||
| chr16:19054904 | C | T | 1 | a0001c0001t0008g0188 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1872-1638C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19054904 | |||||||
| chr16:19054936 | C | T | 1 | a0002c0002t0019g0190 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1872-1606C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19054936 | |||||||
| chr16:19054945 | G | A | 1 | a0001c0017t0033g0247 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1872-1597G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19054945 | |||||||
| chr16:19054976 | G | A | 3 | a0005c0007t0013g0200 a0005c0007t0013g0202 a0005c0007t0021g0203 |
3 | HG02572.hp2 HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1872-1566G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19054976 | |||||||
| chr16:19055021 | T | G | 28 | a0001c0001t0001g0114 a0001c0001t0001g0131 a0001c0001t0001g0132 others(25): Show |
28 | HG01074.hp1 HG01109.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.1872-1521T>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19055021 | |||||||
| chr16:19055048 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1872-1494A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19055048 | |||||||
| chr16:19055054 | T | C | 3 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 |
3 | HG02109.hp2 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1872-1488T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19055054 | |||||||
| chr16:19055202 | A | G | 31 | a0001c0001t0009g0236 a0001c0006t0018g0155 a0001c0006t0018g0156 others(28): Show |
31 | HG00609.hp1 HG00738.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1872-1340A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19055202 | |||||||
| chr16:19055314 | T | G | 135 | a0001c0001t0009g0236 a0001c0005t0002g0164 a0001c0005t0002g0165 others(132): Show |
135 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1872-1228T>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19055314 | |||||||
| chr16:19055342 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1872-1200C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19055342 | |||||||
| chr16:19055547 | G | A | 6 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(3): Show |
6 | HG02615.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1872-995G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19055547 | |||||||
| chr16:19055566 | C | G | 1 | a0002c0002t0002g0088 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1872-976C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19055566 | |||||||
| chr16:19055605 | G | A | 6 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(3): Show |
6 | HG02615.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1872-937G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19055605 | |||||||
| chr16:19055607 | C | T | 3 | a0005c0007t0013g0200 a0005c0007t0013g0202 a0005c0007t0021g0203 |
3 | HG02572.hp2 HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1872-935C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19055607 | |||||||
| chr16:19055633 | C | A | 239 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(236): Show |
240 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1872-909C>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19055633 | |||||||
| chr16:19055889 | C | G | 1 | a0002c0002t0002g0033 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1872-653C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19055889 | |||||||
| chr16:19056023 | C | G | 1 | a0002c0002t0002g0104 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1872-519C>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19056023 | |||||||
| chr16:19056055 | T | A | 1 | a0002c0002t0024g0199 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1872-487T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19056055 | |||||||
| chr16:19056094 | C | CT | 12 | a0001c0001t0006g0011 a0001c0001t0007g0204 a0001c0001t0007g0205 others(9): Show |
12 | HG02132.hp2 HG02451.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1872-436dupT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr16 | 19056094 | ||||||
| chr16:19056111 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1872-431C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19056111 | |||||||
| chr16:19056112 | G | A | 2 | a0001c0001t0003g0013 a0001c0017t0033g0247 |
2 | HG02622.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1872-430G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19056112 | |||||||
| chr16:19056122 | C | T | 146 | a0001c0001t0009g0236 a0001c0001t0010g0209 a0001c0001t0010g0210 others(143): Show |
146 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.1872-420C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19056122 | |||||||
| chr16:19056197 | C | T | 6 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(3): Show |
6 | HG02615.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1872-345C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19056197 | |||||||
| chr16:19056232 | T | C | 1 | a0002c0003t0016g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1872-310T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19056232 | |||||||
| chr16:19056338 | G | A | 121 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0007g0204 others(118): Show |
121 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1872-204G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19056338 | |||||||
| chr16:19056375 | C | T | 1 | a0002c0003t0004g0140 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1872-167C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19056375 | |||||||
| chr16:19056393 | G | A | 5 | a0001c0001t0007g0205 a0003c0004t0006g0252 a0003c0004t0006g0253 others(2): Show |
5 | HG02451.hp1 HG02622.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1872-149G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 13/15 | chr16 | 19056393 | |||||||
| chr16:19056731 | G | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0228 a0001c0001t0001g0259 others(5): Show |
9 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.2027+34G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/15 | chr16 | 19056731 | |||||||
| chr16:19056784 | T | G | 31 | a0001c0001t0009g0236 a0001c0006t0018g0155 a0001c0006t0018g0156 others(28): Show |
31 | HG00609.hp1 HG00738.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.2027+87T>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/15 | chr16 | 19056784 | |||||||
| chr16:19056968 | AT | A | 154 | a0001c0001t0001g0114 a0001c0001t0001g0131 a0001c0001t0001g0132 others(151): Show |
154 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.2027+272delT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/15 | chr16 | 19056968 | |||||||
| chr16:19057002 | G | T | 28 | a0001c0001t0001g0114 a0001c0001t0001g0131 a0001c0001t0001g0132 others(25): Show |
28 | HG01074.hp1 HG01109.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.2027+305G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/15 | chr16 | 19057002 | |||||||
| chr16:19057012 | G | T | 1 | a0007c0018t0002g0015 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2027+315G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/15 | chr16 | 19057012 | |||||||
| chr16:19057053 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2027+356C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/15 | chr16 | 19057053 | |||||||
| chr16:19057226 | A | G | 3 | a0005c0007t0013g0200 a0005c0007t0013g0202 a0005c0007t0021g0203 |
3 | HG02572.hp2 HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2027+529A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/15 | chr16 | 19057226 | |||||||
| chr16:19057228 | C | T | 1 | a0002c0003t0009g0116 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2027+531C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/15 | chr16 | 19057228 | |||||||
| chr16:19057509 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2027+812A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/15 | chr16 | 19057509 | |||||||
| chr16:19057618 | C | T | 1 | a0002c0002t0002g0043 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2027+921C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/15 | chr16 | 19057618 | |||||||
| chr16:19057947 | A | AT | 109 | a0001c0001t0001g0133 a0001c0001t0003g0153 a0001c0001t0010g0210 others(106): Show |
109 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.2027+1265dupT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr16 | 19057947 | ||||||
| chr16:19057947 | A | ATT | 31 | a0001c0001t0001g0114 a0001c0001t0001g0131 a0001c0001t0001g0132 others(28): Show |
31 | HG00738.hp1 HG01069.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.2027+1264_2027+126 others(6): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr16 | 19057947 | ||||||
| chr16:19057947 | AT | A | 5 | a0001c0001t0007g0205 a0003c0004t0006g0252 a0003c0004t0006g0253 others(2): Show |
5 | HG02451.hp1 HG02622.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2027+1265delT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr16 | 19057947 | ||||||
| chr16:19058044 | ACACCAGG | A | 7 | a0002c0002t0002g0017 a0002c0002t0002g0019 a0002c0002t0002g0040 others(4): Show |
7 | HG01257.hp2 HG01928.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2027+1359_2028-135 others(11): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr16 | 19058044 | ||||||
| chr16:19058071 | C | T | 31 | a0001c0001t0009g0236 a0001c0006t0018g0155 a0001c0006t0018g0156 others(28): Show |
31 | HG00609.hp1 HG00738.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.2028-1345C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/15 | chr16 | 19058071 | |||||||
| chr16:19058129 | C | T | 4 | a0001c0001t0001g0272 a0001c0001t0001g0274 a0001c0001t0001g0277 others(1): Show |
4 | NA18940.hp1 NA18975.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.2028-1287C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/15 | chr16 | 19058129 | |||||||
| chr16:19058131 | C | T | 57 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(54): Show |
58 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.2028-1285C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/15 | chr16 | 19058131 | |||||||
| chr16:19058168 | G | T | 1 | a0002c0003t0009g0116 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2028-1248G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/15 | chr16 | 19058168 | |||||||
| chr16:19058239 | A | G | 4 | a0001c0006t0018g0155 a0001c0006t0018g0156 a0001c0006t0034g0154 others(1): Show |
4 | HG00738.hp2 HG01074.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.2028-1177A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/15 | chr16 | 19058239 | |||||||
| chr16:19058399 | AAAAT | A | 31 | a0001c0001t0009g0236 a0001c0006t0018g0155 a0001c0006t0018g0156 others(28): Show |
31 | HG00609.hp1 HG00738.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.2028-1009_2028-100 others(8): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr16 | 19058399 | ||||||
| chr16:19058486 | A | G | 5 | a0001c0001t0007g0205 a0003c0004t0006g0252 a0003c0004t0006g0253 others(2): Show |
5 | HG02451.hp1 HG02622.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2028-930A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/15 | chr16 | 19058486 | |||||||
| chr16:19058496 | C | T | 3 | a0005c0007t0013g0200 a0005c0007t0013g0202 a0005c0007t0021g0203 |
3 | HG02572.hp2 HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2028-920C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/15 | chr16 | 19058496 | |||||||
| chr16:19058604 | T | C | 1 | a0001c0001t0026g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2028-812T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/15 | chr16 | 19058604 | |||||||
| chr16:19058740 | CTG | C | 4 | a0001c0006t0018g0155 a0001c0006t0018g0156 a0001c0006t0034g0154 others(1): Show |
4 | HG00738.hp2 HG01074.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.2028-674_2028-673d others(4): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr16 | 19058740 | ||||||
| chr16:19059066 | C | T | 3 | a0002c0003t0015g0127 a0002c0003t0015g0128 a0002c0003t0016g0129 |
3 | HG02647.hp1 HG02818.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2028-350C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/15 | chr16 | 19059066 | |||||||
| chr16:19059120 | C | T | 31 | a0001c0001t0009g0236 a0001c0006t0018g0155 a0001c0006t0018g0156 others(28): Show |
31 | HG00609.hp1 HG00738.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.2028-296C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/15 | chr16 | 19059120 | |||||||
| chr16:19059129 | C | T | 1 | a0002c0002t0002g0071 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2028-287C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 14/15 | chr16 | 19059129 | |||||||
| chr16:19059623 | C | T | 3 | a0005c0007t0013g0200 a0005c0007t0013g0202 a0005c0007t0021g0203 |
3 | HG02572.hp2 HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2106+129C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 15/15 | chr16 | 19059623 | |||||||
| chr16:19059643 | G | A | 31 | a0001c0001t0009g0236 a0001c0006t0018g0155 a0001c0006t0018g0156 others(28): Show |
31 | HG00609.hp1 HG00738.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.2106+149G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 15/15 | chr16 | 19059643 | |||||||
| chr16:19059699 | G | C | 5 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(2): Show |
5 | HG01081.hp2 HG02109.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2106+205G>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 15/15 | chr16 | 19059699 | |||||||
| chr16:19059742 | C | T | 3 | a0001c0001t0003g0163 a0001c0001t0003g0169 a0001c0001t0003g0254 |
3 | HG02145.hp1 HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2106+248C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 15/15 | chr16 | 19059742 | |||||||
| chr16:19059829 | T | G | 4 | a0001c0006t0018g0155 a0001c0006t0018g0156 a0001c0006t0034g0154 others(1): Show |
4 | HG00738.hp2 HG01074.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.2106+335T>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 15/15 | chr16 | 19059829 | |||||||
| chr16:19059862 | A | T | 28 | a0001c0001t0001g0114 a0001c0001t0001g0131 a0001c0001t0001g0132 others(25): Show |
28 | HG01074.hp1 HG01109.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.2106+368A>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 15/15 | chr16 | 19059862 | |||||||
| chr16:19059969 | T | C | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0187 others(2): Show |
5 | HG02965.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2106+475T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 15/15 | chr16 | 19059969 | |||||||
| chr16:19059998 | T | C | 3 | a0005c0007t0013g0200 a0005c0007t0013g0202 a0005c0007t0021g0203 |
3 | HG02572.hp2 HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2106+504T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 15/15 | chr16 | 19059998 | |||||||
| chr16:19060110 | G | C | 138 | a0001c0001t0009g0236 a0001c0001t0010g0209 a0001c0001t0010g0210 others(135): Show |
138 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.2106+616G>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 15/15 | chr16 | 19060110 | |||||||
| chr16:19060205 | T | A | 232 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(229): Show |
233 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.2106+711T>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 15/15 | chr16 | 19060205 | |||||||
| chr16:19060244 | G | A | 5 | a0001c0001t0007g0205 a0003c0004t0006g0252 a0003c0004t0006g0253 others(2): Show |
5 | HG02451.hp1 HG02622.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2106+750G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 15/15 | chr16 | 19060244 | |||||||
| chr16:19060416 | G | A | 1 | a0002c0002t0002g0098 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2106+922G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 15/15 | chr16 | 19060416 | |||||||
| chr16:19060434 | G | A | 3 | a0005c0007t0013g0200 a0005c0007t0013g0202 a0005c0007t0021g0203 |
3 | HG02572.hp2 HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2106+940G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 15/15 | chr16 | 19060434 | |||||||
| chr16:19060449 | C | T | 2 | a0001c0001t0001g0227 a0001c0001t0001g0260 |
2 | HG01515.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.2106+955C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 15/15 | chr16 | 19060449 | |||||||
| chr16:19060476 | A | G | 4 | a0001c0001t0003g0001 a0001c0001t0003g0152 a0001c0001t0003g0158 others(1): Show |
5 | HG02486.hp2 HG02809.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2106+982A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 15/15 | chr16 | 19060476 | |||||||
| chr16:19060496 | T | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0228 a0001c0001t0001g0259 others(5): Show |
9 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.2106+1002T>C | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 15/15 | chr16 | 19060496 | |||||||
| chr16:19060592 | A | G | 174 | a0001c0001t0001g0114 a0001c0001t0001g0131 a0001c0001t0001g0132 others(171): Show |
174 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.2106+1098A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 15/15 | chr16 | 19060592 | |||||||
| chr16:19060634 | A | G | 31 | a0001c0001t0009g0236 a0001c0006t0018g0155 a0001c0006t0018g0156 others(28): Show |
31 | HG00609.hp1 HG00738.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.2106+1140A>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 15/15 | chr16 | 19060634 | |||||||
| chr16:19060789 | A | AT | 100 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(97): Show |
101 | HG00323.hp1 HG00639.hp1 HG00673.hp2 others(98): Show |
intron_variant | MODIFIER | c.2107-974dupT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 19060789 | ||||||
| chr16:19060789 | A | ATT | 29 | a0001c0001t0001g0274 a0001c0001t0009g0236 a0001c0001t0010g0209 others(26): Show |
29 | HG00423.hp1 HG00609.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.2107-975_2107-974d others(4): Show |
TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 19060789 | ||||||
| chr16:19060789 | A | T | 3 | a0001c0006t0018g0155 a0001c0006t0018g0156 a0001c0006t0034g0154 |
3 | HG00738.hp2 HG01074.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2107-989A>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 15/15 | chr16 | 19060789 | |||||||
| chr16:19060818 | G | T | 31 | a0001c0001t0009g0236 a0001c0006t0018g0155 a0001c0006t0018g0156 others(28): Show |
31 | HG00609.hp1 HG00738.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.2107-960G>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 15/15 | chr16 | 19060818 | |||||||
| chr16:19060841 | C | T | 112 | a0001c0001t0010g0209 a0001c0001t0010g0210 a0001c0001t0010g0211 others(109): Show |
112 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.2107-937C>T | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 15/15 | chr16 | 19060841 | |||||||
| chr16:19060848 | G | A | 31 | a0001c0001t0009g0236 a0001c0006t0018g0155 a0001c0006t0018g0156 others(28): Show |
31 | HG00609.hp1 HG00738.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.2107-930G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 15/15 | chr16 | 19060848 | |||||||
| chr16:19060999 | CT | C | 88 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0062 others(85): Show |
89 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.2107-762delT | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 19060999 | ||||||
| chr16:19061080 | T | G | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 |
3 | HG01361.hp2 HG01516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2107-698T>G | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 15/15 | chr16 | 19061080 | |||||||
| chr16:19061265 | G | A | 4 | a0001c0006t0018g0155 a0001c0006t0018g0156 a0001c0006t0034g0154 others(1): Show |
4 | HG00738.hp2 HG01074.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.2107-513G>A | TMC7 | ENSG00000170537.13 | transcript | ENST00000304381.10 | protein_coding | 15/15 | chr16 | 19061265 |