Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54868 |
| ensemblid | ENSG00000109066.14 |
| hgncid | 25984 |
| symbol | TMEM104 |
| name | transmembrane protein 104 |
| refseq_nuc | NM_017728.4 |
| refseq_prot | NP_060198.3 |
| ensembl_nuc | ENST00000335464.10 |
| ensembl_prot | ENSP00000334849.5 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 74776499 |
| end | 74839753 |
| strand | + |
| ver | v1.2 |
| region | chr17:74776499-74839753 |
| region5000 | chr17:74771499-74844753 |
| regionname0 | TMEM104_chr17_74776499_74839753 |
| regionname5000 | TMEM104_chr17_74771499_74844753 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 496 | 162 | 56 | 32 | 48 | 7 | 18 | 32 | TMEM104_chr17_74771499_74844753 | TMEM104 | MAGEI others(491): Show |
chr17 | 74771499 | 74844753 |
| a0002 | 1/0 | 496 | 134 | 27 | 29 | 48 | 7 | 22 | 33 | TMEM104_chr17_74771499_74844753 | TMEM104 | MAGEI others(491): Show |
chr17 | 74771499 | 74844753 |
| a0003 | 0/0 | 496 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TMEM104_chr17_74771499_74844753 | TMEM104 | MAGEI others(491): Show |
chr17 | 74771499 | 74844753 |
| a0004 | 0/0 | 496 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | MAGEI others(491): Show |
chr17 | 74771499 | 74844753 |
| a0005 | 0/0 | 496 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | MAGEI others(491): Show |
chr17 | 74771499 | 74844753 |
| a0006 | 0/0 | 496 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | MAGEI others(491): Show |
chr17 | 74771499 | 74844753 |
| a0007 | 0/0 | 496 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | MAGEI others(491): Show |
chr17 | 74771499 | 74844753 |
| a0008 | 0/0 | 496 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | MAGEI others(491): Show |
chr17 | 74771499 | 74844753 |
| a0009 | 0/0 | 496 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | MAGEI others(491): Show |
chr17 | 74771499 | 74844753 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1488 | 144 | 45 | 30 | 43 | 7 | 18 | TMEM104_chr17_74771499_74844753 | TMEM104 | ATGGC others(1483): Show |
chr17 | 74771499 | 74844753 | ||
| a0001c0004 | 0/0 | 1488 | 8 | 7 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | ATGGC others(1483): Show |
chr17 | 74771499 | 74844753 | ||
| a0001c0006 | 0/0 | 1488 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | ATGGC others(1483): Show |
chr17 | 74771499 | 74844753 | ||
| a0001c0008 | 0/0 | 1488 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | ATGGC others(1483): Show |
chr17 | 74771499 | 74844753 | ||
| a0001c0010 | 0/0 | 1488 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | ATGGC others(1483): Show |
chr17 | 74771499 | 74844753 | ||
| a0001c0011 | 0/0 | 1488 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | ATGGC others(1483): Show |
chr17 | 74771499 | 74844753 | ||
| a0001c0012 | 0/0 | 1488 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | ATGGC others(1483): Show |
chr17 | 74771499 | 74844753 | ||
| a0001c0017 | 0/0 | 1488 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | ATGGC others(1483): Show |
chr17 | 74771499 | 74844753 | ||
| a0001c0021 | 0/0 | 1488 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | ATGGC others(1483): Show |
chr17 | 74771499 | 74844753 | ||
| a0002c0002 | 1/0 | 1488 | 113 | 17 | 21 | 45 | 7 | 22 | TMEM104_chr17_74771499_74844753 | TMEM104 | ATGGC others(1483): Show |
chr17 | 74771499 | 74844753 | ||
| a0002c0003 | 0/0 | 1488 | 9 | 0 | 7 | 2 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | ATGGC others(1483): Show |
chr17 | 74771499 | 74844753 | ||
| a0002c0005 | 0/0 | 1488 | 8 | 7 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | ATGGC others(1483): Show |
chr17 | 74771499 | 74844753 | ||
| a0002c0007 | 0/0 | 1488 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | ATGGC others(1483): Show |
chr17 | 74771499 | 74844753 | ||
| a0002c0019 | 0/0 | 1488 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | ATGGC others(1483): Show |
chr17 | 74771499 | 74844753 | ||
| a0003c0009 | 0/0 | 1488 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | ATGGC others(1483): Show |
chr17 | 74771499 | 74844753 | ||
| a0004c0015 | 0/0 | 1488 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | ATGGC others(1483): Show |
chr17 | 74771499 | 74844753 | ||
| a0005c0020 | 0/0 | 1488 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | ATGGC others(1483): Show |
chr17 | 74771499 | 74844753 | ||
| a0006c0013 | 0/0 | 1488 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | ATGGC others(1483): Show |
chr17 | 74771499 | 74844753 | ||
| a0007c0018 | 0/0 | 1488 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | ATGGC others(1483): Show |
chr17 | 74771499 | 74844753 | ||
| a0008c0014 | 0/0 | 1488 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | ATGGC others(1483): Show |
chr17 | 74771499 | 74844753 | ||
| a0009c0016 | 0/0 | 1488 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | ATGGC others(1483): Show |
chr17 | 74771499 | 74844753 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4703 | 11 | 2 | 0 | 7 | 0 | 2 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0001c0001t0002 | 0/0 | 4703 | 61 | 11 | 18 | 19 | 3 | 10 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0001c0001t0003 | 0/0 | 4704 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4699): Show |
chr17 | 74771499 | 74844753 |
| a0001c0001t0004 | 0/0 | 4703 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0001c0001t0005 | 0/0 | 4703 | 18 | 8 | 4 | 0 | 3 | 3 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0001c0001t0006 | 0/0 | 4704 | 13 | 0 | 4 | 5 | 1 | 3 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4699): Show |
chr17 | 74771499 | 74844753 |
| a0001c0001t0007 | 0/0 | 4704 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4699): Show |
chr17 | 74771499 | 74844753 |
| a0001c0001t0008 | 0/0 | 4704 | 6 | 4 | 2 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4699): Show |
chr17 | 74771499 | 74844753 |
| a0001c0001t0009 | 0/0 | 4703 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0001c0001t0010 | 0/0 | 4703 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0001c0001t0014 | 0/0 | 4704 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4699): Show |
chr17 | 74771499 | 74844753 |
| a0001c0001t0015 | 0/0 | 4704 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4699): Show |
chr17 | 74771499 | 74844753 |
| a0001c0001t0017 | 0/0 | 4703 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0001c0001t0019 | 0/0 | 4704 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4699): Show |
chr17 | 74771499 | 74844753 |
| a0001c0001t0020 | 0/0 | 4704 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4699): Show |
chr17 | 74771499 | 74844753 |
| a0001c0001t0021 | 0/0 | 4703 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0001c0001t0022 | 0/0 | 4703 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0001c0001t0023 | 0/0 | 4703 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0001c0001t0024 | 0/0 | 4703 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0001c0001t0025 | 0/0 | 4703 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0001c0001t0026 | 0/0 | 4703 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0001c0001t0027 | 0/1 | 4703 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0001c0001t0028 | 0/0 | 4703 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0001c0001t0029 | 0/0 | 4704 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4699): Show |
chr17 | 74771499 | 74844753 |
| a0001c0004t0011 | 0/0 | 4704 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4699): Show |
chr17 | 74771499 | 74844753 |
| a0001c0004t0012 | 0/0 | 4704 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4699): Show |
chr17 | 74771499 | 74844753 |
| a0001c0004t0013 | 0/0 | 4704 | 3 | 2 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4699): Show |
chr17 | 74771499 | 74844753 |
| a0001c0006t0002 | 0/0 | 4703 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0001c0008t0007 | 0/0 | 4704 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4699): Show |
chr17 | 74771499 | 74844753 |
| a0001c0010t0018 | 0/0 | 4703 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0001c0011t0006 | 0/0 | 4704 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4699): Show |
chr17 | 74771499 | 74844753 |
| a0001c0012t0006 | 0/0 | 4704 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4699): Show |
chr17 | 74771499 | 74844753 |
| a0001c0017t0003 | 0/0 | 4704 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4699): Show |
chr17 | 74771499 | 74844753 |
| a0001c0021t0037 | 0/0 | 4704 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4699): Show |
chr17 | 74771499 | 74844753 |
| a0002c0002t0001 | 1/0 | 4703 | 50 | 7 | 13 | 16 | 2 | 11 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0002c0002t0003 | 0/0 | 4704 | 38 | 0 | 7 | 18 | 5 | 8 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4699): Show |
chr17 | 74771499 | 74844753 |
| a0002c0002t0004 | 0/0 | 4703 | 15 | 6 | 1 | 7 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0002c0002t0007 | 0/0 | 4704 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4699): Show |
chr17 | 74771499 | 74844753 |
| a0002c0002t0016 | 0/0 | 4703 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0002c0002t0017 | 0/0 | 4703 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0002c0002t0030 | 0/0 | 4703 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0002c0002t0031 | 0/0 | 4704 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4699): Show |
chr17 | 74771499 | 74844753 |
| a0002c0002t0032 | 0/0 | 4704 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4699): Show |
chr17 | 74771499 | 74844753 |
| a0002c0002t0035 | 0/0 | 4703 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0002c0002t0036 | 0/0 | 4703 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0002c0003t0001 | 0/0 | 4703 | 8 | 0 | 6 | 2 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0002c0003t0033 | 0/0 | 4703 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0002c0005t0001 | 0/0 | 4703 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0002c0005t0004 | 0/0 | 4703 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0002c0005t0007 | 0/0 | 4704 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4699): Show |
chr17 | 74771499 | 74844753 |
| a0002c0005t0034 | 0/0 | 4703 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0002c0007t0012 | 0/0 | 4704 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4699): Show |
chr17 | 74771499 | 74844753 |
| a0002c0019t0003 | 0/0 | 4704 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4699): Show |
chr17 | 74771499 | 74844753 |
| a0003c0009t0002 | 0/0 | 4703 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0003c0009t0006 | 0/0 | 4704 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4699): Show |
chr17 | 74771499 | 74844753 |
| a0004c0015t0008 | 0/0 | 4704 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4699): Show |
chr17 | 74771499 | 74844753 |
| a0005c0020t0001 | 0/0 | 4703 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0006c0013t0002 | 0/0 | 4703 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0007c0018t0001 | 0/0 | 4703 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0008c0014t0009 | 0/0 | 4703 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4698): Show |
chr17 | 74771499 | 74844753 |
| a0009c0016t0006 | 0/0 | 4704 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | GGAAG others(4699): Show |
chr17 | 74771499 | 74844753 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0005g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0005g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0005g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0005g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0005g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0005g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0005g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0005g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0005g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0005g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0006g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0006g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0006g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0006g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0006g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0006g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0006g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0006g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0006g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0006g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0006g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0006g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0006g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0007g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0008g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0008g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0008g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0008g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0008g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0008g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0009g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0009g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0009g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0009g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0010g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0010g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0010g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0014g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0014g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0014g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0015g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0015g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0017g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0019g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0020g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0021g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0022g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0023g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0024g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0025g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0026g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0027g0040 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0028g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0001t0029g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0004t0011g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0004t0011g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0004t0011g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0004t0011g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0004t0012g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0004t0013g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0004t0013g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0004t0013g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0006t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0006t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0006t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0008t0007g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0008t0007g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0010t0018g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0011t0006g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0012t0006g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0017t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0001c0021t0037g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0004 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0004g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0007g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0007g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0016g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0016g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0017g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0030g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0031g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0032g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0035g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0002t0036g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0003t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0003t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0003t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0003t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0003t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0003t0033g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0005t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0005t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0005t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0005t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0005t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0005t0007g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0005t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0005t0034g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0007t0012g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0007t0012g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0007t0012g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0002c0019t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0003c0009t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0003c0009t0006g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0004c0015t0008g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0005c0020t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0006c0013t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0007c0018t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0008c0014t0009g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| a0009c0016t0006g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0003 | g0106 | EUR | GBR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0099 | EUR | GBR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG00323 | hp1 | a0001 | c0001 | t0006 | g0272 | EUR | FIN | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0211 | EUR | FIN | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0101 | EAS | CHS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | CHS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG00423 | hp2 | a0002 | c0002 | t0003 | g0119 | EAS | CHS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG00438 | hp1 | a0004 | c0015 | t0008 | g0273 | EAS | CHS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG00438 | hp2 | a0002 | c0019 | t0003 | g0148 | EAS | CHS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | CHS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG00544 | hp2 | a0002 | c0002 | t0003 | g0127 | EAS | CHS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG00558 | hp1 | a0001 | c0012 | t0006 | g0202 | EAS | CHS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG00639 | hp1 | a0001 | c0011 | t0006 | g0013 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0030 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG00642 | hp1 | a0001 | c0001 | t0006 | g0253 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG00673 | hp1 | a0001 | c0001 | t0017 | g0081 | EAS | CHS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG00673 | hp2 | a0002 | c0002 | t0003 | g0109 | EAS | CHS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0257 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG00733 | hp2 | a0001 | c0001 | t0008 | g0227 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG00735 | hp1 | a0002 | c0002 | t0003 | g0147 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0149 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0015 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0212 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01069 | hp1 | a0002 | c0005 | t0034 | g0066 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0136 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0093 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0097 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01074 | hp1 | a0001 | c0001 | t0006 | g0033 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01099 | hp2 | a0001 | c0001 | t0015 | g0043 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01106 | hp1 | a0001 | c0004 | t0013 | g0019 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01109 | hp2 | a0001 | c0001 | t0008 | g0223 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01168 | hp2 | a0002 | c0002 | t0003 | g0121 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01175 | hp1 | a0002 | c0002 | t0003 | g0155 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0085 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0246 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01256 | hp1 | a0001 | c0001 | t0006 | g0219 | AMR | CLM | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | CLM | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01257 | hp1 | a0002 | c0002 | t0004 | g0084 | AMR | CLM | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01257 | hp2 | a0001 | c0001 | t0021 | g0245 | AMR | CLM | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01346 | hp1 | a0002 | c0003 | t0001 | g0005 | AMR | CLM | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | CLM | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01361 | hp1 | a0002 | c0002 | t0003 | g0146 | AMR | CLM | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01361 | hp2 | a0001 | c0001 | t0006 | g0251 | AMR | CLM | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01433 | hp1 | a0002 | c0002 | t0003 | g0141 | AMR | CLM | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01433 | hp2 | a0002 | c0003 | t0001 | g0132 | AMR | CLM | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01515 | hp1 | a0002 | c0002 | t0003 | g0110 | EUR | IBS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0216 | EUR | IBS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01516 | hp1 | a0001 | c0001 | t0005 | g0270 | EUR | IBS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0226 | EUR | IBS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01517 | hp1 | a0002 | c0002 | t0003 | g0144 | EUR | IBS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01517 | hp2 | a0001 | c0001 | t0005 | g0260 | EUR | IBS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01884 | hp1 | a0002 | c0002 | t0035 | g0074 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0050 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01891 | hp1 | a0001 | c0004 | t0011 | g0290 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01891 | hp2 | a0002 | c0002 | t0004 | g0163 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0112 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01952 | hp1 | a0002 | c0003 | t0033 | g0103 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01952 | hp2 | a0001 | c0001 | t0005 | g0218 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01975 | hp1 | a0002 | c0003 | t0001 | g0088 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0258 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0124 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02004 | hp1 | a0002 | c0003 | t0001 | g0100 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0123 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02015 | hp2 | a0002 | c0002 | t0003 | g0058 | EAS | KHV | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | KHV | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02027 | hp2 | a0001 | c0001 | t0020 | g0193 | EAS | KHV | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0077 | EAS | KHV | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02055 | hp2 | a0001 | c0004 | t0011 | g0285 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | KHV | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02071 | hp2 | a0002 | c0002 | t0003 | g0105 | EAS | KHV | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | KHV | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0189 | EAS | KHV | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | KHV | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0274 | EAS | KHV | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | KHV | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02145 | hp1 | a0002 | c0002 | t0007 | g0060 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02148 | hp1 | a0002 | c0002 | t0003 | g0130 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02165 | hp1 | a0002 | c0002 | t0004 | g0156 | EAS | CDX | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | CDX | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0047 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0269 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02273 | hp1 | a0002 | c0003 | t0001 | g0005 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0089 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02280 | hp1 | a0001 | c0004 | t0011 | g0289 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0266 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02293 | hp1 | a0002 | c0003 | t0001 | g0104 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0098 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02300 | hp2 | a0005 | c0020 | t0001 | g0079 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02451 | hp1 | a0002 | c0005 | t0007 | g0076 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0137 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02572 | hp1 | a0002 | c0002 | t0004 | g0061 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02572 | hp2 | a0001 | c0001 | t0008 | g0037 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0243 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0230 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02615 | hp1 | a0001 | c0001 | t0010 | g0292 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02615 | hp2 | a0002 | c0005 | t0007 | g0067 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02622 | hp1 | a0001 | c0001 | t0019 | g0281 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02622 | hp2 | a0002 | c0005 | t0004 | g0162 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02630 | hp1 | a0001 | c0010 | t0018 | g0286 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02630 | hp2 | a0001 | c0001 | t0010 | g0293 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0239 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02698 | hp2 | a0002 | c0002 | t0003 | g0125 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02717 | hp1 | a0001 | c0004 | t0012 | g0048 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02717 | hp2 | a0001 | c0021 | t0037 | g0010 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0131 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02735 | hp2 | a0002 | c0002 | t0003 | g0142 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0271 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0176 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02809 | hp1 | a0001 | c0001 | t0009 | g0287 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0038 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02818 | hp2 | a0001 | c0001 | t0025 | g0220 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02886 | hp1 | a0002 | c0005 | t0001 | g0075 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02886 | hp2 | a0001 | c0001 | t0029 | g0018 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02896 | hp1 | a0001 | c0001 | t0009 | g0283 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02896 | hp2 | a0001 | c0008 | t0007 | g0164 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02897 | hp1 | a0001 | c0001 | t0009 | g0282 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02897 | hp2 | a0001 | c0008 | t0007 | g0160 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0228 | AFR | ESN | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02922 | hp2 | a0001 | c0004 | t0013 | g0017 | AFR | ESN | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0072 | AFR | ESN | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02965 | hp2 | a0002 | c0007 | t0012 | g0070 | AFR | ESN | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02970 | hp1 | a0001 | c0004 | t0011 | g0284 | AFR | ESN | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0231 | AFR | ESN | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0238 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0174 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03041 | hp2 | a0002 | c0002 | t0004 | g0064 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03098 | hp1 | a0001 | c0001 | t0008 | g0016 | AFR | MSL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03098 | hp2 | a0002 | c0002 | t0004 | g0165 | AFR | MSL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03130 | hp1 | a0002 | c0007 | t0012 | g0068 | AFR | ESN | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03130 | hp2 | a0001 | c0001 | t0010 | g0002 | AFR | ESN | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0071 | AFR | ESN | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03139 | hp2 | a0002 | c0005 | t0001 | g0062 | AFR | ESN | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03195 | hp1 | a0002 | c0002 | t0007 | g0073 | AFR | ESN | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03195 | hp2 | a0002 | c0007 | t0012 | g0069 | AFR | ESN | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03209 | hp1 | a0001 | c0001 | t0015 | g0020 | AFR | MSL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03209 | hp2 | a0001 | c0001 | t0028 | g0197 | AFR | MSL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03225 | hp1 | a0002 | c0005 | t0007 | g0063 | AFR | MSL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0026 | AFR | MSL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | MSL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0051 | AFR | MSL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03490 | hp1 | a0002 | c0002 | t0003 | g0001 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03490 | hp2 | a0006 | c0013 | t0002 | g0229 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03491 | hp1 | a0001 | c0001 | t0006 | g0242 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0168 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03492 | hp1 | a0002 | c0002 | t0003 | g0001 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0169 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0027 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0046 | AFR | MSL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0053 | AFR | MSL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0159 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0263 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0198 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03688 | hp1 | a0002 | c0002 | t0036 | g0117 | SAS | STU | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03688 | hp2 | a0001 | c0001 | t0006 | g0264 | SAS | STU | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0237 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0128 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03710 | hp1 | a0001 | c0001 | t0006 | g0235 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0111 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | BEB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0139 | SAS | BEB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0118 | SAS | BEB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03834 | hp2 | a0002 | c0002 | t0003 | g0158 | SAS | BEB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0233 | SAS | STU | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG04115 | hp2 | a0002 | c0002 | t0003 | g0129 | SAS | STU | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | BEB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG04184 | hp2 | a0002 | c0002 | t0004 | g0181 | SAS | BEB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | STU | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG04199 | hp2 | a0002 | c0002 | t0003 | g0145 | SAS | STU | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG04204 | hp1 | a0007 | c0018 | t0001 | g0113 | SAS | STU | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG04204 | hp2 | a0002 | c0002 | t0003 | g0078 | SAS | STU | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG04228 | hp1 | a0002 | c0002 | t0032 | g0001 | SAS | STU | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | STU | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18522 | hp1 | a0002 | c0002 | t0004 | g0057 | AFR | YRI | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | YRI | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | CHB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18612 | hp2 | a0001 | c0001 | t0026 | g0205 | EAS | CHB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18747 | hp1 | a0002 | c0002 | t0016 | g0096 | EAS | CHB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | YRI | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18906 | hp2 | a0008 | c0014 | t0009 | g0291 | AFR | YRI | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18947 | hp1 | a0003 | c0009 | t0002 | g0024 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18947 | hp2 | a0003 | c0009 | t0006 | g0012 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18948 | hp1 | a0001 | c0001 | t0014 | g0014 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18948 | hp2 | a0001 | c0001 | t0022 | g0250 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18953 | hp1 | a0002 | c0002 | t0003 | g0179 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18960 | hp1 | a0002 | c0002 | t0004 | g0151 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18960 | hp2 | a0001 | c0001 | t0006 | g0215 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18971 | hp1 | a0001 | c0006 | t0002 | g0206 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18973 | hp2 | a0002 | c0002 | t0003 | g0108 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18975 | hp1 | a0002 | c0002 | t0004 | g0152 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18981 | hp1 | a0002 | c0002 | t0004 | g0102 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18983 | hp1 | a0001 | c0006 | t0002 | g0210 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18983 | hp2 | a0009 | c0016 | t0006 | g0021 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18984 | hp1 | a0002 | c0002 | t0003 | g0126 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18984 | hp2 | a0001 | c0001 | t0014 | g0204 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18986 | hp1 | a0001 | c0001 | t0006 | g0203 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18986 | hp2 | a0002 | c0002 | t0017 | g0092 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18992 | hp1 | a0002 | c0002 | t0031 | g0122 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18995 | hp2 | a0001 | c0001 | t0014 | g0032 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18998 | hp1 | a0001 | c0001 | t0006 | g0195 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18999 | hp1 | a0001 | c0001 | t0024 | g0192 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19002 | hp2 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19003 | hp2 | a0002 | c0002 | t0004 | g0054 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19005 | hp1 | a0002 | c0002 | t0003 | g0095 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19005 | hp2 | a0001 | c0001 | t0023 | g0201 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19007 | hp1 | a0002 | c0003 | t0001 | g0087 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19007 | hp2 | a0001 | c0001 | t0006 | g0252 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19009 | hp1 | a0002 | c0003 | t0001 | g0180 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19009 | hp2 | a0002 | c0002 | t0003 | g0157 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19010 | hp1 | a0001 | c0017 | t0003 | g0185 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19010 | hp2 | a0002 | c0002 | t0003 | g0133 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19030 | hp1 | a0001 | c0001 | t0008 | g0191 | AFR | LWK | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19030 | hp2 | a0002 | c0002 | t0030 | g0161 | AFR | LWK | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19043 | hp1 | a0001 | c0001 | t0009 | g0288 | AFR | LWK | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | LWK | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19056 | hp2 | a0001 | c0006 | t0002 | g0194 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19060 | hp1 | a0002 | c0002 | t0003 | g0173 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19060 | hp2 | a0001 | c0001 | t0006 | g0234 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19064 | hp2 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19068 | hp2 | a0002 | c0002 | t0016 | g0177 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19077 | hp2 | a0002 | c0002 | t0003 | g0175 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19082 | hp1 | a0002 | c0002 | t0003 | g0094 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19087 | hp1 | a0002 | c0002 | t0003 | g0143 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19087 | hp2 | a0002 | c0002 | t0004 | g0055 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19240 | hp1 | a0001 | c0001 | t0010 | g0002 | AFR | YRI | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA19240 | hp2 | a0002 | c0005 | t0001 | g0065 | AFR | YRI | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | ASW | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA20129 | hp2 | a0001 | c0001 | t0010 | g0002 | AFR | ASW | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA20752 | hp1 | a0002 | c0002 | t0003 | g0153 | EUR | TSI | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0154 | EUR | TSI | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA20805 | hp1 | a0001 | c0001 | t0005 | g0236 | EUR | TSI | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA20805 | hp2 | a0002 | c0002 | t0003 | g0114 | EUR | TSI | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0120 | SAS | GIH | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0265 | SAS | GIH | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0116 | AMR | CLM | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG01123 | hp2 | a0002 | c0002 | t0003 | g0107 | AMR | CLM | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0224 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0172 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0034 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0225 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG02559 | hp2 | a0001 | c0004 | t0013 | g0011 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0222 | AFR | MSL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | MSL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | USA | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| HG06807 | hp2 | a0002 | c0002 | t0004 | g0170 | AFR | USA | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18955 | hp1 | a0002 | c0002 | t0004 | g0056 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA18955 | hp2 | a0002 | c0002 | t0003 | g0167 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0059 | AFR | LWK | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0190 | AFR | LWK | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0027 | g0040 | REF | REF | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0004 | REF | REF | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:74788793 | G | A | 6 | a0001 a0003 a0004 others(3): Show |
167 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(164): Show |
missense_variant | MODERATE | c.172G>A | p.Val58Met | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/10 | 318/4703 | 172/1491 | 58/496 | chr17 | 74788793 | |||
| chr17:74790224 | A | G | 1 | a0003 | 2 | NA18947.hp1 NA18947.hp2 |
missense_variant | MODERATE | c.274A>G | p.Thr92Ala | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/10 | 420/4703 | 274/1491 | 92/496 | chr17 | 74790224 | |||
| chr17:74790993 | C | A | 1 | a0007 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.384C>A | p.Asp128Glu | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/10 | 530/4703 | 384/1491 | 128/496 | chr17 | 74790993 | |||
| chr17:74795041 | A | G | 1 | a0009 | 1 | NA18983.hp2 | missense_variant | MODERATE | c.457A>G | p.Ile153Val | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 7/10 | 603/4703 | 457/1491 | 153/496 | chr17 | 74795041 | |||
| chr17:74795600 | C | G | 1 | a0005 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.604C>G | p.Leu202Val | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/10 | 750/4703 | 604/1491 | 202/496 | chr17 | 74795600 | |||
| chr17:74836064 | C | A | 1 | a0007 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.868C>A | p.Leu290Met | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 1014/4703 | 868/1491 | 290/496 | chr17 | 74836064 | |||
| chr17:74836445 | G | A | 1 | a0006 | 1 | HG03490.hp2 | missense_variant | MODERATE | c.1249G>A | p.Asp417Asn | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 1395/4703 | 1249/1491 | 417/496 | chr17 | 74836445 | |||
| chr17:74836502 | G | A | 1 | a0008 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.1306G>A | p.Val436Ile | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 1452/4703 | 1306/1491 | 436/496 | chr17 | 74836502 | |||
| chr17:74836511 | G | A | 1 | a0004 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.1315G>A | p.Ala439Thr | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 1461/4703 | 1315/1491 | 439/496 | chr17 | 74836511 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:74785556 | C | T | 1 | a0001c0021 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.120C>T | p.Ala40Ala | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/10 | 266/4703 | 120/1491 | 40/496 | chr17 | 74785556 | |||
| chr17:74788792 | C | T | 1 | a0002c0005 | 8 | HG01069.hp1 HG02451.hp1 HG02615.hp2 others(5): Show |
synonymous_variant | LOW | c.171C>T | p.Phe57Phe | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/10 | 317/4703 | 171/1491 | 57/496 | chr17 | 74788792 | |||
| chr17:74790238 | C | T | 1 | a0001c0017 | 1 | NA19010.hp1 | synonymous_variant | LOW | c.288C>T | p.Ser96Ser | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/10 | 434/4703 | 288/1491 | 96/496 | chr17 | 74790238 | |||
| chr17:74795581 | T | C | 1 | a0001c0010 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.585T>C | p.Thr195Thr | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/10 | 731/4703 | 585/1491 | 195/496 | chr17 | 74795581 | |||
| chr17:74819842 | C | T | 2 | a0001c0006 a0002c0003 |
12 | HG01346.hp1 HG01433.hp2 HG01952.hp1 others(9): Show |
splice_region_variant&synonymous_variant | LOW | c.729C>T | p.Ile243Ile | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/10 | 875/4703 | 729/1491 | 243/496 | chr17 | 74819842 | |||
| chr17:74835997 | G | A | 1 | a0001c0011 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.801G>A | p.Leu267Leu | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 947/4703 | 801/1491 | 267/496 | chr17 | 74835997 | |||
| chr17:74836186 | C | T | 2 | a0001c0004 a0002c0007 |
11 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
synonymous_variant | LOW | c.990C>T | p.Arg330Arg | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 1136/4703 | 990/1491 | 330/496 | chr17 | 74836186 | |||
| chr17:74836225 | G | A | 1 | a0002c0019 | 1 | HG00438.hp2 | synonymous_variant | LOW | c.1029G>A | p.Ala343Ala | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 1175/4703 | 1029/1491 | 343/496 | chr17 | 74836225 | |||
| chr17:74836366 | G | A | 1 | a0001c0012 | 1 | HG00558.hp1 | synonymous_variant | LOW | c.1170G>A | p.Thr390Thr | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 1316/4703 | 1170/1491 | 390/496 | chr17 | 74836366 | |||
| chr17:74836483 | G | A | 1 | a0001c0008 | 2 | HG02896.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.1287G>A | p.Ala429Ala | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 1433/4703 | 1287/1491 | 429/496 | chr17 | 74836483 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:74776559 | G | C | 30 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(27): Show |
141 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(138): Show |
5_prime_UTR_variant | MODIFIER | c.-86G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/10 | 772 | chr17 | 74776559 | ||||||
| chr17:74776568 | T | C | 6 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0019 others(3): Show |
16 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-77T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/10 | 763 | chr17 | 74776568 | ||||||
| chr17:74777283 | C | A | 1 | a0002c0002t0030 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-48C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/10 | 48 | chr17 | 74777283 | ||||||
| chr17:74836744 | G | A | 4 | a0001c0004t0011 a0001c0004t0012 a0001c0004t0013 others(1): Show |
11 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*57G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 57 | chr17 | 74836744 | ||||||
| chr17:74836789 | G | A | 13 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0014 others(10): Show |
66 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*102G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 102 | chr17 | 74836789 | ||||||
| chr17:74836843 | A | AC | 27 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(24): Show |
97 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*159dupC | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 160 | INFO_REALIGN_3_PRIME | chr17 | 74836843 | |||||
| chr17:74837013 | G | T | 1 | a0002c0002t0036 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*326G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 326 | chr17 | 74837013 | ||||||
| chr17:74837027 | A | G | 2 | a0001c0001t0017 a0002c0002t0017 |
2 | HG00673.hp1 NA18986.hp2 |
3_prime_UTR_variant | MODIFIER | c.*340A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 340 | chr17 | 74837027 | ||||||
| chr17:74837152 | G | A | 1 | a0001c0001t0021 | 1 | HG01257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*465G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 465 | chr17 | 74837152 | ||||||
| chr17:74837205 | C | T | 1 | a0001c0001t0028 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*518C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 518 | chr17 | 74837205 | ||||||
| chr17:74837228 | G | T | 1 | a0002c0002t0016 | 2 | NA18747.hp1 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*541G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 541 | chr17 | 74837228 | ||||||
| chr17:74837336 | C | A | 1 | a0002c0003t0033 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*649C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 649 | chr17 | 74837336 | ||||||
| chr17:74837458 | C | T | 1 | a0002c0002t0032 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*771C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 771 | chr17 | 74837458 | ||||||
| chr17:74837508 | C | A | 1 | a0001c0021t0037 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*821C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 821 | chr17 | 74837508 | ||||||
| chr17:74837587 | C | G | 1 | a0001c0001t0015 | 2 | HG01099.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*900C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 900 | chr17 | 74837587 | ||||||
| chr17:74837679 | T | C | 1 | a0001c0001t0029 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*992T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 992 | chr17 | 74837679 | ||||||
| chr17:74837748 | C | G | 1 | a0001c0021t0037 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1061C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 1061 | chr17 | 74837748 | ||||||
| chr17:74837753 | A | G | 1 | a0002c0002t0035 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1066A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 1066 | chr17 | 74837753 | ||||||
| chr17:74838019 | C | G | 5 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0010 others(2): Show |
44 | HG00639.hp2 HG00738.hp2 HG00741.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1332C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 1332 | chr17 | 74838019 | ||||||
| chr17:74838234 | T | A | 1 | a0002c0002t0031 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1547T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 1547 | chr17 | 74838234 | ||||||
| chr17:74838250 | C | G | 1 | a0001c0001t0026 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1563C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 1563 | chr17 | 74838250 | ||||||
| chr17:74838446 | A | G | 30 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(27): Show |
100 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*1759A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 1759 | chr17 | 74838446 | ||||||
| chr17:74838729 | G | A | 1 | a0001c0001t0014 | 3 | NA18948.hp1 NA18984.hp2 NA18995.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2042G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 2042 | chr17 | 74838729 | ||||||
| chr17:74838734 | C | T | 1 | a0002c0005t0034 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2047C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 2047 | chr17 | 74838734 | ||||||
| chr17:74838815 | C | A | 28 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(25): Show |
98 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*2128C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 2128 | chr17 | 74838815 | ||||||
| chr17:74838820 | C | T | 1 | a0002c0002t0030 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2133C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 2133 | chr17 | 74838820 | ||||||
| chr17:74839085 | G | A | 1 | a0001c0001t0022 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2398G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 2398 | chr17 | 74839085 | ||||||
| chr17:74839349 | G | A | 1 | a0001c0001t0020 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2662G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 2662 | chr17 | 74839349 | ||||||
| chr17:74839424 | G | A | 1 | a0001c0001t0023 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2737G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 2737 | chr17 | 74839424 | ||||||
| chr17:74839448 | C | T | 2 | a0001c0001t0025 a0001c0010t0018 |
2 | HG02630.hp1 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2761C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 2761 | chr17 | 74839448 | ||||||
| chr17:74839500 | C | G | 1 | a0001c0010t0018 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2813C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 2813 | chr17 | 74839500 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:74776582 | T | TGGGTC | 14 | a0001c0001t0009g0282 a0001c0001t0009g0283 a0001c0001t0009g0287 others(11): Show |
16 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-68+19_-68+23dupTC others(3): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 74776582 | ||||||
| chr17:74776629 | G | A | 1 | a0001c0021t0037g0010 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-68+52G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/9 | chr17 | 74776629 | |||||||
| chr17:74776636 | T | TGGGGC | 92 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(89): Show |
94 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.-68+72_-68+76dupGG others(3): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 74776636 | ||||||
| chr17:74776671 | C | T | 2 | a0001c0001t0002g0279 a0001c0001t0002g0280 |
2 | NA19068.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-68+94C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/9 | chr17 | 74776671 | |||||||
| chr17:74776709 | T | C | 145 | a0001c0001t0001g0045 a0001c0001t0002g0003 a0001c0001t0002g0008 others(142): Show |
150 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.-68+132T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/9 | chr17 | 74776709 | |||||||
| chr17:74776710 | T | G | 1 | a0001c0004t0013g0011 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-68+133T>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/9 | chr17 | 74776710 | |||||||
| chr17:74776908 | C | T | 45 | a0001c0001t0002g0009 a0001c0001t0002g0232 a0001c0001t0002g0233 others(42): Show |
46 | HG00323.hp1 HG00438.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.-68+331C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/9 | chr17 | 74776908 | |||||||
| chr17:74776971 | G | A | 74 | a0001c0001t0002g0009 a0001c0001t0002g0196 a0001c0001t0002g0199 others(71): Show |
75 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.-67-293G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/9 | chr17 | 74776971 | |||||||
| chr17:74776976 | A | C | 83 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0196 others(80): Show |
85 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-67-288A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/9 | chr17 | 74776976 | |||||||
| chr17:74777016 | G | T | 1 | a0001c0001t0004g0053 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-67-248G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/9 | chr17 | 74777016 | |||||||
| chr17:74777088 | C | T | 1 | a0001c0001t0002g0052 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-67-176C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/9 | chr17 | 74777088 | |||||||
| chr17:74777154 | C | A | 2 | a0001c0001t0009g0282 a0001c0001t0019g0281 |
2 | HG02622.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-67-110C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/9 | chr17 | 74777154 | |||||||
| chr17:74777194 | A | G | 73 | a0001c0001t0002g0009 a0001c0001t0002g0196 a0001c0001t0002g0199 others(70): Show |
74 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.-67-70A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/9 | chr17 | 74777194 | |||||||
| chr17:74777248 | G | A | 112 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(109): Show |
115 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.-67-16G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/9 | chr17 | 74777248 | |||||||
| chr17:74777499 | T | C | 10 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0039 others(7): Show |
10 | HG01099.hp2 HG01243.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.45+124T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74777499 | |||||||
| chr17:74777655 | C | A | 145 | a0001c0001t0001g0045 a0001c0001t0002g0003 a0001c0001t0002g0008 others(142): Show |
150 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.45+280C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74777655 | |||||||
| chr17:74777745 | C | A | 1 | a0001c0001t0001g0045 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.45+370C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74777745 | |||||||
| chr17:74777772 | A | G | 1 | a0002c0002t0001g0190 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.45+397A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74777772 | |||||||
| chr17:74777846 | G | A | 3 | a0002c0002t0004g0054 a0002c0002t0004g0055 a0002c0002t0004g0056 |
3 | NA18955.hp1 NA19003.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.45+471G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74777846 | |||||||
| chr17:74777850 | G | A | 10 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0039 others(7): Show |
10 | HG01099.hp2 HG01243.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.45+475G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74777850 | |||||||
| chr17:74777874 | G | A | 145 | a0001c0001t0001g0045 a0001c0001t0002g0003 a0001c0001t0002g0008 others(142): Show |
150 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.45+499G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74777874 | |||||||
| chr17:74777989 | T | C | 120 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(117): Show |
123 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.45+614T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74777989 | |||||||
| chr17:74778036 | G | A | 112 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(109): Show |
115 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.45+661G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74778036 | |||||||
| chr17:74778043 | TC | T | 3 | a0001c0001t0002g0221 a0001c0001t0005g0222 a0001c0001t0008g0223 |
3 | HG00738.hp1 HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.45+669delC | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74778043 | |||||||
| chr17:74778073 | TA | T | 12 | a0001c0001t0009g0283 a0001c0001t0009g0287 a0001c0001t0009g0288 others(9): Show |
14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.45+699delA | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74778073 | |||||||
| chr17:74778101 | G | A | 1 | a0002c0002t0004g0057 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.45+726G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74778101 | |||||||
| chr17:74778212 | C | T | 1 | a0002c0002t0001g0189 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.45+837C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74778212 | |||||||
| chr17:74778362 | C | T | 2 | a0001c0001t0002g0044 a0001c0001t0015g0043 |
2 | HG01099.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.45+987C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74778362 | |||||||
| chr17:74778419 | G | A | 112 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(109): Show |
115 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.45+1044G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74778419 | |||||||
| chr17:74778421 | A | G | 21 | a0001c0001t0001g0045 a0001c0001t0002g0035 a0001c0001t0002g0036 others(18): Show |
21 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.45+1046A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74778421 | |||||||
| chr17:74778538 | C | G | 83 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0196 others(80): Show |
85 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.45+1163C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74778538 | |||||||
| chr17:74778599 | C | G | 157 | a0001c0001t0001g0045 a0001c0001t0001g0182 a0001c0001t0001g0183 others(154): Show |
162 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.45+1224C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74778599 | |||||||
| chr17:74778639 | C | CT | 28 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0276 others(25): Show |
28 | HG00408.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.45+1290dupT | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 74778639 | ||||||
| chr17:74778639 | C | CTT | 12 | a0001c0001t0009g0283 a0001c0001t0009g0287 a0001c0001t0009g0288 others(9): Show |
14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.45+1289_45+1290dup others(2): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 74778639 | ||||||
| chr17:74778639 | CT | C | 13 | a0001c0001t0001g0045 a0001c0001t0002g0031 a0001c0001t0002g0042 others(10): Show |
13 | HG01074.hp1 HG01109.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.45+1290delT | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 74778639 | ||||||
| chr17:74778639 | CTT | C | 42 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0023 others(39): Show |
43 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.45+1289_45+1290del others(2): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 74778639 | ||||||
| chr17:74778639 | CTTT | C | 74 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0196 others(71): Show |
76 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.45+1288_45+1290del others(3): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 74778639 | ||||||
| chr17:74778782 | CCCCACCC others(1): Show |
C | 21 | a0001c0001t0001g0045 a0001c0001t0002g0035 a0001c0001t0002g0036 others(18): Show |
21 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.45+1412_45+1419del others(8): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 74778782 | ||||||
| chr17:74778960 | A | G | 145 | a0001c0001t0001g0045 a0001c0001t0002g0003 a0001c0001t0002g0008 others(142): Show |
150 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.45+1585A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74778960 | |||||||
| chr17:74779201 | C | G | 112 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(109): Show |
115 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.45+1826C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74779201 | |||||||
| chr17:74779219 | G | A | 145 | a0001c0001t0001g0045 a0001c0001t0002g0003 a0001c0001t0002g0008 others(142): Show |
150 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.45+1844G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74779219 | |||||||
| chr17:74779279 | C | T | 1 | a0002c0002t0001g0159 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.45+1904C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74779279 | |||||||
| chr17:74779295 | C | T | 2 | a0001c0001t0010g0292 a0001c0001t0010g0293 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.45+1920C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74779295 | |||||||
| chr17:74779375 | G | C | 1 | a0001c0004t0013g0011 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.45+2000G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74779375 | |||||||
| chr17:74779497 | G | A | 1 | a0002c0002t0001g0189 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.45+2122G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74779497 | |||||||
| chr17:74779529 | G | A | 1 | a0003c0009t0006g0012 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.45+2154G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74779529 | |||||||
| chr17:74779546 | G | A | 1 | a0001c0021t0037g0010 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.45+2171G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74779546 | |||||||
| chr17:74779654 | C | T | 1 | a0002c0002t0003g0158 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.45+2279C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74779654 | |||||||
| chr17:74779772 | A | G | 121 | a0001c0001t0001g0082 a0001c0001t0001g0182 a0001c0001t0001g0183 others(118): Show |
125 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.45+2397A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74779772 | |||||||
| chr17:74779883 | A | C | 2 | a0001c0001t0009g0282 a0001c0001t0019g0281 |
2 | HG02622.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.45+2508A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74779883 | |||||||
| chr17:74780134 | C | T | 1 | a0001c0001t0005g0230 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.45+2759C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74780134 | |||||||
| chr17:74780372 | G | A | 8 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0039 others(5): Show |
8 | HG01243.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.45+2997G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74780372 | |||||||
| chr17:74780549 | G | A | 1 | a0001c0001t0002g0232 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.45+3174G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74780549 | |||||||
| chr17:74780631 | T | C | 8 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0039 others(5): Show |
8 | HG01243.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.45+3256T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74780631 | |||||||
| chr17:74780867 | T | G | 1 | a0001c0001t0002g0233 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.45+3492T>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74780867 | |||||||
| chr17:74780928 | A | G | 1 | a0002c0005t0007g0076 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.45+3553A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74780928 | |||||||
| chr17:74781286 | T | G | 1 | a0001c0011t0006g0013 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.45+3911T>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74781286 | |||||||
| chr17:74781658 | G | T | 1 | a0002c0002t0004g0181 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.46-3824G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74781658 | |||||||
| chr17:74781666 | C | G | 1 | a0001c0001t0002g0269 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.46-3816C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74781666 | |||||||
| chr17:74781668 | C | T | 1 | a0001c0001t0002g0269 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.46-3814C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74781668 | |||||||
| chr17:74781748 | G | C | 1 | a0002c0002t0001g0077 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.46-3734G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74781748 | |||||||
| chr17:74781867 | C | T | 1 | a0002c0002t0003g0157 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.46-3615C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74781867 | |||||||
| chr17:74781906 | G | A | 12 | a0001c0001t0009g0283 a0001c0001t0009g0287 a0001c0001t0009g0288 others(9): Show |
14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.46-3576G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74781906 | |||||||
| chr17:74782073 | C | T | 12 | a0001c0001t0009g0283 a0001c0001t0009g0287 a0001c0001t0009g0288 others(9): Show |
14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.46-3409C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74782073 | |||||||
| chr17:74782109 | C | T | 1 | a0001c0001t0004g0053 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.46-3373C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74782109 | |||||||
| chr17:74782213 | G | T | 1 | a0001c0004t0013g0011 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.46-3269G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74782213 | |||||||
| chr17:74782456 | T | G | 2 | a0002c0002t0003g0078 a0005c0020t0001g0079 |
2 | HG02300.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.46-3026T>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74782456 | |||||||
| chr17:74782462 | G | A | 1 | a0002c0002t0001g0190 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.46-3020G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74782462 | |||||||
| chr17:74782476 | G | A | 1 | a0001c0004t0013g0011 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.46-3006G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74782476 | |||||||
| chr17:74782498 | G | A | 10 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0039 others(7): Show |
10 | HG01099.hp2 HG01243.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.46-2984G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74782498 | |||||||
| chr17:74782665 | G | A | 1 | a0002c0002t0004g0054 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.46-2817G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74782665 | |||||||
| chr17:74782822 | G | A | 12 | a0001c0001t0009g0283 a0001c0001t0009g0287 a0001c0001t0009g0288 others(9): Show |
14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.46-2660G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74782822 | |||||||
| chr17:74783117 | G | A | 10 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0039 others(7): Show |
10 | HG01099.hp2 HG01243.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.46-2365G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74783117 | |||||||
| chr17:74783404 | C | T | 1 | a0002c0002t0004g0156 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.46-2078C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74783404 | |||||||
| chr17:74783721 | C | CT | 45 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0277 others(42): Show |
46 | HG00408.hp1 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.46-1734dupT | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 74783721 | ||||||
| chr17:74783721 | CT | C | 29 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0023 others(26): Show |
30 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.46-1734delT | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 74783721 | ||||||
| chr17:74783721 | CTTT | C | 23 | a0001c0001t0001g0045 a0001c0001t0002g0035 a0001c0001t0002g0036 others(20): Show |
25 | HG01099.hp2 HG01243.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.46-1736_46-1734del others(3): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 74783721 | ||||||
| chr17:74783721 | CTTTT | C | 7 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0049 others(4): Show |
7 | HG01884.hp2 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-1737_46-1734del others(4): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 74783721 | ||||||
| chr17:74783721 | CTTTTTTT others(2): Show |
C | 85 | a0001c0001t0001g0082 a0001c0001t0002g0008 a0001c0001t0002g0009 others(82): Show |
87 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.46-1742_46-1734del others(9): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 74783721 | ||||||
| chr17:74783721 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0004g0053 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.46-1744_46-1734del others(11): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 74783721 | ||||||
| chr17:74783729 | T | C | 1 | a0001c0004t0013g0011 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.46-1753T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74783729 | |||||||
| chr17:74783734 | T | C | 23 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0023 others(20): Show |
24 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.46-1748T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74783734 | |||||||
| chr17:74783762 | G | T | 7 | a0001c0001t0001g0045 a0001c0001t0004g0046 a0001c0001t0004g0047 others(4): Show |
7 | HG01884.hp2 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-1720G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74783762 | |||||||
| chr17:74783791 | C | T | 2 | a0001c0001t0009g0282 a0001c0001t0019g0281 |
2 | HG02622.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.46-1691C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74783791 | |||||||
| chr17:74783930 | T | C | 17 | a0001c0001t0002g0221 a0001c0001t0005g0030 a0001c0001t0005g0222 others(14): Show |
19 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.46-1552T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74783930 | |||||||
| chr17:74783986 | C | T | 21 | a0001c0001t0001g0045 a0001c0001t0002g0035 a0001c0001t0002g0036 others(18): Show |
21 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.46-1496C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74783986 | |||||||
| chr17:74784023 | G | A | 21 | a0001c0001t0001g0045 a0001c0001t0002g0035 a0001c0001t0002g0036 others(18): Show |
21 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.46-1459G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74784023 | |||||||
| chr17:74784038 | T | TA | 112 | a0001c0001t0001g0082 a0001c0001t0002g0003 a0001c0001t0002g0008 others(109): Show |
115 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.46-1431dupA | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 74784038 | ||||||
| chr17:74784052 | C | A | 6 | a0001c0001t0002g0221 a0001c0001t0005g0030 a0001c0001t0005g0222 others(3): Show |
6 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-1430C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74784052 | |||||||
| chr17:74784266 | A | G | 1 | a0002c0002t0003g0158 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.46-1216A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74784266 | |||||||
| chr17:74784352 | G | A | 86 | a0001c0001t0001g0082 a0001c0001t0002g0008 a0001c0001t0002g0009 others(83): Show |
88 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.46-1130G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74784352 | |||||||
| chr17:74784613 | G | A | 1 | a0001c0001t0006g0234 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.46-869G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74784613 | |||||||
| chr17:74784672 | A | G | 1 | a0001c0001t0002g0266 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.46-810A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74784672 | |||||||
| chr17:74784680 | C | A | 12 | a0001c0001t0009g0283 a0001c0001t0009g0287 a0001c0001t0009g0288 others(9): Show |
14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.46-802C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74784680 | |||||||
| chr17:74784691 | T | C | 160 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0182 others(157): Show |
165 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.46-791T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74784691 | |||||||
| chr17:74784788 | C | T | 3 | a0001c0001t0002g0221 a0001c0001t0005g0222 a0001c0001t0008g0223 |
3 | HG00738.hp1 HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.46-694C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74784788 | |||||||
| chr17:74784836 | G | T | 1 | a0002c0002t0003g0155 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.46-646G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74784836 | |||||||
| chr17:74784959 | T | TC | 5 | a0001c0001t0002g0221 a0001c0001t0005g0030 a0001c0001t0005g0222 others(2): Show |
5 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-523_46-522insC | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74784959 | |||||||
| chr17:74784965 | T | A | 5 | a0001c0001t0002g0221 a0001c0001t0005g0030 a0001c0001t0005g0222 others(2): Show |
5 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-517T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74784965 | |||||||
| chr17:74784965 | T | TA | 12 | a0001c0001t0009g0283 a0001c0001t0009g0287 a0001c0001t0009g0288 others(9): Show |
14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.46-517_46-516insA | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74784965 | |||||||
| chr17:74784966 | T | A | 17 | a0001c0001t0002g0221 a0001c0001t0005g0030 a0001c0001t0005g0222 others(14): Show |
19 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.46-516T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74784966 | |||||||
| chr17:74784966 | T | TA | 141 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0182 others(138): Show |
144 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.46-511dupA | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 74784966 | ||||||
| chr17:74785044 | A | G | 1 | a0001c0021t0037g0010 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.46-438A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74785044 | |||||||
| chr17:74785069 | A | G | 150 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0002g0003 others(147): Show |
155 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.46-413A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74785069 | |||||||
| chr17:74785148 | G | T | 2 | a0002c0002t0003g0127 a0002c0002t0003g0175 |
2 | HG00544.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.46-334G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74785148 | |||||||
| chr17:74785153 | C | G | 143 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0182 others(140): Show |
146 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.46-329C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74785153 | |||||||
| chr17:74785288 | G | A | 1 | a0002c0002t0004g0084 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.46-194G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74785288 | |||||||
| chr17:74785642 | T | C | 1 | a0002c0002t0001g0085 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.167+39T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74785642 | |||||||
| chr17:74785655 | A | T | 1 | a0001c0021t0037g0010 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.167+52A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74785655 | |||||||
| chr17:74785673 | G | A | 148 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0002g0003 others(145): Show |
153 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.167+70G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74785673 | |||||||
| chr17:74785722 | G | A | 2 | a0001c0001t0004g0046 a0001c0001t0004g0051 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.167+119G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74785722 | |||||||
| chr17:74785883 | C | A | 2 | a0001c0001t0009g0282 a0001c0001t0019g0281 |
2 | HG02622.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.167+280C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74785883 | |||||||
| chr17:74785885 | C | G | 10 | a0001c0001t0001g0045 a0001c0001t0004g0046 a0001c0001t0004g0047 others(7): Show |
10 | HG01884.hp2 HG02258.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.167+282C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74785885 | |||||||
| chr17:74786077 | T | C | 127 | a0001c0001t0001g0082 a0001c0001t0001g0182 a0001c0001t0001g0183 others(124): Show |
130 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.167+474T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74786077 | |||||||
| chr17:74786098 | C | T | 1 | a0002c0002t0001g0159 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.167+495C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74786098 | |||||||
| chr17:74786229 | G | A | 4 | a0001c0008t0007g0160 a0001c0008t0007g0164 a0002c0002t0001g0059 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.167+626G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74786229 | |||||||
| chr17:74786260 | C | T | 1 | a0001c0001t0002g0280 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.167+657C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74786260 | |||||||
| chr17:74786337 | T | A | 98 | a0001c0001t0001g0082 a0001c0001t0001g0182 a0001c0001t0001g0183 others(95): Show |
100 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.167+734T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74786337 | |||||||
| chr17:74786342 | AGGAGCAC others(2): Show |
A | 89 | a0001c0001t0001g0082 a0001c0001t0001g0182 a0001c0001t0001g0183 others(86): Show |
90 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.167+743_167+751del others(9): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr17 | 74786342 | ||||||
| chr17:74786362 | C | T | 89 | a0001c0001t0001g0082 a0001c0001t0001g0182 a0001c0001t0001g0183 others(86): Show |
90 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.167+759C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74786362 | |||||||
| chr17:74786566 | G | A | 11 | a0001c0001t0001g0045 a0001c0001t0004g0046 a0001c0001t0004g0047 others(8): Show |
11 | HG01884.hp2 HG02258.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.167+963G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74786566 | |||||||
| chr17:74786587 | C | G | 148 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0002g0003 others(145): Show |
153 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.167+984C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74786587 | |||||||
| chr17:74786818 | G | T | 1 | a0001c0004t0013g0011 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.167+1215G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74786818 | |||||||
| chr17:74786999 | G | A | 12 | a0001c0001t0009g0283 a0001c0001t0009g0287 a0001c0001t0009g0288 others(9): Show |
14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.167+1396G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74786999 | |||||||
| chr17:74787012 | GTC | G | 3 | a0002c0007t0012g0068 a0002c0007t0012g0069 a0002c0007t0012g0070 |
3 | HG02965.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.167+1413_167+1414d others(4): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr17 | 74787012 | ||||||
| chr17:74787128 | C | A | 8 | a0001c0001t0002g0233 a0001c0001t0002g0238 a0001c0001t0002g0239 others(5): Show |
8 | HG01074.hp2 HG02258.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.167+1525C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787128 | |||||||
| chr17:74787238 | C | T | 2 | a0001c0001t0010g0292 a0001c0001t0010g0293 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.168-1551C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787238 | |||||||
| chr17:74787246 | T | C | 160 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0182 others(157): Show |
165 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.168-1543T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787246 | |||||||
| chr17:74787297 | AGTCTGCT others(94): Show |
A | 10 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0039 others(7): Show |
10 | HG01099.hp2 HG01243.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.168-1490_168-1390d others(2): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr17 | 74787297 | ||||||
| chr17:74787344 | C | T | 2 | a0002c0002t0003g0145 a0002c0002t0032g0001 |
2 | HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.168-1445C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787344 | |||||||
| chr17:74787349 | G | A | 6 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0207 others(3): Show |
6 | HG00323.hp2 HG00741.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.168-1440G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787349 | |||||||
| chr17:74787361 | A | G | 150 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0182 others(147): Show |
155 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.168-1428A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787361 | |||||||
| chr17:74787394 | A | G | 150 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0182 others(147): Show |
155 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.168-1395A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787394 | |||||||
| chr17:74787426 | T | A | 12 | a0001c0001t0009g0283 a0001c0001t0009g0287 a0001c0001t0009g0288 others(9): Show |
14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.168-1363T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787426 | |||||||
| chr17:74787479 | G | A | 21 | a0001c0001t0001g0045 a0001c0001t0002g0035 a0001c0001t0002g0036 others(18): Show |
21 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.168-1310G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787479 | |||||||
| chr17:74787592 | G | A | 1 | a0001c0001t0002g0241 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.168-1197G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787592 | |||||||
| chr17:74787607 | C | T | 1 | a0001c0004t0013g0011 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.168-1182C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787607 | |||||||
| chr17:74787623 | C | T | 7 | a0001c0001t0001g0045 a0001c0001t0004g0046 a0001c0001t0004g0047 others(4): Show |
7 | HG01884.hp2 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.168-1166C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787623 | |||||||
| chr17:74787628 | CA | C | 158 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0182 others(155): Show |
163 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.168-1146delA | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr17 | 74787628 | ||||||
| chr17:74787630 | A | C | 21 | a0001c0001t0001g0045 a0001c0001t0002g0035 a0001c0001t0002g0036 others(18): Show |
21 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.168-1159A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787630 | |||||||
| chr17:74787659 | A | C | 160 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0182 others(157): Show |
165 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.168-1130A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787659 | |||||||
| chr17:74787682 | G | A | 10 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0039 others(7): Show |
10 | HG01099.hp2 HG01243.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.168-1107G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787682 | |||||||
| chr17:74787797 | C | CT | 104 | a0002c0002t0001g0007 a0002c0002t0001g0077 a0002c0002t0001g0083 others(101): Show |
108 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.168-978dupT | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr17 | 74787797 | ||||||
| chr17:74787797 | CT | C | 159 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0182 others(156): Show |
164 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.168-978delT | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr17 | 74787797 | ||||||
| chr17:74787816 | C | T | 1 | a0002c0002t0003g0158 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.168-973C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787816 | |||||||
| chr17:74787856 | C | T | 160 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0182 others(157): Show |
165 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.168-933C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787856 | |||||||
| chr17:74787985 | G | A | 1 | a0002c0002t0001g0128 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.168-804G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787985 | |||||||
| chr17:74787985 | G | T | 12 | a0001c0001t0009g0283 a0001c0001t0009g0287 a0001c0001t0009g0288 others(9): Show |
14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.168-804G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787985 | |||||||
| chr17:74788029 | T | G | 8 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0039 others(5): Show |
8 | HG01243.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.168-760T>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74788029 | |||||||
| chr17:74788315 | G | A | 1 | a0001c0001t0004g0053 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.168-474G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74788315 | |||||||
| chr17:74788324 | G | A | 1 | a0001c0021t0037g0010 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.168-465G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74788324 | |||||||
| chr17:74788491 | A | G | 160 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0182 others(157): Show |
165 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.168-298A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74788491 | |||||||
| chr17:74788510 | C | T | 88 | a0001c0001t0001g0082 a0001c0001t0001g0182 a0001c0001t0001g0183 others(85): Show |
89 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.168-279C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74788510 | |||||||
| chr17:74788566 | A | C | 1 | a0002c0005t0001g0075 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.168-223A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74788566 | |||||||
| chr17:74788580 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.168-209C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74788580 | |||||||
| chr17:74788588 | G | A | 1 | a0008c0014t0009g0291 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.168-201G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74788588 | |||||||
| chr17:74788596 | G | A | 1 | a0001c0001t0024g0192 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.168-193G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74788596 | |||||||
| chr17:74788705 | G | T | 1 | a0002c0002t0004g0181 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.168-84G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74788705 | |||||||
| chr17:74788718 | A | G | 7 | a0001c0001t0001g0045 a0001c0001t0004g0046 a0001c0001t0004g0047 others(4): Show |
7 | HG01884.hp2 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.168-71A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74788718 | |||||||
| chr17:74788751 | C | A | 1 | a0001c0001t0001g0182 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.168-38C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74788751 | |||||||
| chr17:74788929 | C | T | 1 | a0002c0005t0007g0067 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.249+59C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | chr17 | 74788929 | |||||||
| chr17:74788933 | C | T | 1 | a0001c0001t0004g0053 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.249+63C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | chr17 | 74788933 | |||||||
| chr17:74788958 | A | G | 1 | a0001c0001t0002g0214 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.249+88A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | chr17 | 74788958 | |||||||
| chr17:74789256 | G | A | 10 | a0001c0001t0001g0045 a0001c0001t0004g0046 a0001c0001t0004g0047 others(7): Show |
10 | HG01884.hp2 HG02258.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.249+386G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | chr17 | 74789256 | |||||||
| chr17:74789258 | G | A | 2 | a0002c0003t0001g0087 a0002c0003t0001g0088 |
2 | HG01975.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.249+388G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | chr17 | 74789258 | |||||||
| chr17:74789394 | ATGATG | A | 5 | a0001c0001t0002g0221 a0001c0001t0005g0030 a0001c0001t0005g0222 others(2): Show |
5 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+527_249+531del others(5): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr17 | 74789394 | ||||||
| chr17:74789447 | G | A | 2 | a0001c0001t0009g0282 a0001c0001t0019g0281 |
2 | HG02622.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.249+577G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | chr17 | 74789447 | |||||||
| chr17:74789543 | C | CA | 14 | a0001c0001t0009g0283 a0001c0001t0009g0287 a0001c0001t0009g0288 others(11): Show |
16 | HG01175.hp1 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.250-639dupA | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr17 | 74789543 | ||||||
| chr17:74789543 | CA | C | 135 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0002g0003 others(132): Show |
138 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.250-639delA | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr17 | 74789543 | ||||||
| chr17:74789738 | G | A | 1 | a0002c0002t0004g0055 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.250-462G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | chr17 | 74789738 | |||||||
| chr17:74789809 | C | T | 2 | a0002c0005t0001g0065 a0002c0005t0001g0075 |
2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.250-391C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | chr17 | 74789809 | |||||||
| chr17:74789845 | C | CA | 23 | a0001c0001t0001g0183 a0001c0001t0001g0187 a0001c0001t0001g0277 others(20): Show |
24 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.250-333dupA | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr17 | 74789845 | ||||||
| chr17:74789845 | CA | C | 12 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0039 others(9): Show |
12 | HG01099.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.250-333delA | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr17 | 74789845 | ||||||
| chr17:74789845 | CAA | C | 12 | a0001c0001t0009g0283 a0001c0001t0009g0287 a0001c0001t0009g0288 others(9): Show |
14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-334_250-333del others(2): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr17 | 74789845 | ||||||
| chr17:74789890 | T | C | 160 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0182 others(157): Show |
165 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.250-310T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | chr17 | 74789890 | |||||||
| chr17:74789917 | C | CT | 10 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0039 others(7): Show |
10 | HG01099.hp2 HG01243.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.250-274dupT | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr17 | 74789917 | ||||||
| chr17:74789940 | C | CT | 3 | a0001c0001t0002g0025 a0001c0001t0002g0213 a0001c0001t0004g0053 |
3 | HG02145.hp2 HG03579.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.250-254dupT | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr17 | 74789940 | ||||||
| chr17:74789947 | G | T | 138 | a0001c0001t0001g0082 a0001c0001t0002g0003 a0001c0001t0002g0008 others(135): Show |
143 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.250-253G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | chr17 | 74789947 | |||||||
| chr17:74789955 | G | T | 22 | a0001c0001t0001g0045 a0001c0001t0004g0046 a0001c0001t0004g0047 others(19): Show |
24 | HG00741.hp1 HG01884.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.250-245G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | chr17 | 74789955 | |||||||
| chr17:74789963 | GT | G | 12 | a0001c0001t0009g0283 a0001c0001t0009g0287 a0001c0001t0009g0288 others(9): Show |
14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-230delT | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr17 | 74789963 | ||||||
| chr17:74790018 | A | G | 12 | a0001c0001t0009g0283 a0001c0001t0009g0287 a0001c0001t0009g0288 others(9): Show |
14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-182A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | chr17 | 74790018 | |||||||
| chr17:74790079 | A | G | 1 | a0001c0001t0004g0053 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.250-121A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | chr17 | 74790079 | |||||||
| chr17:74790334 | C | T | 1 | a0001c0001t0002g0266 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.346+38C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/9 | chr17 | 74790334 | |||||||
| chr17:74790384 | C | T | 1 | a0001c0001t0002g0280 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.346+88C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/9 | chr17 | 74790384 | |||||||
| chr17:74790385 | G | A | 1 | a0002c0002t0001g0131 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.346+89G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/9 | chr17 | 74790385 | |||||||
| chr17:74790472 | G | T | 106 | a0002c0002t0001g0007 a0002c0002t0001g0077 a0002c0002t0001g0083 others(103): Show |
110 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.346+176G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/9 | chr17 | 74790472 | |||||||
| chr17:74790609 | G | A | 1 | a0001c0004t0013g0011 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.346+313G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/9 | chr17 | 74790609 | |||||||
| chr17:74790694 | T | C | 1 | a0001c0001t0008g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.347-262T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/9 | chr17 | 74790694 | |||||||
| chr17:74790770 | C | CT | 17 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0035 others(14): Show |
17 | HG00738.hp2 HG01106.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.347-184dupT | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr17 | 74790770 | ||||||
| chr17:74790772 | T | TTA | 3 | a0001c0001t0002g0031 a0001c0001t0005g0034 a0009c0016t0006g0021 |
3 | HG02486.hp2 NA18983.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.347-184_347-183ins others(2): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/9 | chr17 | 74790772 | |||||||
| chr17:74790772 | TA | T | 31 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0002g0211 others(28): Show |
33 | HG00323.hp1 HG00323.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.347-164delA | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr17 | 74790772 | ||||||
| chr17:74790773 | A | T | 118 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(115): Show |
121 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.347-183A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/9 | chr17 | 74790773 | |||||||
| chr17:74790774 | A | T | 20 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0002g0211 others(17): Show |
22 | HG00323.hp1 HG00323.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.347-182A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/9 | chr17 | 74790774 | |||||||
| chr17:74790775 | A | T | 1 | a0001c0001t0009g0283 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.347-181A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/9 | chr17 | 74790775 | |||||||
| chr17:74790776 | A | T | 1 | a0001c0006t0002g0210 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.347-180A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/9 | chr17 | 74790776 | |||||||
| chr17:74790891 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.347-65C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/9 | chr17 | 74790891 | |||||||
| chr17:74791254 | T | TAGCGGAA others(89): Show |
5 | a0001c0001t0002g0221 a0001c0001t0005g0030 a0001c0001t0005g0222 others(2): Show |
5 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.427+225_427+320dup others(96): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 74791254 | ||||||
| chr17:74791324 | G | GGGTCAGG others(25): Show |
1 | a0002c0002t0003g0167 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.427+317_427+348dup others(32): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 74791324 | ||||||
| chr17:74791353 | C | T | 13 | a0001c0001t0009g0283 a0001c0001t0009g0287 a0001c0001t0009g0288 others(10): Show |
15 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.427+317C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791353 | |||||||
| chr17:74791354 | G | A | 1 | a0002c0003t0001g0132 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.427+318G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791354 | |||||||
| chr17:74791355 | G | A | 13 | a0001c0001t0009g0283 a0001c0001t0009g0287 a0001c0001t0009g0288 others(10): Show |
15 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.427+319G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791355 | |||||||
| chr17:74791356 | A | AAGTCAGG others(121): Show |
23 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0023 others(20): Show |
24 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.427+320_427+321ins others(128): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791356 | |||||||
| chr17:74791356 | A | AGGTCAGG others(25): Show |
1 | a0002c0002t0030g0161 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.427+322_427+353dup others(32): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 74791356 | ||||||
| chr17:74791356 | A | G | 13 | a0001c0001t0009g0283 a0001c0001t0009g0287 a0001c0001t0009g0288 others(10): Show |
15 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.427+320A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791356 | |||||||
| chr17:74791358 | GTCAGGAA others(25): Show |
G | 9 | a0001c0001t0001g0045 a0001c0001t0004g0046 a0001c0001t0004g0047 others(6): Show |
9 | HG01884.hp2 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.427+354_427+385del others(32): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 74791358 | ||||||
| chr17:74791385 | T | C | 12 | a0001c0001t0009g0283 a0001c0001t0009g0287 a0001c0001t0009g0288 others(9): Show |
14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.427+349T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791385 | |||||||
| chr17:74791387 | A | G | 12 | a0001c0001t0009g0283 a0001c0001t0009g0287 a0001c0001t0009g0288 others(9): Show |
14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.427+351A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791387 | |||||||
| chr17:74791388 | G | A | 12 | a0001c0001t0009g0283 a0001c0001t0009g0287 a0001c0001t0009g0288 others(9): Show |
14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.427+352G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791388 | |||||||
| chr17:74791390 | T | G | 151 | a0001c0001t0001g0082 a0001c0001t0001g0182 a0001c0001t0001g0183 others(148): Show |
156 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.427+354T>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791390 | |||||||
| chr17:74791459 | G | T | 1 | a0001c0001t0002g0232 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.427+423G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791459 | |||||||
| chr17:74791545 | T | C | 98 | a0001c0001t0001g0082 a0001c0001t0001g0182 a0001c0001t0001g0183 others(95): Show |
100 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.427+509T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791545 | |||||||
| chr17:74791600 | C | A | 1 | a0001c0001t0002g0025 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.427+564C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791600 | |||||||
| chr17:74791680 | C | A | 1 | a0002c0002t0004g0061 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.427+644C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791680 | |||||||
| chr17:74791875 | G | A | 9 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(6): Show |
9 | HG00738.hp2 HG01106.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.427+839G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791875 | |||||||
| chr17:74791893 | T | C | 7 | a0001c0001t0001g0045 a0001c0001t0004g0046 a0001c0001t0004g0047 others(4): Show |
7 | HG01884.hp2 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.427+857T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791893 | |||||||
| chr17:74791912 | C | T | 3 | a0002c0002t0001g0120 a0002c0002t0003g0121 a0002c0002t0003g0125 |
3 | HG01168.hp2 HG02698.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.427+876C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791912 | |||||||
| chr17:74791959 | A | C | 3 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0051 |
3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.427+923A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791959 | |||||||
| chr17:74792033 | C | G | 1 | a0001c0001t0002g0209 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.427+997C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792033 | |||||||
| chr17:74792103 | G | A | 2 | a0001c0001t0009g0282 a0001c0001t0019g0281 |
2 | HG02622.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.427+1067G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792103 | |||||||
| chr17:74792105 | C | T | 5 | a0001c0001t0002g0243 a0001c0001t0002g0265 a0001c0001t0002g0266 others(2): Show |
5 | HG00323.hp1 HG02280.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.427+1069C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792105 | |||||||
| chr17:74792123 | G | A | 10 | a0001c0001t0002g0003 a0001c0001t0002g0025 a0001c0001t0002g0028 others(7): Show |
11 | HG00639.hp1 HG01106.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.427+1087G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792123 | |||||||
| chr17:74792230 | C | T | 87 | a0001c0001t0001g0082 a0001c0001t0002g0008 a0001c0001t0002g0009 others(84): Show |
89 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.427+1194C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792230 | |||||||
| chr17:74792392 | A | G | 2 | a0002c0002t0001g0150 a0002c0002t0003g0119 |
2 | HG00423.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.427+1356A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792392 | |||||||
| chr17:74792494 | C | T | 2 | a0002c0002t0001g0149 a0002c0002t0001g0154 |
2 | HG00735.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.427+1458C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792494 | |||||||
| chr17:74792568 | G | A | 1 | a0001c0001t0004g0053 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.427+1532G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792568 | |||||||
| chr17:74792605 | G | A | 1 | a0002c0002t0001g0089 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.427+1569G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792605 | |||||||
| chr17:74792607 | G | A | 12 | a0001c0001t0009g0283 a0001c0001t0009g0287 a0001c0001t0009g0288 others(9): Show |
14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.427+1571G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792607 | |||||||
| chr17:74792635 | C | G | 2 | a0001c0001t0005g0222 a0001c0001t0008g0223 |
2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.427+1599C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792635 | |||||||
| chr17:74792635 | C | T | 1 | a0002c0002t0030g0161 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.427+1599C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792635 | |||||||
| chr17:74792665 | G | C | 86 | a0001c0001t0001g0082 a0001c0001t0002g0008 a0001c0001t0002g0009 others(83): Show |
88 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.427+1629G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792665 | |||||||
| chr17:74792732 | T | A | 1 | a0002c0002t0003g0133 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.427+1696T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792732 | |||||||
| chr17:74792752 | C | T | 12 | a0001c0001t0009g0283 a0001c0001t0009g0287 a0001c0001t0009g0288 others(9): Show |
14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.427+1716C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792752 | |||||||
| chr17:74792907 | G | A | 1 | a0001c0021t0037g0010 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.427+1871G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792907 | |||||||
| chr17:74792999 | C | T | 1 | a0002c0002t0004g0084 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.427+1963C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792999 | |||||||
| chr17:74793094 | C | G | 2 | a0002c0002t0001g0118 a0002c0002t0036g0117 |
2 | HG03688.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.428-1918C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74793094 | |||||||
| chr17:74793173 | C | T | 29 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0023 others(26): Show |
30 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.428-1839C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74793173 | |||||||
| chr17:74793444 | G | A | 1 | a0001c0021t0037g0010 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.428-1568G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74793444 | |||||||
| chr17:74793663 | C | T | 1 | a0002c0002t0001g0116 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.428-1349C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74793663 | |||||||
| chr17:74793676 | G | A | 1 | a0001c0021t0037g0010 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.428-1336G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74793676 | |||||||
| chr17:74793738 | C | G | 1 | a0002c0019t0003g0148 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.428-1274C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74793738 | |||||||
| chr17:74793749 | C | T | 2 | a0002c0002t0001g0166 a0002c0002t0003g0173 |
2 | NA18994.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.428-1263C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74793749 | |||||||
| chr17:74793877 | C | T | 2 | a0002c0005t0007g0067 a0002c0005t0034g0066 |
2 | HG01069.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.428-1135C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74793877 | |||||||
| chr17:74794158 | C | G | 1 | a0002c0002t0001g0115 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.428-854C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794158 | |||||||
| chr17:74794191 | ATTC | A | 4 | a0001c0001t0001g0045 a0001c0001t0004g0049 a0001c0001t0007g0050 others(1): Show |
4 | HG01884.hp2 HG02717.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.428-816_428-814del others(3): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 74794191 | ||||||
| chr17:74794234 | T | C | 290 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0182 others(287): Show |
299 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.428-778T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794234 | |||||||
| chr17:74794247 | C | G | 3 | a0001c0001t0010g0002 a0001c0004t0011g0289 a0001c0004t0011g0290 |
5 | HG01891.hp1 HG02280.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.428-765C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794247 | |||||||
| chr17:74794327 | G | A | 1 | a0001c0021t0037g0010 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.428-685G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794327 | |||||||
| chr17:74794399 | G | A | 12 | a0001c0001t0009g0283 a0001c0001t0009g0287 a0001c0001t0009g0288 others(9): Show |
14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.428-613G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794399 | |||||||
| chr17:74794401 | A | G | 1 | a0001c0001t0007g0050 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.428-611A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794401 | |||||||
| chr17:74794424 | G | A | 111 | a0001c0001t0001g0082 a0001c0001t0002g0003 a0001c0001t0002g0008 others(108): Show |
114 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.428-588G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794424 | |||||||
| chr17:74794494 | G | A | 1 | a0001c0001t0004g0053 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.428-518G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794494 | |||||||
| chr17:74794544 | C | T | 5 | a0001c0001t0002g0221 a0001c0001t0005g0030 a0001c0001t0005g0222 others(2): Show |
5 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.428-468C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794544 | |||||||
| chr17:74794603 | T | G | 1 | a0002c0002t0004g0057 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.428-409T>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794603 | |||||||
| chr17:74794604 | AGAGCCCG others(27): Show |
A | 1 | a0002c0002t0004g0057 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.428-407_428-374del others(34): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794604 | |||||||
| chr17:74794625 | C | G | 12 | a0001c0001t0009g0283 a0001c0001t0009g0287 a0001c0001t0009g0288 others(9): Show |
14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.428-387C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794625 | |||||||
| chr17:74794698 | A | T | 14 | a0001c0001t0004g0053 a0001c0001t0009g0283 a0001c0001t0009g0287 others(11): Show |
16 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.428-314A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794698 | |||||||
| chr17:74794780 | C | T | 2 | a0002c0005t0001g0065 a0002c0005t0001g0075 |
2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.428-232C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794780 | |||||||
| chr17:74794797 | T | A | 5 | a0001c0001t0002g0221 a0001c0001t0005g0030 a0001c0001t0005g0222 others(2): Show |
5 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.428-215T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794797 | |||||||
| chr17:74794949 | A | AG | 172 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0184 others(169): Show |
177 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.428-63_428-62insG | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794949 | |||||||
| chr17:74794950 | A | G | 8 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0187 others(5): Show |
8 | HG00408.hp1 HG01069.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.428-62A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794950 | |||||||
| chr17:74795125 | T | C | 1 | a0001c0001t0028g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.527+14T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 7/9 | chr17 | 74795125 | |||||||
| chr17:74795127 | G | A | 215 | a0001c0001t0001g0082 a0001c0001t0001g0182 a0001c0001t0001g0183 others(212): Show |
222 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.527+16G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 7/9 | chr17 | 74795127 | |||||||
| chr17:74795470 | A | G | 3 | a0001c0001t0006g0195 a0001c0001t0017g0081 a0001c0001t0020g0193 |
3 | HG00673.hp1 HG02027.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.528-54A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 7/9 | chr17 | 74795470 | |||||||
| chr17:74795479 | A | G | 211 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0182 others(208): Show |
219 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.528-45A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 7/9 | chr17 | 74795479 | |||||||
| chr17:74795738 | A | G | 1 | a0002c0005t0007g0063 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.636+106A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74795738 | |||||||
| chr17:74795763 | A | G | 1 | a0002c0005t0007g0063 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.636+131A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74795763 | |||||||
| chr17:74795799 | G | A | 1 | a0002c0002t0003g0126 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.636+167G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74795799 | |||||||
| chr17:74795932 | G | A | 93 | a0001c0001t0001g0082 a0001c0001t0001g0275 a0001c0001t0002g0035 others(90): Show |
95 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.636+300G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74795932 | |||||||
| chr17:74796029 | G | A | 1 | a0002c0002t0001g0118 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.636+397G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74796029 | |||||||
| chr17:74796045 | G | A | 65 | a0001c0001t0001g0184 a0001c0001t0001g0188 a0001c0001t0002g0008 others(62): Show |
68 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.636+413G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74796045 | |||||||
| chr17:74796104 | C | G | 2 | a0001c0001t0001g0183 a0001c0001t0001g0187 |
2 | HG00408.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.636+472C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74796104 | |||||||
| chr17:74796149 | G | A | 2 | a0001c0001t0002g0254 a0001c0001t0003g0274 |
2 | HG01256.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.636+517G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74796149 | |||||||
| chr17:74796387 | G | A | 1 | a0001c0001t0002g0267 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.636+755G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74796387 | |||||||
| chr17:74796614 | A | G | 80 | a0001c0001t0001g0275 a0001c0001t0002g0029 a0001c0001t0002g0035 others(77): Show |
82 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.636+982A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74796614 | |||||||
| chr17:74796806 | G | A | 1 | a0002c0002t0035g0074 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.636+1174G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74796806 | |||||||
| chr17:74796976 | G | A | 1 | a0002c0005t0007g0063 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.636+1344G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74796976 | |||||||
| chr17:74797130 | G | A | 1 | a0001c0001t0006g0242 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.636+1498G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74797130 | |||||||
| chr17:74797259 | C | T | 4 | a0001c0001t0002g0035 a0001c0001t0002g0042 a0001c0001t0005g0026 others(1): Show |
4 | HG01109.hp2 HG01243.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.636+1627C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74797259 | |||||||
| chr17:74797422 | A | T | 3 | a0001c0021t0037g0010 a0002c0002t0001g0059 a0002c0002t0004g0165 |
3 | HG02717.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.636+1790A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74797422 | |||||||
| chr17:74797429 | G | A | 1 | a0002c0002t0004g0061 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.636+1797G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74797429 | |||||||
| chr17:74797529 | G | A | 1 | a0001c0001t0002g0213 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.636+1897G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74797529 | |||||||
| chr17:74797594 | A | G | 109 | a0001c0001t0001g0275 a0001c0001t0002g0029 a0001c0001t0002g0035 others(106): Show |
111 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.636+1962A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74797594 | |||||||
| chr17:74797640 | G | A | 1 | a0007c0018t0001g0113 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.636+2008G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74797640 | |||||||
| chr17:74797644 | G | A | 1 | a0001c0001t0004g0049 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.636+2012G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74797644 | |||||||
| chr17:74797819 | C | T | 1 | a0001c0001t0002g0208 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.636+2187C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74797819 | |||||||
| chr17:74797859 | C | G | 1 | a0001c0001t0008g0037 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.636+2227C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74797859 | |||||||
| chr17:74797862 | G | A | 1 | a0002c0002t0004g0061 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.636+2230G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74797862 | |||||||
| chr17:74797974 | T | G | 2 | a0001c0001t0023g0201 a0001c0006t0002g0194 |
2 | NA19005.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.636+2342T>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74797974 | |||||||
| chr17:74798079 | G | A | 2 | a0001c0001t0019g0281 a0002c0002t0004g0061 |
2 | HG02572.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.636+2447G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74798079 | |||||||
| chr17:74798235 | A | G | 78 | a0001c0001t0001g0275 a0001c0001t0002g0035 a0001c0001t0002g0042 others(75): Show |
80 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.636+2603A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74798235 | |||||||
| chr17:74798518 | C | T | 8 | a0001c0001t0008g0016 a0001c0001t0015g0020 a0001c0001t0015g0043 others(5): Show |
8 | HG01099.hp2 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.636+2886C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74798518 | |||||||
| chr17:74798534 | C | A | 3 | a0001c0001t0009g0287 a0001c0001t0009g0288 a0008c0014t0009g0291 |
3 | HG02809.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.636+2902C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74798534 | |||||||
| chr17:74798579 | G | A | 1 | a0002c0002t0035g0074 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.636+2947G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74798579 | |||||||
| chr17:74798883 | AAC | A | 8 | a0001c0001t0002g0035 a0001c0001t0002g0042 a0001c0001t0005g0026 others(5): Show |
8 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.636+3255_636+3256d others(4): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr17 | 74798883 | ||||||
| chr17:74799059 | A | G | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.636+3427A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74799059 | |||||||
| chr17:74799179 | G | A | 1 | a0001c0001t0005g0015 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.636+3547G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74799179 | |||||||
| chr17:74799190 | GCTGAAAG others(3): Show |
G | 1 | a0001c0001t0028g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.636+3571_636+3580d others(12): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr17 | 74799190 | ||||||
| chr17:74799326 | C | T | 14 | a0001c0001t0004g0046 a0001c0001t0004g0049 a0001c0001t0004g0051 others(11): Show |
14 | HG01099.hp2 HG02055.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.636+3694C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74799326 | |||||||
| chr17:74799332 | T | G | 4 | a0002c0002t0004g0054 a0002c0002t0004g0055 a0002c0002t0004g0056 others(1): Show |
4 | NA18955.hp1 NA18981.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.636+3700T>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74799332 | |||||||
| chr17:74799634 | C | T | 3 | a0001c0001t0004g0046 a0001c0001t0004g0049 a0001c0001t0004g0051 |
3 | HG03486.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.636+4002C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74799634 | |||||||
| chr17:74799775 | T | C | 1 | a0002c0002t0004g0181 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.636+4143T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74799775 | |||||||
| chr17:74799905 | C | T | 2 | a0001c0001t0007g0050 a0002c0002t0007g0060 |
2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.636+4273C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74799905 | |||||||
| chr17:74800527 | G | C | 40 | a0001c0001t0001g0188 a0001c0001t0002g0196 a0001c0001t0002g0226 others(37): Show |
42 | HG00544.hp1 HG00639.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.636+4895G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74800527 | |||||||
| chr17:74800528 | C | T | 40 | a0001c0001t0001g0188 a0001c0001t0002g0196 a0001c0001t0002g0226 others(37): Show |
42 | HG00544.hp1 HG00639.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.636+4896C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74800528 | |||||||
| chr17:74800563 | G | A | 78 | a0001c0001t0001g0275 a0001c0001t0002g0035 a0001c0001t0002g0042 others(75): Show |
80 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.636+4931G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74800563 | |||||||
| chr17:74800781 | G | A | 1 | a0001c0001t0002g0199 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.636+5149G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74800781 | |||||||
| chr17:74800795 | T | TG | 124 | a0001c0001t0001g0082 a0001c0001t0001g0275 a0001c0001t0001g0276 others(121): Show |
126 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.636+5164dupG | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr17 | 74800795 | ||||||
| chr17:74800914 | T | C | 1 | a0001c0001t0004g0051 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.636+5282T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74800914 | |||||||
| chr17:74801086 | C | T | 4 | a0001c0001t0008g0027 a0001c0001t0008g0037 a0002c0005t0007g0067 others(1): Show |
4 | HG02451.hp1 HG02572.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.636+5454C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74801086 | |||||||
| chr17:74801227 | G | A | 18 | a0001c0001t0004g0046 a0001c0001t0004g0049 a0001c0001t0004g0051 others(15): Show |
18 | HG01099.hp2 HG02055.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.636+5595G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74801227 | |||||||
| chr17:74801254 | T | C | 17 | a0001c0001t0001g0082 a0001c0001t0001g0276 a0001c0001t0001g0277 others(14): Show |
17 | HG00438.hp1 HG00733.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.636+5622T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74801254 | |||||||
| chr17:74801333 | A | G | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.636+5701A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74801333 | |||||||
| chr17:74801385 | CGAGGTGT others(82): Show |
C | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.636+5807_636+5895d others(91): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr17 | 74801385 | ||||||
| chr17:74801521 | T | C | 1 | a0001c0001t0002g0041 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.636+5889T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74801521 | |||||||
| chr17:74801643 | G | A | 1 | a0002c0002t0030g0161 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.636+6011G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74801643 | |||||||
| chr17:74801764 | A | G | 2 | a0001c0001t0007g0050 a0002c0002t0007g0060 |
2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.636+6132A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74801764 | |||||||
| chr17:74801861 | G | A | 4 | a0001c0001t0008g0027 a0001c0001t0008g0037 a0002c0005t0007g0067 others(1): Show |
4 | HG02451.hp1 HG02572.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.636+6229G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74801861 | |||||||
| chr17:74801968 | G | A | 1 | a0001c0001t0009g0283 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.636+6336G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74801968 | |||||||
| chr17:74801974 | C | A | 1 | a0001c0001t0001g0082 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.636+6342C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74801974 | |||||||
| chr17:74802021 | A | G | 107 | a0001c0001t0001g0275 a0001c0001t0002g0029 a0001c0001t0002g0035 others(104): Show |
109 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.636+6389A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74802021 | |||||||
| chr17:74802082 | G | A | 1 | a0002c0002t0003g0141 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.636+6450G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74802082 | |||||||
| chr17:74802095 | C | T | 78 | a0001c0001t0001g0275 a0001c0001t0002g0035 a0001c0001t0002g0042 others(75): Show |
80 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.636+6463C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74802095 | |||||||
| chr17:74802123 | T | G | 1 | a0002c0002t0004g0156 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.636+6491T>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74802123 | |||||||
| chr17:74802231 | A | G | 3 | a0001c0001t0009g0287 a0001c0001t0009g0288 a0008c0014t0009g0291 |
3 | HG02809.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.636+6599A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74802231 | |||||||
| chr17:74802259 | G | A | 76 | a0001c0001t0001g0275 a0001c0001t0002g0035 a0001c0001t0002g0042 others(73): Show |
78 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.636+6627G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74802259 | |||||||
| chr17:74802293 | A | G | 77 | a0001c0001t0001g0275 a0001c0001t0002g0035 a0001c0001t0002g0042 others(74): Show |
79 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.636+6661A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74802293 | |||||||
| chr17:74802304 | G | A | 2 | a0001c0001t0002g0008 a0001c0001t0002g0023 |
3 | HG00642.hp2 HG01934.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.636+6672G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74802304 | |||||||
| chr17:74802341 | A | G | 1 | a0001c0001t0008g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.636+6709A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74802341 | |||||||
| chr17:74802508 | G | A | 1 | a0001c0001t0002g0247 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.636+6876G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74802508 | |||||||
| chr17:74802539 | G | C | 1 | a0001c0001t0002g0221 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.636+6907G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74802539 | |||||||
| chr17:74802701 | G | T | 1 | a0002c0003t0001g0104 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.636+7069G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74802701 | |||||||
| chr17:74802760 | G | A | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.636+7128G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74802760 | |||||||
| chr17:74802886 | C | T | 1 | a0003c0009t0002g0024 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.636+7254C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74802886 | |||||||
| chr17:74803165 | T | C | 1 | a0002c0005t0034g0066 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.636+7533T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74803165 | |||||||
| chr17:74803201 | G | A | 99 | a0001c0001t0001g0275 a0001c0001t0002g0035 a0001c0001t0002g0042 others(96): Show |
101 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.636+7569G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74803201 | |||||||
| chr17:74803283 | C | G | 1 | a0002c0002t0001g0176 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.636+7651C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74803283 | |||||||
| chr17:74803355 | T | C | 2 | a0001c0001t0007g0050 a0002c0002t0007g0060 |
2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.636+7723T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74803355 | |||||||
| chr17:74803474 | G | A | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.636+7842G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74803474 | |||||||
| chr17:74803499 | A | T | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.636+7867A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74803499 | |||||||
| chr17:74803606 | C | A | 1 | a0001c0001t0005g0034 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.636+7974C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74803606 | |||||||
| chr17:74803702 | A | G | 1 | a0001c0001t0002g0217 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.636+8070A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74803702 | |||||||
| chr17:74803724 | C | T | 1 | a0001c0001t0002g0029 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.636+8092C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74803724 | |||||||
| chr17:74804005 | T | C | 68 | a0001c0001t0001g0275 a0001c0001t0002g0243 a0001c0001t0003g0080 others(65): Show |
70 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.636+8373T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74804005 | |||||||
| chr17:74804011 | A | G | 1 | a0001c0001t0002g0208 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.636+8379A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74804011 | |||||||
| chr17:74804149 | T | C | 4 | a0001c0001t0008g0027 a0001c0001t0008g0037 a0002c0005t0007g0067 others(1): Show |
4 | HG02451.hp1 HG02572.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.636+8517T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74804149 | |||||||
| chr17:74804191 | A | G | 1 | a0002c0005t0007g0063 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.636+8559A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74804191 | |||||||
| chr17:74804195 | G | T | 1 | a0001c0001t0001g0275 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.636+8563G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74804195 | |||||||
| chr17:74804213 | T | A | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.636+8581T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74804213 | |||||||
| chr17:74804288 | T | C | 273 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0182 others(270): Show |
282 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.636+8656T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74804288 | |||||||
| chr17:74804499 | G | A | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.636+8867G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74804499 | |||||||
| chr17:74804615 | G | C | 16 | a0001c0001t0001g0082 a0001c0001t0001g0276 a0001c0001t0001g0277 others(13): Show |
16 | HG00438.hp1 HG00733.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.636+8983G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74804615 | |||||||
| chr17:74804739 | C | T | 1 | a0002c0002t0001g0171 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.636+9107C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74804739 | |||||||
| chr17:74804768 | A | G | 78 | a0001c0001t0001g0275 a0001c0001t0002g0035 a0001c0001t0002g0042 others(75): Show |
80 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.636+9136A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74804768 | |||||||
| chr17:74804808 | G | A | 2 | a0001c0001t0002g0029 a0001c0001t0002g0052 |
2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.636+9176G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74804808 | |||||||
| chr17:74804916 | T | C | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.636+9284T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74804916 | |||||||
| chr17:74804983 | G | A | 74 | a0001c0001t0001g0275 a0001c0001t0002g0035 a0001c0001t0002g0042 others(71): Show |
76 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.636+9351G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74804983 | |||||||
| chr17:74805172 | C | T | 3 | a0002c0002t0003g0006 a0002c0002t0003g0095 a0002c0019t0003g0148 |
4 | HG00438.hp2 NA19002.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.636+9540C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74805172 | |||||||
| chr17:74805248 | T | C | 102 | a0001c0001t0001g0275 a0001c0001t0002g0029 a0001c0001t0002g0035 others(99): Show |
104 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.636+9616T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74805248 | |||||||
| chr17:74805371 | A | C | 3 | a0001c0001t0004g0046 a0001c0001t0004g0049 a0001c0001t0004g0051 |
3 | HG03486.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.636+9739A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74805371 | |||||||
| chr17:74805375 | G | T | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.636+9743G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74805375 | |||||||
| chr17:74805417 | T | C | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.636+9785T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74805417 | |||||||
| chr17:74805470 | G | A | 99 | a0001c0001t0001g0275 a0001c0001t0002g0035 a0001c0001t0002g0042 others(96): Show |
101 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.636+9838G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74805470 | |||||||
| chr17:74805567 | G | C | 99 | a0001c0001t0001g0275 a0001c0001t0002g0035 a0001c0001t0002g0042 others(96): Show |
101 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.636+9935G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74805567 | |||||||
| chr17:74805647 | C | A | 2 | a0001c0001t0002g0029 a0001c0001t0002g0052 |
2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.636+10015C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74805647 | |||||||
| chr17:74805657 | C | T | 2 | a0001c0001t0002g0246 a0002c0002t0001g0120 |
2 | HG01192.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.636+10025C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74805657 | |||||||
| chr17:74805758 | C | T | 1 | a0002c0002t0001g0176 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.636+10126C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74805758 | |||||||
| chr17:74805769 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.636+10137G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74805769 | |||||||
| chr17:74806003 | C | G | 3 | a0001c0001t0009g0287 a0001c0001t0009g0288 a0008c0014t0009g0291 |
3 | HG02809.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.636+10371C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74806003 | |||||||
| chr17:74806054 | T | C | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.636+10422T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74806054 | |||||||
| chr17:74806297 | C | T | 2 | a0001c0001t0002g0029 a0001c0001t0002g0052 |
2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.636+10665C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74806297 | |||||||
| chr17:74806376 | G | A | 1 | a0001c0004t0013g0017 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.636+10744G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74806376 | |||||||
| chr17:74806425 | G | C | 4 | a0001c0001t0008g0027 a0001c0001t0008g0037 a0002c0005t0007g0067 others(1): Show |
4 | HG02451.hp1 HG02572.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.636+10793G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74806425 | |||||||
| chr17:74806497 | C | T | 1 | a0002c0002t0001g0176 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.636+10865C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74806497 | |||||||
| chr17:74806590 | A | T | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.636+10958A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74806590 | |||||||
| chr17:74806626 | T | C | 101 | a0001c0001t0001g0275 a0001c0001t0002g0029 a0001c0001t0002g0035 others(98): Show |
103 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.636+10994T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74806626 | |||||||
| chr17:74806640 | C | T | 3 | a0001c0001t0008g0191 a0001c0001t0015g0020 a0001c0001t0015g0043 |
3 | HG01099.hp2 HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.636+11008C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74806640 | |||||||
| chr17:74806751 | C | T | 1 | a0001c0001t0006g0219 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.636+11119C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74806751 | |||||||
| chr17:74806864 | C | T | 3 | a0001c0001t0004g0053 a0001c0001t0025g0220 a0001c0010t0018g0286 |
3 | HG02630.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.636+11232C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74806864 | |||||||
| chr17:74806888 | G | A | 2 | a0001c0001t0002g0209 a0001c0001t0002g0214 |
2 | HG02040.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.636+11256G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74806888 | |||||||
| chr17:74806930 | C | T | 1 | a0001c0011t0006g0013 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.636+11298C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74806930 | |||||||
| chr17:74807069 | G | T | 2 | a0002c0002t0001g0099 a0002c0002t0001g0116 |
2 | HG00140.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.636+11437G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74807069 | |||||||
| chr17:74807086 | C | G | 3 | a0001c0001t0002g0240 a0001c0001t0005g0236 a0002c0002t0001g0137 |
3 | HG01074.hp2 HG02451.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.636+11454C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74807086 | |||||||
| chr17:74807208 | G | C | 167 | a0001c0001t0001g0082 a0001c0001t0001g0188 a0001c0001t0001g0275 others(164): Show |
171 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.636+11576G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74807208 | |||||||
| chr17:74807386 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.636+11754G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74807386 | |||||||
| chr17:74807443 | G | A | 1 | a0001c0001t0002g0265 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.636+11811G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74807443 | |||||||
| chr17:74807606 | C | G | 1 | a0002c0005t0001g0062 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.636+11974C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74807606 | |||||||
| chr17:74807635 | T | C | 1 | a0001c0001t0002g0035 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.636+12003T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74807635 | |||||||
| chr17:74807755 | C | A | 3 | a0001c0001t0004g0046 a0001c0001t0004g0049 a0001c0001t0004g0051 |
3 | HG03486.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.637-11995C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74807755 | |||||||
| chr17:74807755 | C | T | 14 | a0001c0001t0002g0035 a0001c0001t0002g0042 a0001c0001t0003g0274 others(11): Show |
14 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.637-11995C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74807755 | |||||||
| chr17:74807925 | C | G | 2 | a0001c0001t0002g0029 a0001c0001t0002g0052 |
2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.637-11825C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74807925 | |||||||
| chr17:74807937 | G | A | 1 | a0001c0001t0002g0254 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.637-11813G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74807937 | |||||||
| chr17:74807985 | A | G | 2 | a0001c0001t0002g0029 a0001c0001t0002g0052 |
2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.637-11765A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74807985 | |||||||
| chr17:74808006 | G | A | 1 | a0001c0021t0037g0010 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.637-11744G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74808006 | |||||||
| chr17:74808122 | G | A | 2 | a0001c0001t0002g0029 a0001c0001t0002g0052 |
2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.637-11628G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74808122 | |||||||
| chr17:74808506 | T | G | 7 | a0001c0004t0011g0284 a0001c0004t0011g0285 a0001c0004t0012g0048 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.637-11244T>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74808506 | |||||||
| chr17:74808545 | G | A | 2 | a0001c0001t0008g0191 a0002c0002t0001g0138 |
2 | NA18959.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.637-11205G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74808545 | |||||||
| chr17:74808665 | T | A | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-11085T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74808665 | |||||||
| chr17:74808670 | T | C | 1 | a0008c0014t0009g0291 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.637-11080T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74808670 | |||||||
| chr17:74808688 | C | T | 1 | a0002c0002t0001g0101 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.637-11062C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74808688 | |||||||
| chr17:74808785 | T | C | 6 | a0001c0001t0007g0050 a0001c0004t0011g0284 a0001c0004t0011g0285 others(3): Show |
6 | HG01884.hp2 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.637-10965T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74808785 | |||||||
| chr17:74808935 | G | T | 1 | a0002c0002t0016g0096 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.637-10815G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74808935 | |||||||
| chr17:74809125 | A | G | 1 | a0001c0004t0011g0284 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.637-10625A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74809125 | |||||||
| chr17:74809128 | T | A | 1 | a0001c0001t0004g0053 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.637-10622T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74809128 | |||||||
| chr17:74809144 | G | A | 1 | a0002c0002t0001g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.637-10606G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74809144 | |||||||
| chr17:74809310 | T | C | 2 | a0001c0001t0002g0029 a0001c0001t0002g0052 |
2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.637-10440T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74809310 | |||||||
| chr17:74809588 | G | A | 4 | a0002c0002t0004g0054 a0002c0002t0004g0055 a0002c0002t0004g0056 others(1): Show |
4 | NA18955.hp1 NA18981.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-10162G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74809588 | |||||||
| chr17:74809627 | C | T | 97 | a0001c0001t0001g0275 a0001c0001t0002g0035 a0001c0001t0002g0042 others(94): Show |
99 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.637-10123C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74809627 | |||||||
| chr17:74809644 | C | T | 159 | a0001c0001t0001g0082 a0001c0001t0001g0275 a0001c0001t0001g0276 others(156): Show |
163 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.637-10106C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74809644 | |||||||
| chr17:74809841 | C | T | 2 | a0001c0001t0002g0029 a0001c0001t0002g0052 |
2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.637-9909C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74809841 | |||||||
| chr17:74809966 | G | A | 2 | a0001c0001t0008g0027 a0002c0005t0007g0067 |
2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.637-9784G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74809966 | |||||||
| chr17:74809967 | A | G | 2 | a0001c0001t0007g0050 a0002c0002t0007g0060 |
2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.637-9783A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74809967 | |||||||
| chr17:74810083 | C | T | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-9667C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74810083 | |||||||
| chr17:74810306 | C | T | 1 | a0002c0002t0001g0111 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.637-9444C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74810306 | |||||||
| chr17:74810433 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.637-9317A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74810433 | |||||||
| chr17:74810619 | A | T | 1 | a0002c0002t0031g0122 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.637-9131A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74810619 | |||||||
| chr17:74810701 | C | T | 2 | a0001c0001t0002g0029 a0001c0001t0002g0052 |
2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.637-9049C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74810701 | |||||||
| chr17:74810719 | G | A | 2 | a0001c0001t0002g0209 a0001c0001t0002g0214 |
2 | HG02040.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.637-9031G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74810719 | |||||||
| chr17:74810775 | G | A | 1 | a0001c0001t0002g0028 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.637-8975G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74810775 | |||||||
| chr17:74810785 | G | A | 1 | a0002c0002t0001g0140 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.637-8965G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74810785 | |||||||
| chr17:74810880 | C | T | 4 | a0001c0001t0004g0049 a0001c0001t0015g0020 a0001c0001t0015g0043 others(1): Show |
4 | HG01099.hp2 HG02622.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-8870C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74810880 | |||||||
| chr17:74810882 | G | A | 104 | a0001c0001t0001g0275 a0001c0001t0002g0035 a0001c0001t0002g0042 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.637-8868G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74810882 | |||||||
| chr17:74810898 | G | A | 13 | a0001c0001t0001g0082 a0001c0001t0001g0276 a0001c0001t0001g0277 others(10): Show |
13 | HG00733.hp2 HG00738.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.637-8852G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74810898 | |||||||
| chr17:74810901 | T | C | 1 | a0001c0001t0009g0283 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.637-8849T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74810901 | |||||||
| chr17:74811037 | A | C | 40 | a0001c0001t0002g0023 a0001c0001t0002g0226 a0001c0001t0004g0047 others(37): Show |
42 | HG00639.hp2 HG00741.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.637-8713A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74811037 | |||||||
| chr17:74811045 | T | C | 82 | a0001c0001t0001g0275 a0001c0001t0002g0035 a0001c0001t0002g0042 others(79): Show |
84 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.637-8705T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74811045 | |||||||
| chr17:74811087 | T | C | 2 | a0001c0001t0002g0209 a0001c0001t0002g0214 |
2 | HG02040.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.637-8663T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74811087 | |||||||
| chr17:74811155 | C | A | 1 | a0002c0005t0007g0063 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.637-8595C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74811155 | |||||||
| chr17:74811425 | C | T | 105 | a0001c0001t0001g0275 a0001c0001t0002g0029 a0001c0001t0002g0035 others(102): Show |
107 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.637-8325C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74811425 | |||||||
| chr17:74811463 | G | C | 82 | a0001c0001t0001g0275 a0001c0001t0002g0035 a0001c0001t0002g0042 others(79): Show |
84 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.637-8287G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74811463 | |||||||
| chr17:74811749 | G | T | 2 | a0002c0002t0001g0071 a0002c0002t0001g0072 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.637-8001G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74811749 | |||||||
| chr17:74811770 | G | A | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-7980G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74811770 | |||||||
| chr17:74811875 | A | T | 1 | a0001c0001t0003g0274 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.637-7875A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74811875 | |||||||
| chr17:74811878 | T | A | 2 | a0002c0002t0003g0114 a0002c0002t0003g0153 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.637-7872T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74811878 | |||||||
| chr17:74811891 | A | C | 1 | a0001c0001t0006g0234 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.637-7859A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74811891 | |||||||
| chr17:74811928 | C | T | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-7822C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74811928 | |||||||
| chr17:74811978 | C | G | 17 | a0001c0001t0004g0046 a0001c0001t0004g0049 a0001c0001t0004g0051 others(14): Show |
17 | HG01099.hp2 HG02055.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.637-7772C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74811978 | |||||||
| chr17:74812051 | G | A | 1 | a0002c0002t0001g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.637-7699G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74812051 | |||||||
| chr17:74812242 | G | A | 14 | a0001c0001t0008g0027 a0001c0001t0008g0037 a0001c0004t0011g0284 others(11): Show |
14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.637-7508G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74812242 | |||||||
| chr17:74812248 | G | A | 12 | a0001c0001t0002g0226 a0001c0001t0005g0212 a0001c0004t0011g0284 others(9): Show |
12 | HG00741.hp1 HG01516.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.637-7502G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74812248 | |||||||
| chr17:74812508 | C | T | 68 | a0001c0001t0001g0275 a0001c0001t0002g0271 a0001c0001t0003g0186 others(65): Show |
70 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.637-7242C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74812508 | |||||||
| chr17:74812631 | G | A | 14 | a0001c0001t0008g0027 a0001c0001t0008g0037 a0001c0004t0011g0284 others(11): Show |
14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.637-7119G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74812631 | |||||||
| chr17:74812637 | G | A | 1 | a0001c0001t0002g0209 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.637-7113G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74812637 | |||||||
| chr17:74812638 | C | T | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-7112C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74812638 | |||||||
| chr17:74812735 | G | A | 2 | a0001c0001t0007g0050 a0002c0002t0007g0060 |
2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.637-7015G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74812735 | |||||||
| chr17:74812750 | A | G | 2 | a0002c0002t0003g0114 a0002c0002t0003g0153 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.637-7000A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74812750 | |||||||
| chr17:74813115 | G | A | 5 | a0001c0001t0004g0053 a0001c0001t0005g0034 a0001c0001t0005g0038 others(2): Show |
5 | HG02486.hp2 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-6635G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74813115 | |||||||
| chr17:74813166 | G | A | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-6584G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74813166 | |||||||
| chr17:74813224 | A | G | 1 | a0002c0002t0001g0190 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.637-6526A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74813224 | |||||||
| chr17:74813284 | C | T | 1 | a0001c0001t0002g0243 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.637-6466C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74813284 | |||||||
| chr17:74813340 | G | T | 2 | a0001c0001t0005g0236 a0002c0002t0004g0181 |
2 | HG04184.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.637-6410G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74813340 | |||||||
| chr17:74813345 | A | C | 1 | a0002c0002t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.637-6405A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74813345 | |||||||
| chr17:74813596 | G | T | 2 | a0001c0001t0002g0031 a0002c0002t0001g0178 |
2 | NA18998.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.637-6154G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74813596 | |||||||
| chr17:74813931 | G | A | 60 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0187 others(57): Show |
63 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.637-5819G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74813931 | |||||||
| chr17:74813964 | G | A | 1 | a0002c0002t0003g0129 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.637-5786G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74813964 | |||||||
| chr17:74814103 | T | C | 4 | a0001c0001t0002g0233 a0001c0001t0002g0238 a0001c0001t0002g0240 others(1): Show |
4 | HG01074.hp2 HG02451.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-5647T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74814103 | |||||||
| chr17:74814228 | C | T | 1 | a0001c0001t0004g0053 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.637-5522C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74814228 | |||||||
| chr17:74814242 | TCCCAGGC others(43): Show |
T | 2 | a0002c0002t0001g0111 a0002c0002t0001g0128 |
2 | HG03704.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.637-5472_637-5423d others(52): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr17 | 74814242 | ||||||
| chr17:74814242 | TCCCAGGC others(102): Show |
T | 3 | a0002c0002t0003g0006 a0002c0002t0003g0095 a0002c0019t0003g0148 |
4 | HG00438.hp2 NA19002.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-5469_637-5361d others(2): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr17 | 74814242 | ||||||
| chr17:74814553 | G | A | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-5197G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74814553 | |||||||
| chr17:74814615 | C | T | 1 | a0001c0001t0002g0258 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.637-5135C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74814615 | |||||||
| chr17:74814658 | G | A | 1 | a0002c0002t0001g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.637-5092G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74814658 | |||||||
| chr17:74814685 | T | G | 14 | a0001c0001t0004g0053 a0001c0001t0005g0030 a0001c0001t0005g0034 others(11): Show |
16 | HG00639.hp2 HG01074.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.637-5065T>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74814685 | |||||||
| chr17:74814939 | C | G | 2 | a0002c0005t0001g0065 a0002c0005t0001g0075 |
2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.637-4811C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74814939 | |||||||
| chr17:74815193 | G | A | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-4557G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815193 | |||||||
| chr17:74815195 | G | A | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-4555G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815195 | |||||||
| chr17:74815204 | A | G | 73 | a0001c0001t0001g0275 a0001c0001t0003g0080 a0001c0001t0003g0186 others(70): Show |
75 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.637-4546A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815204 | |||||||
| chr17:74815332 | A | G | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-4418A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815332 | |||||||
| chr17:74815336 | G | A | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-4414G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815336 | |||||||
| chr17:74815378 | G | A | 10 | a0001c0001t0006g0251 a0001c0001t0006g0253 a0002c0002t0003g0001 others(7): Show |
11 | HG00140.hp1 HG00642.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.637-4372G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815378 | |||||||
| chr17:74815444 | T | C | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 |
3 | HG02055.hp1 HG04184.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.637-4306T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815444 | |||||||
| chr17:74815547 | C | T | 1 | a0002c0002t0017g0092 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.637-4203C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815547 | |||||||
| chr17:74815557 | G | A | 1 | a0001c0004t0011g0289 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.637-4193G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815557 | |||||||
| chr17:74815563 | C | T | 1 | a0002c0002t0001g0138 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.637-4187C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815563 | |||||||
| chr17:74815574 | C | T | 1 | a0001c0001t0002g0259 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.637-4176C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815574 | |||||||
| chr17:74815920 | G | A | 1 | a0001c0001t0009g0282 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.637-3830G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815920 | |||||||
| chr17:74815936 | C | T | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-3814C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815936 | |||||||
| chr17:74815962 | C | T | 1 | a0002c0002t0001g0166 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.637-3788C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815962 | |||||||
| chr17:74815991 | G | A | 1 | a0002c0002t0001g0124 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.637-3759G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815991 | |||||||
| chr17:74816186 | C | T | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-3564C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74816186 | |||||||
| chr17:74816234 | A | G | 1 | a0001c0001t0009g0282 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.637-3516A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74816234 | |||||||
| chr17:74816386 | C | T | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-3364C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74816386 | |||||||
| chr17:74816391 | G | T | 1 | a0002c0002t0001g0139 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.637-3359G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74816391 | |||||||
| chr17:74816401 | C | T | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-3349C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74816401 | |||||||
| chr17:74816629 | C | T | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-3121C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74816629 | |||||||
| chr17:74816677 | G | GT | 9 | a0001c0001t0002g0029 a0001c0001t0002g0035 a0001c0001t0002g0042 others(6): Show |
9 | HG01109.hp2 HG01243.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.637-3064dupT | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr17 | 74816677 | ||||||
| chr17:74816711 | C | T | 11 | a0001c0006t0002g0194 a0001c0006t0002g0206 a0001c0006t0002g0210 others(8): Show |
12 | HG01346.hp1 HG01433.hp2 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.637-3039C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74816711 | |||||||
| chr17:74816714 | C | T | 2 | a0002c0002t0003g0167 a0002c0002t0003g0179 |
2 | NA18953.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.637-3036C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74816714 | |||||||
| chr17:74816840 | T | C | 38 | a0001c0001t0001g0275 a0001c0001t0003g0080 a0001c0001t0003g0186 others(35): Show |
39 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.637-2910T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74816840 | |||||||
| chr17:74816850 | G | T | 1 | a0002c0002t0001g0131 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.637-2900G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74816850 | |||||||
| chr17:74817021 | G | C | 290 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0182 others(287): Show |
299 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.637-2729G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74817021 | |||||||
| chr17:74817063 | C | T | 1 | a0001c0001t0002g0035 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.637-2687C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74817063 | |||||||
| chr17:74817101 | G | A | 3 | a0001c0001t0008g0227 a0001c0021t0037g0010 a0002c0002t0001g0059 |
3 | HG00733.hp2 HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.637-2649G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74817101 | |||||||
| chr17:74817202 | G | A | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-2548G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74817202 | |||||||
| chr17:74817301 | C | T | 2 | a0002c0002t0001g0168 a0002c0002t0001g0169 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.637-2449C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74817301 | |||||||
| chr17:74817420 | G | C | 15 | a0001c0001t0008g0027 a0001c0001t0008g0037 a0001c0004t0011g0284 others(12): Show |
15 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.637-2330G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74817420 | |||||||
| chr17:74817688 | G | C | 64 | a0001c0001t0001g0275 a0001c0001t0003g0080 a0001c0001t0003g0186 others(61): Show |
66 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.637-2062G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74817688 | |||||||
| chr17:74817874 | C | A | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-1876C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74817874 | |||||||
| chr17:74817945 | C | A | 1 | a0002c0002t0036g0117 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.637-1805C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74817945 | |||||||
| chr17:74817996 | G | A | 11 | a0001c0004t0011g0284 a0001c0004t0011g0285 a0001c0004t0011g0289 others(8): Show |
11 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.637-1754G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74817996 | |||||||
| chr17:74818033 | A | G | 1 | a0001c0001t0002g0249 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.637-1717A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74818033 | |||||||
| chr17:74818192 | C | T | 2 | a0001c0001t0007g0050 a0002c0002t0007g0060 |
2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.637-1558C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74818192 | |||||||
| chr17:74818248 | A | G | 104 | a0001c0001t0001g0275 a0001c0001t0002g0240 a0001c0001t0003g0080 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.637-1502A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74818248 | |||||||
| chr17:74818340 | G | T | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-1410G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74818340 | |||||||
| chr17:74818427 | A | T | 2 | a0001c0001t0017g0081 a0002c0002t0017g0092 |
2 | HG00673.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.637-1323A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74818427 | |||||||
| chr17:74818437 | A | G | 165 | a0001c0001t0001g0082 a0001c0001t0001g0275 a0001c0001t0001g0276 others(162): Show |
169 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.637-1313A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74818437 | |||||||
| chr17:74818452 | A | G | 16 | a0001c0001t0001g0275 a0001c0001t0006g0219 a0001c0001t0006g0234 others(13): Show |
17 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(14): Show |
intron_variant | MODIFIER | c.637-1298A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74818452 | |||||||
| chr17:74818483 | C | T | 3 | a0001c0001t0006g0195 a0003c0009t0006g0012 a0009c0016t0006g0021 |
3 | NA18947.hp2 NA18983.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.637-1267C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74818483 | |||||||
| chr17:74818533 | G | A | 1 | a0001c0001t0021g0245 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.637-1217G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74818533 | |||||||
| chr17:74818658 | C | T | 1 | a0002c0002t0004g0163 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.637-1092C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74818658 | |||||||
| chr17:74819010 | C | G | 2 | a0001c0001t0007g0050 a0002c0002t0007g0060 |
2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.637-740C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74819010 | |||||||
| chr17:74819055 | G | A | 15 | a0001c0001t0002g0207 a0001c0001t0002g0233 a0001c0001t0002g0238 others(12): Show |
15 | HG00735.hp2 HG01069.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.637-695G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74819055 | |||||||
| chr17:74819333 | A | T | 2 | a0001c0004t0012g0048 a0002c0007t0012g0068 |
2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.637-417A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74819333 | |||||||
| chr17:74819464 | G | C | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-286G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74819464 | |||||||
| chr17:74819517 | C | T | 1 | a0003c0009t0002g0024 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.637-233C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74819517 | |||||||
| chr17:74819662 | G | A | 2 | a0001c0001t0005g0228 a0001c0001t0005g0231 |
2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.637-88G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74819662 | |||||||
| chr17:74819690 | G | A | 2 | a0002c0002t0001g0168 a0002c0002t0001g0169 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.637-60G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74819690 | |||||||
| chr17:74819874 | G | A | 11 | a0001c0001t0001g0082 a0001c0001t0001g0276 a0001c0001t0001g0277 others(8): Show |
11 | HG01069.hp1 HG01192.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.730+31G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74819874 | |||||||
| chr17:74819996 | A | C | 2 | a0001c0001t0015g0020 a0001c0001t0015g0043 |
2 | HG01099.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.730+153A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74819996 | |||||||
| chr17:74820074 | G | A | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.730+231G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74820074 | |||||||
| chr17:74820153 | A | G | 6 | a0001c0001t0008g0016 a0001c0001t0008g0191 a0001c0001t0029g0018 others(3): Show |
6 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.730+310A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74820153 | |||||||
| chr17:74820241 | G | A | 1 | a0001c0001t0004g0047 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.730+398G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74820241 | |||||||
| chr17:74820402 | C | T | 1 | a0001c0004t0013g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.730+559C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74820402 | |||||||
| chr17:74820628 | C | T | 73 | a0001c0001t0001g0275 a0001c0001t0003g0080 a0001c0001t0003g0186 others(70): Show |
75 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.730+785C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74820628 | |||||||
| chr17:74820810 | G | A | 22 | a0001c0001t0004g0049 a0001c0001t0008g0027 a0001c0001t0008g0037 others(19): Show |
22 | HG00733.hp2 HG01099.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.730+967G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74820810 | |||||||
| chr17:74820915 | C | T | 1 | a0001c0001t0002g0039 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.730+1072C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74820915 | |||||||
| chr17:74820928 | T | A | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.730+1085T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74820928 | |||||||
| chr17:74821021 | G | A | 3 | a0001c0001t0008g0227 a0001c0021t0037g0010 a0002c0002t0001g0059 |
3 | HG00733.hp2 HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.730+1178G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74821021 | |||||||
| chr17:74821121 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0002g0035 |
2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.730+1278G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74821121 | |||||||
| chr17:74821246 | C | G | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.730+1403C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74821246 | |||||||
| chr17:74821711 | A | G | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.730+1868A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74821711 | |||||||
| chr17:74821875 | G | A | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.730+2032G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74821875 | |||||||
| chr17:74821986 | T | C | 16 | a0001c0001t0005g0224 a0001c0001t0008g0027 a0001c0001t0008g0037 others(13): Show |
16 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.730+2143T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74821986 | |||||||
| chr17:74822101 | G | T | 2 | a0001c0001t0002g0029 a0001c0001t0002g0052 |
2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.730+2258G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74822101 | |||||||
| chr17:74822143 | C | T | 6 | a0001c0001t0008g0016 a0001c0001t0008g0191 a0001c0001t0029g0018 others(3): Show |
6 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.730+2300C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74822143 | |||||||
| chr17:74822213 | G | T | 1 | a0001c0001t0002g0257 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.730+2370G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74822213 | |||||||
| chr17:74822341 | C | A | 1 | a0002c0002t0003g0095 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.730+2498C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74822341 | |||||||
| chr17:74822360 | C | A | 2 | a0001c0001t0002g0025 a0001c0001t0002g0221 |
2 | HG00738.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.730+2517C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74822360 | |||||||
| chr17:74822641 | A | G | 3 | a0001c0001t0008g0227 a0001c0021t0037g0010 a0002c0002t0001g0059 |
3 | HG00733.hp2 HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.730+2798A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74822641 | |||||||
| chr17:74822738 | G | T | 1 | a0001c0001t0001g0184 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.730+2895G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74822738 | |||||||
| chr17:74822865 | C | T | 49 | a0001c0001t0001g0045 a0001c0001t0001g0182 a0001c0001t0001g0188 others(46): Show |
51 | HG00408.hp2 HG00544.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.730+3022C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74822865 | |||||||
| chr17:74822881 | C | A | 1 | a0001c0001t0002g0213 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.730+3038C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74822881 | |||||||
| chr17:74822894 | C | T | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.730+3051C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74822894 | |||||||
| chr17:74822925 | G | C | 9 | a0001c0001t0002g0233 a0001c0001t0002g0238 a0001c0001t0002g0240 others(6): Show |
9 | HG01069.hp2 HG01071.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.730+3082G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74822925 | |||||||
| chr17:74822940 | G | A | 13 | a0001c0001t0001g0082 a0001c0001t0001g0276 a0001c0001t0001g0277 others(10): Show |
13 | HG00423.hp2 HG01069.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.730+3097G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74822940 | |||||||
| chr17:74822994 | C | T | 1 | a0001c0001t0002g0262 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.730+3151C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74822994 | |||||||
| chr17:74823043 | A | G | 36 | a0001c0001t0001g0182 a0001c0001t0002g0036 a0001c0001t0002g0039 others(33): Show |
37 | HG00408.hp2 HG00673.hp1 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.730+3200A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74823043 | |||||||
| chr17:74823119 | C | A | 1 | a0001c0001t0002g0268 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.730+3276C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74823119 | |||||||
| chr17:74823136 | G | A | 1 | a0002c0002t0001g0149 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.730+3293G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74823136 | |||||||
| chr17:74823205 | C | T | 1 | a0001c0001t0002g0200 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.730+3362C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74823205 | |||||||
| chr17:74823424 | C | G | 5 | a0001c0001t0008g0016 a0001c0001t0029g0018 a0001c0008t0007g0160 others(2): Show |
5 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.730+3581C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74823424 | |||||||
| chr17:74823957 | A | G | 282 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0182 others(279): Show |
291 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.730+4114A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74823957 | |||||||
| chr17:74823962 | G | A | 1 | a0002c0002t0016g0096 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.730+4119G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74823962 | |||||||
| chr17:74824125 | T | C | 16 | a0001c0001t0005g0030 a0001c0001t0015g0020 a0001c0001t0015g0043 others(13): Show |
16 | HG00639.hp2 HG01099.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.730+4282T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824125 | |||||||
| chr17:74824199 | G | A | 1 | a0002c0002t0004g0170 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.730+4356G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824199 | |||||||
| chr17:74824215 | T | C | 1 | a0001c0001t0002g0028 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.730+4372T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824215 | |||||||
| chr17:74824230 | C | A | 1 | a0002c0002t0001g0134 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.730+4387C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824230 | |||||||
| chr17:74824295 | C | T | 3 | a0001c0001t0015g0020 a0001c0001t0015g0043 a0001c0001t0019g0281 |
3 | HG01099.hp2 HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.730+4452C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824295 | |||||||
| chr17:74824368 | A | G | 2 | a0001c0001t0007g0050 a0002c0002t0007g0060 |
2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.730+4525A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824368 | |||||||
| chr17:74824426 | C | A | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.730+4583C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824426 | |||||||
| chr17:74824453 | T | C | 39 | a0001c0001t0003g0274 a0001c0001t0007g0050 a0001c0001t0008g0016 others(36): Show |
39 | HG00639.hp1 HG00733.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.730+4610T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824453 | |||||||
| chr17:74824454 | G | C | 14 | a0001c0001t0003g0274 a0001c0001t0008g0016 a0001c0001t0008g0191 others(11): Show |
14 | HG00639.hp1 HG02015.hp2 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.730+4611G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824454 | |||||||
| chr17:74824455 | C | A | 5 | a0001c0001t0003g0274 a0002c0002t0003g0058 a0002c0002t0003g0114 others(2): Show |
5 | HG02015.hp2 HG02132.hp1 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.730+4612C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824455 | |||||||
| chr17:74824462 | G | A | 2 | a0002c0002t0001g0093 a0002c0002t0001g0136 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.730+4619G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824462 | |||||||
| chr17:74824527 | G | A | 2 | a0002c0002t0003g0114 a0002c0002t0003g0153 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.730+4684G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824527 | |||||||
| chr17:74824562 | G | A | 59 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0187 others(56): Show |
62 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.730+4719G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824562 | |||||||
| chr17:74824601 | G | A | 15 | a0001c0001t0008g0027 a0001c0001t0008g0037 a0001c0004t0011g0284 others(12): Show |
15 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.730+4758G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824601 | |||||||
| chr17:74824660 | C | T | 3 | a0001c0001t0004g0047 a0001c0001t0005g0026 a0002c0002t0004g0064 |
3 | HG02258.hp1 HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.730+4817C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824660 | |||||||
| chr17:74824865 | G | A | 1 | a0002c0002t0004g0055 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.730+5022G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824865 | |||||||
| chr17:74825257 | A | T | 6 | a0001c0001t0001g0183 a0001c0001t0001g0187 a0001c0001t0002g0248 others(3): Show |
6 | HG00408.hp1 NA18612.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.730+5414A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74825257 | |||||||
| chr17:74825285 | G | C | 1 | a0002c0002t0001g0139 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.730+5442G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74825285 | |||||||
| chr17:74825540 | T | A | 20 | a0001c0001t0008g0027 a0001c0001t0008g0037 a0001c0001t0008g0223 others(17): Show |
20 | HG00438.hp1 HG01099.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.730+5697T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74825540 | |||||||
| chr17:74825607 | G | A | 5 | a0001c0001t0006g0242 a0001c0001t0006g0264 a0001c0001t0006g0272 others(2): Show |
5 | HG00323.hp1 HG00735.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.730+5764G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74825607 | |||||||
| chr17:74825634 | G | A | 1 | a0002c0002t0001g0176 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.730+5791G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74825634 | |||||||
| chr17:74825765 | C | G | 3 | a0001c0001t0010g0292 a0001c0001t0010g0293 a0002c0005t0004g0162 |
3 | HG02615.hp1 HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.730+5922C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74825765 | |||||||
| chr17:74825769 | C | A | 10 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 others(7): Show |
10 | HG01069.hp1 HG01192.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.730+5926C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74825769 | |||||||
| chr17:74825817 | G | C | 71 | a0001c0001t0003g0080 a0001c0001t0003g0186 a0001c0001t0003g0274 others(68): Show |
73 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.730+5974G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74825817 | |||||||
| chr17:74825874 | C | T | 6 | a0001c0001t0002g0025 a0001c0001t0002g0029 a0001c0001t0002g0052 others(3): Show |
6 | HG00738.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.730+6031C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74825874 | |||||||
| chr17:74825977 | G | A | 1 | a0001c0001t0005g0236 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.730+6134G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74825977 | |||||||
| chr17:74826150 | A | G | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.730+6307A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74826150 | |||||||
| chr17:74826239 | G | A | 1 | a0001c0001t0002g0207 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.730+6396G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74826239 | |||||||
| chr17:74826300 | GCTGCCAC others(3): Show |
G | 2 | a0001c0001t0015g0020 a0001c0001t0015g0043 |
2 | HG01099.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.730+6466_730+6475d others(12): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 74826300 | ||||||
| chr17:74826328 | G | A | 1 | a0001c0001t0005g0212 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.730+6485G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74826328 | |||||||
| chr17:74826364 | T | C | 97 | a0001c0001t0003g0080 a0001c0001t0003g0186 a0001c0001t0003g0274 others(94): Show |
99 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.730+6521T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74826364 | |||||||
| chr17:74826399 | C | G | 97 | a0001c0001t0003g0080 a0001c0001t0003g0186 a0001c0001t0003g0274 others(94): Show |
99 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.730+6556C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74826399 | |||||||
| chr17:74826421 | C | T | 3 | a0001c0001t0009g0287 a0001c0001t0009g0288 a0008c0014t0009g0291 |
3 | HG02809.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.730+6578C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74826421 | |||||||
| chr17:74826507 | C | G | 1 | a0001c0001t0008g0223 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.730+6664C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74826507 | |||||||
| chr17:74826556 | A | C | 71 | a0001c0001t0003g0080 a0001c0001t0003g0186 a0001c0001t0003g0274 others(68): Show |
73 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.730+6713A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74826556 | |||||||
| chr17:74826577 | C | G | 1 | a0001c0001t0008g0223 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.730+6734C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74826577 | |||||||
| chr17:74826589 | G | A | 97 | a0001c0001t0003g0080 a0001c0001t0003g0186 a0001c0001t0003g0274 others(94): Show |
99 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.730+6746G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74826589 | |||||||
| chr17:74826817 | G | A | 63 | a0001c0001t0003g0080 a0001c0001t0003g0186 a0001c0001t0003g0274 others(60): Show |
65 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.730+6974G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74826817 | |||||||
| chr17:74826880 | G | A | 97 | a0001c0001t0003g0080 a0001c0001t0003g0186 a0001c0001t0003g0274 others(94): Show |
99 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.730+7037G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74826880 | |||||||
| chr17:74827066 | T | C | 71 | a0001c0001t0003g0080 a0001c0001t0003g0186 a0001c0001t0003g0274 others(68): Show |
73 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.730+7223T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74827066 | |||||||
| chr17:74827174 | G | A | 1 | a0001c0001t0005g0030 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.730+7331G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74827174 | |||||||
| chr17:74827175 | C | A | 1 | a0001c0001t0006g0251 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.730+7332C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74827175 | |||||||
| chr17:74827220 | G | A | 1 | a0001c0001t0002g0255 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.730+7377G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74827220 | |||||||
| chr17:74827298 | CT | C | 6 | a0001c0001t0002g0268 a0001c0001t0004g0053 a0001c0001t0006g0242 others(3): Show |
6 | HG03195.hp2 HG03491.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.730+7471delT | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 74827298 | ||||||
| chr17:74827510 | G | A | 3 | a0001c0001t0015g0020 a0001c0001t0015g0043 a0001c0001t0019g0281 |
3 | HG01099.hp2 HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.730+7667G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74827510 | |||||||
| chr17:74827597 | C | T | 4 | a0001c0006t0002g0194 a0001c0006t0002g0206 a0001c0006t0002g0210 others(1): Show |
4 | NA18971.hp1 NA18983.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.730+7754C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74827597 | |||||||
| chr17:74827890 | A | G | 1 | a0002c0002t0001g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.731-8037A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74827890 | |||||||
| chr17:74827911 | A | AT | 97 | a0001c0001t0003g0080 a0001c0001t0003g0186 a0001c0001t0003g0274 others(94): Show |
99 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.731-8016_731-8015i others(3): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74827911 | |||||||
| chr17:74827926 | C | T | 3 | a0001c0001t0009g0287 a0001c0001t0009g0288 a0008c0014t0009g0291 |
3 | HG02809.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.731-8001C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74827926 | |||||||
| chr17:74827983 | C | T | 1 | a0001c0001t0008g0227 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.731-7944C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74827983 | |||||||
| chr17:74828137 | C | T | 1 | a0001c0001t0003g0080 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.731-7790C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74828137 | |||||||
| chr17:74828304 | G | T | 1 | a0002c0002t0003g0107 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.731-7623G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74828304 | |||||||
| chr17:74828361 | T | A | 1 | a0001c0001t0028g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.731-7566T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74828361 | |||||||
| chr17:74828477 | C | G | 1 | a0001c0001t0001g0188 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.731-7450C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74828477 | |||||||
| chr17:74828744 | GAGA | G | 5 | a0001c0001t0002g0003 a0001c0001t0002g0028 a0001c0001t0002g0042 others(2): Show |
6 | HG01243.hp2 HG02818.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.731-7180_731-7178d others(5): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 74828744 | ||||||
| chr17:74828809 | A | C | 2 | a0001c0001t0007g0050 a0002c0002t0007g0060 |
2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.731-7118A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74828809 | |||||||
| chr17:74828904 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.731-7023C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74828904 | |||||||
| chr17:74828958 | C | T | 15 | a0001c0001t0008g0027 a0001c0001t0008g0037 a0001c0004t0011g0284 others(12): Show |
15 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.731-6969C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74828958 | |||||||
| chr17:74829096 | G | A | 1 | a0001c0001t0002g0213 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.731-6831G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829096 | |||||||
| chr17:74829155 | G | A | 2 | a0001c0001t0025g0220 a0001c0010t0018g0286 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.731-6772G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829155 | |||||||
| chr17:74829269 | G | A | 11 | a0001c0004t0011g0284 a0001c0004t0011g0285 a0001c0004t0011g0289 others(8): Show |
11 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.731-6658G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829269 | |||||||
| chr17:74829334 | G | A | 39 | a0001c0001t0004g0047 a0001c0001t0004g0053 a0001c0001t0005g0015 others(36): Show |
41 | HG00639.hp2 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.731-6593G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829334 | |||||||
| chr17:74829395 | A | G | 4 | a0001c0001t0002g0022 a0001c0001t0002g0257 a0001c0001t0002g0266 others(1): Show |
4 | HG00733.hp1 HG01106.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.731-6532A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829395 | |||||||
| chr17:74829538 | C | T | 3 | a0001c0001t0014g0014 a0001c0001t0014g0032 a0001c0001t0014g0204 |
3 | NA18948.hp1 NA18984.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.731-6389C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829538 | |||||||
| chr17:74829540 | A | G | 1 | a0002c0002t0001g0171 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.731-6387A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829540 | |||||||
| chr17:74829672 | A | C | 1 | a0004c0015t0008g0273 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.731-6255A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829672 | |||||||
| chr17:74829721 | G | T | 21 | a0001c0001t0008g0027 a0001c0001t0008g0037 a0001c0001t0008g0223 others(18): Show |
21 | HG00733.hp2 HG01099.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.731-6206G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829721 | |||||||
| chr17:74829742 | C | T | 2 | a0001c0001t0005g0218 a0002c0002t0001g0089 |
2 | HG01952.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.731-6185C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829742 | |||||||
| chr17:74829762 | C | T | 1 | a0001c0001t0002g0025 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.731-6165C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829762 | |||||||
| chr17:74829767 | A | C | 1 | a0001c0001t0002g0268 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.731-6160A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829767 | |||||||
| chr17:74829810 | C | T | 1 | a0002c0003t0001g0100 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.731-6117C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829810 | |||||||
| chr17:74829820 | T | G | 1 | a0001c0001t0005g0198 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.731-6107T>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829820 | |||||||
| chr17:74829993 | G | A | 1 | a0001c0001t0029g0018 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.731-5934G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829993 | |||||||
| chr17:74830104 | G | A | 1 | a0002c0002t0001g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.731-5823G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74830104 | |||||||
| chr17:74830150 | A | G | 1 | a0001c0001t0005g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.731-5777A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74830150 | |||||||
| chr17:74830605 | A | G | 1 | a0002c0002t0003g0133 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.731-5322A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74830605 | |||||||
| chr17:74830636 | C | T | 2 | a0001c0001t0002g0256 a0001c0001t0021g0245 |
2 | HG01168.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.731-5291C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74830636 | |||||||
| chr17:74830713 | G | T | 1 | a0001c0001t0002g0039 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.731-5214G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74830713 | |||||||
| chr17:74830939 | G | A | 71 | a0001c0001t0003g0080 a0001c0001t0003g0186 a0001c0001t0003g0274 others(68): Show |
73 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.731-4988G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74830939 | |||||||
| chr17:74831132 | A | ACC | 11 | a0001c0004t0011g0284 a0001c0004t0011g0285 a0001c0004t0011g0289 others(8): Show |
11 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.731-4794_731-4793d others(4): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 74831132 | ||||||
| chr17:74831134 | C | G | 1 | a0001c0001t0002g0031 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.731-4793C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74831134 | |||||||
| chr17:74831184 | T | A | 97 | a0001c0001t0003g0080 a0001c0001t0003g0186 a0001c0001t0003g0274 others(94): Show |
99 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.731-4743T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74831184 | |||||||
| chr17:74831185 | C | T | 97 | a0001c0001t0003g0080 a0001c0001t0003g0186 a0001c0001t0003g0274 others(94): Show |
99 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.731-4742C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74831185 | |||||||
| chr17:74831222 | G | A | 2 | a0002c0002t0001g0099 a0002c0002t0001g0116 |
2 | HG00140.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.731-4705G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74831222 | |||||||
| chr17:74831304 | C | A | 71 | a0001c0001t0003g0080 a0001c0001t0003g0186 a0001c0001t0003g0274 others(68): Show |
73 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.731-4623C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74831304 | |||||||
| chr17:74831407 | C | T | 2 | a0001c0001t0002g0031 a0002c0002t0001g0178 |
2 | NA18998.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.731-4520C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74831407 | |||||||
| chr17:74831408 | A | G | 1 | a0002c0002t0001g0135 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.731-4519A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74831408 | |||||||
| chr17:74831525 | C | T | 1 | a0002c0002t0003g0142 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.731-4402C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74831525 | |||||||
| chr17:74831546 | C | G | 97 | a0001c0001t0003g0080 a0001c0001t0003g0186 a0001c0001t0003g0274 others(94): Show |
99 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.731-4381C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74831546 | |||||||
| chr17:74831742 | G | A | 2 | a0001c0001t0002g0256 a0001c0001t0021g0245 |
2 | HG01168.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.731-4185G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74831742 | |||||||
| chr17:74832012 | T | C | 13 | a0001c0001t0008g0227 a0001c0004t0011g0284 a0001c0004t0011g0285 others(10): Show |
13 | HG00733.hp2 HG01106.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.731-3915T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74832012 | |||||||
| chr17:74832074 | C | CA | 71 | a0001c0001t0003g0080 a0001c0001t0003g0186 a0001c0001t0003g0274 others(68): Show |
73 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.731-3851dupA | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 74832074 | ||||||
| chr17:74832133 | A | G | 1 | a0002c0002t0001g0128 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.731-3794A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74832133 | |||||||
| chr17:74832246 | C | T | 1 | a0001c0001t0002g0265 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.731-3681C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74832246 | |||||||
| chr17:74832532 | A | G | 1 | a0002c0002t0001g0149 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.731-3395A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74832532 | |||||||
| chr17:74832611 | G | A | 1 | a0007c0018t0001g0113 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.731-3316G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74832611 | |||||||
| chr17:74832664 | G | A | 1 | a0002c0002t0004g0057 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.731-3263G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74832664 | |||||||
| chr17:74832761 | C | T | 1 | a0002c0002t0004g0181 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.731-3166C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74832761 | |||||||
| chr17:74832834 | G | A | 4 | a0001c0001t0002g0280 a0002c0002t0001g0083 a0002c0002t0001g0090 others(1): Show |
4 | NA18968.hp1 NA19056.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.731-3093G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74832834 | |||||||
| chr17:74832950 | A | G | 2 | a0001c0001t0007g0050 a0002c0002t0007g0060 |
2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.731-2977A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74832950 | |||||||
| chr17:74832993 | T | C | 4 | a0001c0001t0015g0020 a0001c0001t0015g0043 a0001c0001t0019g0281 others(1): Show |
4 | HG00438.hp1 HG01099.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.731-2934T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74832993 | |||||||
| chr17:74832998 | T | C | 1 | a0001c0001t0008g0223 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.731-2929T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74832998 | |||||||
| chr17:74833015 | G | GACTT | 87 | a0001c0001t0003g0080 a0001c0001t0003g0186 a0001c0001t0003g0274 others(84): Show |
89 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.731-2912_731-2911i others(6): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833015 | |||||||
| chr17:74833015 | G | GACTTGTT others(1): Show |
6 | a0001c0001t0015g0020 a0001c0001t0015g0043 a0001c0001t0019g0281 others(3): Show |
6 | HG00438.hp1 HG01099.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.731-2912_731-2911i others(10): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833015 | |||||||
| chr17:74833017 | C | CTTGT | 3 | a0001c0001t0007g0050 a0002c0002t0001g0176 a0002c0002t0007g0060 |
3 | HG01884.hp2 HG02145.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.731-2891_731-2888d others(6): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 74833017 | ||||||
| chr17:74833017 | C | T | 93 | a0001c0001t0003g0080 a0001c0001t0003g0186 a0001c0001t0003g0274 others(90): Show |
95 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.731-2910C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833017 | |||||||
| chr17:74833086 | C | T | 2 | a0002c0002t0001g0168 a0002c0002t0001g0169 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.731-2841C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833086 | |||||||
| chr17:74833323 | T | C | 1 | a0002c0002t0001g0176 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.731-2604T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833323 | |||||||
| chr17:74833595 | G | A | 4 | a0001c0001t0015g0020 a0001c0001t0015g0043 a0001c0001t0019g0281 others(1): Show |
4 | HG00438.hp1 HG01099.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.731-2332G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833595 | |||||||
| chr17:74833612 | G | C | 1 | a0001c0004t0011g0290 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.731-2315G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833612 | |||||||
| chr17:74833627 | A | T | 3 | a0001c0001t0009g0287 a0001c0001t0009g0288 a0008c0014t0009g0291 |
3 | HG02809.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.731-2300A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833627 | |||||||
| chr17:74833668 | T | C | 1 | a0002c0019t0003g0148 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.731-2259T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833668 | |||||||
| chr17:74833703 | C | T | 1 | a0001c0001t0003g0080 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.731-2224C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833703 | |||||||
| chr17:74833746 | A | G | 93 | a0001c0001t0003g0080 a0001c0001t0003g0186 a0001c0001t0003g0274 others(90): Show |
95 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.731-2181A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833746 | |||||||
| chr17:74833864 | C | G | 1 | a0001c0001t0008g0227 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.731-2063C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833864 | |||||||
| chr17:74833882 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.731-2045G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833882 | |||||||
| chr17:74833967 | C | T | 4 | a0001c0001t0005g0034 a0001c0001t0005g0038 a0001c0001t0005g0228 others(1): Show |
4 | HG02486.hp2 HG02809.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.731-1960C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833967 | |||||||
| chr17:74833989 | C | A | 1 | a0002c0002t0004g0170 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.731-1938C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833989 | |||||||
| chr17:74834107 | G | C | 1 | a0001c0001t0002g0240 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.731-1820G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74834107 | |||||||
| chr17:74834259 | T | C | 97 | a0001c0001t0003g0080 a0001c0001t0003g0186 a0001c0001t0003g0274 others(94): Show |
99 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.731-1668T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74834259 | |||||||
| chr17:74834293 | G | A | 66 | a0001c0001t0003g0080 a0001c0001t0003g0186 a0001c0001t0003g0274 others(63): Show |
68 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.731-1634G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74834293 | |||||||
| chr17:74834412 | C | T | 1 | a0002c0005t0004g0162 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.731-1515C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74834412 | |||||||
| chr17:74834719 | G | C | 3 | a0001c0001t0006g0253 a0002c0002t0003g0001 a0002c0002t0032g0001 |
4 | HG00642.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.731-1208G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74834719 | |||||||
| chr17:74834732 | G | A | 97 | a0001c0001t0003g0080 a0001c0001t0003g0186 a0001c0001t0003g0274 others(94): Show |
99 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.731-1195G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74834732 | |||||||
| chr17:74834833 | C | T | 2 | a0002c0002t0001g0071 a0002c0002t0001g0072 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.731-1094C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74834833 | |||||||
| chr17:74834899 | C | T | 2 | a0001c0004t0012g0048 a0002c0007t0012g0068 |
2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.731-1028C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74834899 | |||||||
| chr17:74834985 | C | T | 2 | a0001c0001t0004g0053 a0001c0001t0005g0030 |
2 | HG00639.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.731-942C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74834985 | |||||||
| chr17:74835019 | C | T | 1 | a0002c0002t0003g0133 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.731-908C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74835019 | |||||||
| chr17:74835304 | C | G | 1 | a0001c0001t0008g0223 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.731-623C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74835304 | |||||||
| chr17:74835761 | G | A | 1 | a0002c0002t0004g0057 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.731-166G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74835761 | |||||||
| chr17:74835801 | A | G | 1 | a0001c0001t0022g0250 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.731-126A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74835801 | |||||||
| chr17:74835845 | C | T | 1 | a0002c0002t0035g0074 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.731-82C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74835845 | |||||||
| chr17:74835854 | G | A | 4 | a0001c0001t0002g0233 a0001c0001t0002g0238 a0001c0001t0002g0240 others(1): Show |
4 | HG01074.hp2 HG02451.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.731-73G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74835854 | |||||||
| chr17:74835893 | C | G | 74 | a0001c0001t0003g0080 a0001c0001t0003g0186 a0001c0001t0003g0274 others(71): Show |
76 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.731-34C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74835893 |