Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 123591 |
| ensemblid | ENSG00000169758.13 |
| hgncid | 26763 |
| symbol | TMEM266 |
| name | transmembrane protein 266 |
| refseq_nuc | NM_152335.5 |
| refseq_prot | NP_689548.3 |
| ensembl_nuc | ENST00000388942.9 |
| ensembl_prot | ENSP00000373594.4 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 76059985 |
| end | 76204963 |
| strand | + |
| ver | v1.2 |
| region | chr15:76059985-76204963 |
| region5000 | chr15:76054985-76209963 |
| regionname0 | TMEM266_chr15_76059985_76204963 |
| regionname5000 | TMEM266_chr15_76054985_76209963 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 523 | 170 | 66 | 28 | 52 | 7 | 15 | 32 | TMEM266_chr15_76054985_76209963 | TMEM266 | MTNPQ others(518): Show |
chr15 | 76054985 | 76209963 |
| a0002 | 0/0 | 523 | 101 | 18 | 22 | 48 | 5 | 8 | 32 | TMEM266_chr15_76054985_76209963 | TMEM266 | MTNPQ others(518): Show |
chr15 | 76054985 | 76209963 |
| a0003 | 0/0 | 523 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | MTNPQ others(518): Show |
chr15 | 76054985 | 76209963 |
| a0004 | 0/0 | 523 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | MTNPQ others(518): Show |
chr15 | 76054985 | 76209963 |
| a0005 | 0/0 | 523 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | MTNPQ others(518): Show |
chr15 | 76054985 | 76209963 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1569 | 170 | 66 | 28 | 52 | 7 | 15 | TMEM266_chr15_76054985_76209963 | TMEM266 | ATGAC others(1564): Show |
chr15 | 76054985 | 76209963 | ||
| a0002c0002 | 0/0 | 1569 | 99 | 17 | 22 | 47 | 5 | 8 | TMEM266_chr15_76054985_76209963 | TMEM266 | ATGAC others(1564): Show |
chr15 | 76054985 | 76209963 | ||
| a0002c0003 | 0/0 | 1569 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | ATGAC others(1564): Show |
chr15 | 76054985 | 76209963 | ||
| a0002c0007 | 0/0 | 1569 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | ATGAC others(1564): Show |
chr15 | 76054985 | 76209963 | ||
| a0003c0004 | 0/0 | 1569 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM266_chr15_76054985_76209963 | TMEM266 | ATGAC others(1564): Show |
chr15 | 76054985 | 76209963 | ||
| a0004c0005 | 0/0 | 1569 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | ATGAC others(1564): Show |
chr15 | 76054985 | 76209963 | ||
| a0005c0006 | 0/0 | 1569 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | ATGAC others(1564): Show |
chr15 | 76054985 | 76209963 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2372 | 59 | 42 | 8 | 4 | 1 | 4 | TMEM266_chr15_76054985_76209963 | TMEM266 | AGAGC others(2367): Show |
chr15 | 76054985 | 76209963 |
| a0001c0001t0002 | 0/1 | 2372 | 89 | 9 | 20 | 42 | 6 | 11 | TMEM266_chr15_76054985_76209963 | TMEM266 | AGAGC others(2367): Show |
chr15 | 76054985 | 76209963 |
| a0001c0001t0003 | 1/0 | 2372 | 6 | 5 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | AGAGC others(2367): Show |
chr15 | 76054985 | 76209963 |
| a0001c0001t0004 | 0/0 | 2372 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | AGAGC others(2367): Show |
chr15 | 76054985 | 76209963 |
| a0001c0001t0005 | 0/0 | 2372 | 5 | 0 | 0 | 5 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | AGAGC others(2367): Show |
chr15 | 76054985 | 76209963 |
| a0001c0001t0007 | 0/0 | 2372 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | AGAGC others(2367): Show |
chr15 | 76054985 | 76209963 |
| a0001c0001t0008 | 0/0 | 2372 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | AGAGC others(2367): Show |
chr15 | 76054985 | 76209963 |
| a0001c0001t0009 | 0/0 | 2372 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | AGAGC others(2367): Show |
chr15 | 76054985 | 76209963 |
| a0001c0001t0011 | 0/0 | 2372 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | AGAGC others(2367): Show |
chr15 | 76054985 | 76209963 |
| a0002c0002t0001 | 0/0 | 2372 | 90 | 16 | 21 | 40 | 5 | 8 | TMEM266_chr15_76054985_76209963 | TMEM266 | AGAGC others(2367): Show |
chr15 | 76054985 | 76209963 |
| a0002c0002t0002 | 0/0 | 2372 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | AGAGC others(2367): Show |
chr15 | 76054985 | 76209963 |
| a0002c0002t0006 | 0/0 | 2372 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | AGAGC others(2367): Show |
chr15 | 76054985 | 76209963 |
| a0002c0002t0010 | 0/0 | 2372 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | AGAGC others(2367): Show |
chr15 | 76054985 | 76209963 |
| a0002c0002t0012 | 0/0 | 2372 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | AGAGC others(2367): Show |
chr15 | 76054985 | 76209963 |
| a0002c0003t0001 | 0/0 | 2372 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | AGAGC others(2367): Show |
chr15 | 76054985 | 76209963 |
| a0002c0007t0001 | 0/0 | 2372 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | AGAGC others(2367): Show |
chr15 | 76054985 | 76209963 |
| a0003c0004t0001 | 0/0 | 2372 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM266_chr15_76054985_76209963 | TMEM266 | AGAGC others(2367): Show |
chr15 | 76054985 | 76209963 |
| a0004c0005t0001 | 0/0 | 2372 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | AGAGC others(2367): Show |
chr15 | 76054985 | 76209963 |
| a0005c0006t0001 | 0/0 | 2372 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | AGAGC others(2367): Show |
chr15 | 76054985 | 76209963 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0077 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0003g0101 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0005g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0005g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0007g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0007g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0008g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0008g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0009g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0001c0001t0011g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0006g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0006g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0006g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0010g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0002t0012g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0003t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0002c0007t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0003c0004t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0004c0005t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| a0005c0006t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0183 | EUR | GBR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0064 | EUR | GBR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0100 | EUR | GBR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0126 | EUR | GBR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0112 | EUR | FIN | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0225 | EUR | FIN | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | CHS | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | CHS | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | CHS | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | CHS | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG00597 | hp1 | a0001 | c0001 | t0005 | g0097 | EAS | CHS | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | CHS | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | CHS | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | CHS | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | CHS | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG00733 | hp2 | a0002 | c0002 | t0010 | g0103 | AMR | PUR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0161 | AMR | PUR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | PUR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0162 | AMR | PUR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0222 | AMR | PUR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0181 | AMR | PUR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0059 | AMR | PUR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0223 | AMR | PUR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0259 | AMR | PUR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0125 | AMR | PUR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0227 | AMR | PUR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0141 | AMR | PUR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0221 | AMR | PUR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0208 | AMR | PUR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | CLM | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0049 | AMR | CLM | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | CLM | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0069 | AMR | CLM | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0209 | AMR | CLM | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0262 | AMR | CLM | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0164 | AMR | CLM | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | CLM | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0123 | EUR | IBS | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0171 | EUR | IBS | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0108 | EUR | IBS | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0067 | EUR | IBS | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | ACB | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0087 | AFR | ACB | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0245 | AFR | ACB | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0155 | AMR | PEL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PEL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0204 | AMR | PEL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | PEL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0048 | AMR | PEL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0163 | AMR | PEL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0206 | EAS | KHV | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02015 | hp2 | a0001 | c0001 | t0005 | g0061 | EAS | KHV | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | KHV | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | KHV | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | KHV | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | KHV | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | KHV | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0039 | EAS | KHV | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | KHV | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0242 | EAS | KHV | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | KHV | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | KHV | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | KHV | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0194 | EAS | KHV | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | KHV | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | ACB | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | CDX | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | CDX | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | CDX | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | CDX | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02257 | hp1 | a0002 | c0003 | t0001 | g0015 | AFR | ACB | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0239 | AMR | PEL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PEL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0268 | AFR | ACB | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0253 | AFR | ACB | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02523 | hp1 | a0002 | c0007 | t0001 | g0212 | EAS | KHV | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | KHV | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0086 | AFR | GWD | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0040 | AFR | GWD | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0176 | SAS | PJL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | GWD | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0252 | AFR | GWD | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0193 | SAS | PJL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0218 | SAS | PJL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | GWD | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0174 | AFR | GWD | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | PJL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0217 | SAS | PJL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0263 | AFR | GWD | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0128 | AFR | GWD | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0175 | AFR | ESN | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02965 | hp1 | a0001 | c0001 | t0011 | g0199 | AFR | ESN | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0053 | AFR | ESN | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03017 | hp1 | a0003 | c0004 | t0001 | g0159 | SAS | PJL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0254 | AFR | GWD | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0270 | AFR | GWD | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | MSL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | MSL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | ESN | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0131 | AFR | ESN | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0265 | AFR | MSL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | MSL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0178 | SAS | PJL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0250 | AFR | MSL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0127 | AFR | MSL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ESN | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | GWD | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0180 | SAS | PJL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0246 | SAS | PJL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0170 | SAS | PJL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0179 | SAS | STU | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | STU | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0182 | SAS | PJL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | PJL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0215 | SAS | BEB | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | BEB | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | YRI | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | YRI | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | CHB | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | CHB | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18965 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18967 | hp1 | a0001 | c0001 | t0005 | g0186 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18969 | hp2 | a0001 | c0001 | t0005 | g0121 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18970 | hp2 | a0001 | c0001 | t0009 | g0091 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18971 | hp1 | a0002 | c0002 | t0006 | g0195 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0238 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18973 | hp2 | a0002 | c0002 | t0006 | g0145 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA19030 | hp2 | a0001 | c0001 | t0008 | g0249 | AFR | LWK | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA19043 | hp1 | a0002 | c0002 | t0012 | g0267 | AFR | LWK | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA19057 | hp1 | a0002 | c0002 | t0006 | g0150 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA19057 | hp2 | a0001 | c0001 | t0005 | g0084 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA19058 | hp1 | a0002 | c0002 | t0006 | g0026 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0237 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ASW | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ASW | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0226 | EUR | TSI | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0166 | EUR | TSI | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0216 | SAS | GIH | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0236 | SAS | GIH | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0220 | AMR | CLM | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | CLM | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0248 | AFR | ACB | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | ACB | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | MSL | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | USA | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | USA | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA20300 | hp1 | a0001 | c0001 | t0007 | g0251 | AFR | USA | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | USA | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA21309 | hp1 | a0004 | c0005 | t0001 | g0211 | AFR | LWK | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| NA21309 | hp2 | a0005 | c0006 | t0001 | g0110 | AFR | LWK | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0077 | REF | REF | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0101 | REF | REF | TMEM266_chr15_76054985_76209963 | TMEM266 | chr15 | 76054985 | 76209963 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:76192157 | G | A | 1 | a0003 | 1 | HG03017.hp1 | missense_variant&splice_region_variant | MODERATE | c.934G>A | p.Glu312Lys | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/11 | 1086/2372 | 934/1572 | 312/523 | chr15 | 76192157 | |||
| chr15:76203891 | G | A | 2 | a0002 a0003 |
102 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(99): Show |
missense_variant | MODERATE | c.1148G>A | p.Arg383His | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 11/11 | 1300/2372 | 1148/1572 | 383/523 | chr15 | 76203891 | |||
| chr15:76203930 | C | T | 1 | a0005 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1187C>T | p.Thr396Met | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 11/11 | 1339/2372 | 1187/1572 | 396/523 | chr15 | 76203930 | |||
| chr15:76203962 | C | T | 1 | a0004 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1219C>T | p.Arg407Cys | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 11/11 | 1371/2372 | 1219/1572 | 407/523 | chr15 | 76203962 | |||
| chr15:76203999 | C | T | 2 | a0002 a0003 |
102 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(99): Show |
missense_variant | MODERATE | c.1256C>T | p.Pro419Leu | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 11/11 | 1408/2372 | 1256/1572 | 419/523 | chr15 | 76203999 | |||
| chr15:76204073 | T | C | 1 | a0004 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1330T>C | p.Cys444Arg | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 11/11 | 1482/2372 | 1330/1572 | 444/523 | chr15 | 76204073 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:76137884 | C | T | 1 | a0002c0007 | 1 | HG02523.hp1 | synonymous_variant | LOW | c.192C>T | p.Tyr64Tyr | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/11 | 344/2372 | 192/1572 | 64/523 | chr15 | 76137884 | |||
| chr15:76192024 | C | A | 1 | a0002c0003 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.801C>A | p.Ala267Ala | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/11 | 953/2372 | 801/1572 | 267/523 | chr15 | 76192024 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:76059990 | C | A | 3 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 |
9 | HG02451.hp2 HG02486.hp1 HG02630.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-147C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/11 | 74298 | chr15 | 76059990 | ||||||
| chr15:76134172 | C | G | 1 | a0002c0002t0012 | 1 | NA19043.hp1 | 5_prime_UTR_variant | MODIFIER | c.-116C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/11 | 116 | chr15 | 76134172 | ||||||
| chr15:76134184 | G | C | 2 | a0001c0001t0009 a0002c0002t0006 |
5 | NA18970.hp2 NA18971.hp1 NA18973.hp2 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-104G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/11 | chr15 | 76134184 | |||||||
| chr15:76204455 | C | T | 1 | a0001c0001t0005 | 5 | HG00597.hp1 HG02015.hp2 NA18967.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*140C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 11/11 | 140 | chr15 | 76204455 | ||||||
| chr15:76204502 | C | G | 1 | a0001c0001t0011 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*187C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 11/11 | 187 | chr15 | 76204502 | ||||||
| chr15:76204636 | G | C | 17 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(14): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
3_prime_UTR_variant | MODIFIER | c.*321G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 11/11 | 321 | chr15 | 76204636 | ||||||
| chr15:76204837 | G | A | 1 | a0002c0002t0010 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*522G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 11/11 | 522 | chr15 | 76204837 | ||||||
| chr15:76204876 | C | T | 12 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0011 others(9): Show |
166 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*561C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 11/11 | 561 | chr15 | 76204876 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:76060069 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0002g0004 |
2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-121+53G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76060069 | |||||||
| chr15:76060089 | G | C | 2 | a0001c0001t0004g0005 a0001c0001t0004g0006 |
2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-121+73G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76060089 | |||||||
| chr15:76060093 | T | C | 1 | a0002c0002t0001g0007 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-121+77T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76060093 | |||||||
| chr15:76060134 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
2 | HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-121+118G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76060134 | |||||||
| chr15:76060181 | G | C | 1 | a0002c0002t0002g0010 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-121+165G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76060181 | |||||||
| chr15:76060184 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0002g0004 |
2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-121+168G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76060184 | |||||||
| chr15:76060363 | G | T | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-121+347G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76060363 | |||||||
| chr15:76060496 | AG | A | 11 | a0001c0001t0001g0261 a0001c0001t0001g0264 a0001c0001t0001g0266 others(8): Show |
11 | HG01243.hp2 HG01346.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-121+481delG | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76060496 | |||||||
| chr15:76060510 | G | T | 5 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-121+494G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76060510 | |||||||
| chr15:76060948 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-121+932A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76060948 | |||||||
| chr15:76061117 | C | A | 5 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-121+1101C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76061117 | |||||||
| chr15:76061210 | C | T | 9 | a0001c0001t0004g0005 a0001c0001t0004g0006 a0001c0001t0004g0248 others(6): Show |
9 | HG02451.hp2 HG02486.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-121+1194C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76061210 | |||||||
| chr15:76061355 | T | C | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-121+1339T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76061355 | |||||||
| chr15:76061505 | G | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0003g0014 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-121+1489G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76061505 | |||||||
| chr15:76061834 | T | G | 10 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0256 others(7): Show |
11 | HG01167.hp2 HG01169.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-121+1818T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76061834 | |||||||
| chr15:76061837 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-121+1821C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76061837 | |||||||
| chr15:76061859 | C | T | 1 | a0001c0001t0002g0001 | 2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-121+1843C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76061859 | |||||||
| chr15:76062029 | AT | A | 10 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0256 others(7): Show |
11 | HG01167.hp2 HG01169.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-121+2020delT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76062029 | ||||||
| chr15:76062222 | A | T | 10 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0256 others(7): Show |
11 | HG01167.hp2 HG01169.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-121+2206A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76062222 | |||||||
| chr15:76062453 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0002g0004 |
2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-121+2437G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76062453 | |||||||
| chr15:76062768 | G | A | 10 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0256 others(7): Show |
11 | HG01167.hp2 HG01169.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-121+2752G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76062768 | |||||||
| chr15:76062820 | A | C | 2 | a0001c0001t0002g0245 a0001c0001t0002g0246 |
2 | HG01891.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-121+2804A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76062820 | |||||||
| chr15:76062837 | T | G | 1 | a0002c0002t0001g0016 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-121+2821T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76062837 | |||||||
| chr15:76062906 | C | T | 15 | a0001c0001t0001g0230 a0001c0001t0001g0234 a0001c0001t0001g0241 others(12): Show |
15 | HG02080.hp1 HG02155.hp2 HG02300.hp1 others(12): Show |
intron_variant | MODIFIER | c.-121+2890C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76062906 | |||||||
| chr15:76062911 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-121+2895C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76062911 | |||||||
| chr15:76062921 | C | A | 1 | a0001c0001t0002g0001 | 2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-121+2905C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76062921 | |||||||
| chr15:76063105 | G | A | 15 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(12): Show |
16 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.-121+3089G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76063105 | |||||||
| chr15:76063252 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-121+3236T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76063252 | |||||||
| chr15:76063289 | C | T | 1 | a0001c0001t0002g0228 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-121+3273C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76063289 | |||||||
| chr15:76063359 | C | T | 10 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0256 others(7): Show |
11 | HG01167.hp2 HG01169.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-121+3343C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76063359 | |||||||
| chr15:76063371 | A | G | 7 | a0001c0001t0002g0224 a0001c0001t0002g0226 a0002c0002t0001g0221 others(4): Show |
7 | HG00280.hp2 HG01069.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.-121+3355A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76063371 | |||||||
| chr15:76063381 | T | C | 11 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0230 others(8): Show |
12 | HG01167.hp2 HG01169.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-121+3365T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76063381 | |||||||
| chr15:76063514 | A | G | 1 | a0001c0001t0002g0220 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-121+3498A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76063514 | |||||||
| chr15:76063523 | C | T | 1 | a0001c0001t0002g0219 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-121+3507C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76063523 | |||||||
| chr15:76063766 | A | G | 1 | a0001c0001t0004g0254 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-121+3750A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76063766 | |||||||
| chr15:76063798 | C | T | 10 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0256 others(7): Show |
11 | HG01167.hp2 HG01169.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-121+3782C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76063798 | |||||||
| chr15:76063956 | T | C | 2 | a0001c0001t0001g0017 a0001c0001t0001g0018 |
2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-121+3940T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76063956 | |||||||
| chr15:76064001 | A | G | 4 | a0002c0002t0001g0215 a0002c0002t0001g0216 a0002c0002t0001g0217 others(1): Show |
4 | HG02683.hp2 HG02735.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-121+3985A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76064001 | |||||||
| chr15:76064076 | C | T | 1 | a0001c0001t0002g0214 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-121+4060C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76064076 | |||||||
| chr15:76064210 | G | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0271 a0001c0001t0001g0272 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-121+4194G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76064210 | |||||||
| chr15:76064271 | G | T | 1 | a0001c0001t0002g0001 | 2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-121+4255G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76064271 | |||||||
| chr15:76064280 | C | G | 1 | a0001c0001t0002g0001 | 2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-121+4264C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76064280 | |||||||
| chr15:76064280 | C | T | 1 | a0001c0001t0002g0213 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-121+4264C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76064280 | |||||||
| chr15:76064397 | CT | C | 7 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(4): Show |
7 | HG01891.hp2 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-121+4384delT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76064397 | ||||||
| chr15:76064445 | A | G | 1 | a0002c0007t0001g0212 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-121+4429A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76064445 | |||||||
| chr15:76064572 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-121+4556C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76064572 | |||||||
| chr15:76064746 | A | C | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-121+4730A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76064746 | |||||||
| chr15:76064797 | C | T | 1 | a0004c0005t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-121+4781C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76064797 | |||||||
| chr15:76064858 | T | C | 1 | a0001c0001t0002g0001 | 2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-121+4842T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76064858 | |||||||
| chr15:76064902 | A | G | 18 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(15): Show |
18 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.-121+4886A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76064902 | |||||||
| chr15:76064903 | A | G | 7 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(4): Show |
7 | HG01891.hp2 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-121+4887A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76064903 | |||||||
| chr15:76064960 | A | G | 1 | a0001c0001t0002g0210 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-121+4944A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76064960 | |||||||
| chr15:76065003 | G | A | 1 | a0002c0002t0001g0215 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-121+4987G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76065003 | |||||||
| chr15:76065013 | A | G | 7 | a0001c0001t0004g0248 a0001c0001t0004g0253 a0001c0001t0004g0254 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-121+4997A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76065013 | |||||||
| chr15:76065173 | A | G | 15 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0271 others(12): Show |
15 | HG02257.hp1 HG02451.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-121+5157A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76065173 | |||||||
| chr15:76065193 | C | T | 15 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0271 others(12): Show |
15 | HG02257.hp1 HG02451.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-121+5177C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76065193 | |||||||
| chr15:76065260 | T | C | 1 | a0002c0002t0006g0026 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-121+5244T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76065260 | |||||||
| chr15:76065471 | G | GCGGTGTC | 5 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0003g0014 others(2): Show |
5 | HG02257.hp1 HG02647.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-121+5458_-121+546 others(11): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76065471 | ||||||
| chr15:76065479 | C | T | 1 | a0002c0002t0001g0209 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-121+5463C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76065479 | |||||||
| chr15:76065484 | C | T | 1 | a0002c0003t0001g0015 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-121+5468C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76065484 | |||||||
| chr15:76065714 | A | G | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-121+5698A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76065714 | |||||||
| chr15:76065723 | A | AT | 5 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0003g0014 others(2): Show |
5 | HG02257.hp1 HG02647.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-121+5716dupT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76065723 | ||||||
| chr15:76065823 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0003g0014 |
3 | HG02647.hp1 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-121+5807C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76065823 | |||||||
| chr15:76065837 | A | G | 1 | a0001c0001t0001g0008 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-121+5821A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76065837 | |||||||
| chr15:76065945 | A | G | 9 | a0001c0001t0004g0005 a0001c0001t0004g0006 a0001c0001t0004g0248 others(6): Show |
9 | HG02451.hp2 HG02486.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-121+5929A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76065945 | |||||||
| chr15:76066159 | C | A | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-121+6143C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76066159 | |||||||
| chr15:76066175 | C | T | 2 | a0001c0001t0004g0253 a0001c0001t0004g0254 |
2 | HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-121+6159C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76066175 | |||||||
| chr15:76066266 | C | T | 26 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(23): Show |
27 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.-121+6250C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76066266 | |||||||
| chr15:76066350 | A | G | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-121+6334A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76066350 | |||||||
| chr15:76066614 | G | T | 1 | a0001c0001t0001g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-121+6598G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76066614 | |||||||
| chr15:76066615 | A | T | 1 | a0001c0001t0001g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-121+6599A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76066615 | |||||||
| chr15:76066640 | TA | T | 22 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0021 others(19): Show |
23 | HG01891.hp2 HG02015.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.-121+6641delA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76066640 | ||||||
| chr15:76066714 | C | T | 79 | a0001c0001t0001g0153 a0001c0001t0001g0157 a0001c0001t0001g0158 others(76): Show |
79 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.-121+6698C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76066714 | |||||||
| chr15:76066976 | G | A | 2 | a0001c0001t0002g0027 a0001c0001t0002g0028 |
2 | HG02080.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.-121+6960G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76066976 | |||||||
| chr15:76067313 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-121+7297G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76067313 | |||||||
| chr15:76067463 | A | T | 2 | a0001c0001t0004g0005 a0001c0001t0004g0006 |
2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-121+7447A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76067463 | |||||||
| chr15:76067515 | T | C | 1 | a0001c0001t0002g0001 | 2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-121+7499T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76067515 | |||||||
| chr15:76067627 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-121+7611C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76067627 | |||||||
| chr15:76067644 | AAAAAAG | A | 14 | a0001c0001t0001g0143 a0001c0001t0001g0269 a0001c0001t0001g0271 others(11): Show |
14 | HG01243.hp2 HG02257.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-121+7633_-121+763 others(10): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76067644 | ||||||
| chr15:76067644 | AAAAAAGA others(9): Show |
A | 1 | a0002c0002t0001g0016 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-121+7633_-121+764 others(20): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76067644 | ||||||
| chr15:76067645 | AAAAAG | A | 200 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(197): Show |
201 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.-121+7654_-121+765 others(9): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76067645 | ||||||
| chr15:76067645 | AAAAAGAA others(3): Show |
A | 2 | a0002c0002t0001g0175 a0002c0002t0001g0215 |
2 | HG02922.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-121+7649_-121+765 others(14): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76067645 | ||||||
| chr15:76067646 | AAAAG | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0261 a0001c0001t0002g0151 others(5): Show |
8 | HG00597.hp2 HG01346.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-121+7634_-121+763 others(8): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76067646 | ||||||
| chr15:76067687 | G | GT | 16 | a0001c0001t0001g0132 a0001c0001t0001g0135 a0001c0001t0001g0137 others(13): Show |
16 | HG00735.hp1 HG00738.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.-121+7684dupT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76067687 | ||||||
| chr15:76067688 | T | G | 5 | a0001c0001t0001g0264 a0001c0001t0002g0263 a0001c0001t0003g0265 others(2): Show |
5 | HG01346.hp2 HG02258.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-121+7672T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76067688 | |||||||
| chr15:76067706 | T | A | 9 | a0001c0001t0002g0147 a0001c0001t0002g0151 a0002c0002t0001g0144 others(6): Show |
9 | HG00597.hp2 NA18957.hp1 NA18967.hp2 others(6): Show |
intron_variant | MODIFIER | c.-121+7690T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76067706 | |||||||
| chr15:76067988 | A | G | 1 | a0001c0001t0001g0207 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-121+7972A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76067988 | |||||||
| chr15:76068011 | T | A | 2 | a0002c0002t0001g0216 a0002c0002t0001g0217 |
2 | HG02735.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-121+7995T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76068011 | |||||||
| chr15:76068022 | C | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0271 a0001c0001t0002g0001 |
4 | HG02615.hp1 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-121+8006C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76068022 | |||||||
| chr15:76068137 | G | C | 4 | a0001c0001t0001g0132 a0001c0001t0001g0229 a0002c0002t0001g0029 others(1): Show |
4 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-121+8121G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76068137 | |||||||
| chr15:76068265 | T | C | 1 | a0001c0001t0002g0030 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-121+8249T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76068265 | |||||||
| chr15:76068458 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-121+8442G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76068458 | |||||||
| chr15:76068494 | A | G | 1 | a0002c0002t0001g0131 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-121+8478A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76068494 | |||||||
| chr15:76068992 | T | C | 1 | a0001c0001t0003g0031 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-121+8976T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76068992 | |||||||
| chr15:76069081 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-121+9065A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76069081 | |||||||
| chr15:76069283 | T | A | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-121+9267T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76069283 | |||||||
| chr15:76069328 | T | C | 2 | a0001c0001t0001g0143 a0001c0001t0001g0269 |
2 | HG01243.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-121+9312T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76069328 | |||||||
| chr15:76069400 | T | G | 4 | a0001c0001t0001g0132 a0001c0001t0001g0229 a0002c0002t0001g0029 others(1): Show |
4 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-121+9384T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76069400 | |||||||
| chr15:76069411 | T | G | 1 | a0001c0001t0002g0032 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-121+9395T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76069411 | |||||||
| chr15:76069452 | A | G | 1 | a0002c0002t0001g0217 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-121+9436A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76069452 | |||||||
| chr15:76069677 | A | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0271 a0001c0001t0002g0001 others(1): Show |
5 | HG02615.hp1 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-121+9661A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76069677 | |||||||
| chr15:76069684 | G | C | 1 | a0001c0001t0002g0152 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-121+9668G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76069684 | |||||||
| chr15:76069705 | C | T | 1 | a0002c0002t0001g0204 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-121+9689C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76069705 | |||||||
| chr15:76069823 | A | AG | 2 | a0001c0001t0002g0001 a0001c0001t0002g0004 |
3 | HG02809.hp1 HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-121+9808dupG | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76069823 | ||||||
| chr15:76069883 | A | G | 7 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(4): Show |
7 | HG01891.hp2 HG02922.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-121+9867A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76069883 | |||||||
| chr15:76070007 | T | G | 1 | a0001c0001t0001g0256 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-121+9991T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76070007 | |||||||
| chr15:76070206 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-121+10190C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76070206 | |||||||
| chr15:76070403 | A | G | 2 | a0001c0001t0001g0132 a0002c0002t0001g0029 |
2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-121+10387A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76070403 | |||||||
| chr15:76070741 | T | C | 2 | a0001c0001t0001g0153 a0002c0002t0001g0209 |
2 | HG01106.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.-121+10725T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76070741 | |||||||
| chr15:76070833 | T | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0143 a0001c0001t0001g0269 others(3): Show |
7 | HG01243.hp2 HG02615.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-121+10817T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76070833 | |||||||
| chr15:76070837 | C | T | 4 | a0001c0001t0001g0129 a0001c0001t0001g0142 a0002c0002t0001g0127 others(1): Show |
4 | HG02818.hp2 HG02976.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-121+10821C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76070837 | |||||||
| chr15:76070975 | C | T | 34 | a0001c0001t0001g0008 a0001c0001t0001g0109 a0001c0001t0001g0137 others(31): Show |
34 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.-121+10959C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76070975 | |||||||
| chr15:76071019 | C | T | 1 | a0001c0001t0004g0253 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-121+11003C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76071019 | |||||||
| chr15:76071074 | A | G | 2 | a0001c0001t0004g0005 a0001c0001t0004g0006 |
2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-121+11058A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76071074 | |||||||
| chr15:76071201 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-121+11185G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76071201 | |||||||
| chr15:76071245 | G | C | 31 | a0001c0001t0001g0038 a0001c0001t0001g0230 a0001c0001t0001g0234 others(28): Show |
31 | HG00558.hp1 HG01167.hp2 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.-121+11229G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76071245 | |||||||
| chr15:76071491 | G | C | 6 | a0001c0001t0001g0009 a0001c0001t0001g0143 a0001c0001t0001g0269 others(3): Show |
7 | HG01243.hp2 HG02615.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-121+11475G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76071491 | |||||||
| chr15:76071512 | AGGGCTCC others(18): Show |
A | 1 | a0001c0001t0002g0126 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-121+11499_-121+11 others(31): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76071512 | ||||||
| chr15:76071541 | G | T | 3 | a0001c0001t0001g0102 a0001c0001t0002g0104 a0002c0002t0010g0103 |
3 | HG00733.hp2 HG01978.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.-121+11525G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76071541 | |||||||
| chr15:76071591 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-121+11575A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76071591 | |||||||
| chr15:76071734 | C | A | 155 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0012 others(152): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.-121+11718C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76071734 | |||||||
| chr15:76071746 | A | G | 227 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(224): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.-121+11730A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76071746 | |||||||
| chr15:76071819 | C | T | 1 | a0004c0005t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-121+11803C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76071819 | |||||||
| chr15:76071908 | A | ATT | 6 | a0001c0001t0001g0009 a0001c0001t0001g0143 a0001c0001t0001g0269 others(3): Show |
7 | HG01243.hp2 HG02615.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-121+11903_-121+11 others(8): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76071908 | ||||||
| chr15:76072052 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-121+12036G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76072052 | |||||||
| chr15:76072205 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-121+12189G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76072205 | |||||||
| chr15:76072237 | G | T | 6 | a0001c0001t0001g0009 a0001c0001t0001g0143 a0001c0001t0001g0269 others(3): Show |
7 | HG01243.hp2 HG02615.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-121+12221G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76072237 | |||||||
| chr15:76072255 | A | G | 131 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0020 others(128): Show |
132 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.-121+12239A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76072255 | |||||||
| chr15:76072336 | G | T | 1 | a0001c0001t0001g0008 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-121+12320G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76072336 | |||||||
| chr15:76072394 | C | T | 1 | a0002c0002t0001g0075 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-121+12378C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76072394 | |||||||
| chr15:76072438 | C | CA | 45 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0102 others(42): Show |
47 | HG00438.hp2 HG00733.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.-121+12444dupA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76072438 | ||||||
| chr15:76072706 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-121+12690C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76072706 | |||||||
| chr15:76072782 | T | G | 1 | a0001c0001t0001g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-121+12766T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76072782 | |||||||
| chr15:76072856 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-121+12840T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76072856 | |||||||
| chr15:76072885 | C | A | 2 | a0001c0001t0004g0005 a0001c0001t0004g0006 |
2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-121+12869C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76072885 | |||||||
| chr15:76072963 | C | G | 1 | a0002c0002t0001g0016 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-121+12947C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76072963 | |||||||
| chr15:76072975 | G | A | 6 | a0001c0001t0001g0009 a0001c0001t0001g0143 a0001c0001t0001g0269 others(3): Show |
7 | HG01243.hp2 HG02615.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-121+12959G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76072975 | |||||||
| chr15:76072994 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-121+12978T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76072994 | |||||||
| chr15:76073041 | C | T | 1 | a0001c0001t0002g0056 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-121+13025C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76073041 | |||||||
| chr15:76073078 | T | C | 1 | a0001c0001t0002g0056 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-121+13062T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76073078 | |||||||
| chr15:76073233 | C | CT | 32 | a0001c0001t0001g0038 a0001c0001t0001g0230 a0001c0001t0001g0234 others(29): Show |
32 | HG00558.hp1 HG00741.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.-121+13232dupT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76073233 | ||||||
| chr15:76073233 | CT | C | 149 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(146): Show |
150 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-121+13232delT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76073233 | ||||||
| chr15:76073385 | A | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0143 a0001c0001t0001g0269 others(3): Show |
7 | HG01243.hp2 HG02615.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-121+13369A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76073385 | |||||||
| chr15:76073410 | T | C | 1 | a0001c0001t0002g0057 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-121+13394T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76073410 | |||||||
| chr15:76073421 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-121+13405C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76073421 | |||||||
| chr15:76073441 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-121+13425C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76073441 | |||||||
| chr15:76073481 | C | T | 1 | a0001c0001t0002g0001 | 2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-121+13465C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76073481 | |||||||
| chr15:76073512 | T | C | 6 | a0001c0001t0001g0009 a0001c0001t0001g0143 a0001c0001t0001g0269 others(3): Show |
7 | HG01243.hp2 HG02615.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-121+13496T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76073512 | |||||||
| chr15:76073524 | T | C | 6 | a0001c0001t0001g0009 a0001c0001t0001g0143 a0001c0001t0001g0269 others(3): Show |
7 | HG01243.hp2 HG02615.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-121+13508T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76073524 | |||||||
| chr15:76073796 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-121+13780G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76073796 | |||||||
| chr15:76073911 | ATGAGGCC others(4548): Show |
A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0135 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-121+13899_-121+18 others(6): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76073911 | ||||||
| chr15:76074001 | G | A | 3 | a0001c0001t0001g0257 a0001c0001t0001g0260 a0001c0001t0002g0259 |
3 | HG01167.hp2 HG01169.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-121+13985G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76074001 | |||||||
| chr15:76074145 | A | T | 1 | a0001c0001t0001g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-121+14129A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76074145 | |||||||
| chr15:76074290 | C | A | 1 | a0004c0005t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-121+14274C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76074290 | |||||||
| chr15:76074427 | ACT | A | 2 | a0001c0001t0002g0001 a0001c0001t0002g0004 |
3 | HG02809.hp1 HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-121+14414_-121+14 others(8): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76074427 | ||||||
| chr15:76074535 | C | T | 35 | a0001c0001t0001g0008 a0001c0001t0001g0109 a0001c0001t0001g0137 others(32): Show |
35 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.-121+14519C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76074535 | |||||||
| chr15:76074536 | G | A | 1 | a0001c0001t0002g0240 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-121+14520G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76074536 | |||||||
| chr15:76074570 | T | C | 4 | a0001c0001t0001g0143 a0001c0001t0001g0269 a0001c0001t0002g0001 others(1): Show |
5 | HG01243.hp2 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-121+14554T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76074570 | |||||||
| chr15:76074593 | T | C | 6 | a0001c0001t0001g0009 a0001c0001t0001g0143 a0001c0001t0001g0269 others(3): Show |
7 | HG01243.hp2 HG02615.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-121+14577T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76074593 | |||||||
| chr15:76074665 | A | G | 1 | a0001c0001t0002g0140 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-121+14649A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76074665 | |||||||
| chr15:76075062 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-121+15046A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76075062 | |||||||
| chr15:76075080 | A | G | 2 | a0001c0001t0002g0001 a0001c0001t0002g0004 |
3 | HG02809.hp1 HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-121+15064A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76075080 | |||||||
| chr15:76075211 | A | G | 2 | a0001c0001t0001g0229 a0002c0002t0001g0208 |
2 | HG01243.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-121+15195A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76075211 | |||||||
| chr15:76075266 | G | A | 1 | a0002c0002t0001g0046 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-121+15250G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76075266 | |||||||
| chr15:76075354 | G | A | 220 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(217): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.-121+15338G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76075354 | |||||||
| chr15:76075513 | A | G | 1 | a0001c0001t0002g0001 | 2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-121+15497A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76075513 | |||||||
| chr15:76075662 | C | G | 4 | a0001c0001t0002g0002 a0001c0001t0002g0051 a0001c0001t0002g0052 others(1): Show |
5 | HG00733.hp1 HG00735.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.-121+15646C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76075662 | |||||||
| chr15:76075806 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-121+15790C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76075806 | |||||||
| chr15:76075834 | CA | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 |
3 | HG01891.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-121+15819delA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76075834 | |||||||
| chr15:76075835 | A | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0130 a0002c0002t0001g0022 others(1): Show |
4 | HG02922.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-121+15819A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76075835 | |||||||
| chr15:76075836 | G | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0130 a0002c0002t0001g0022 others(1): Show |
4 | HG02922.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-121+15820G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76075836 | |||||||
| chr15:76075837 | C | CT | 53 | a0001c0001t0001g0012 a0001c0001t0001g0079 a0001c0001t0001g0083 others(50): Show |
54 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.-121+15858dupT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76075837 | ||||||
| chr15:76075837 | C | CTT | 65 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0068 others(62): Show |
65 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.-121+15857_-121+15 others(8): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76075837 | ||||||
| chr15:76075837 | C | CTTT | 13 | a0001c0001t0001g0020 a0001c0001t0001g0272 a0001c0001t0002g0104 others(10): Show |
13 | HG01978.hp1 HG02040.hp2 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.-121+15856_-121+15 others(9): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76075837 | ||||||
| chr15:76075837 | C | CTTTT | 6 | a0001c0001t0001g0229 a0001c0001t0002g0114 a0001c0001t0002g0139 others(3): Show |
6 | HG02056.hp2 HG02630.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-121+15855_-121+15 others(10): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76075837 | ||||||
| chr15:76075837 | C | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0130 a0002c0002t0001g0022 others(1): Show |
4 | HG02922.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-121+15821C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76075837 | |||||||
| chr15:76075837 | CT | C | 17 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0080 others(14): Show |
17 | HG01255.hp2 HG01884.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-121+15858delT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76075837 | ||||||
| chr15:76075837 | CTTTTT | C | 12 | a0001c0001t0001g0003 a0001c0001t0001g0230 a0001c0001t0001g0256 others(9): Show |
12 | HG02027.hp2 HG02055.hp2 HG03139.hp2 others(9): Show |
intron_variant | MODIFIER | c.-121+15854_-121+15 others(11): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76075837 | ||||||
| chr15:76075837 | CTTTTTT | C | 17 | a0001c0001t0001g0234 a0001c0001t0001g0241 a0001c0001t0001g0244 others(14): Show |
17 | HG00558.hp1 HG02080.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.-121+15853_-121+15 others(12): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76075837 | ||||||
| chr15:76075837 | CTTTTTTT | C | 12 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0132 others(9): Show |
12 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.-121+15852_-121+15 others(13): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76075837 | ||||||
| chr15:76075837 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0271 |
2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-121+15848_-121+15 others(17): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76075837 | ||||||
| chr15:76075837 | CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0002c0002t0001g0075 |
4 | HG02809.hp1 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-121+15847_-121+15 others(18): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76075837 | ||||||
| chr15:76075837 | CTTTTTTT others(7): Show |
C | 2 | a0002c0002t0001g0039 a0002c0002t0001g0164 |
2 | HG01496.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.-121+15845_-121+15 others(20): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76075837 | ||||||
| chr15:76075837 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0005g0061 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-121+15844_-121+15 others(21): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76075837 | ||||||
| chr15:76075837 | CTTTTTTT others(9): Show |
C | 2 | a0002c0002t0001g0168 a0002c0002t0001g0169 |
2 | HG02040.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.-121+15843_-121+15 others(22): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76075837 | ||||||
| chr15:76075837 | CTTTTTTT others(12): Show |
C | 1 | a0001c0001t0001g0177 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-121+15840_-121+15 others(25): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76075837 | ||||||
| chr15:76075881 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-121+15865C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76075881 | |||||||
| chr15:76075882 | G | A | 2 | a0002c0002t0006g0145 a0002c0002t0006g0150 |
2 | NA18973.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-121+15866G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76075882 | |||||||
| chr15:76075884 | G | C | 268 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(265): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-121+15868G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76075884 | |||||||
| chr15:76075889 | T | C | 268 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(265): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-121+15873T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76075889 | |||||||
| chr15:76075891 | T | C | 268 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(265): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-121+15875T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76075891 | |||||||
| chr15:76075928 | G | C | 268 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(265): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-121+15912G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76075928 | |||||||
| chr15:76075975 | A | G | 268 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(265): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-121+15959A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76075975 | |||||||
| chr15:76076039 | G | A | 2 | a0001c0001t0004g0005 a0001c0001t0004g0006 |
2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-121+16023G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76076039 | |||||||
| chr15:76076085 | T | G | 1 | a0001c0001t0002g0167 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-121+16069T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76076085 | |||||||
| chr15:76076195 | T | G | 4 | a0001c0001t0001g0143 a0001c0001t0001g0269 a0001c0001t0002g0001 others(1): Show |
5 | HG01243.hp2 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-121+16179T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76076195 | |||||||
| chr15:76076303 | A | G | 2 | a0001c0001t0002g0001 a0001c0001t0002g0004 |
3 | HG02809.hp1 HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-121+16287A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76076303 | |||||||
| chr15:76076626 | C | G | 1 | a0001c0001t0002g0219 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-121+16610C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76076626 | |||||||
| chr15:76076887 | A | G | 1 | a0001c0001t0001g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-121+16871A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76076887 | |||||||
| chr15:76076953 | G | T | 1 | a0001c0001t0001g0003 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-121+16937G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76076953 | |||||||
| chr15:76076954 | T | G | 1 | a0001c0001t0001g0003 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-121+16938T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76076954 | |||||||
| chr15:76076978 | T | G | 8 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.-121+16962T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76076978 | |||||||
| chr15:76077029 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-121+17013A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76077029 | |||||||
| chr15:76077162 | G | A | 2 | a0001c0001t0002g0220 a0002c0002t0001g0011 |
2 | HG01123.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-121+17146G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76077162 | |||||||
| chr15:76077265 | T | C | 10 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0004g0248 others(7): Show |
10 | HG02257.hp1 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-121+17249T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76077265 | |||||||
| chr15:76077298 | A | T | 1 | a0001c0001t0002g0106 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-121+17282A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76077298 | |||||||
| chr15:76077454 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-121+17438C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76077454 | |||||||
| chr15:76077529 | A | G | 16 | a0001c0001t0001g0261 a0001c0001t0001g0264 a0001c0001t0002g0063 others(13): Show |
16 | HG00609.hp2 HG01346.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-121+17513A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76077529 | |||||||
| chr15:76077569 | A | C | 1 | a0001c0001t0001g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-121+17553A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76077569 | |||||||
| chr15:76077661 | C | G | 2 | a0001c0001t0002g0001 a0001c0001t0002g0004 |
3 | HG02809.hp1 HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-121+17645C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76077661 | |||||||
| chr15:76077689 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-121+17673C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76077689 | |||||||
| chr15:76077700 | G | A | 1 | a0002c0002t0001g0215 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-121+17684G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76077700 | |||||||
| chr15:76077771 | T | C | 2 | a0001c0001t0001g0143 a0001c0001t0001g0269 |
2 | HG01243.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-121+17755T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76077771 | |||||||
| chr15:76077893 | T | C | 6 | a0001c0001t0001g0009 a0001c0001t0001g0143 a0001c0001t0001g0269 others(3): Show |
7 | HG01243.hp2 HG02615.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-121+17877T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76077893 | |||||||
| chr15:76078303 | C | G | 2 | a0001c0001t0001g0132 a0002c0002t0001g0029 |
2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-121+18287C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76078303 | |||||||
| chr15:76078343 | A | G | 1 | a0001c0001t0001g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-121+18327A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76078343 | |||||||
| chr15:76078345 | A | G | 1 | a0001c0001t0002g0191 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-121+18329A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76078345 | |||||||
| chr15:76078466 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-121+18450C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76078466 | |||||||
| chr15:76078815 | A | G | 1 | a0002c0002t0001g0125 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-121+18799A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76078815 | |||||||
| chr15:76078818 | T | G | 1 | a0001c0001t0001g0158 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-121+18802T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76078818 | |||||||
| chr15:76078885 | A | T | 1 | a0001c0001t0001g0158 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-121+18869A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76078885 | |||||||
| chr15:76078943 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-121+18927A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76078943 | |||||||
| chr15:76079045 | C | T | 1 | a0001c0001t0002g0074 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-121+19029C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76079045 | |||||||
| chr15:76079046 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-121+19030G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76079046 | |||||||
| chr15:76079232 | A | G | 1 | a0002c0002t0001g0198 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-121+19216A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76079232 | |||||||
| chr15:76079311 | G | A | 1 | a0002c0002t0001g0198 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-121+19295G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76079311 | |||||||
| chr15:76079352 | CA | C | 227 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(224): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.-121+19347delA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76079352 | ||||||
| chr15:76079390 | C | T | 3 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0008g0249 |
4 | HG02809.hp1 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-121+19374C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76079390 | |||||||
| chr15:76079392 | G | C | 34 | a0001c0001t0001g0008 a0001c0001t0001g0109 a0001c0001t0001g0137 others(31): Show |
34 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.-121+19376G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76079392 | |||||||
| chr15:76079479 | G | T | 1 | a0001c0001t0001g0003 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-121+19463G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76079479 | |||||||
| chr15:76079535 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-121+19519G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76079535 | |||||||
| chr15:76079586 | A | C | 1 | a0004c0005t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-121+19570A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76079586 | |||||||
| chr15:76079751 | G | A | 9 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(6): Show |
9 | HG01891.hp2 HG02145.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.-121+19735G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76079751 | |||||||
| chr15:76079771 | C | CA | 16 | a0001c0001t0001g0060 a0001c0001t0001g0229 a0001c0001t0002g0214 others(13): Show |
16 | HG00738.hp1 HG00741.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.-121+19774dupA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76079771 | ||||||
| chr15:76079886 | T | C | 1 | a0002c0002t0001g0163 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-121+19870T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76079886 | |||||||
| chr15:76079945 | A | G | 1 | a0001c0001t0002g0124 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-121+19929A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76079945 | |||||||
| chr15:76079967 | C | A | 1 | a0001c0001t0002g0124 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-121+19951C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76079967 | |||||||
| chr15:76079993 | A | G | 1 | a0002c0002t0001g0198 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-121+19977A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76079993 | |||||||
| chr15:76080304 | A | ATGCAGTG others(165): Show |
86 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(83): Show |
86 | HG00558.hp1 HG00597.hp1 HG00741.hp1 others(83): Show |
intron_variant | MODIFIER | c.-121+20295_-121+20 others(178): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76080304 | ||||||
| chr15:76080304 | A | ATGCAGTG others(165): Show |
1 | a0002c0002t0001g0133 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-121+20295_-121+20 others(178): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76080304 | ||||||
| chr15:76080304 | A | ATGCAGTG others(166): Show |
1 | a0001c0001t0002g0243 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-121+20295_-121+20 others(179): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76080304 | ||||||
| chr15:76080304 | A | ATGCAGTG others(164): Show |
9 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0004g0248 others(6): Show |
9 | HG02257.hp1 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-121+20295_-121+20 others(177): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76080304 | ||||||
| chr15:76080336 | T | A | 1 | a0001c0001t0001g0247 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-121+20320T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76080336 | |||||||
| chr15:76080462 | G | C | 1 | a0004c0005t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-121+20446G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76080462 | |||||||
| chr15:76080465 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-121+20449G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76080465 | |||||||
| chr15:76080468 | C | T | 4 | a0002c0002t0001g0156 a0002c0002t0001g0196 a0002c0002t0001g0197 others(1): Show |
4 | NA18940.hp2 NA18971.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.-121+20452C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76080468 | |||||||
| chr15:76080479 | G | A | 6 | a0001c0001t0001g0143 a0001c0001t0001g0269 a0001c0001t0004g0248 others(3): Show |
6 | HG01243.hp2 HG02486.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-121+20463G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76080479 | |||||||
| chr15:76080491 | C | T | 2 | a0001c0001t0001g0260 a0001c0001t0002g0259 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-121+20475C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76080491 | |||||||
| chr15:76080496 | G | A | 63 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(60): Show |
63 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.-121+20480G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76080496 | |||||||
| chr15:76080660 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-121+20644T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76080660 | |||||||
| chr15:76080686 | G | A | 16 | a0001c0001t0001g0261 a0001c0001t0001g0264 a0001c0001t0002g0035 others(13): Show |
16 | HG01346.hp2 HG02040.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-121+20670G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76080686 | |||||||
| chr15:76080800 | G | A | 21 | a0001c0001t0001g0008 a0001c0001t0001g0076 a0001c0001t0001g0078 others(18): Show |
21 | HG01167.hp2 HG01169.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.-121+20784G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76080800 | |||||||
| chr15:76080912 | AT | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0256 a0001c0001t0001g0258 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-121+20910delT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76080912 | ||||||
| chr15:76080947 | CA | C | 186 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(183): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.-121+20932delA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76080947 | |||||||
| chr15:76080950 | T | G | 186 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(183): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.-121+20934T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76080950 | |||||||
| chr15:76080988 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-121+20972C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76080988 | |||||||
| chr15:76081039 | C | T | 4 | a0001c0001t0001g0132 a0001c0001t0001g0229 a0002c0002t0001g0029 others(1): Show |
4 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-121+21023C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76081039 | |||||||
| chr15:76081076 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-121+21060T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76081076 | |||||||
| chr15:76081155 | A | G | 1 | a0001c0001t0002g0032 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-121+21139A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76081155 | |||||||
| chr15:76081204 | C | G | 107 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0038 others(104): Show |
108 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.-121+21188C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76081204 | |||||||
| chr15:76081245 | A | G | 1 | a0001c0001t0001g0003 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-121+21229A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76081245 | |||||||
| chr15:76081285 | T | C | 211 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(208): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.-121+21269T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76081285 | |||||||
| chr15:76081304 | T | C | 1 | a0001c0001t0001g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-121+21288T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76081304 | |||||||
| chr15:76081308 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-121+21292G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76081308 | |||||||
| chr15:76081479 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-121+21463C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76081479 | |||||||
| chr15:76081534 | C | G | 1 | a0002c0002t0001g0016 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-121+21518C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76081534 | |||||||
| chr15:76081714 | C | T | 208 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(205): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-121+21698C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76081714 | |||||||
| chr15:76081971 | G | A | 2 | a0001c0001t0001g0132 a0002c0002t0001g0029 |
2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-121+21955G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76081971 | |||||||
| chr15:76082002 | A | T | 1 | a0001c0001t0001g0003 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-121+21986A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76082002 | |||||||
| chr15:76082099 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-121+22083C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76082099 | |||||||
| chr15:76082156 | T | C | 187 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(184): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.-121+22140T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76082156 | |||||||
| chr15:76082221 | G | A | 4 | a0001c0001t0001g0261 a0001c0001t0002g0167 a0002c0002t0001g0268 others(1): Show |
4 | HG02145.hp2 HG02451.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-121+22205G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76082221 | |||||||
| chr15:76082227 | T | G | 22 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0076 others(19): Show |
22 | HG01167.hp2 HG01169.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.-121+22211T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76082227 | |||||||
| chr15:76082370 | G | C | 4 | a0001c0001t0001g0132 a0001c0001t0001g0229 a0002c0002t0001g0029 others(1): Show |
4 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-121+22354G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76082370 | |||||||
| chr15:76082500 | C | T | 3 | a0001c0001t0001g0068 a0001c0001t0004g0005 a0001c0001t0004g0006 |
3 | HG02559.hp1 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-121+22484C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76082500 | |||||||
| chr15:76082637 | TGAAA | T | 185 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(182): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.-121+22625_-121+22 others(10): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76082637 | ||||||
| chr15:76082797 | T | C | 209 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(206): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.-121+22781T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76082797 | |||||||
| chr15:76082892 | C | A | 1 | a0001c0001t0001g0177 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-121+22876C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76082892 | |||||||
| chr15:76082970 | A | AAAC | 46 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0109 others(43): Show |
46 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.-121+22979_-121+22 others(9): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76082970 | ||||||
| chr15:76083064 | A | G | 1 | a0002c0002t0001g0237 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-121+23048A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76083064 | |||||||
| chr15:76083079 | C | G | 1 | a0001c0001t0001g0038 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-121+23063C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76083079 | |||||||
| chr15:76083233 | C | CTT | 18 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0076 others(15): Show |
18 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-121+23232_-121+23 others(8): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76083233 | ||||||
| chr15:76083233 | C | CTTT | 5 | a0001c0001t0001g0003 a0001c0001t0001g0257 a0001c0001t0001g0260 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.-121+23231_-121+23 others(9): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76083233 | ||||||
| chr15:76083627 | T | G | 5 | a0001c0001t0001g0234 a0001c0001t0002g0243 a0002c0002t0001g0232 others(2): Show |
5 | NA18940.hp1 NA18946.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.-121+23611T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76083627 | |||||||
| chr15:76083650 | C | T | 1 | a0002c0002t0001g0099 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-121+23634C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76083650 | |||||||
| chr15:76083736 | G | A | 21 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0076 others(18): Show |
21 | HG01167.hp2 HG01169.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.-121+23720G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76083736 | |||||||
| chr15:76083775 | A | G | 209 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(206): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.-121+23759A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76083775 | |||||||
| chr15:76083812 | G | C | 1 | a0001c0001t0001g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-121+23796G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76083812 | |||||||
| chr15:76083825 | C | T | 1 | a0002c0002t0001g0131 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-121+23809C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76083825 | |||||||
| chr15:76083946 | T | C | 4 | a0001c0001t0001g0132 a0001c0001t0001g0229 a0002c0002t0001g0029 others(1): Show |
4 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-121+23930T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76083946 | |||||||
| chr15:76084041 | G | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0076 others(19): Show |
22 | HG01167.hp2 HG01169.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.-121+24025G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084041 | |||||||
| chr15:76084121 | T | C | 1 | a0001c0001t0002g0200 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-121+24105T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084121 | |||||||
| chr15:76084162 | A | G | 21 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0076 others(18): Show |
21 | HG01167.hp2 HG01169.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.-121+24146A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084162 | |||||||
| chr15:76084267 | T | G | 27 | a0001c0001t0001g0060 a0001c0001t0001g0153 a0001c0001t0001g0157 others(24): Show |
28 | HG00099.hp2 HG00280.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.-121+24251T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084267 | |||||||
| chr15:76084479 | G | A | 3 | a0001c0001t0001g0102 a0001c0001t0002g0104 a0002c0002t0010g0103 |
3 | HG00733.hp2 HG01978.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.-121+24463G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084479 | |||||||
| chr15:76084479 | G | C | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24463G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084479 | |||||||
| chr15:76084481 | A | T | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24465A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084481 | |||||||
| chr15:76084482 | T | C | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24466T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084482 | |||||||
| chr15:76084485 | G | T | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24469G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084485 | |||||||
| chr15:76084486 | G | T | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24470G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084486 | |||||||
| chr15:76084489 | A | C | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24473A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084489 | |||||||
| chr15:76084490 | A | C | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24474A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084490 | |||||||
| chr15:76084491 | A | T | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24475A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084491 | |||||||
| chr15:76084494 | G | T | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24478G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084494 | |||||||
| chr15:76084496 | A | T | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24480A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084496 | |||||||
| chr15:76084497 | A | T | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24481A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084497 | |||||||
| chr15:76084498 | G | A | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24482G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084498 | |||||||
| chr15:76084502 | T | A | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24486T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084502 | |||||||
| chr15:76084504 | A | T | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24488A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084504 | |||||||
| chr15:76084505 | G | C | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24489G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084505 | |||||||
| chr15:76084509 | G | T | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24493G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084509 | |||||||
| chr15:76084510 | G | T | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24494G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084510 | |||||||
| chr15:76084511 | G | A | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24495G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084511 | |||||||
| chr15:76084514 | A | T | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24498A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084514 | |||||||
| chr15:76084517 | G | T | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24501G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084517 | |||||||
| chr15:76084518 | G | T | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24502G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084518 | |||||||
| chr15:76084521 | C | A | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24505C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084521 | |||||||
| chr15:76084524 | A | C | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24508A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084524 | |||||||
| chr15:76084525 | G | C | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24509G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084525 | |||||||
| chr15:76084526 | G | T | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24510G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084526 | |||||||
| chr15:76084529 | A | C | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24513A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084529 | |||||||
| chr15:76084540 | T | G | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24524T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084540 | |||||||
| chr15:76084541 | G | C | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24525G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084541 | |||||||
| chr15:76084543 | C | A | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24527C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084543 | |||||||
| chr15:76084544 | T | G | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24528T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084544 | |||||||
| chr15:76084546 | T | A | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24530T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084546 | |||||||
| chr15:76084548 | T | G | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24532T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084548 | |||||||
| chr15:76084550 | T | C | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24534T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084550 | |||||||
| chr15:76084551 | G | A | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24535G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084551 | |||||||
| chr15:76084552 | G | T | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24536G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084552 | |||||||
| chr15:76084556 | A | T | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24540A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084556 | |||||||
| chr15:76084557 | A | C | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24541A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084557 | |||||||
| chr15:76084563 | A | C | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24547A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084563 | |||||||
| chr15:76084565 | A | T | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24549A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084565 | |||||||
| chr15:76084571 | A | C | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24555A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084571 | |||||||
| chr15:76084577 | C | T | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24561C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084577 | |||||||
| chr15:76084579 | G | A | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24563G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084579 | |||||||
| chr15:76084582 | A | C | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24566A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084582 | |||||||
| chr15:76084584 | G | C | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24568G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084584 | |||||||
| chr15:76084586 | G | T | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24570G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084586 | |||||||
| chr15:76084587 | G | C | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24571G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084587 | |||||||
| chr15:76084588 | G | C | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24572G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084588 | |||||||
| chr15:76084589 | T | G | 1 | a0002c0003t0001g0015 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-121+24573T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084589 | |||||||
| chr15:76084597 | G | C | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24581G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084597 | |||||||
| chr15:76084597 | G | T | 1 | a0001c0001t0001g0003 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-121+24581G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084597 | |||||||
| chr15:76084598 | G | GGT | 46 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0109 others(43): Show |
46 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.-121+24582_-121+24 others(8): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084598 | |||||||
| chr15:76084598 | G | GT | 6 | a0001c0001t0001g0020 a0001c0001t0001g0068 a0001c0001t0002g0246 others(3): Show |
6 | HG00438.hp2 HG02559.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-121+24595dupT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76084598 | ||||||
| chr15:76084598 | G | T | 3 | a0001c0001t0001g0003 a0001c0001t0002g0044 a0001c0001t0002g0063 |
3 | HG02055.hp2 HG03688.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.-121+24582G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084598 | |||||||
| chr15:76084599 | T | G | 1 | a0002c0002t0001g0075 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-121+24583T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084599 | |||||||
| chr15:76084600 | T | G | 2 | a0001c0001t0002g0027 a0001c0001t0002g0028 |
2 | HG02080.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.-121+24584T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084600 | |||||||
| chr15:76084602 | T | A | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24586T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084602 | |||||||
| chr15:76084607 | T | G | 1 | a0001c0001t0003g0031 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-121+24591T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084607 | |||||||
| chr15:76084607 | T | TG | 22 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0076 others(19): Show |
22 | HG01167.hp2 HG01169.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.-121+24591_-121+24 others(7): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084607 | |||||||
| chr15:76084608 | T | G | 47 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0109 others(44): Show |
47 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.-121+24592T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084608 | |||||||
| chr15:76084612 | G | T | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24596G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084612 | |||||||
| chr15:76084613 | T | C | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24597T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084613 | |||||||
| chr15:76084635 | G | C | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24619G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084635 | |||||||
| chr15:76084636 | T | G | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24620T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084636 | |||||||
| chr15:76084637 | G | T | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-121+24621G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084637 | |||||||
| chr15:76084704 | A | G | 208 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(205): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-121+24688A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084704 | |||||||
| chr15:76084725 | C | A | 3 | a0002c0002t0001g0221 a0002c0002t0001g0222 a0002c0002t0001g0223 |
3 | HG01069.hp1 HG01106.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.-121+24709C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084725 | |||||||
| chr15:76084811 | C | T | 9 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0004g0248 others(6): Show |
9 | HG02257.hp1 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-121+24795C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76084811 | |||||||
| chr15:76085020 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-121+25004C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76085020 | |||||||
| chr15:76085062 | G | C | 1 | a0001c0001t0002g0082 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-121+25046G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76085062 | |||||||
| chr15:76085251 | G | A | 48 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0083 others(45): Show |
48 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.-121+25235G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76085251 | |||||||
| chr15:76085542 | A | G | 1 | a0001c0001t0001g0003 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-121+25526A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76085542 | |||||||
| chr15:76085567 | G | A | 1 | a0001c0001t0002g0062 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-121+25551G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76085567 | |||||||
| chr15:76085668 | T | C | 2 | a0001c0001t0002g0122 a0002c0002t0001g0042 |
2 | NA18942.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.-121+25652T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76085668 | |||||||
| chr15:76085813 | G | A | 137 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0038 others(134): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.-121+25797G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76085813 | |||||||
| chr15:76085921 | G | A | 27 | a0001c0001t0001g0060 a0001c0001t0001g0153 a0001c0001t0001g0157 others(24): Show |
28 | HG00099.hp2 HG00280.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.-121+25905G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76085921 | |||||||
| chr15:76086053 | G | GA | 69 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(66): Show |
69 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.-121+26050dupA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76086053 | ||||||
| chr15:76086120 | A | T | 36 | a0001c0001t0001g0109 a0001c0001t0001g0137 a0001c0001t0001g0247 others(33): Show |
36 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.-121+26104A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76086120 | |||||||
| chr15:76086229 | T | A | 1 | a0001c0001t0005g0084 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-121+26213T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76086229 | |||||||
| chr15:76086261 | C | A | 70 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.-121+26245C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76086261 | |||||||
| chr15:76086639 | A | G | 70 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.-121+26623A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76086639 | |||||||
| chr15:76086653 | G | T | 1 | a0001c0001t0001g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-121+26637G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76086653 | |||||||
| chr15:76086861 | T | G | 3 | a0001c0001t0001g0068 a0001c0001t0004g0005 a0001c0001t0004g0006 |
3 | HG02559.hp1 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-121+26845T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76086861 | |||||||
| chr15:76086885 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-121+26869T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76086885 | |||||||
| chr15:76086928 | C | CG | 30 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0109 others(27): Show |
30 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.-121+26922dupG | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76086928 | ||||||
| chr15:76086928 | C | CGG | 22 | a0001c0001t0001g0076 a0001c0001t0001g0098 a0001c0001t0001g0137 others(19): Show |
22 | HG00621.hp2 HG00738.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.-121+26921_-121+26 others(8): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76086928 | ||||||
| chr15:76086928 | C | T | 2 | a0001c0001t0002g0054 a0002c0002t0001g0194 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.-121+26912C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76086928 | |||||||
| chr15:76086932 | G | GA | 137 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(134): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.-121+26916_-121+26 others(7): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76086932 | |||||||
| chr15:76086936 | G | T | 1 | a0001c0001t0001g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-121+26920G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76086936 | |||||||
| chr15:76086940 | G | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0004g0248 others(6): Show |
9 | HG02257.hp1 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-121+26924G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76086940 | |||||||
| chr15:76087123 | G | A | 208 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(205): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-121+27107G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76087123 | |||||||
| chr15:76087159 | T | G | 1 | a0002c0002t0001g0178 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-121+27143T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76087159 | |||||||
| chr15:76087281 | A | T | 1 | a0002c0007t0001g0212 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-121+27265A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76087281 | |||||||
| chr15:76087804 | A | T | 1 | a0001c0001t0011g0199 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-121+27788A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76087804 | |||||||
| chr15:76088199 | T | A | 209 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(206): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.-121+28183T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76088199 | |||||||
| chr15:76088555 | G | C | 1 | a0001c0001t0001g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-121+28539G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76088555 | |||||||
| chr15:76088577 | A | G | 1 | a0001c0001t0001g0130 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-121+28561A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76088577 | |||||||
| chr15:76088639 | T | G | 1 | a0001c0001t0001g0003 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-121+28623T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76088639 | |||||||
| chr15:76088687 | C | T | 4 | a0001c0001t0002g0193 a0002c0002t0001g0215 a0002c0002t0001g0216 others(1): Show |
4 | HG02683.hp1 HG02735.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-121+28671C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76088687 | |||||||
| chr15:76088763 | C | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0076 others(19): Show |
22 | HG01167.hp2 HG01169.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.-121+28747C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76088763 | |||||||
| chr15:76088953 | G | A | 2 | a0001c0001t0001g0229 a0002c0002t0001g0208 |
2 | HG01243.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-121+28937G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76088953 | |||||||
| chr15:76088975 | C | T | 160 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(157): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.-121+28959C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76088975 | |||||||
| chr15:76089093 | C | CA | 124 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(121): Show |
126 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.-121+29098dupA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76089093 | ||||||
| chr15:76089093 | C | CAA | 71 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(68): Show |
71 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(68): Show |
intron_variant | MODIFIER | c.-121+29097_-121+29 others(8): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76089093 | ||||||
| chr15:76089093 | C | CAAA | 11 | a0001c0001t0001g0021 a0001c0001t0001g0229 a0001c0001t0001g0230 others(8): Show |
11 | HG00438.hp1 HG00621.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.-121+29096_-121+29 others(9): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76089093 | ||||||
| chr15:76089109 | A | G | 2 | a0001c0001t0004g0005 a0001c0001t0004g0006 |
2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-121+29093A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76089109 | |||||||
| chr15:76089234 | G | A | 6 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0025 others(3): Show |
6 | HG02922.hp2 HG03098.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-121+29218G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76089234 | |||||||
| chr15:76089342 | G | A | 47 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(44): Show |
47 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.-121+29326G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76089342 | |||||||
| chr15:76089416 | A | G | 1 | a0002c0002t0001g0198 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-121+29400A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76089416 | |||||||
| chr15:76089435 | T | C | 208 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(205): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-121+29419T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76089435 | |||||||
| chr15:76089473 | T | A | 1 | a0001c0001t0001g0143 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-121+29457T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76089473 | |||||||
| chr15:76089521 | A | G | 1 | a0001c0001t0002g0236 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-121+29505A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76089521 | |||||||
| chr15:76089564 | T | C | 1 | a0001c0001t0002g0064 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-121+29548T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76089564 | |||||||
| chr15:76089574 | T | G | 1 | a0004c0005t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-121+29558T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76089574 | |||||||
| chr15:76089674 | G | A | 7 | a0002c0002t0001g0069 a0002c0002t0001g0123 a0002c0002t0001g0161 others(4): Show |
7 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.-121+29658G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76089674 | |||||||
| chr15:76089712 | T | G | 1 | a0001c0001t0002g0106 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-121+29696T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76089712 | |||||||
| chr15:76089823 | C | A | 47 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(44): Show |
47 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.-121+29807C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76089823 | |||||||
| chr15:76089988 | A | G | 47 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(44): Show |
47 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.-121+29972A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76089988 | |||||||
| chr15:76090057 | G | A | 2 | a0001c0001t0008g0249 a0004c0005t0001g0211 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-121+30041G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76090057 | |||||||
| chr15:76090199 | A | G | 47 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(44): Show |
47 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.-121+30183A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76090199 | |||||||
| chr15:76090270 | T | C | 4 | a0001c0001t0001g0230 a0001c0001t0001g0241 a0001c0001t0001g0266 others(1): Show |
4 | HG02809.hp2 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-121+30254T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76090270 | |||||||
| chr15:76090312 | C | T | 1 | a0002c0002t0001g0055 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-121+30296C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76090312 | |||||||
| chr15:76090319 | T | C | 206 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(203): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.-121+30303T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76090319 | |||||||
| chr15:76090337 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-121+30321C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76090337 | |||||||
| chr15:76090491 | C | CA | 31 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0076 others(28): Show |
31 | HG00597.hp2 HG01074.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-121+30494dupA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76090491 | ||||||
| chr15:76090491 | C | CAA | 37 | a0001c0001t0001g0003 a0001c0001t0001g0068 a0001c0001t0001g0078 others(34): Show |
38 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.-121+30493_-121+30 others(8): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76090491 | ||||||
| chr15:76090491 | CA | C | 13 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(10): Show |
13 | HG00621.hp1 HG02257.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-121+30494delA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76090491 | ||||||
| chr15:76090692 | T | A | 47 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(44): Show |
47 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.-121+30676T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76090692 | |||||||
| chr15:76090711 | G | A | 2 | a0002c0002t0001g0168 a0002c0002t0001g0169 |
2 | HG02040.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.-121+30695G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76090711 | |||||||
| chr15:76090750 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-121+30734G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76090750 | |||||||
| chr15:76091003 | G | A | 1 | a0001c0001t0002g0062 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-121+30987G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76091003 | |||||||
| chr15:76091111 | ACATAT | A | 10 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0004g0248 others(7): Show |
10 | HG02257.hp1 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-121+31098_-121+31 others(11): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76091111 | ||||||
| chr15:76091118 | A | G | 10 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0004g0248 others(7): Show |
10 | HG02257.hp1 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-121+31102A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76091118 | |||||||
| chr15:76091120 | GA | G | 10 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0004g0248 others(7): Show |
10 | HG02257.hp1 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-121+31105delA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76091120 | |||||||
| chr15:76091353 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-121+31337A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76091353 | |||||||
| chr15:76091407 | G | A | 1 | a0001c0001t0002g0136 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-121+31391G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76091407 | |||||||
| chr15:76091423 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-121+31407G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76091423 | |||||||
| chr15:76091482 | C | T | 47 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(44): Show |
47 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.-121+31466C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76091482 | |||||||
| chr15:76091505 | G | A | 36 | a0001c0001t0001g0109 a0001c0001t0001g0137 a0001c0001t0001g0247 others(33): Show |
36 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.-121+31489G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76091505 | |||||||
| chr15:76091627 | T | C | 1 | a0002c0002t0001g0198 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-121+31611T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76091627 | |||||||
| chr15:76091714 | C | T | 1 | a0001c0001t0002g0033 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-121+31698C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76091714 | |||||||
| chr15:76091844 | A | G | 7 | a0001c0001t0002g0002 a0001c0001t0002g0051 a0001c0001t0002g0052 others(4): Show |
8 | HG00733.hp1 HG00735.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.-121+31828A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76091844 | |||||||
| chr15:76092027 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-121+32011G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76092027 | |||||||
| chr15:76092228 | G | A | 1 | a0001c0001t0008g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-121+32212G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76092228 | |||||||
| chr15:76092460 | C | T | 1 | a0001c0001t0002g0191 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-121+32444C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76092460 | |||||||
| chr15:76092517 | C | A | 158 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(155): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.-121+32501C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76092517 | |||||||
| chr15:76092635 | A | G | 2 | a0001c0001t0001g0229 a0002c0002t0001g0208 |
2 | HG01243.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-121+32619A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76092635 | |||||||
| chr15:76092667 | G | A | 104 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0038 others(101): Show |
105 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.-121+32651G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76092667 | |||||||
| chr15:76092756 | A | C | 2 | a0001c0001t0001g0260 a0001c0001t0002g0259 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-121+32740A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76092756 | |||||||
| chr15:76092792 | A | G | 1 | a0004c0005t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-121+32776A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76092792 | |||||||
| chr15:76092804 | C | CT | 15 | a0001c0001t0001g0009 a0001c0001t0001g0207 a0001c0001t0002g0050 others(12): Show |
15 | HG00597.hp1 HG01123.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.-121+32809dupT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76092804 | ||||||
| chr15:76092804 | CT | C | 28 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0079 others(25): Show |
28 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.-121+32809delT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76092804 | ||||||
| chr15:76093086 | G | A | 47 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(44): Show |
47 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.-121+33070G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76093086 | |||||||
| chr15:76093259 | G | A | 1 | a0001c0001t0002g0182 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-121+33243G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76093259 | |||||||
| chr15:76093384 | C | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0076 a0001c0001t0001g0078 others(17): Show |
20 | HG01167.hp2 HG01169.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.-121+33368C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76093384 | |||||||
| chr15:76093519 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-121+33503G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76093519 | |||||||
| chr15:76093558 | G | C | 139 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0021 others(136): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.-121+33542G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76093558 | |||||||
| chr15:76093698 | C | T | 27 | a0001c0001t0001g0060 a0001c0001t0001g0153 a0001c0001t0001g0157 others(24): Show |
28 | HG00099.hp2 HG00280.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.-121+33682C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76093698 | |||||||
| chr15:76093736 | TA | T | 47 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(44): Show |
47 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.-121+33725delA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76093736 | ||||||
| chr15:76093751 | T | A | 1 | a0002c0002t0001g0055 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-121+33735T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76093751 | |||||||
| chr15:76093806 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-121+33790T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76093806 | |||||||
| chr15:76093872 | T | A | 1 | a0004c0005t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-121+33856T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76093872 | |||||||
| chr15:76093941 | T | C | 1 | a0001c0001t0001g0003 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-121+33925T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76093941 | |||||||
| chr15:76094122 | T | A | 1 | a0001c0001t0001g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-121+34106T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76094122 | |||||||
| chr15:76094220 | G | C | 20 | a0001c0001t0001g0008 a0001c0001t0001g0076 a0001c0001t0001g0078 others(17): Show |
20 | HG01167.hp2 HG01169.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.-121+34204G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76094220 | |||||||
| chr15:76094309 | G | T | 1 | a0001c0001t0001g0083 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-121+34293G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76094309 | |||||||
| chr15:76094503 | G | A | 136 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0021 others(133): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.-121+34487G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76094503 | |||||||
| chr15:76094586 | C | T | 2 | a0001c0001t0001g0137 a0001c0001t0002g0108 |
2 | HG01516.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.-121+34570C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76094586 | |||||||
| chr15:76094906 | G | A | 1 | a0001c0001t0002g0063 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-121+34890G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76094906 | |||||||
| chr15:76095025 | G | A | 1 | a0001c0001t0002g0085 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-121+35009G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76095025 | |||||||
| chr15:76095051 | A | T | 15 | a0001c0001t0002g0002 a0001c0001t0002g0041 a0001c0001t0002g0044 others(12): Show |
16 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.-121+35035A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76095051 | |||||||
| chr15:76095130 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-121+35114A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76095130 | |||||||
| chr15:76095192 | A | C | 1 | a0001c0001t0001g0003 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-121+35176A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76095192 | |||||||
| chr15:76095450 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-121+35434C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76095450 | |||||||
| chr15:76095464 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-121+35448C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76095464 | |||||||
| chr15:76095465 | G | A | 3 | a0001c0001t0001g0068 a0001c0001t0004g0005 a0001c0001t0004g0006 |
3 | HG02559.hp1 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-121+35449G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76095465 | |||||||
| chr15:76095474 | G | A | 1 | a0001c0001t0001g0003 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-121+35458G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76095474 | |||||||
| chr15:76095537 | C | T | 4 | a0001c0001t0001g0132 a0001c0001t0001g0229 a0002c0002t0001g0029 others(1): Show |
4 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-121+35521C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76095537 | |||||||
| chr15:76095546 | T | G | 47 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(44): Show |
47 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.-121+35530T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76095546 | |||||||
| chr15:76095637 | T | C | 47 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(44): Show |
47 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.-121+35621T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76095637 | |||||||
| chr15:76095685 | A | T | 1 | a0001c0001t0001g0003 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-121+35669A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76095685 | |||||||
| chr15:76095699 | C | T | 3 | a0001c0001t0001g0068 a0001c0001t0004g0005 a0001c0001t0004g0006 |
3 | HG02559.hp1 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-121+35683C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76095699 | |||||||
| chr15:76095722 | C | T | 130 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0021 others(127): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.-121+35706C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76095722 | |||||||
| chr15:76096302 | A | T | 45 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0109 others(42): Show |
45 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.-121+36286A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76096302 | |||||||
| chr15:76096306 | T | C | 1 | a0002c0002t0001g0016 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-121+36290T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76096306 | |||||||
| chr15:76096534 | T | C | 2 | a0001c0001t0001g0256 a0001c0001t0001g0258 |
2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-121+36518T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76096534 | |||||||
| chr15:76096537 | A | G | 1 | a0002c0002t0001g0189 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-121+36521A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76096537 | |||||||
| chr15:76096581 | T | C | 1 | a0001c0001t0004g0248 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-121+36565T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76096581 | |||||||
| chr15:76096661 | G | T | 47 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(44): Show |
47 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.-121+36645G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76096661 | |||||||
| chr15:76096696 | G | A | 1 | a0002c0002t0001g0016 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-121+36680G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76096696 | |||||||
| chr15:76096741 | A | G | 1 | a0001c0001t0001g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-121+36725A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76096741 | |||||||
| chr15:76096932 | A | AT | 116 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0012 others(113): Show |
117 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.-121+36933dupT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76096932 | ||||||
| chr15:76096932 | A | ATT | 11 | a0001c0001t0001g0188 a0001c0001t0001g0271 a0001c0001t0002g0035 others(8): Show |
11 | HG00597.hp2 HG00735.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.-121+36932_-121+36 others(8): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76096932 | ||||||
| chr15:76096961 | T | G | 208 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(205): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-121+36945T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76096961 | |||||||
| chr15:76097026 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-121+37010C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76097026 | |||||||
| chr15:76097259 | T | C | 1 | a0001c0001t0001g0003 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-120-36909T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76097259 | |||||||
| chr15:76097396 | T | C | 1 | a0002c0002t0001g0215 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-120-36772T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76097396 | |||||||
| chr15:76097602 | T | C | 159 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(156): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.-120-36566T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76097602 | |||||||
| chr15:76097604 | G | A | 3 | a0002c0002t0001g0155 a0002c0002t0001g0163 a0002c0002t0001g0204 |
3 | HG01928.hp1 HG01943.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.-120-36564G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76097604 | |||||||
| chr15:76097609 | G | T | 46 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0109 others(43): Show |
46 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.-120-36559G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76097609 | |||||||
| chr15:76097661 | A | G | 1 | a0001c0001t0001g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-120-36507A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76097661 | |||||||
| chr15:76097662 | G | A | 1 | a0001c0001t0001g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-120-36506G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76097662 | |||||||
| chr15:76097663 | T | A | 1 | a0001c0001t0001g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-120-36505T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76097663 | |||||||
| chr15:76097664 | T | C | 1 | a0001c0001t0001g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-120-36504T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76097664 | |||||||
| chr15:76097665 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-120-36503C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76097665 | |||||||
| chr15:76097832 | C | G | 3 | a0001c0001t0001g0068 a0001c0001t0004g0005 a0001c0001t0004g0006 |
3 | HG02559.hp1 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-120-36336C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76097832 | |||||||
| chr15:76098307 | C | T | 2 | a0001c0001t0008g0249 a0004c0005t0001g0211 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-120-35861C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76098307 | |||||||
| chr15:76098343 | T | A | 1 | a0002c0002t0001g0208 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-120-35825T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76098343 | |||||||
| chr15:76098395 | G | T | 139 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0021 others(136): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.-120-35773G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76098395 | |||||||
| chr15:76098405 | C | A | 1 | a0004c0005t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-120-35763C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76098405 | |||||||
| chr15:76098473 | T | C | 1 | a0001c0001t0001g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-120-35695T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76098473 | |||||||
| chr15:76098543 | A | G | 3 | a0001c0001t0001g0068 a0001c0001t0004g0005 a0001c0001t0004g0006 |
3 | HG02559.hp1 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-120-35625A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76098543 | |||||||
| chr15:76098684 | G | A | 2 | a0001c0001t0002g0245 a0001c0001t0002g0246 |
2 | HG01891.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-120-35484G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76098684 | |||||||
| chr15:76098848 | A | G | 3 | a0001c0001t0001g0068 a0001c0001t0004g0005 a0001c0001t0004g0006 |
3 | HG02559.hp1 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-120-35320A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76098848 | |||||||
| chr15:76098961 | C | T | 1 | a0002c0002t0001g0164 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-120-35207C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76098961 | |||||||
| chr15:76099066 | G | A | 10 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0004g0248 others(7): Show |
10 | HG02257.hp1 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-120-35102G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76099066 | |||||||
| chr15:76099167 | C | T | 2 | a0001c0001t0001g0132 a0002c0002t0001g0029 |
2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-120-35001C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76099167 | |||||||
| chr15:76099207 | G | A | 48 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0020 others(45): Show |
48 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.-120-34961G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76099207 | |||||||
| chr15:76099236 | G | A | 1 | a0002c0002t0001g0016 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-120-34932G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76099236 | |||||||
| chr15:76099243 | G | A | 207 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(204): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.-120-34925G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76099243 | |||||||
| chr15:76099471 | T | C | 216 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(213): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-120-34697T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76099471 | |||||||
| chr15:76099488 | G | A | 15 | a0001c0001t0001g0060 a0001c0001t0001g0158 a0001c0001t0002g0065 others(12): Show |
15 | HG00280.hp2 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.-120-34680G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76099488 | |||||||
| chr15:76099783 | C | T | 48 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0020 others(45): Show |
48 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.-120-34385C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76099783 | |||||||
| chr15:76099900 | C | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0076 a0001c0001t0001g0078 others(17): Show |
20 | HG01167.hp2 HG01169.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.-120-34268C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76099900 | |||||||
| chr15:76099991 | T | C | 68 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(65): Show |
68 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.-120-34177T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76099991 | |||||||
| chr15:76100083 | T | C | 1 | a0001c0001t0002g0074 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-120-34085T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76100083 | |||||||
| chr15:76100135 | C | G | 208 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(205): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.-120-34033C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76100135 | |||||||
| chr15:76100257 | C | G | 1 | a0002c0002t0001g0113 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-120-33911C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76100257 | |||||||
| chr15:76100382 | A | G | 36 | a0001c0001t0001g0109 a0001c0001t0001g0137 a0001c0001t0001g0247 others(33): Show |
36 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.-120-33786A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76100382 | |||||||
| chr15:76101193 | C | T | 4 | a0001c0001t0001g0068 a0001c0001t0001g0261 a0001c0001t0004g0005 others(1): Show |
4 | HG02559.hp1 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120-32975C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76101193 | |||||||
| chr15:76101326 | T | C | 6 | a0001c0001t0001g0102 a0001c0001t0002g0063 a0001c0001t0002g0104 others(3): Show |
6 | HG00733.hp2 HG01978.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.-120-32842T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76101326 | |||||||
| chr15:76101349 | C | T | 4 | a0001c0001t0001g0068 a0001c0001t0001g0261 a0001c0001t0004g0005 others(1): Show |
4 | HG02559.hp1 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120-32819C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76101349 | |||||||
| chr15:76101506 | G | A | 1 | a0002c0002t0001g0231 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-120-32662G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76101506 | |||||||
| chr15:76101662 | G | A | 1 | a0001c0001t0004g0005 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-120-32506G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76101662 | |||||||
| chr15:76101730 | G | A | 1 | a0002c0002t0001g0120 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-120-32438G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76101730 | |||||||
| chr15:76101780 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-120-32388A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76101780 | |||||||
| chr15:76101820 | G | A | 2 | a0001c0001t0001g0229 a0002c0002t0001g0208 |
2 | HG01243.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-120-32348G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76101820 | |||||||
| chr15:76101893 | C | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0076 a0001c0001t0001g0078 others(17): Show |
20 | HG01167.hp2 HG01169.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.-120-32275C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76101893 | |||||||
| chr15:76101945 | A | G | 199 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(196): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.-120-32223A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76101945 | |||||||
| chr15:76102038 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-120-32130G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76102038 | |||||||
| chr15:76102078 | T | C | 199 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(196): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.-120-32090T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76102078 | |||||||
| chr15:76102092 | G | A | 20 | a0001c0001t0001g0008 a0001c0001t0001g0076 a0001c0001t0001g0078 others(17): Show |
20 | HG01167.hp2 HG01169.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.-120-32076G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76102092 | |||||||
| chr15:76102229 | T | G | 1 | a0001c0001t0008g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-120-31939T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76102229 | |||||||
| chr15:76102322 | A | G | 2 | a0002c0002t0001g0170 a0002c0002t0001g0171 |
2 | HG01515.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-120-31846A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76102322 | |||||||
| chr15:76102347 | A | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0271 |
2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-120-31821A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76102347 | |||||||
| chr15:76102837 | C | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0076 a0001c0001t0001g0078 others(17): Show |
20 | HG01167.hp2 HG01169.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.-120-31331C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76102837 | |||||||
| chr15:76102840 | C | CA | 37 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0019 others(34): Show |
38 | HG00438.hp1 HG00621.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.-120-31308dupA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76102840 | ||||||
| chr15:76102840 | CA | C | 18 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0078 others(15): Show |
18 | HG00597.hp1 HG00609.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.-120-31308delA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76102840 | ||||||
| chr15:76102969 | T | C | 20 | a0001c0001t0001g0166 a0001c0001t0001g0234 a0001c0001t0001g0244 others(17): Show |
20 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.-120-31199T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76102969 | |||||||
| chr15:76103090 | G | A | 130 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0021 others(127): Show |
132 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.-120-31078G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76103090 | |||||||
| chr15:76103145 | C | A | 1 | a0001c0001t0001g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-120-31023C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76103145 | |||||||
| chr15:76103146 | A | C | 1 | a0001c0001t0008g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-120-31022A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76103146 | |||||||
| chr15:76103195 | G | A | 20 | a0001c0001t0001g0008 a0001c0001t0001g0076 a0001c0001t0001g0078 others(17): Show |
20 | HG01167.hp2 HG01169.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.-120-30973G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76103195 | |||||||
| chr15:76103216 | G | A | 67 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(64): Show |
67 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.-120-30952G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76103216 | |||||||
| chr15:76103329 | C | A | 94 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0021 others(91): Show |
95 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.-120-30839C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76103329 | |||||||
| chr15:76103340 | CA | C | 68 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(65): Show |
68 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.-120-30817delA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76103340 | ||||||
| chr15:76103397 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0003g0014 |
3 | HG02647.hp1 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-120-30771G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76103397 | |||||||
| chr15:76103570 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-120-30598C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76103570 | |||||||
| chr15:76103656 | A | T | 48 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0020 others(45): Show |
48 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.-120-30512A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76103656 | |||||||
| chr15:76103761 | AATTAGC | A | 3 | a0001c0001t0001g0166 a0001c0001t0002g0165 a0002c0002t0001g0100 |
3 | HG00140.hp1 HG01074.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-120-30406_-120-30 others(12): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76103761 | |||||||
| chr15:76103857 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-120-30311A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76103857 | |||||||
| chr15:76103910 | C | CA | 9 | a0001c0001t0001g0009 a0001c0001t0001g0068 a0001c0001t0001g0098 others(6): Show |
9 | HG01109.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-120-30243dupA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76103910 | ||||||
| chr15:76103910 | C | CAA | 31 | a0001c0001t0001g0003 a0001c0001t0001g0060 a0001c0001t0001g0153 others(28): Show |
32 | HG00099.hp2 HG00280.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.-120-30244_-120-30 others(8): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76103910 | ||||||
| chr15:76103910 | CA | C | 66 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(63): Show |
66 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.-120-30243delA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76103910 | ||||||
| chr15:76103981 | G | C | 20 | a0001c0001t0001g0008 a0001c0001t0001g0076 a0001c0001t0001g0078 others(17): Show |
20 | HG01167.hp2 HG01169.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.-120-30187G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76103981 | |||||||
| chr15:76103990 | G | A | 2 | a0001c0001t0001g0157 a0001c0001t0002g0173 |
2 | HG01175.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-120-30178G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76103990 | |||||||
| chr15:76103996 | AG | A | 48 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0020 others(45): Show |
48 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.-120-30170delG | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76103996 | ||||||
| chr15:76104016 | G | A | 1 | a0001c0001t0002g0036 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-120-30152G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76104016 | |||||||
| chr15:76104182 | G | A | 2 | a0001c0001t0005g0084 a0001c0001t0005g0097 |
2 | HG00597.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-120-29986G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76104182 | |||||||
| chr15:76104205 | C | CA | 19 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0076 others(16): Show |
19 | HG01167.hp2 HG01169.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.-120-29950dupA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76104205 | ||||||
| chr15:76104205 | C | CAAAAA | 38 | a0001c0001t0001g0020 a0001c0001t0001g0109 a0001c0001t0001g0137 others(35): Show |
38 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.-120-29954_-120-29 others(11): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76104205 | ||||||
| chr15:76104205 | CA | C | 126 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0021 others(123): Show |
128 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.-120-29950delA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76104205 | ||||||
| chr15:76104205 | CAA | C | 10 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0004g0248 others(7): Show |
10 | HG02257.hp1 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-120-29951_-120-29 others(8): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76104205 | ||||||
| chr15:76104219 | T | A | 18 | a0001c0001t0001g0008 a0001c0001t0001g0076 a0001c0001t0001g0078 others(15): Show |
18 | HG01167.hp2 HG01169.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.-120-29949T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76104219 | |||||||
| chr15:76104231 | G | A | 1 | a0002c0002t0001g0174 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-120-29937G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76104231 | |||||||
| chr15:76104355 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0271 |
2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-120-29813C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76104355 | |||||||
| chr15:76104424 | A | G | 2 | a0001c0001t0001g0229 a0002c0002t0001g0208 |
2 | HG01243.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-120-29744A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76104424 | |||||||
| chr15:76104454 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-120-29714T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76104454 | |||||||
| chr15:76104487 | T | G | 1 | a0002c0002t0001g0123 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-120-29681T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76104487 | |||||||
| chr15:76104544 | C | T | 2 | a0002c0002t0001g0161 a0002c0002t0001g0162 |
2 | HG00738.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.-120-29624C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76104544 | |||||||
| chr15:76104547 | G | C | 20 | a0001c0001t0001g0008 a0001c0001t0001g0076 a0001c0001t0001g0078 others(17): Show |
20 | HG01167.hp2 HG01169.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.-120-29621G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76104547 | |||||||
| chr15:76104589 | C | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0076 a0001c0001t0001g0078 others(17): Show |
20 | HG01167.hp2 HG01169.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.-120-29579C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76104589 | |||||||
| chr15:76104645 | C | T | 68 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(65): Show |
68 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.-120-29523C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76104645 | |||||||
| chr15:76105017 | A | G | 68 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(65): Show |
68 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.-120-29151A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76105017 | |||||||
| chr15:76105049 | C | T | 91 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0021 others(88): Show |
92 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.-120-29119C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76105049 | |||||||
| chr15:76105114 | C | T | 3 | a0001c0001t0001g0157 a0001c0001t0002g0173 a0001c0001t0002g0176 |
3 | HG01175.hp2 HG02486.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.-120-29054C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76105114 | |||||||
| chr15:76105202 | C | T | 1 | a0001c0001t0002g0213 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-120-28966C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76105202 | |||||||
| chr15:76105405 | C | T | 2 | a0002c0002t0001g0125 a0002c0002t0001g0141 |
2 | HG01169.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.-120-28763C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76105405 | |||||||
| chr15:76105424 | C | T | 1 | a0001c0001t0008g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-120-28744C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76105424 | |||||||
| chr15:76105430 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-120-28738A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76105430 | |||||||
| chr15:76105452 | T | C | 1 | a0001c0001t0001g0003 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-120-28716T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76105452 | |||||||
| chr15:76105560 | C | T | 2 | a0001c0001t0001g0229 a0002c0002t0001g0208 |
2 | HG01243.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-120-28608C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76105560 | |||||||
| chr15:76105562 | A | G | 20 | a0001c0001t0001g0008 a0001c0001t0001g0076 a0001c0001t0001g0078 others(17): Show |
20 | HG01167.hp2 HG01169.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.-120-28606A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76105562 | |||||||
| chr15:76105613 | G | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0271 others(1): Show |
4 | HG01891.hp2 HG02615.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-120-28555G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76105613 | |||||||
| chr15:76105706 | A | G | 27 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(24): Show |
27 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.-120-28462A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76105706 | |||||||
| chr15:76105840 | T | C | 1 | a0002c0002t0001g0270 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-120-28328T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76105840 | |||||||
| chr15:76105852 | A | G | 176 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(173): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.-120-28316A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76105852 | |||||||
| chr15:76105865 | C | T | 173 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(170): Show |
175 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.-120-28303C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76105865 | |||||||
| chr15:76105868 | T | G | 1 | a0001c0001t0008g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-120-28300T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76105868 | |||||||
| chr15:76105988 | G | A | 1 | a0001c0001t0001g0003 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-120-28180G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76105988 | |||||||
| chr15:76106043 | A | G | 205 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(202): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.-120-28125A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76106043 | |||||||
| chr15:76106051 | A | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(204): Show |
209 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.-120-28117A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76106051 | |||||||
| chr15:76106224 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-120-27944A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76106224 | |||||||
| chr15:76106267 | A | G | 266 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(263): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.-120-27901A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76106267 | |||||||
| chr15:76106284 | G | A | 2 | a0001c0001t0001g0068 a0002c0002t0001g0164 |
2 | HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-120-27884G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76106284 | |||||||
| chr15:76106340 | A | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0258 a0001c0001t0002g0001 others(2): Show |
6 | HG02809.hp1 HG02886.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-120-27828A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76106340 | |||||||
| chr15:76106545 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-120-27623T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76106545 | |||||||
| chr15:76106646 | A | G | 83 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(80): Show |
83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.-120-27522A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76106646 | |||||||
| chr15:76106673 | C | T | 63 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0102 others(60): Show |
63 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.-120-27495C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76106673 | |||||||
| chr15:76106742 | A | G | 1 | a0002c0002t0001g0169 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-120-27426A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76106742 | |||||||
| chr15:76106831 | T | G | 1 | a0001c0001t0003g0031 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-120-27337T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76106831 | |||||||
| chr15:76106996 | C | G | 1 | a0001c0001t0001g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-120-27172C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76106996 | |||||||
| chr15:76107066 | C | T | 3 | a0001c0001t0001g0076 a0001c0001t0001g0135 a0001c0001t0001g0229 |
3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-120-27102C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76107066 | |||||||
| chr15:76107178 | G | A | 135 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(132): Show |
135 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.-120-26990G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76107178 | |||||||
| chr15:76107340 | C | T | 27 | a0001c0001t0002g0002 a0001c0001t0002g0027 a0001c0001t0002g0028 others(24): Show |
28 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.-120-26828C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76107340 | |||||||
| chr15:76107343 | G | A | 1 | a0001c0001t0002g0167 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-120-26825G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76107343 | |||||||
| chr15:76107684 | G | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0078 others(3): Show |
6 | HG01891.hp2 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-120-26484G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76107684 | |||||||
| chr15:76107718 | T | C | 1 | a0002c0002t0001g0048 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-120-26450T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76107718 | |||||||
| chr15:76107754 | G | T | 7 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0023 others(4): Show |
7 | HG02922.hp1 HG02970.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.-120-26414G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76107754 | |||||||
| chr15:76108028 | C | T | 10 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0023 others(7): Show |
10 | HG02451.hp2 HG02647.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.-120-26140C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76108028 | |||||||
| chr15:76108068 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-120-26100A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76108068 | |||||||
| chr15:76108145 | G | A | 12 | a0001c0001t0002g0030 a0001c0001t0002g0082 a0001c0001t0002g0085 others(9): Show |
12 | HG02071.hp2 HG02083.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.-120-26023G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76108145 | |||||||
| chr15:76108205 | C | T | 2 | a0001c0001t0002g0165 a0002c0002t0001g0100 |
2 | HG00140.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.-120-25963C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76108205 | |||||||
| chr15:76108316 | G | A | 5 | a0001c0001t0001g0093 a0001c0001t0001g0129 a0001c0001t0001g0142 others(2): Show |
5 | HG02818.hp2 HG02976.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-120-25852G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76108316 | |||||||
| chr15:76108335 | C | T | 1 | a0001c0001t0002g0116 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-120-25833C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76108335 | |||||||
| chr15:76108482 | T | G | 1 | a0001c0001t0002g0041 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-120-25686T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76108482 | |||||||
| chr15:76108938 | C | G | 1 | a0001c0001t0001g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-120-25230C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76108938 | |||||||
| chr15:76109139 | T | C | 3 | a0002c0002t0002g0010 a0002c0002t0002g0107 a0002c0002t0002g0138 |
3 | NA18965.hp1 NA18970.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-120-25029T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76109139 | |||||||
| chr15:76109269 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-120-24899T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76109269 | |||||||
| chr15:76109300 | A | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0038 others(1): Show |
4 | HG02280.hp2 HG02647.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120-24868A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76109300 | |||||||
| chr15:76109302 | G | A | 1 | a0001c0001t0004g0254 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-120-24866G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76109302 | |||||||
| chr15:76109408 | A | C | 24 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(21): Show |
24 | HG02056.hp1 HG02129.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.-120-24760A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76109408 | |||||||
| chr15:76109562 | T | C | 37 | a0001c0001t0001g0076 a0001c0001t0001g0135 a0001c0001t0001g0143 others(34): Show |
39 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.-120-24606T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76109562 | |||||||
| chr15:76109644 | G | T | 5 | a0001c0001t0001g0068 a0001c0001t0004g0248 a0002c0002t0001g0011 others(2): Show |
5 | HG02486.hp1 HG02559.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-120-24524G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76109644 | |||||||
| chr15:76109663 | A | G | 24 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0023 others(21): Show |
24 | HG02056.hp1 HG02129.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.-120-24505A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76109663 | |||||||
| chr15:76109711 | C | CT | 6 | a0001c0001t0001g0132 a0001c0001t0002g0045 a0001c0001t0008g0249 others(3): Show |
6 | HG01109.hp1 HG01884.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-120-24441dupT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76109711 | ||||||
| chr15:76109711 | CT | C | 47 | a0001c0001t0001g0060 a0001c0001t0001g0076 a0001c0001t0001g0081 others(44): Show |
49 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.-120-24441delT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76109711 | ||||||
| chr15:76109816 | G | A | 1 | a0002c0002t0001g0218 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-120-24352G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76109816 | |||||||
| chr15:76109897 | C | T | 3 | a0001c0001t0001g0241 a0002c0002t0012g0267 a0002c0003t0001g0015 |
3 | HG02257.hp1 HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-120-24271C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76109897 | |||||||
| chr15:76109947 | G | A | 7 | a0001c0001t0001g0234 a0001c0001t0002g0095 a0001c0001t0002g0235 others(4): Show |
7 | HG02155.hp2 NA18940.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.-120-24221G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76109947 | |||||||
| chr15:76109953 | C | G | 1 | a0001c0001t0001g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-120-24215C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76109953 | |||||||
| chr15:76110039 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-120-24129G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76110039 | |||||||
| chr15:76110063 | G | A | 1 | a0002c0002t0001g0048 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-120-24105G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76110063 | |||||||
| chr15:76110133 | G | A | 144 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(141): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.-120-24035G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76110133 | |||||||
| chr15:76110166 | AT | A | 7 | a0001c0001t0001g0234 a0001c0001t0002g0095 a0001c0001t0002g0235 others(4): Show |
7 | HG02155.hp2 NA18940.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.-120-23992delT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76110166 | ||||||
| chr15:76110283 | A | G | 146 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(143): Show |
148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-120-23885A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76110283 | |||||||
| chr15:76110382 | C | T | 1 | a0001c0001t0002g0187 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-120-23786C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76110382 | |||||||
| chr15:76110454 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-120-23714C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76110454 | |||||||
| chr15:76110490 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0023 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-120-23678C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76110490 | |||||||
| chr15:76110584 | A | G | 8 | a0001c0001t0001g0143 a0001c0001t0001g0269 a0001c0001t0002g0045 others(5): Show |
8 | HG01243.hp2 HG01884.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-120-23584A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76110584 | |||||||
| chr15:76110638 | G | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0038 others(1): Show |
4 | HG02280.hp2 HG02647.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120-23530G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76110638 | |||||||
| chr15:76110696 | C | T | 3 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0126 |
3 | HG00140.hp2 HG00280.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.-120-23472C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76110696 | |||||||
| chr15:76110761 | A | G | 86 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0060 others(83): Show |
86 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.-120-23407A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76110761 | |||||||
| chr15:76111033 | T | C | 2 | a0001c0001t0001g0271 a0004c0005t0001g0211 |
2 | HG02615.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-120-23135T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76111033 | |||||||
| chr15:76111048 | G | A | 1 | a0001c0001t0002g0050 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-120-23120G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76111048 | |||||||
| chr15:76111075 | C | T | 1 | a0002c0002t0001g0160 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-120-23093C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76111075 | |||||||
| chr15:76111083 | C | CT | 144 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(141): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.-120-23071dupT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76111083 | ||||||
| chr15:76111111 | G | C | 2 | a0001c0001t0002g0045 a0002c0002t0001g0053 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-120-23057G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76111111 | |||||||
| chr15:76111200 | C | T | 4 | a0001c0001t0002g0070 a0001c0001t0002g0116 a0001c0001t0002g0210 others(1): Show |
4 | HG00609.hp2 HG00621.hp2 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120-22968C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76111200 | |||||||
| chr15:76111269 | C | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0269 |
2 | HG01243.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-120-22899C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76111269 | |||||||
| chr15:76111446 | T | C | 146 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(143): Show |
148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-120-22722T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76111446 | |||||||
| chr15:76111447 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-120-22721G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76111447 | |||||||
| chr15:76111472 | C | T | 5 | a0001c0001t0001g0102 a0001c0001t0001g0153 a0001c0001t0001g0158 others(2): Show |
5 | HG00735.hp2 HG01106.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.-120-22696C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76111472 | |||||||
| chr15:76111552 | C | T | 144 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(141): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.-120-22616C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76111552 | |||||||
| chr15:76111553 | G | A | 4 | a0001c0001t0002g0070 a0001c0001t0002g0116 a0001c0001t0002g0210 others(1): Show |
4 | HG00609.hp2 HG00621.hp2 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120-22615G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76111553 | |||||||
| chr15:76111573 | G | A | 156 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(153): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-120-22595G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76111573 | |||||||
| chr15:76111589 | A | G | 146 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(143): Show |
148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-120-22579A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76111589 | |||||||
| chr15:76111748 | C | A | 2 | a0001c0001t0002g0045 a0002c0002t0001g0053 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-120-22420C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76111748 | |||||||
| chr15:76111752 | A | G | 146 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(143): Show |
148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-120-22416A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76111752 | |||||||
| chr15:76111942 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-120-22226C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76111942 | |||||||
| chr15:76111979 | G | C | 5 | a0001c0001t0001g0009 a0001c0001t0001g0266 a0001c0001t0004g0005 others(2): Show |
5 | HG02922.hp1 HG02970.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-120-22189G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76111979 | |||||||
| chr15:76112029 | A | C | 1 | a0001c0001t0001g0068 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-120-22139A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76112029 | |||||||
| chr15:76112321 | T | C | 1 | a0002c0002t0001g0094 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-120-21847T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76112321 | |||||||
| chr15:76112378 | A | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0078 others(3): Show |
6 | HG01891.hp2 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-120-21790A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76112378 | |||||||
| chr15:76112424 | G | A | 149 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(146): Show |
151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.-120-21744G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76112424 | |||||||
| chr15:76112833 | A | G | 1 | a0001c0001t0002g0070 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-120-21335A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76112833 | |||||||
| chr15:76113044 | G | A | 1 | a0001c0001t0002g0220 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-120-21124G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76113044 | |||||||
| chr15:76113053 | C | T | 1 | a0001c0001t0002g0203 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-120-21115C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76113053 | |||||||
| chr15:76113229 | G | A | 144 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(141): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.-120-20939G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76113229 | |||||||
| chr15:76113550 | G | T | 29 | a0001c0001t0001g0083 a0001c0001t0002g0030 a0001c0001t0002g0035 others(26): Show |
29 | HG00099.hp1 HG00741.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.-120-20618G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76113550 | |||||||
| chr15:76113587 | A | T | 2 | a0001c0001t0001g0271 a0004c0005t0001g0211 |
2 | HG02615.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-120-20581A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76113587 | |||||||
| chr15:76113705 | C | A | 1 | a0001c0001t0002g0104 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-120-20463C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76113705 | |||||||
| chr15:76113772 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-120-20396G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76113772 | |||||||
| chr15:76113772 | G | C | 12 | a0001c0001t0001g0093 a0001c0001t0001g0129 a0001c0001t0001g0142 others(9): Show |
12 | HG02056.hp1 HG02129.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-120-20396G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76113772 | |||||||
| chr15:76113962 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-120-20206A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76113962 | |||||||
| chr15:76113988 | G | A | 153 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(150): Show |
155 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-120-20180G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76113988 | |||||||
| chr15:76114009 | C | G | 1 | a0002c0002t0012g0267 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-120-20159C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76114009 | |||||||
| chr15:76114043 | C | T | 2 | a0001c0001t0001g0271 a0004c0005t0001g0211 |
2 | HG02615.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-120-20125C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76114043 | |||||||
| chr15:76114100 | T | G | 3 | a0001c0001t0002g0043 a0001c0001t0002g0122 a0002c0002t0001g0042 |
3 | HG02132.hp1 NA18942.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.-120-20068T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76114100 | |||||||
| chr15:76114260 | T | C | 144 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(141): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.-120-19908T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76114260 | |||||||
| chr15:76114328 | T | G | 1 | a0001c0001t0001g0098 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-120-19840T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76114328 | |||||||
| chr15:76114410 | C | G | 2 | a0001c0001t0001g0271 a0004c0005t0001g0211 |
2 | HG02615.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-120-19758C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76114410 | |||||||
| chr15:76114412 | C | T | 2 | a0001c0001t0002g0119 a0001c0001t0002g0147 |
2 | HG00438.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.-120-19756C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76114412 | |||||||
| chr15:76114502 | A | G | 2 | a0001c0001t0001g0271 a0004c0005t0001g0211 |
2 | HG02615.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-120-19666A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76114502 | |||||||
| chr15:76114610 | A | C | 144 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(141): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.-120-19558A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76114610 | |||||||
| chr15:76114665 | T | C | 2 | a0002c0002t0001g0170 a0002c0002t0001g0171 |
2 | HG01515.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-120-19503T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76114665 | |||||||
| chr15:76114779 | T | C | 118 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0019 others(115): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.-120-19389T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76114779 | |||||||
| chr15:76114822 | T | C | 43 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0078 others(40): Show |
44 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.-120-19346T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76114822 | |||||||
| chr15:76114854 | A | T | 4 | a0001c0001t0002g0070 a0001c0001t0002g0116 a0001c0001t0002g0210 others(1): Show |
4 | HG00609.hp2 HG00621.hp2 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120-19314A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76114854 | |||||||
| chr15:76114893 | T | A | 2 | a0001c0001t0001g0098 a0004c0005t0001g0211 |
2 | HG02055.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-120-19275T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76114893 | |||||||
| chr15:76114947 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-120-19221G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76114947 | |||||||
| chr15:76114980 | T | C | 1 | a0001c0001t0002g0151 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-120-19188T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76114980 | |||||||
| chr15:76115494 | T | G | 1 | a0001c0001t0001g0081 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-120-18674T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76115494 | |||||||
| chr15:76115496 | C | CT | 7 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0098 others(4): Show |
7 | HG02055.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-120-18666dupT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76115496 | ||||||
| chr15:76115741 | C | T | 3 | a0001c0001t0001g0132 a0002c0002t0001g0029 a0002c0002t0001g0040 |
3 | HG01109.hp1 HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-120-18427C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76115741 | |||||||
| chr15:76115749 | G | A | 130 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(127): Show |
132 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.-120-18419G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76115749 | |||||||
| chr15:76115751 | AT | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0038 others(1): Show |
4 | HG02280.hp2 HG02647.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120-18414delT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76115751 | ||||||
| chr15:76115846 | G | T | 11 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0023 others(8): Show |
11 | HG02055.hp1 HG02451.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-120-18322G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76115846 | |||||||
| chr15:76115962 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-120-18206C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76115962 | |||||||
| chr15:76116003 | G | T | 6 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0023 others(3): Show |
6 | HG02970.hp2 HG03098.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-120-18165G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76116003 | |||||||
| chr15:76116207 | T | C | 152 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(149): Show |
154 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(151): Show |
intron_variant | MODIFIER | c.-120-17961T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76116207 | |||||||
| chr15:76116224 | C | T | 1 | a0001c0001t0008g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-120-17944C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76116224 | |||||||
| chr15:76116277 | CT | C | 182 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(179): Show |
184 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(181): Show |
intron_variant | MODIFIER | c.-120-17888delT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76116277 | ||||||
| chr15:76116322 | G | T | 1 | a0005c0006t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-120-17846G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76116322 | |||||||
| chr15:76116358 | A | G | 145 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(142): Show |
147 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(144): Show |
intron_variant | MODIFIER | c.-120-17810A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76116358 | |||||||
| chr15:76116365 | T | C | 145 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(142): Show |
147 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(144): Show |
intron_variant | MODIFIER | c.-120-17803T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76116365 | |||||||
| chr15:76116473 | G | A | 148 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(145): Show |
150 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(147): Show |
intron_variant | MODIFIER | c.-120-17695G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76116473 | |||||||
| chr15:76116536 | C | T | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-120-17632C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76116536 | |||||||
| chr15:76116537 | G | A | 3 | a0001c0001t0001g0132 a0002c0002t0001g0029 a0002c0002t0001g0040 |
3 | HG01109.hp1 HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-120-17631G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76116537 | |||||||
| chr15:76116790 | T | C | 133 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(130): Show |
135 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(132): Show |
intron_variant | MODIFIER | c.-120-17378T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76116790 | |||||||
| chr15:76116896 | CT | C | 69 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(66): Show |
71 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.-120-17252delT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76116896 | ||||||
| chr15:76116899 | T | A | 59 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0102 others(56): Show |
59 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.-120-17269T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76116899 | |||||||
| chr15:76116899 | T | C | 6 | a0001c0001t0001g0098 a0001c0001t0003g0014 a0001c0001t0004g0006 others(3): Show |
6 | HG02055.hp1 HG02647.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.-120-17269T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76116899 | |||||||
| chr15:76116900 | T | A | 60 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(57): Show |
62 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.-120-17268T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76116900 | |||||||
| chr15:76116900 | T | C | 5 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0023 others(2): Show |
5 | HG02451.hp2 HG03098.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-120-17268T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76116900 | |||||||
| chr15:76116901 | T | A | 1 | a0001c0001t0003g0265 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-120-17267T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76116901 | |||||||
| chr15:76116921 | C | T | 133 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(130): Show |
135 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(132): Show |
intron_variant | MODIFIER | c.-120-17247C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76116921 | |||||||
| chr15:76116929 | C | T | 63 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0102 others(60): Show |
63 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.-120-17239C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76116929 | |||||||
| chr15:76116952 | T | C | 133 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(130): Show |
135 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(132): Show |
intron_variant | MODIFIER | c.-120-17216T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76116952 | |||||||
| chr15:76116969 | G | T | 133 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(130): Show |
135 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(132): Show |
intron_variant | MODIFIER | c.-120-17199G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76116969 | |||||||
| chr15:76116993 | G | A | 3 | a0001c0001t0002g0224 a0001c0001t0002g0226 a0002c0002t0001g0067 |
3 | HG01099.hp1 HG01516.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-120-17175G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76116993 | |||||||
| chr15:76117057 | G | A | 6 | a0001c0001t0001g0098 a0001c0001t0003g0014 a0001c0001t0004g0253 others(3): Show |
6 | HG02055.hp1 HG02451.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-120-17111G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76117057 | |||||||
| chr15:76117059 | C | T | 1 | a0001c0001t0002g0126 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-120-17109C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76117059 | |||||||
| chr15:76117065 | A | C | 17 | a0001c0001t0001g0060 a0001c0001t0001g0137 a0001c0001t0001g0157 others(14): Show |
17 | HG00738.hp2 HG01069.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.-120-17103A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76117065 | |||||||
| chr15:76117081 | C | T | 138 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(135): Show |
140 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.-120-17087C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76117081 | |||||||
| chr15:76117088 | A | G | 138 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(135): Show |
140 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.-120-17080A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76117088 | |||||||
| chr15:76117090 | C | T | 126 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(123): Show |
128 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.-120-17078C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76117090 | |||||||
| chr15:76117110 | G | T | 1 | a0001c0001t0004g0248 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-120-17058G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76117110 | |||||||
| chr15:76117151 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-120-17017G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76117151 | |||||||
| chr15:76117211 | G | T | 3 | a0001c0001t0002g0001 a0001c0001t0003g0265 a0001c0001t0007g0252 |
4 | HG02630.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120-16957G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76117211 | |||||||
| chr15:76117247 | A | AT | 132 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(129): Show |
134 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.-120-16911dupT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76117247 | ||||||
| chr15:76117327 | G | A | 12 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0023 others(9): Show |
12 | HG02055.hp1 HG02451.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.-120-16841G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76117327 | |||||||
| chr15:76117410 | C | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0038 others(1): Show |
4 | HG02280.hp2 HG02647.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120-16758C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76117410 | |||||||
| chr15:76117439 | C | T | 138 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(135): Show |
140 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.-120-16729C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76117439 | |||||||
| chr15:76117520 | A | C | 138 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(135): Show |
140 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.-120-16648A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76117520 | |||||||
| chr15:76117584 | C | T | 138 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(135): Show |
140 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.-120-16584C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76117584 | |||||||
| chr15:76117592 | G | A | 138 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(135): Show |
140 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.-120-16576G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76117592 | |||||||
| chr15:76117624 | T | C | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-120-16544T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76117624 | |||||||
| chr15:76117818 | T | C | 4 | a0001c0001t0001g0098 a0001c0001t0003g0014 a0001c0001t0004g0253 others(1): Show |
4 | HG02055.hp1 HG02451.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-120-16350T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76117818 | |||||||
| chr15:76117967 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-120-16201T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76117967 | |||||||
| chr15:76118032 | A | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0023 others(3): Show |
6 | HG02970.hp2 HG03098.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-120-16136A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76118032 | |||||||
| chr15:76118124 | C | T | 20 | a0001c0001t0001g0081 a0001c0001t0001g0093 a0001c0001t0001g0129 others(17): Show |
20 | HG01243.hp1 HG01255.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.-120-16044C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76118124 | |||||||
| chr15:76118135 | T | G | 20 | a0001c0001t0001g0081 a0001c0001t0001g0093 a0001c0001t0001g0129 others(17): Show |
20 | HG01243.hp1 HG01255.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.-120-16033T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76118135 | |||||||
| chr15:76118138 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-120-16030C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76118138 | |||||||
| chr15:76118381 | G | A | 1 | a0002c0002t0001g0180 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-120-15787G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76118381 | |||||||
| chr15:76118384 | A | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0021 others(2): Show |
5 | HG01891.hp2 HG02055.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-120-15784A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76118384 | |||||||
| chr15:76118390 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-120-15778C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76118390 | |||||||
| chr15:76118431 | C | T | 5 | a0001c0001t0001g0098 a0001c0001t0001g0132 a0001c0001t0008g0249 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-120-15737C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76118431 | |||||||
| chr15:76118460 | A | G | 24 | a0001c0001t0001g0081 a0001c0001t0001g0093 a0001c0001t0001g0129 others(21): Show |
24 | HG01243.hp1 HG01255.hp2 HG02056.hp1 others(21): Show |
intron_variant | MODIFIER | c.-120-15708A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76118460 | |||||||
| chr15:76118467 | A | G | 24 | a0001c0001t0001g0081 a0001c0001t0001g0093 a0001c0001t0001g0129 others(21): Show |
24 | HG01243.hp1 HG01255.hp2 HG02056.hp1 others(21): Show |
intron_variant | MODIFIER | c.-120-15701A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76118467 | |||||||
| chr15:76118478 | G | A | 3 | a0001c0001t0001g0076 a0001c0001t0001g0135 a0001c0001t0001g0229 |
3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-120-15690G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76118478 | |||||||
| chr15:76118538 | A | G | 22 | a0001c0001t0001g0081 a0001c0001t0001g0093 a0001c0001t0001g0129 others(19): Show |
22 | HG01243.hp1 HG01255.hp2 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.-120-15630A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76118538 | |||||||
| chr15:76118756 | T | A | 1 | a0001c0001t0001g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-120-15412T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76118756 | |||||||
| chr15:76118842 | G | C | 2 | a0002c0002t0001g0016 a0004c0005t0001g0211 |
2 | NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-120-15326G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76118842 | |||||||
| chr15:76118895 | A | T | 22 | a0001c0001t0001g0081 a0001c0001t0001g0093 a0001c0001t0001g0129 others(19): Show |
22 | HG01243.hp1 HG01255.hp2 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.-120-15273A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76118895 | |||||||
| chr15:76118985 | T | A | 22 | a0001c0001t0001g0081 a0001c0001t0001g0093 a0001c0001t0001g0129 others(19): Show |
22 | HG01243.hp1 HG01255.hp2 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.-120-15183T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76118985 | |||||||
| chr15:76119108 | G | A | 22 | a0001c0001t0001g0081 a0001c0001t0001g0093 a0001c0001t0001g0129 others(19): Show |
22 | HG01243.hp1 HG01255.hp2 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.-120-15060G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76119108 | |||||||
| chr15:76119179 | G | A | 1 | a0002c0002t0001g0181 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-120-14989G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76119179 | |||||||
| chr15:76119276 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-120-14892C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76119276 | |||||||
| chr15:76119296 | C | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0018 |
2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-120-14872C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76119296 | |||||||
| chr15:76119344 | T | C | 8 | a0001c0001t0001g0098 a0001c0001t0001g0132 a0001c0001t0002g0045 others(5): Show |
8 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-120-14824T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76119344 | |||||||
| chr15:76119367 | C | A | 22 | a0001c0001t0001g0081 a0001c0001t0001g0093 a0001c0001t0001g0129 others(19): Show |
22 | HG01243.hp1 HG01255.hp2 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.-120-14801C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76119367 | |||||||
| chr15:76119391 | C | CA | 52 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0023 others(49): Show |
52 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.-120-14756dupA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76119391 | ||||||
| chr15:76119391 | CA | C | 13 | a0001c0001t0001g0098 a0001c0001t0001g0132 a0001c0001t0001g0255 others(10): Show |
13 | HG00280.hp1 HG01109.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.-120-14756delA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76119391 | ||||||
| chr15:76119391 | CAA | C | 14 | a0001c0001t0001g0093 a0001c0001t0001g0129 a0001c0001t0001g0142 others(11): Show |
14 | HG01243.hp1 HG01255.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.-120-14757_-120-14 others(8): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76119391 | ||||||
| chr15:76119391 | CAAAAAAA others(1): Show |
C | 115 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(112): Show |
117 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.-120-14763_-120-14 others(14): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76119391 | ||||||
| chr15:76119406 | A | G | 3 | a0001c0001t0002g0236 a0002c0002t0001g0141 a0003c0004t0001g0159 |
3 | HG01192.hp1 HG03017.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-120-14762A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76119406 | |||||||
| chr15:76119411 | A | G | 1 | a0002c0002t0001g0120 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-120-14757A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76119411 | |||||||
| chr15:76119493 | G | A | 2 | a0001c0001t0002g0070 a0001c0001t0002g0210 |
2 | HG00609.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.-120-14675G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76119493 | |||||||
| chr15:76119495 | G | A | 1 | a0004c0005t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-120-14673G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76119495 | |||||||
| chr15:76119574 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-120-14594C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76119574 | |||||||
| chr15:76119635 | A | C | 37 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.-120-14533A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76119635 | |||||||
| chr15:76119641 | C | G | 63 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0102 others(60): Show |
63 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.-120-14527C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76119641 | |||||||
| chr15:76119766 | C | CAAAA | 15 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(12): Show |
15 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.-120-14395_-120-14 others(10): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76119766 | ||||||
| chr15:76120067 | AT | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0021 others(2): Show |
5 | HG01891.hp2 HG02055.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-120-14098delT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76120067 | ||||||
| chr15:76120161 | T | C | 13 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(10): Show |
13 | HG01109.hp1 HG02055.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-120-14007T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76120161 | |||||||
| chr15:76120243 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-120-13925A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76120243 | |||||||
| chr15:76120305 | A | G | 1 | a0001c0001t0002g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-120-13863A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76120305 | |||||||
| chr15:76120393 | A | G | 2 | a0001c0001t0002g0045 a0002c0002t0001g0053 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-120-13775A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76120393 | |||||||
| chr15:76120496 | C | G | 3 | a0002c0002t0001g0221 a0002c0002t0001g0222 a0002c0002t0001g0223 |
3 | HG01069.hp1 HG01106.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.-120-13672C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76120496 | |||||||
| chr15:76120581 | C | T | 1 | a0001c0001t0002g0167 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-120-13587C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76120581 | |||||||
| chr15:76120582 | G | A | 2 | a0001c0001t0001g0256 a0001c0001t0001g0258 |
2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-120-13586G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76120582 | |||||||
| chr15:76120680 | G | T | 13 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(10): Show |
13 | HG01109.hp1 HG02055.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-120-13488G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76120680 | |||||||
| chr15:76120758 | C | CA | 28 | a0001c0001t0001g0020 a0001c0001t0001g0081 a0001c0001t0001g0093 others(25): Show |
28 | HG01109.hp2 HG01123.hp1 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.-120-13387dupA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76120758 | ||||||
| chr15:76120758 | C | CAA | 9 | a0001c0001t0001g0098 a0001c0001t0001g0132 a0001c0001t0001g0142 others(6): Show |
9 | HG01109.hp1 HG02055.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-120-13388_-120-13 others(8): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76120758 | ||||||
| chr15:76120758 | CA | C | 67 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(64): Show |
67 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.-120-13387delA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76120758 | ||||||
| chr15:76120782 | G | T | 2 | a0001c0001t0001g0256 a0001c0001t0001g0258 |
2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-120-13386G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76120782 | |||||||
| chr15:76120946 | T | C | 16 | a0001c0001t0001g0025 a0001c0001t0001g0079 a0001c0001t0001g0080 others(13): Show |
17 | HG01123.hp1 HG01243.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.-120-13222T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76120946 | |||||||
| chr15:76121055 | A | AG | 3 | a0001c0001t0002g0043 a0001c0001t0002g0122 a0002c0002t0001g0042 |
3 | HG02132.hp1 NA18942.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.-120-13110dupG | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76121055 | ||||||
| chr15:76121098 | C | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0038 others(1): Show |
4 | HG02280.hp2 HG02647.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120-13070C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76121098 | |||||||
| chr15:76121116 | T | C | 13 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(10): Show |
13 | HG01109.hp1 HG02055.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-120-13052T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76121116 | |||||||
| chr15:76121188 | G | A | 158 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(155): Show |
160 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(157): Show |
intron_variant | MODIFIER | c.-120-12980G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76121188 | |||||||
| chr15:76121239 | A | G | 2 | a0001c0001t0003g0014 a0001c0001t0004g0253 |
2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-120-12929A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76121239 | |||||||
| chr15:76121288 | GTAT | G | 13 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(10): Show |
13 | HG01109.hp1 HG02055.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-120-12875_-120-12 others(9): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76121288 | ||||||
| chr15:76121294 | T | C | 22 | a0001c0001t0001g0081 a0001c0001t0001g0093 a0001c0001t0001g0129 others(19): Show |
22 | HG01243.hp1 HG01255.hp2 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.-120-12874T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76121294 | |||||||
| chr15:76121346 | A | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0023 others(3): Show |
6 | HG02970.hp2 HG03098.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-120-12822A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76121346 | |||||||
| chr15:76121492 | C | T | 1 | a0002c0002t0001g0218 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-120-12676C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76121492 | |||||||
| chr15:76121599 | T | C | 13 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(10): Show |
13 | HG01109.hp1 HG02055.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-120-12569T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76121599 | |||||||
| chr15:76121604 | G | A | 35 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(32): Show |
35 | HG01109.hp1 HG01243.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.-120-12564G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76121604 | |||||||
| chr15:76121771 | G | A | 2 | a0001c0001t0003g0014 a0001c0001t0004g0253 |
2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-120-12397G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76121771 | |||||||
| chr15:76121923 | A | G | 1 | a0001c0001t0002g0193 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-120-12245A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76121923 | |||||||
| chr15:76122025 | C | G | 1 | a0001c0001t0001g0130 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-120-12143C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76122025 | |||||||
| chr15:76122506 | C | A | 35 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(32): Show |
35 | HG01109.hp1 HG01243.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.-120-11662C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76122506 | |||||||
| chr15:76122531 | T | C | 4 | a0001c0001t0002g0045 a0001c0001t0003g0014 a0001c0001t0004g0253 others(1): Show |
4 | HG01884.hp1 HG02451.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-120-11637T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76122531 | |||||||
| chr15:76122548 | T | G | 14 | a0001c0001t0001g0025 a0001c0001t0001g0076 a0001c0001t0001g0079 others(11): Show |
14 | HG01123.hp1 HG01346.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.-120-11620T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76122548 | |||||||
| chr15:76122708 | T | C | 5 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0037 others(2): Show |
5 | NA18948.hp1 NA18957.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-120-11460T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76122708 | |||||||
| chr15:76122821 | A | C | 36 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(33): Show |
36 | HG01109.hp1 HG01243.hp1 HG01255.hp2 others(33): Show |
intron_variant | MODIFIER | c.-120-11347A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76122821 | |||||||
| chr15:76122916 | C | T | 1 | a0002c0002t0001g0016 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-120-11252C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76122916 | |||||||
| chr15:76122943 | A | G | 13 | a0001c0001t0001g0093 a0001c0001t0001g0129 a0001c0001t0001g0142 others(10): Show |
13 | HG02056.hp1 HG02129.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-120-11225A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76122943 | |||||||
| chr15:76122988 | A | G | 23 | a0001c0001t0001g0081 a0001c0001t0001g0093 a0001c0001t0001g0129 others(20): Show |
23 | HG01243.hp1 HG01255.hp2 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.-120-11180A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76122988 | |||||||
| chr15:76123039 | CA | C | 13 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(10): Show |
13 | HG01109.hp1 HG02055.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-120-11128delA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76123039 | |||||||
| chr15:76123108 | G | C | 5 | a0001c0001t0001g0060 a0001c0001t0001g0137 a0001c0001t0002g0065 others(2): Show |
5 | HG01074.hp2 HG01167.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.-120-11060G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76123108 | |||||||
| chr15:76123398 | C | T | 23 | a0001c0001t0001g0081 a0001c0001t0001g0093 a0001c0001t0001g0129 others(20): Show |
23 | HG01243.hp1 HG01255.hp2 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.-120-10770C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76123398 | |||||||
| chr15:76123448 | C | A | 9 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(6): Show |
9 | HG02055.hp1 HG02970.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.-120-10720C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76123448 | |||||||
| chr15:76123667 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-120-10501G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76123667 | |||||||
| chr15:76123699 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-120-10469C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76123699 | |||||||
| chr15:76123713 | C | CT | 12 | a0001c0001t0001g0025 a0001c0001t0001g0079 a0001c0001t0001g0080 others(9): Show |
12 | HG01123.hp1 HG01346.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.-120-10444dupT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76123713 | ||||||
| chr15:76123713 | C | CTTT | 20 | a0001c0001t0001g0093 a0001c0001t0001g0129 a0001c0001t0001g0142 others(17): Show |
20 | HG01243.hp1 HG01255.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.-120-10446_-120-10 others(9): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76123713 | ||||||
| chr15:76123902 | G | A | 23 | a0001c0001t0001g0081 a0001c0001t0001g0093 a0001c0001t0001g0129 others(20): Show |
23 | HG01243.hp1 HG01255.hp2 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.-120-10266G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76123902 | |||||||
| chr15:76123909 | C | T | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-120-10259C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76123909 | |||||||
| chr15:76123910 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-120-10258G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76123910 | |||||||
| chr15:76123919 | G | C | 13 | a0001c0001t0001g0025 a0001c0001t0001g0076 a0001c0001t0001g0079 others(10): Show |
13 | HG01123.hp1 HG01346.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-120-10249G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76123919 | |||||||
| chr15:76123932 | C | T | 13 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(10): Show |
13 | HG01109.hp1 HG02055.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-120-10236C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76123932 | |||||||
| chr15:76123984 | A | T | 4 | a0001c0001t0001g0255 a0001c0001t0004g0248 a0002c0002t0001g0175 others(1): Show |
4 | HG02486.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120-10184A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76123984 | |||||||
| chr15:76124010 | G | T | 31 | a0001c0001t0002g0002 a0001c0001t0002g0027 a0001c0001t0002g0028 others(28): Show |
32 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-120-10158G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76124010 | |||||||
| chr15:76124060 | T | C | 23 | a0001c0001t0001g0081 a0001c0001t0001g0093 a0001c0001t0001g0129 others(20): Show |
23 | HG01243.hp1 HG01255.hp2 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.-120-10108T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76124060 | |||||||
| chr15:76124189 | T | C | 6 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0023 others(3): Show |
6 | HG02970.hp2 HG03098.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-120-9979T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76124189 | |||||||
| chr15:76124572 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-120-9596G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76124572 | |||||||
| chr15:76124669 | C | T | 13 | a0001c0001t0001g0093 a0001c0001t0001g0129 a0001c0001t0001g0142 others(10): Show |
13 | HG02056.hp1 HG02129.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-120-9499C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76124669 | |||||||
| chr15:76124685 | G | C | 23 | a0001c0001t0001g0081 a0001c0001t0001g0093 a0001c0001t0001g0129 others(20): Show |
23 | HG01243.hp1 HG01255.hp2 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.-120-9483G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76124685 | |||||||
| chr15:76124905 | GA | G | 23 | a0001c0001t0001g0081 a0001c0001t0001g0093 a0001c0001t0001g0129 others(20): Show |
23 | HG01243.hp1 HG01255.hp2 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.-120-9256delA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76124905 | ||||||
| chr15:76124987 | A | T | 1 | a0002c0002t0002g0010 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-120-9181A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76124987 | |||||||
| chr15:76125018 | G | A | 6 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0023 others(3): Show |
6 | HG02970.hp2 HG03098.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-120-9150G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76125018 | |||||||
| chr15:76125103 | C | T | 23 | a0001c0001t0001g0081 a0001c0001t0001g0093 a0001c0001t0001g0129 others(20): Show |
23 | HG01243.hp1 HG01255.hp2 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.-120-9065C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76125103 | |||||||
| chr15:76125224 | G | T | 1 | a0002c0002t0001g0016 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-120-8944G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76125224 | |||||||
| chr15:76125359 | G | T | 1 | a0002c0002t0001g0174 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-120-8809G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76125359 | |||||||
| chr15:76125392 | C | G | 23 | a0001c0001t0001g0081 a0001c0001t0001g0093 a0001c0001t0001g0129 others(20): Show |
23 | HG01243.hp1 HG01255.hp2 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.-120-8776C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76125392 | |||||||
| chr15:76125394 | G | A | 6 | a0001c0001t0001g0098 a0001c0001t0001g0132 a0001c0001t0008g0249 others(3): Show |
6 | HG01109.hp1 HG02055.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-120-8774G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76125394 | |||||||
| chr15:76125503 | A | G | 5 | a0001c0001t0001g0098 a0001c0001t0001g0132 a0001c0001t0008g0249 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-120-8665A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76125503 | |||||||
| chr15:76125763 | G | C | 13 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(10): Show |
13 | HG01109.hp1 HG02055.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-120-8405G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76125763 | |||||||
| chr15:76125772 | C | T | 6 | a0001c0001t0001g0081 a0001c0001t0001g0271 a0001c0001t0002g0057 others(3): Show |
6 | HG01243.hp1 HG01255.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-120-8396C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76125772 | |||||||
| chr15:76125839 | C | A | 2 | a0001c0001t0003g0014 a0001c0001t0004g0253 |
2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-120-8329C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76125839 | |||||||
| chr15:76125840 | T | G | 6 | a0001c0001t0001g0081 a0001c0001t0001g0271 a0001c0001t0002g0057 others(3): Show |
6 | HG01243.hp1 HG01255.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-120-8328T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76125840 | |||||||
| chr15:76125846 | T | TA | 16 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0080 others(13): Show |
16 | HG01175.hp2 HG01928.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-120-8304dupA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76125846 | ||||||
| chr15:76125846 | TA | T | 10 | a0001c0001t0001g0081 a0001c0001t0001g0271 a0001c0001t0002g0045 others(7): Show |
10 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-120-8304delA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76125846 | ||||||
| chr15:76125873 | G | T | 6 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0023 others(3): Show |
6 | HG02970.hp2 HG03098.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-120-8295G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76125873 | |||||||
| chr15:76125953 | T | C | 3 | a0001c0001t0002g0001 a0001c0001t0003g0265 a0001c0001t0007g0252 |
4 | HG02630.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120-8215T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76125953 | |||||||
| chr15:76126272 | C | T | 6 | a0001c0001t0001g0081 a0001c0001t0001g0271 a0001c0001t0002g0057 others(3): Show |
6 | HG01243.hp1 HG01255.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-120-7896C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76126272 | |||||||
| chr15:76126336 | C | A | 5 | a0001c0001t0001g0247 a0001c0001t0002g0074 a0001c0001t0002g0106 others(2): Show |
5 | HG01255.hp1 HG01257.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-120-7832C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76126336 | |||||||
| chr15:76126365 | A | C | 6 | a0001c0001t0001g0081 a0001c0001t0001g0271 a0001c0001t0002g0057 others(3): Show |
6 | HG01243.hp1 HG01255.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-120-7803A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76126365 | |||||||
| chr15:76126367 | C | A | 2 | a0001c0001t0001g0244 a0002c0002t0001g0099 |
2 | NA18948.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-120-7801C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76126367 | |||||||
| chr15:76126374 | C | CAT | 15 | a0001c0001t0001g0130 a0001c0001t0001g0272 a0001c0001t0002g0045 others(12): Show |
15 | HG00099.hp2 HG00558.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.-120-7768_-120-776 others(6): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76126374 | ||||||
| chr15:76126374 | C | CATAT | 4 | a0001c0001t0002g0033 a0001c0001t0002g0165 a0002c0002t0001g0100 others(1): Show |
4 | HG00140.hp1 HG01074.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120-7770_-120-776 others(8): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76126374 | ||||||
| chr15:76126374 | C | CATATATA others(5): Show |
2 | a0001c0001t0001g0098 a0001c0001t0008g0249 |
2 | HG02055.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-120-7778_-120-776 others(16): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76126374 | ||||||
| chr15:76126374 | C | CATATATA others(9): Show |
1 | a0001c0001t0001g0257 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-120-7782_-120-776 others(20): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76126374 | ||||||
| chr15:76126374 | C | CATATATA others(17): Show |
1 | a0001c0001t0001g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-120-7790_-120-776 others(28): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76126374 | ||||||
| chr15:76126374 | C | CATATATA others(21): Show |
1 | a0002c0002t0001g0029 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-120-7767_-120-776 others(32): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76126374 | ||||||
| chr15:76126374 | C | CATATATA others(23): Show |
2 | a0002c0002t0001g0011 a0002c0002t0001g0040 |
2 | HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-120-7767_-120-776 others(34): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76126374 | ||||||
| chr15:76126374 | CATAT | C | 8 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0023 others(5): Show |
8 | HG02451.hp2 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.-120-7770_-120-776 others(8): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76126374 | ||||||
| chr15:76126374 | CATATATA others(1): Show |
C | 6 | a0001c0001t0001g0081 a0001c0001t0001g0129 a0001c0001t0001g0271 others(3): Show |
6 | HG01243.hp1 HG01255.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.-120-7774_-120-776 others(12): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76126374 | ||||||
| chr15:76126374 | CATATATA others(3): Show |
C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(136): Show |
141 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.-120-7776_-120-776 others(14): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76126374 | ||||||
| chr15:76126505 | A | T | 1 | a0001c0001t0001g0025 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-120-7663A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76126505 | |||||||
| chr15:76126534 | AT | A | 41 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(38): Show |
42 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.-120-7618delT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76126534 | ||||||
| chr15:76126566 | C | G | 5 | a0001c0001t0002g0056 a0002c0002t0001g0073 a0002c0002t0001g0075 others(2): Show |
5 | HG02083.hp1 NA18747.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.-120-7602C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76126566 | |||||||
| chr15:76126612 | T | G | 3 | a0001c0001t0001g0060 a0001c0001t0002g0065 a0001c0001t0002g0066 |
3 | HG01167.hp1 HG01261.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-120-7556T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76126612 | |||||||
| chr15:76126613 | C | G | 3 | a0001c0001t0001g0060 a0001c0001t0002g0065 a0001c0001t0002g0066 |
3 | HG01167.hp1 HG01261.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-120-7555C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76126613 | |||||||
| chr15:76126617 | C | T | 3 | a0001c0001t0001g0081 a0002c0002t0001g0016 a0004c0005t0001g0211 |
3 | HG03486.hp1 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-120-7551C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76126617 | |||||||
| chr15:76126625 | G | T | 2 | a0001c0001t0008g0249 a0002c0002t0001g0011 |
2 | NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-120-7543G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76126625 | |||||||
| chr15:76126656 | T | C | 1 | a0005c0006t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-120-7512T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76126656 | |||||||
| chr15:76126658 | A | G | 1 | a0005c0006t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-120-7510A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76126658 | |||||||
| chr15:76126736 | C | T | 2 | a0001c0001t0001g0081 a0004c0005t0001g0211 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-120-7432C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76126736 | |||||||
| chr15:76126809 | G | A | 4 | a0001c0001t0001g0081 a0001c0001t0002g0057 a0002c0002t0001g0208 others(1): Show |
4 | HG01243.hp1 HG01255.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-120-7359G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76126809 | |||||||
| chr15:76126822 | C | G | 42 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0025 others(39): Show |
43 | HG01109.hp1 HG01123.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.-120-7346C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76126822 | |||||||
| chr15:76127144 | G | A | 4 | a0001c0001t0002g0001 a0001c0001t0003g0265 a0001c0001t0007g0252 others(1): Show |
5 | HG02630.hp2 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-120-7024G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76127144 | |||||||
| chr15:76127265 | G | A | 2 | a0001c0001t0002g0152 a0001c0001t0002g0154 |
2 | HG00558.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.-120-6903G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76127265 | |||||||
| chr15:76127323 | C | CT | 58 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0020 others(55): Show |
60 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.-120-6829dupT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76127323 | ||||||
| chr15:76127323 | C | CTT | 21 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0023 others(18): Show |
21 | HG01243.hp1 HG01255.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.-120-6830_-120-682 others(6): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76127323 | ||||||
| chr15:76127395 | T | G | 1 | a0002c0002t0001g0164 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-120-6773T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76127395 | |||||||
| chr15:76127419 | C | T | 4 | a0001c0001t0001g0271 a0001c0001t0002g0057 a0002c0002t0001g0011 others(1): Show |
4 | HG01243.hp1 HG01255.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-120-6749C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76127419 | |||||||
| chr15:76127420 | G | A | 1 | a0001c0001t0001g0244 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-120-6748G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76127420 | |||||||
| chr15:76127577 | C | T | 7 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0271 others(4): Show |
7 | HG01243.hp1 HG01255.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-120-6591C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76127577 | |||||||
| chr15:76127677 | A | G | 3 | a0001c0001t0001g0132 a0002c0002t0001g0029 a0002c0002t0001g0040 |
3 | HG01109.hp1 HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-120-6491A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76127677 | |||||||
| chr15:76127735 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0023 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-120-6433C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76127735 | |||||||
| chr15:76127767 | T | G | 80 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(77): Show |
82 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.-120-6401T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76127767 | |||||||
| chr15:76127945 | C | T | 7 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0271 others(4): Show |
7 | HG01243.hp1 HG01255.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-120-6223C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76127945 | |||||||
| chr15:76127990 | A | G | 2 | a0001c0001t0002g0027 a0001c0001t0002g0028 |
2 | HG02080.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.-120-6178A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76127990 | |||||||
| chr15:76128120 | AC | A | 7 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0271 others(4): Show |
7 | HG01243.hp1 HG01255.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-120-6046delC | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76128120 | ||||||
| chr15:76128170 | C | T | 7 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0271 others(4): Show |
7 | HG01243.hp1 HG01255.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-120-5998C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76128170 | |||||||
| chr15:76128216 | G | T | 1 | a0001c0001t0002g0240 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-120-5952G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76128216 | |||||||
| chr15:76128397 | C | T | 4 | a0001c0001t0001g0271 a0001c0001t0002g0057 a0002c0002t0001g0011 others(1): Show |
4 | HG01243.hp1 HG01255.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-120-5771C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76128397 | |||||||
| chr15:76128417 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0021 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-120-5751G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76128417 | |||||||
| chr15:76128563 | T | G | 1 | a0002c0002t0001g0208 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-120-5605T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76128563 | |||||||
| chr15:76128581 | T | C | 86 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(83): Show |
88 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.-120-5587T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76128581 | |||||||
| chr15:76128591 | G | A | 1 | a0002c0002t0001g0113 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-120-5577G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76128591 | |||||||
| chr15:76128608 | T | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0266 a0001c0001t0004g0005 others(1): Show |
4 | HG02970.hp2 HG03098.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120-5560T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76128608 | |||||||
| chr15:76128627 | G | A | 1 | a0002c0002t0001g0016 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-120-5541G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76128627 | |||||||
| chr15:76128771 | C | A | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-120-5397C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76128771 | |||||||
| chr15:76128783 | C | T | 1 | a0002c0002t0001g0180 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-120-5385C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76128783 | |||||||
| chr15:76128844 | A | G | 74 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(71): Show |
76 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.-120-5324A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76128844 | |||||||
| chr15:76129078 | A | AGTCT | 162 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(159): Show |
164 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(161): Show |
intron_variant | MODIFIER | c.-120-5088_-120-508 others(8): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76129078 | ||||||
| chr15:76129162 | A | C | 7 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0271 others(4): Show |
7 | HG01243.hp1 HG01255.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-120-5006A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76129162 | |||||||
| chr15:76129193 | A | C | 7 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0271 others(4): Show |
7 | HG01243.hp1 HG01255.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-120-4975A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76129193 | |||||||
| chr15:76129355 | A | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0266 a0001c0001t0004g0005 others(1): Show |
4 | HG02970.hp2 HG03098.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120-4813A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76129355 | |||||||
| chr15:76129359 | A | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0266 a0001c0001t0004g0005 others(1): Show |
4 | HG02970.hp2 HG03098.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120-4809A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76129359 | |||||||
| chr15:76129360 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0266 a0001c0001t0004g0005 others(1): Show |
4 | HG02970.hp2 HG03098.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120-4808G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76129360 | |||||||
| chr15:76129374 | G | C | 7 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0271 others(4): Show |
7 | HG01243.hp1 HG01255.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-120-4794G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76129374 | |||||||
| chr15:76129417 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-120-4751G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76129417 | |||||||
| chr15:76129498 | G | A | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-120-4670G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76129498 | |||||||
| chr15:76129513 | T | C | 69 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0102 others(66): Show |
69 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.-120-4655T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76129513 | |||||||
| chr15:76129536 | G | A | 1 | a0001c0001t0003g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-120-4632G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76129536 | |||||||
| chr15:76129537 | A | G | 1 | a0001c0001t0003g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-120-4631A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76129537 | |||||||
| chr15:76129544 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0269 |
2 | HG01243.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-120-4624G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76129544 | |||||||
| chr15:76129592 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0023 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-120-4576G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76129592 | |||||||
| chr15:76129615 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-120-4553C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76129615 | |||||||
| chr15:76129732 | C | T | 7 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0271 others(4): Show |
7 | HG01243.hp1 HG01255.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-120-4436C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76129732 | |||||||
| chr15:76129812 | T | G | 39 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0025 others(36): Show |
40 | HG01123.hp1 HG01243.hp2 HG01346.hp2 others(37): Show |
intron_variant | MODIFIER | c.-120-4356T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76129812 | |||||||
| chr15:76129876 | T | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0003g0014 |
3 | HG02647.hp1 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-120-4292T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76129876 | |||||||
| chr15:76129889 | A | G | 69 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0102 others(66): Show |
69 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.-120-4279A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76129889 | |||||||
| chr15:76129901 | G | A | 69 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0025 others(66): Show |
71 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.-120-4267G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76129901 | |||||||
| chr15:76130043 | C | G | 7 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0271 others(4): Show |
7 | HG01243.hp1 HG01255.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-120-4125C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130043 | |||||||
| chr15:76130061 | A | G | 3 | a0001c0001t0001g0271 a0001c0001t0002g0057 a0002c0002t0001g0208 |
3 | HG01243.hp1 HG01255.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-120-4107A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130061 | |||||||
| chr15:76130083 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0023 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-120-4085G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130083 | |||||||
| chr15:76130088 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-120-4080G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130088 | |||||||
| chr15:76130127 | G | A | 1 | a0001c0001t0003g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-120-4041G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130127 | |||||||
| chr15:76130173 | G | A | 1 | a0001c0001t0003g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-120-3995G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130173 | |||||||
| chr15:76130218 | C | CA | 10 | a0001c0001t0001g0188 a0001c0001t0002g0064 a0001c0001t0002g0136 others(7): Show |
10 | HG00099.hp2 HG00735.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.-120-3914dupA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76130218 | ||||||
| chr15:76130236 | AAAAAAAA others(12): Show |
A | 1 | a0002c0002t0001g0197 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-120-3931_-120-391 others(23): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130236 | |||||||
| chr15:76130238 | AAAAAAAA others(10): Show |
A | 1 | a0001c0001t0001g0098 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-120-3929_-120-391 others(21): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130238 | |||||||
| chr15:76130239 | AAAAAAAA others(9): Show |
A | 1 | a0002c0002t0001g0216 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-120-3928_-120-391 others(20): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130239 | |||||||
| chr15:76130243 | AAAAAAAA others(5): Show |
A | 42 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0025 others(39): Show |
42 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.-120-3924_-120-391 others(16): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130243 | |||||||
| chr15:76130244 | AAAAAAAA others(4): Show |
A | 25 | a0001c0001t0001g0038 a0001c0001t0001g0093 a0001c0001t0001g0129 others(22): Show |
26 | HG00733.hp1 HG01346.hp2 HG01928.hp2 others(23): Show |
intron_variant | MODIFIER | c.-120-3923_-120-391 others(15): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130244 | |||||||
| chr15:76130245 | A | C | 1 | a0002c0002t0001g0179 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-120-3923A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130245 | |||||||
| chr15:76130245 | AAAAAAAA others(3): Show |
A | 8 | a0001c0001t0001g0023 a0001c0001t0001g0271 a0001c0001t0002g0043 others(5): Show |
8 | HG01123.hp1 HG01255.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.-120-3922_-120-391 others(14): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130245 | |||||||
| chr15:76130248 | A | C | 1 | a0002c0002t0001g0178 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-120-3920A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130248 | |||||||
| chr15:76130252 | AAAC | A | 16 | a0001c0001t0001g0009 a0001c0001t0001g0153 a0001c0001t0001g0158 others(13): Show |
16 | HG01099.hp1 HG01106.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.-120-3915_-120-391 others(7): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130252 | |||||||
| chr15:76130253 | AAC | A | 44 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.-120-3914_-120-391 others(6): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130253 | |||||||
| chr15:76130254 | AC | A | 70 | a0001c0001t0001g0083 a0001c0001t0001g0089 a0001c0001t0001g0102 others(67): Show |
70 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.-120-3912delC | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76130254 | ||||||
| chr15:76130255 | C | A | 59 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0021 others(56): Show |
59 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.-120-3913C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130255 | |||||||
| chr15:76130367 | G | A | 3 | a0001c0001t0001g0264 a0001c0001t0002g0263 a0001c0001t0003g0031 |
3 | HG02258.hp2 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-120-3801G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130367 | |||||||
| chr15:76130397 | TG | T | 31 | a0001c0001t0002g0002 a0001c0001t0002g0027 a0001c0001t0002g0028 others(28): Show |
32 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-120-3768delG | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76130397 | ||||||
| chr15:76130508 | C | T | 70 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0025 others(67): Show |
72 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-120-3660C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130508 | |||||||
| chr15:76130512 | C | T | 15 | a0001c0001t0001g0272 a0001c0001t0002g0004 a0001c0001t0002g0063 others(12): Show |
15 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-120-3656C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130512 | |||||||
| chr15:76130537 | C | G | 7 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0271 others(4): Show |
7 | HG01243.hp1 HG01255.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-120-3631C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130537 | |||||||
| chr15:76130551 | T | A | 4 | a0001c0001t0001g0255 a0001c0001t0004g0248 a0002c0002t0001g0175 others(1): Show |
4 | HG02486.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120-3617T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130551 | |||||||
| chr15:76130582 | A | G | 7 | a0001c0001t0001g0244 a0001c0001t0002g0041 a0002c0002t0001g0094 others(4): Show |
7 | NA18948.hp2 NA18968.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.-120-3586A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130582 | |||||||
| chr15:76130682 | G | A | 2 | a0001c0001t0001g0098 a0004c0005t0001g0211 |
2 | HG02055.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-120-3486G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130682 | |||||||
| chr15:76130698 | C | A | 4 | a0001c0001t0001g0271 a0001c0001t0002g0057 a0002c0002t0001g0011 others(1): Show |
4 | HG01243.hp1 HG01255.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-120-3470C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130698 | |||||||
| chr15:76130730 | A | G | 162 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(159): Show |
164 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(161): Show |
intron_variant | MODIFIER | c.-120-3438A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130730 | |||||||
| chr15:76130741 | C | T | 81 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(78): Show |
83 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.-120-3427C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130741 | |||||||
| chr15:76130794 | T | C | 2 | a0001c0001t0002g0045 a0002c0002t0001g0053 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-120-3374T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130794 | |||||||
| chr15:76130808 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0023 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-120-3360C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130808 | |||||||
| chr15:76130812 | CT | C | 7 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0271 others(4): Show |
7 | HG01243.hp1 HG01255.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-120-3355delT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130812 | |||||||
| chr15:76130863 | A | G | 3 | a0001c0001t0001g0271 a0001c0001t0002g0057 a0002c0002t0001g0208 |
3 | HG01243.hp1 HG01255.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-120-3305A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130863 | |||||||
| chr15:76130915 | A | C | 3 | a0001c0001t0001g0132 a0002c0002t0001g0029 a0002c0002t0001g0040 |
3 | HG01109.hp1 HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-120-3253A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130915 | |||||||
| chr15:76130919 | C | T | 162 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(159): Show |
164 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(161): Show |
intron_variant | MODIFIER | c.-120-3249C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76130919 | |||||||
| chr15:76131041 | A | G | 1 | a0001c0001t0001g0130 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-120-3127A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76131041 | |||||||
| chr15:76131044 | A | C | 3 | a0001c0001t0001g0271 a0001c0001t0002g0057 a0002c0002t0001g0208 |
3 | HG01243.hp1 HG01255.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-120-3124A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76131044 | |||||||
| chr15:76131044 | A | G | 4 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0003g0014 others(1): Show |
4 | HG02647.hp1 HG03209.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-120-3124A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76131044 | |||||||
| chr15:76131169 | G | A | 1 | a0001c0001t0003g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-120-2999G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76131169 | |||||||
| chr15:76131228 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0003g0014 |
3 | HG02647.hp1 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-120-2940G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76131228 | |||||||
| chr15:76131323 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0230 |
3 | HG02647.hp2 HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-120-2845C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76131323 | |||||||
| chr15:76131343 | T | C | 3 | a0001c0001t0001g0132 a0002c0002t0001g0029 a0002c0002t0001g0040 |
3 | HG01109.hp1 HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-120-2825T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76131343 | |||||||
| chr15:76131375 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-120-2793A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76131375 | |||||||
| chr15:76131536 | A | G | 1 | a0001c0001t0003g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-120-2632A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76131536 | |||||||
| chr15:76131626 | TG | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0266 a0001c0001t0004g0005 others(1): Show |
4 | HG02970.hp2 HG03098.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120-2540delG | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76131626 | ||||||
| chr15:76131825 | G | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0023 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-120-2343G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76131825 | |||||||
| chr15:76132065 | G | C | 7 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0271 others(4): Show |
7 | HG01243.hp1 HG01255.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-120-2103G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76132065 | |||||||
| chr15:76132113 | A | AT | 5 | a0001c0001t0001g0009 a0001c0001t0001g0266 a0001c0001t0004g0005 others(2): Show |
5 | HG02970.hp2 HG03098.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-120-2042dupT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76132113 | ||||||
| chr15:76132113 | A | ATT | 70 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0025 others(67): Show |
72 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-120-2043_-120-204 others(6): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76132113 | ||||||
| chr15:76132133 | G | T | 2 | a0001c0001t0002g0004 a0001c0001t0007g0251 |
2 | HG03453.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-120-2035G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76132133 | |||||||
| chr15:76132224 | T | G | 1 | a0001c0001t0001g0109 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-120-1944T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76132224 | |||||||
| chr15:76132384 | T | C | 7 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0271 others(4): Show |
7 | HG01243.hp1 HG01255.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-120-1784T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76132384 | |||||||
| chr15:76132399 | G | A | 2 | a0001c0001t0001g0172 a0001c0001t0001g0207 |
2 | HG02886.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-120-1769G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76132399 | |||||||
| chr15:76132400 | C | T | 1 | a0002c0002t0001g0120 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-120-1768C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76132400 | |||||||
| chr15:76132401 | G | A | 5 | a0001c0001t0002g0032 a0001c0001t0002g0056 a0002c0002t0001g0073 others(2): Show |
5 | HG02083.hp1 NA18747.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.-120-1767G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76132401 | |||||||
| chr15:76132566 | C | T | 77 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(74): Show |
79 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.-120-1602C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76132566 | |||||||
| chr15:76132733 | T | C | 40 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0025 others(37): Show |
41 | HG01123.hp1 HG01243.hp2 HG01346.hp2 others(38): Show |
intron_variant | MODIFIER | c.-120-1435T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76132733 | |||||||
| chr15:76132746 | A | C | 21 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0038 others(18): Show |
21 | HG02257.hp1 HG02280.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.-120-1422A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76132746 | |||||||
| chr15:76132781 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0002c0002t0001g0011 |
3 | HG03209.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-120-1387C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76132781 | |||||||
| chr15:76132811 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0266 a0001c0001t0004g0005 others(1): Show |
4 | HG02970.hp2 HG03098.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120-1357G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76132811 | |||||||
| chr15:76132813 | A | AAT | 3 | a0001c0001t0001g0266 a0001c0001t0004g0005 a0001c0001t0004g0006 |
3 | HG02970.hp2 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-120-1354_-120-135 others(6): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76132813 | ||||||
| chr15:76132813 | A | AATT | 65 | a0001c0001t0001g0020 a0001c0001t0001g0060 a0001c0001t0001g0089 others(62): Show |
65 | HG00597.hp2 HG00621.hp1 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.-120-1320_-120-131 others(7): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76132813 | ||||||
| chr15:76132813 | A | AATTATT | 17 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0102 others(14): Show |
17 | HG00280.hp2 HG01074.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.-120-1323_-120-131 others(10): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76132813 | ||||||
| chr15:76132813 | A | AATTATTA others(2): Show |
3 | a0001c0001t0001g0137 a0001c0001t0001g0158 a0001c0001t0001g0188 |
3 | HG00735.hp2 HG02257.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.-120-1326_-120-131 others(13): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76132813 | ||||||
| chr15:76132813 | AATT | A | 12 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0078 others(9): Show |
12 | HG00438.hp1 HG01891.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-120-1320_-120-131 others(7): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76132813 | ||||||
| chr15:76132813 | AATTATTA others(2): Show |
A | 14 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0271 others(11): Show |
14 | HG00099.hp1 HG00741.hp1 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.-120-1326_-120-131 others(13): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76132813 | ||||||
| chr15:76132813 | AATTATTA others(5): Show |
A | 69 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0025 others(66): Show |
71 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.-120-1329_-120-131 others(16): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76132813 | ||||||
| chr15:76132833 | T | C | 1 | a0002c0002t0001g0118 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-120-1335T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76132833 | |||||||
| chr15:76133006 | C | T | 5 | a0001c0001t0002g0104 a0002c0002t0001g0221 a0002c0002t0001g0222 others(2): Show |
5 | HG00733.hp2 HG01069.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.-120-1162C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76133006 | |||||||
| chr15:76133052 | C | T | 1 | a0001c0001t0003g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-120-1116C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76133052 | |||||||
| chr15:76133054 | A | C | 13 | a0001c0001t0001g0083 a0001c0001t0001g0109 a0001c0001t0001g0157 others(10): Show |
13 | HG00438.hp1 HG01175.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.-120-1114A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76133054 | |||||||
| chr15:76133131 | C | CATAA | 31 | a0001c0001t0002g0002 a0001c0001t0002g0027 a0001c0001t0002g0028 others(28): Show |
32 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-120-1022_-120-101 others(8): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76133131 | ||||||
| chr15:76133160 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0266 a0001c0001t0004g0005 others(1): Show |
4 | HG02970.hp2 HG03098.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120-1008G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76133160 | |||||||
| chr15:76133161 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0266 a0001c0001t0004g0005 others(1): Show |
4 | HG02970.hp2 HG03098.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120-1007C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76133161 | |||||||
| chr15:76133199 | C | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0266 a0001c0001t0003g0014 others(2): Show |
5 | HG02647.hp1 HG02970.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-120-969C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76133199 | |||||||
| chr15:76133204 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0266 a0001c0001t0004g0005 others(1): Show |
4 | HG02970.hp2 HG03098.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120-964C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76133204 | |||||||
| chr15:76133232 | G | A | 7 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0271 others(4): Show |
7 | HG01243.hp1 HG01255.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-120-936G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76133232 | |||||||
| chr15:76133258 | A | G | 79 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(76): Show |
81 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.-120-910A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76133258 | |||||||
| chr15:76133287 | T | G | 31 | a0001c0001t0002g0002 a0001c0001t0002g0027 a0001c0001t0002g0028 others(28): Show |
32 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-120-881T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76133287 | |||||||
| chr15:76133351 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-120-817C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76133351 | |||||||
| chr15:76133435 | T | TA | 78 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(75): Show |
80 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-120-725dupA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 76133435 | ||||||
| chr15:76133604 | A | G | 79 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(76): Show |
81 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.-120-564A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76133604 | |||||||
| chr15:76133616 | G | T | 1 | a0002c0002t0001g0204 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-120-552G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76133616 | |||||||
| chr15:76133687 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0023 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-120-481C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76133687 | |||||||
| chr15:76133804 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0023 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-120-364G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76133804 | |||||||
| chr15:76133858 | G | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0132 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.-120-310G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76133858 | |||||||
| chr15:76133908 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0023 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-120-260C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76133908 | |||||||
| chr15:76134120 | A | T | 1 | a0002c0002t0001g0227 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-120-48A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 1/10 | chr15 | 76134120 | |||||||
| chr15:76134498 | C | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0023 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.14+197C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76134498 | |||||||
| chr15:76134572 | A | C | 4 | a0001c0001t0001g0271 a0001c0001t0002g0057 a0002c0002t0001g0011 others(1): Show |
4 | HG01243.hp1 HG01255.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.14+271A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76134572 | |||||||
| chr15:76135053 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.14+752C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76135053 | |||||||
| chr15:76135126 | G | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0266 a0001c0001t0004g0005 others(1): Show |
4 | HG02970.hp2 HG03098.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.14+825G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76135126 | |||||||
| chr15:76135152 | C | G | 86 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(83): Show |
88 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.14+851C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76135152 | |||||||
| chr15:76135319 | C | T | 81 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(78): Show |
83 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.14+1018C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76135319 | |||||||
| chr15:76135379 | C | T | 1 | a0001c0001t0003g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.14+1078C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76135379 | |||||||
| chr15:76135653 | C | T | 158 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(155): Show |
160 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(157): Show |
intron_variant | MODIFIER | c.14+1352C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76135653 | |||||||
| chr15:76135832 | G | T | 81 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(78): Show |
83 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.14+1531G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76135832 | |||||||
| chr15:76135873 | T | A | 4 | a0001c0001t0001g0255 a0001c0001t0004g0248 a0002c0002t0001g0175 others(1): Show |
4 | HG02486.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.14+1572T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76135873 | |||||||
| chr15:76135942 | G | GT | 73 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(70): Show |
73 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.14+1654dupT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 76135942 | ||||||
| chr15:76136036 | C | T | 3 | a0001c0001t0001g0271 a0001c0001t0002g0057 a0002c0002t0001g0208 |
3 | HG01243.hp1 HG01255.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.15-1671C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76136036 | |||||||
| chr15:76136037 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0266 a0001c0001t0004g0005 others(1): Show |
4 | HG02970.hp2 HG03098.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.15-1670G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76136037 | |||||||
| chr15:76136047 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0023 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.15-1660G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76136047 | |||||||
| chr15:76136066 | C | A | 1 | a0001c0001t0002g0236 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.15-1641C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76136066 | |||||||
| chr15:76136092 | C | T | 1 | a0002c0002t0001g0227 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.15-1615C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76136092 | |||||||
| chr15:76136143 | A | G | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.15-1564A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76136143 | |||||||
| chr15:76136223 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.15-1484G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76136223 | |||||||
| chr15:76136233 | A | G | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.15-1474A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76136233 | |||||||
| chr15:76136344 | G | A | 4 | a0001c0001t0002g0041 a0001c0001t0002g0044 a0002c0002t0001g0046 others(1): Show |
4 | NA18968.hp1 NA18978.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.15-1363G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76136344 | |||||||
| chr15:76136347 | C | T | 2 | a0002c0002t0001g0170 a0002c0002t0001g0171 |
2 | HG01515.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.15-1360C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76136347 | |||||||
| chr15:76136355 | T | A | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.15-1352T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76136355 | |||||||
| chr15:76136474 | G | A | 1 | a0001c0001t0002g0139 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.15-1233G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76136474 | |||||||
| chr15:76136516 | A | C | 3 | a0001c0001t0002g0152 a0001c0001t0002g0154 a0001c0001t0002g0191 |
3 | HG00558.hp1 HG02056.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.15-1191A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76136516 | |||||||
| chr15:76136618 | A | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0023 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.15-1089A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76136618 | |||||||
| chr15:76136716 | C | T | 2 | a0001c0001t0001g0244 a0002c0002t0001g0099 |
2 | NA18948.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.15-991C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76136716 | |||||||
| chr15:76136727 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.15-980C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76136727 | |||||||
| chr15:76136839 | G | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0255 a0001c0001t0004g0248 others(2): Show |
5 | HG02486.hp1 HG02559.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.15-868G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76136839 | |||||||
| chr15:76136865 | A | G | 3 | a0001c0001t0001g0132 a0002c0002t0001g0029 a0002c0002t0001g0040 |
3 | HG01109.hp1 HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.15-842A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76136865 | |||||||
| chr15:76136974 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.15-733C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76136974 | |||||||
| chr15:76137068 | G | A | 1 | a0001c0001t0002g0070 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.15-639G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76137068 | |||||||
| chr15:76137162 | C | A | 70 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(67): Show |
70 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.15-545C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76137162 | |||||||
| chr15:76137202 | A | G | 1 | a0002c0002t0001g0197 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.15-505A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76137202 | |||||||
| chr15:76137444 | C | T | 40 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0025 others(37): Show |
41 | HG01123.hp1 HG01243.hp2 HG01346.hp2 others(38): Show |
intron_variant | MODIFIER | c.15-263C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76137444 | |||||||
| chr15:76137694 | C | T | 1 | a0002c0002t0001g0046 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.15-13C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 2/10 | chr15 | 76137694 | |||||||
| chr15:76137949 | C | G | 4 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0038 others(1): Show |
4 | HG02280.hp2 HG02647.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.203+54C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76137949 | |||||||
| chr15:76137949 | C | T | 1 | a0002c0002t0001g0118 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.203+54C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76137949 | |||||||
| chr15:76137993 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0023 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.203+98G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76137993 | |||||||
| chr15:76138020 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0023 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.203+125G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76138020 | |||||||
| chr15:76138025 | C | T | 30 | a0001c0001t0002g0002 a0001c0001t0002g0027 a0001c0001t0002g0028 others(27): Show |
31 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.203+130C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76138025 | |||||||
| chr15:76138097 | C | T | 1 | a0001c0001t0002g0235 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.203+202C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76138097 | |||||||
| chr15:76138173 | A | G | 77 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(74): Show |
79 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.203+278A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76138173 | |||||||
| chr15:76138222 | C | CA | 6 | a0001c0001t0002g0092 a0001c0001t0002g0203 a0001c0001t0002g0263 others(3): Show |
6 | HG00733.hp2 HG01123.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.203+355dupA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 76138222 | ||||||
| chr15:76138222 | CA | C | 39 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0060 others(36): Show |
39 | HG01074.hp1 HG01074.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.203+355delA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 76138222 | ||||||
| chr15:76138222 | CAA | C | 91 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0020 others(88): Show |
92 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.203+354_203+355del others(2): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 76138222 | ||||||
| chr15:76138222 | CAAA | C | 12 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0023 others(9): Show |
12 | HG01243.hp1 HG01257.hp1 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.203+353_203+355del others(3): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 76138222 | ||||||
| chr15:76138222 | CAAAAA | C | 17 | a0001c0001t0001g0025 a0001c0001t0001g0076 a0001c0001t0001g0079 others(14): Show |
17 | HG01123.hp1 HG01255.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.203+351_203+355del others(5): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 76138222 | ||||||
| chr15:76138222 | CAAAAAA | C | 6 | a0001c0001t0001g0269 a0001c0001t0002g0001 a0001c0001t0003g0014 others(3): Show |
7 | HG01243.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.203+350_203+355del others(6): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 76138222 | ||||||
| chr15:76138222 | CAAAAAAA | C | 20 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0038 others(17): Show |
20 | HG02257.hp1 HG02280.hp2 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.203+349_203+355del others(7): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 76138222 | ||||||
| chr15:76138222 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0002g0154 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.203+346_203+355del others(10): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 76138222 | ||||||
| chr15:76138271 | A | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0011g0199 |
3 | HG02965.hp1 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.203+376A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76138271 | |||||||
| chr15:76138271 | ATC | A | 32 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0002g0002 others(29): Show |
33 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.203+378_203+379del others(2): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 76138271 | ||||||
| chr15:76138620 | C | T | 3 | a0001c0001t0001g0132 a0002c0002t0001g0029 a0002c0002t0001g0040 |
3 | HG01109.hp1 HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.203+725C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76138620 | |||||||
| chr15:76138797 | G | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0271 a0001c0001t0002g0057 others(1): Show |
4 | HG01243.hp1 HG01255.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.203+902G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76138797 | |||||||
| chr15:76138987 | T | G | 41 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0025 others(38): Show |
42 | HG01123.hp1 HG01243.hp2 HG01346.hp2 others(39): Show |
intron_variant | MODIFIER | c.203+1092T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76138987 | |||||||
| chr15:76139011 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0266 a0001c0001t0004g0005 others(1): Show |
4 | HG02970.hp2 HG03098.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.203+1116C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76139011 | |||||||
| chr15:76139017 | C | A | 1 | a0002c0002t0001g0231 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.203+1122C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76139017 | |||||||
| chr15:76139364 | A | C | 30 | a0001c0001t0002g0002 a0001c0001t0002g0027 a0001c0001t0002g0028 others(27): Show |
31 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.203+1469A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76139364 | |||||||
| chr15:76139516 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.203+1621C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76139516 | |||||||
| chr15:76139532 | C | T | 1 | a0001c0001t0003g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.203+1637C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76139532 | |||||||
| chr15:76139567 | T | C | 1 | a0001c0001t0001g0207 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.203+1672T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76139567 | |||||||
| chr15:76139691 | A | G | 5 | a0001c0001t0002g0047 a0001c0001t0005g0061 a0001c0001t0005g0084 others(2): Show |
5 | HG00597.hp1 HG02015.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.203+1796A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76139691 | |||||||
| chr15:76139731 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.203+1836C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76139731 | |||||||
| chr15:76139888 | G | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0023 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.203+1993G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76139888 | |||||||
| chr15:76140026 | A | G | 4 | a0001c0001t0001g0020 a0001c0001t0001g0271 a0001c0001t0002g0057 others(1): Show |
4 | HG01243.hp1 HG01255.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.203+2131A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76140026 | |||||||
| chr15:76140460 | G | A | 3 | a0001c0001t0001g0076 a0001c0001t0001g0135 a0001c0001t0001g0229 |
3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.203+2565G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76140460 | |||||||
| chr15:76140482 | C | T | 32 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0002g0002 others(29): Show |
33 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.203+2587C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76140482 | |||||||
| chr15:76140609 | A | G | 1 | a0001c0001t0003g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.203+2714A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76140609 | |||||||
| chr15:76140677 | C | T | 6 | a0001c0001t0001g0009 a0001c0001t0001g0266 a0001c0001t0003g0014 others(3): Show |
6 | HG02647.hp1 HG02970.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.203+2782C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76140677 | |||||||
| chr15:76140741 | G | T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0271 a0001c0001t0002g0057 others(1): Show |
4 | HG01243.hp1 HG01255.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.203+2846G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76140741 | |||||||
| chr15:76140797 | G | A | 30 | a0001c0001t0002g0002 a0001c0001t0002g0027 a0001c0001t0002g0028 others(27): Show |
31 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.203+2902G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76140797 | |||||||
| chr15:76140871 | CA | C | 79 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(76): Show |
79 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.203+2992delA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 76140871 | ||||||
| chr15:76140871 | CAAA | C | 56 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(53): Show |
57 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.203+2990_203+2992d others(5): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 76140871 | ||||||
| chr15:76140871 | CAAAA | C | 16 | a0001c0001t0001g0025 a0001c0001t0001g0076 a0001c0001t0001g0079 others(13): Show |
17 | HG01123.hp1 HG01243.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.203+2989_203+2992d others(6): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 76140871 | ||||||
| chr15:76140896 | G | C | 30 | a0001c0001t0002g0002 a0001c0001t0002g0027 a0001c0001t0002g0028 others(27): Show |
31 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.203+3001G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76140896 | |||||||
| chr15:76141061 | C | T | 1 | a0001c0001t0002g0167 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.203+3166C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76141061 | |||||||
| chr15:76141236 | C | CT | 83 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(80): Show |
83 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.203+3358dupT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 76141236 | ||||||
| chr15:76141236 | CT | C | 58 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(55): Show |
60 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.203+3358delT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 76141236 | ||||||
| chr15:76141245 | T | G | 3 | a0001c0001t0002g0074 a0001c0001t0002g0106 a0001c0001t0002g0108 |
3 | HG01257.hp2 HG01516.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.203+3350T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76141245 | |||||||
| chr15:76141275 | G | A | 2 | a0002c0002t0001g0168 a0002c0002t0001g0169 |
2 | HG02040.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.203+3380G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76141275 | |||||||
| chr15:76141525 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.203+3630C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76141525 | |||||||
| chr15:76141622 | C | T | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.203+3727C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76141622 | |||||||
| chr15:76141790 | C | T | 3 | a0001c0001t0001g0271 a0001c0001t0002g0057 a0002c0002t0001g0208 |
3 | HG01243.hp1 HG01255.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.203+3895C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76141790 | |||||||
| chr15:76141820 | A | G | 5 | a0001c0001t0001g0093 a0001c0001t0001g0241 a0002c0002t0001g0174 others(2): Show |
5 | HG02257.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.203+3925A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76141820 | |||||||
| chr15:76142011 | G | A | 3 | a0001c0001t0001g0271 a0001c0001t0002g0057 a0002c0002t0001g0208 |
3 | HG01243.hp1 HG01255.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.203+4116G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76142011 | |||||||
| chr15:76142111 | G | A | 88 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(85): Show |
90 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.203+4216G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76142111 | |||||||
| chr15:76142143 | C | T | 1 | a0001c0001t0001g0244 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.203+4248C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76142143 | |||||||
| chr15:76142260 | A | G | 1 | a0001c0001t0002g0062 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.203+4365A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76142260 | |||||||
| chr15:76142345 | CGCAGCCA others(2): Show |
C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0266 a0001c0001t0004g0005 others(1): Show |
4 | HG02970.hp2 HG03098.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.203+4454_203+4462d others(11): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 76142345 | ||||||
| chr15:76142348 | A | G | 1 | a0002c0002t0001g0125 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.203+4453A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76142348 | |||||||
| chr15:76142569 | T | C | 41 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0025 others(38): Show |
42 | HG01123.hp1 HG01243.hp2 HG01346.hp2 others(39): Show |
intron_variant | MODIFIER | c.203+4674T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76142569 | |||||||
| chr15:76142756 | C | T | 1 | a0001c0001t0002g0183 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.203+4861C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76142756 | |||||||
| chr15:76142867 | G | A | 49 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(46): Show |
50 | HG01123.hp1 HG01243.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.203+4972G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76142867 | |||||||
| chr15:76142960 | C | T | 84 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(81): Show |
86 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.203+5065C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76142960 | |||||||
| chr15:76143002 | T | C | 158 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(155): Show |
160 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(157): Show |
intron_variant | MODIFIER | c.203+5107T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76143002 | |||||||
| chr15:76143112 | G | A | 35 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0132 others(32): Show |
36 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.203+5217G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76143112 | |||||||
| chr15:76143293 | C | A | 32 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0002g0002 others(29): Show |
33 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.203+5398C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76143293 | |||||||
| chr15:76143299 | G | A | 84 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(81): Show |
86 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.203+5404G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76143299 | |||||||
| chr15:76143336 | C | T | 1 | a0002c0002t0001g0179 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.203+5441C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76143336 | |||||||
| chr15:76143407 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.203+5512T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76143407 | |||||||
| chr15:76143451 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0011g0199 |
3 | HG02965.hp1 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.203+5556G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76143451 | |||||||
| chr15:76143768 | G | A | 1 | a0002c0002t0001g0073 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.203+5873G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76143768 | |||||||
| chr15:76143907 | G | T | 48 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(45): Show |
49 | HG01123.hp1 HG01243.hp2 HG01346.hp2 others(46): Show |
intron_variant | MODIFIER | c.203+6012G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76143907 | |||||||
| chr15:76144168 | C | T | 88 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(85): Show |
90 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.203+6273C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76144168 | |||||||
| chr15:76144210 | C | G | 39 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0132 others(36): Show |
40 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.203+6315C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76144210 | |||||||
| chr15:76144217 | T | TTAC | 158 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(155): Show |
160 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(157): Show |
intron_variant | MODIFIER | c.203+6323_203+6325d others(5): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 76144217 | ||||||
| chr15:76144224 | A | C | 158 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(155): Show |
160 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(157): Show |
intron_variant | MODIFIER | c.203+6329A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76144224 | |||||||
| chr15:76144226 | T | TGA | 158 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(155): Show |
160 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(157): Show |
intron_variant | MODIFIER | c.203+6332_203+6333i others(4): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 76144226 | ||||||
| chr15:76144240 | T | C | 158 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(155): Show |
160 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(157): Show |
intron_variant | MODIFIER | c.203+6345T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76144240 | |||||||
| chr15:76144307 | C | T | 8 | a0001c0001t0002g0092 a0001c0001t0002g0096 a0001c0001t0002g0140 others(5): Show |
8 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.203+6412C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76144307 | |||||||
| chr15:76144320 | G | A | 17 | a0001c0001t0001g0083 a0001c0001t0001g0109 a0001c0001t0001g0157 others(14): Show |
17 | HG00438.hp1 HG01099.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.203+6425G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76144320 | |||||||
| chr15:76144329 | TG | T | 3 | a0001c0001t0001g0271 a0001c0001t0002g0057 a0002c0002t0001g0208 |
3 | HG01243.hp1 HG01255.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.203+6435delG | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76144329 | |||||||
| chr15:76144332 | G | C | 3 | a0001c0001t0001g0271 a0001c0001t0002g0057 a0002c0002t0001g0208 |
3 | HG01243.hp1 HG01255.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.203+6437G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76144332 | |||||||
| chr15:76144412 | C | G | 1 | a0001c0001t0001g0137 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.203+6517C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76144412 | |||||||
| chr15:76144444 | G | A | 14 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0021 others(11): Show |
14 | HG01243.hp1 HG01255.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.203+6549G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76144444 | |||||||
| chr15:76144482 | G | C | 34 | a0001c0001t0001g0132 a0001c0001t0002g0002 a0001c0001t0002g0027 others(31): Show |
35 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.203+6587G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76144482 | |||||||
| chr15:76144579 | C | T | 78 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(75): Show |
78 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.203+6684C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76144579 | |||||||
| chr15:76144954 | T | C | 1 | a0002c0002t0001g0216 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.203+7059T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76144954 | |||||||
| chr15:76144981 | A | G | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.203+7086A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76144981 | |||||||
| chr15:76145065 | A | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0021 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.203+7170A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76145065 | |||||||
| chr15:76145199 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.203+7304A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76145199 | |||||||
| chr15:76145221 | C | T | 52 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(49): Show |
53 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.203+7326C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76145221 | |||||||
| chr15:76145245 | T | C | 3 | a0001c0001t0002g0152 a0001c0001t0002g0154 a0001c0001t0002g0191 |
3 | HG00558.hp1 HG02056.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.203+7350T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76145245 | |||||||
| chr15:76145335 | A | G | 1 | a0001c0001t0004g0254 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.203+7440A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76145335 | |||||||
| chr15:76145335 | AGTGATTT others(12): Show |
A | 35 | a0001c0001t0001g0132 a0001c0001t0002g0002 a0001c0001t0002g0027 others(32): Show |
36 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.203+7455_203+7473d others(21): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 76145335 | ||||||
| chr15:76145369 | T | G | 1 | a0001c0001t0003g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.203+7474T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76145369 | |||||||
| chr15:76145413 | C | T | 34 | a0001c0001t0001g0132 a0001c0001t0002g0002 a0001c0001t0002g0027 others(31): Show |
35 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.203+7518C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76145413 | |||||||
| chr15:76145629 | A | G | 86 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(83): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.203+7734A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76145629 | |||||||
| chr15:76145642 | T | G | 30 | a0001c0001t0001g0025 a0001c0001t0001g0079 a0001c0001t0001g0080 others(27): Show |
31 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.203+7747T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76145642 | |||||||
| chr15:76145741 | T | C | 1 | a0002c0002t0001g0194 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.203+7846T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76145741 | |||||||
| chr15:76145828 | G | C | 2 | a0002c0002t0001g0170 a0002c0002t0001g0171 |
2 | HG01515.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.203+7933G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76145828 | |||||||
| chr15:76145896 | G | T | 1 | a0001c0001t0001g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.203+8001G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76145896 | |||||||
| chr15:76146308 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.203+8413C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76146308 | |||||||
| chr15:76146322 | T | C | 1 | a0004c0005t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.203+8427T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76146322 | |||||||
| chr15:76146652 | A | G | 1 | a0001c0001t0002g0213 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.203+8757A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76146652 | |||||||
| chr15:76146794 | C | G | 168 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(165): Show |
170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.203+8899C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76146794 | |||||||
| chr15:76146849 | C | G | 25 | a0001c0001t0001g0025 a0001c0001t0001g0079 a0001c0001t0001g0080 others(22): Show |
25 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(22): Show |
intron_variant | MODIFIER | c.203+8954C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76146849 | |||||||
| chr15:76146938 | C | T | 2 | a0002c0002t0001g0094 a0002c0002t0001g0105 |
2 | NA19068.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.203+9043C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76146938 | |||||||
| chr15:76146955 | C | T | 1 | a0001c0001t0002g0095 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.203+9060C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76146955 | |||||||
| chr15:76147204 | T | C | 3 | a0001c0001t0001g0266 a0001c0001t0004g0005 a0001c0001t0004g0006 |
3 | HG02970.hp2 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.203+9309T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76147204 | |||||||
| chr15:76147401 | G | A | 52 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(49): Show |
53 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.204-9203G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76147401 | |||||||
| chr15:76147446 | G | A | 52 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(49): Show |
53 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.204-9158G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76147446 | |||||||
| chr15:76147731 | C | T | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.204-8873C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76147731 | |||||||
| chr15:76147769 | GC | G | 6 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0255 others(3): Show |
6 | HG02486.hp1 HG02922.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.204-8833delC | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 76147769 | ||||||
| chr15:76147824 | A | C | 4 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0038 others(1): Show |
4 | HG02280.hp2 HG02647.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.204-8780A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76147824 | |||||||
| chr15:76148293 | GATCATGG others(14): Show |
G | 1 | a0001c0001t0008g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.204-8310_204-8290d others(23): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76148293 | |||||||
| chr15:76148321 | C | A | 1 | a0001c0001t0008g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.204-8283C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76148321 | |||||||
| chr15:76148322 | C | A | 1 | a0001c0001t0008g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.204-8282C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76148322 | |||||||
| chr15:76148323 | A | G | 1 | a0001c0001t0008g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.204-8281A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76148323 | |||||||
| chr15:76148324 | C | G | 1 | a0001c0001t0008g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.204-8280C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76148324 | |||||||
| chr15:76148385 | A | T | 1 | a0001c0001t0001g0102 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.204-8219A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76148385 | |||||||
| chr15:76148473 | A | C | 52 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(49): Show |
53 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.204-8131A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76148473 | |||||||
| chr15:76148602 | C | T | 1 | a0001c0001t0004g0248 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.204-8002C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76148602 | |||||||
| chr15:76148700 | A | C | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.204-7904A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76148700 | |||||||
| chr15:76148733 | C | A | 5 | a0001c0001t0001g0093 a0001c0001t0001g0241 a0002c0002t0001g0174 others(2): Show |
5 | HG02257.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.204-7871C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76148733 | |||||||
| chr15:76148733 | C | T | 1 | a0002c0002t0001g0016 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.204-7871C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76148733 | |||||||
| chr15:76148921 | C | G | 1 | a0001c0001t0002g0004 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.204-7683C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76148921 | |||||||
| chr15:76149341 | A | G | 4 | a0001c0001t0002g0092 a0001c0001t0002g0096 a0001c0001t0002g0183 others(1): Show |
4 | HG00099.hp1 HG00741.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.204-7263A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76149341 | |||||||
| chr15:76149439 | C | A | 1 | a0001c0001t0001g0130 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.204-7165C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76149439 | |||||||
| chr15:76149483 | C | T | 2 | a0001c0001t0002g0057 a0002c0002t0001g0208 |
2 | HG01243.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.204-7121C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76149483 | |||||||
| chr15:76149524 | A | G | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.204-7080A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76149524 | |||||||
| chr15:76149641 | T | C | 32 | a0001c0001t0002g0002 a0001c0001t0002g0027 a0001c0001t0002g0028 others(29): Show |
33 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.204-6963T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76149641 | |||||||
| chr15:76149704 | C | T | 3 | a0001c0001t0002g0044 a0002c0002t0001g0046 a0002c0002t0001g0189 |
3 | NA18978.hp1 NA18990.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.204-6900C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76149704 | |||||||
| chr15:76150115 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.204-6489G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76150115 | |||||||
| chr15:76150252 | T | G | 4 | a0001c0001t0001g0129 a0001c0001t0001g0142 a0002c0002t0001g0127 others(1): Show |
4 | HG02818.hp2 HG02976.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.204-6352T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76150252 | |||||||
| chr15:76150594 | G | T | 1 | a0001c0001t0001g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.204-6010G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76150594 | |||||||
| chr15:76150947 | C | T | 1 | a0002c0002t0001g0215 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.204-5657C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76150947 | |||||||
| chr15:76151007 | C | T | 2 | a0001c0001t0002g0057 a0002c0002t0001g0208 |
2 | HG01243.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.204-5597C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76151007 | |||||||
| chr15:76151066 | G | A | 60 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(57): Show |
61 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.204-5538G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76151066 | |||||||
| chr15:76151287 | C | G | 1 | a0002c0002t0001g0231 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.204-5317C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76151287 | |||||||
| chr15:76151323 | A | G | 174 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(171): Show |
176 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.204-5281A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76151323 | |||||||
| chr15:76151349 | T | G | 1 | a0001c0001t0002g0184 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.204-5255T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76151349 | |||||||
| chr15:76151465 | A | G | 32 | a0001c0001t0002g0002 a0001c0001t0002g0027 a0001c0001t0002g0028 others(29): Show |
33 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.204-5139A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76151465 | |||||||
| chr15:76151520 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.204-5084C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76151520 | |||||||
| chr15:76151617 | T | C | 118 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(115): Show |
120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.204-4987T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76151617 | |||||||
| chr15:76151623 | G | A | 31 | a0001c0001t0001g0025 a0001c0001t0001g0079 a0001c0001t0001g0080 others(28): Show |
32 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.204-4981G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76151623 | |||||||
| chr15:76151689 | C | A | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.204-4915C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76151689 | |||||||
| chr15:76151897 | G | A | 15 | a0001c0001t0001g0083 a0001c0001t0001g0109 a0001c0001t0001g0157 others(12): Show |
15 | HG00438.hp1 HG01099.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.204-4707G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76151897 | |||||||
| chr15:76152079 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.204-4525A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76152079 | |||||||
| chr15:76152228 | G | A | 1 | a0001c0001t0002g0139 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.204-4376G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76152228 | |||||||
| chr15:76152278 | G | A | 1 | a0002c0002t0001g0141 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.204-4326G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76152278 | |||||||
| chr15:76152342 | C | T | 136 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(133): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.204-4262C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76152342 | |||||||
| chr15:76152354 | C | T | 134 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(131): Show |
135 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.204-4250C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76152354 | |||||||
| chr15:76152542 | T | C | 180 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(177): Show |
182 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.204-4062T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76152542 | |||||||
| chr15:76152614 | A | G | 2 | a0001c0001t0002g0045 a0002c0002t0001g0053 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.204-3990A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76152614 | |||||||
| chr15:76152693 | CGCTTTCT others(11): Show |
C | 31 | a0001c0001t0002g0030 a0001c0001t0002g0035 a0001c0001t0002g0036 others(28): Show |
31 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.204-3907_204-3890d others(20): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 76152693 | ||||||
| chr15:76152754 | G | A | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.204-3850G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76152754 | |||||||
| chr15:76152790 | G | T | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.204-3814G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76152790 | |||||||
| chr15:76153009 | G | A | 32 | a0001c0001t0002g0002 a0001c0001t0002g0027 a0001c0001t0002g0028 others(29): Show |
33 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.204-3595G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76153009 | |||||||
| chr15:76153018 | T | C | 65 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0102 others(62): Show |
65 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.204-3586T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76153018 | |||||||
| chr15:76153084 | CACCTCCT others(11): Show |
C | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.204-3516_204-3499d others(20): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 76153084 | ||||||
| chr15:76153134 | C | CA | 169 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(166): Show |
171 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.204-3459dupA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 76153134 | ||||||
| chr15:76153134 | C | CAA | 10 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0076 others(7): Show |
10 | HG01243.hp1 HG01255.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.204-3460_204-3459d others(4): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 76153134 | ||||||
| chr15:76153157 | C | T | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.204-3447C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76153157 | |||||||
| chr15:76153189 | T | C | 1 | a0002c0002t0001g0170 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.204-3415T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76153189 | |||||||
| chr15:76153210 | A | G | 1 | a0001c0001t0002g0054 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.204-3394A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76153210 | |||||||
| chr15:76153348 | C | T | 31 | a0001c0001t0002g0002 a0001c0001t0002g0027 a0001c0001t0002g0028 others(28): Show |
32 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.204-3256C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76153348 | |||||||
| chr15:76153377 | G | A | 3 | a0002c0002t0001g0221 a0002c0002t0001g0222 a0002c0002t0001g0223 |
3 | HG01069.hp1 HG01106.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.204-3227G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76153377 | |||||||
| chr15:76153522 | C | T | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.204-3082C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76153522 | |||||||
| chr15:76153550 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.204-3054A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76153550 | |||||||
| chr15:76153636 | C | T | 5 | a0001c0001t0001g0076 a0001c0001t0001g0135 a0001c0001t0001g0229 others(2): Show |
5 | HG01243.hp1 HG01255.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.204-2968C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76153636 | |||||||
| chr15:76153791 | G | A | 24 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0038 others(21): Show |
24 | HG01074.hp1 HG01167.hp2 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.204-2813G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76153791 | |||||||
| chr15:76153865 | G | A | 62 | a0001c0001t0001g0102 a0001c0001t0001g0137 a0001c0001t0001g0153 others(59): Show |
62 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.204-2739G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76153865 | |||||||
| chr15:76153866 | C | A | 62 | a0001c0001t0001g0102 a0001c0001t0001g0137 a0001c0001t0001g0153 others(59): Show |
62 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.204-2738C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76153866 | |||||||
| chr15:76153867 | T | C | 133 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(130): Show |
134 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.204-2737T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76153867 | |||||||
| chr15:76153887 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0260 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.204-2717G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76153887 | |||||||
| chr15:76153925 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.204-2679C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76153925 | |||||||
| chr15:76153962 | G | A | 31 | a0001c0001t0002g0002 a0001c0001t0002g0027 a0001c0001t0002g0028 others(28): Show |
32 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.204-2642G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76153962 | |||||||
| chr15:76154058 | C | T | 10 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0076 others(7): Show |
10 | HG01243.hp1 HG01255.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.204-2546C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76154058 | |||||||
| chr15:76154111 | C | G | 1 | a0001c0001t0001g0076 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.204-2493C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76154111 | |||||||
| chr15:76154365 | T | G | 31 | a0001c0001t0002g0002 a0001c0001t0002g0027 a0001c0001t0002g0028 others(28): Show |
32 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.204-2239T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76154365 | |||||||
| chr15:76154366 | G | A | 24 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0038 others(21): Show |
24 | HG01074.hp1 HG01167.hp2 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.204-2238G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76154366 | |||||||
| chr15:76154576 | T | G | 5 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0011g0199 others(2): Show |
5 | HG02572.hp2 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.204-2028T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76154576 | |||||||
| chr15:76154586 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.204-2018G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76154586 | |||||||
| chr15:76154606 | C | T | 2 | a0002c0002t0001g0175 a0002c0002t0001g0270 |
2 | HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.204-1998C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76154606 | |||||||
| chr15:76154616 | C | G | 30 | a0001c0001t0002g0002 a0001c0001t0002g0027 a0001c0001t0002g0028 others(27): Show |
31 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.204-1988C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76154616 | |||||||
| chr15:76154895 | G | A | 1 | a0001c0001t0001g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.204-1709G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76154895 | |||||||
| chr15:76154975 | G | C | 3 | a0001c0001t0002g0043 a0001c0001t0002g0056 a0001c0001t0002g0122 |
3 | HG02132.hp1 NA18942.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.204-1629G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76154975 | |||||||
| chr15:76155311 | C | T | 6 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0255 others(3): Show |
6 | HG02486.hp1 HG02922.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.204-1293C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76155311 | |||||||
| chr15:76155328 | T | A | 1 | a0002c0002t0001g0046 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.204-1276T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76155328 | |||||||
| chr15:76155412 | T | C | 135 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(132): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.204-1192T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76155412 | |||||||
| chr15:76155413 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.204-1191G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76155413 | |||||||
| chr15:76155467 | G | C | 134 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(131): Show |
135 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.204-1137G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76155467 | |||||||
| chr15:76155558 | A | G | 2 | a0002c0002t0001g0215 a0002c0002t0001g0217 |
2 | HG02735.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.204-1046A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76155558 | |||||||
| chr15:76155562 | G | A | 65 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(62): Show |
66 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.204-1042G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76155562 | |||||||
| chr15:76155573 | C | T | 1 | a0002c0002t0001g0016 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.204-1031C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76155573 | |||||||
| chr15:76155927 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.204-677C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76155927 | |||||||
| chr15:76155957 | C | T | 1 | a0001c0001t0009g0091 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.204-647C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76155957 | |||||||
| chr15:76156062 | G | T | 1 | a0002c0002t0001g0170 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.204-542G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76156062 | |||||||
| chr15:76156219 | G | A | 1 | a0002c0002t0001g0194 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.204-385G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76156219 | |||||||
| chr15:76156241 | C | A | 1 | a0001c0001t0002g0106 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.204-363C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76156241 | |||||||
| chr15:76156435 | C | T | 150 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(147): Show |
151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.204-169C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76156435 | |||||||
| chr15:76156440 | C | T | 1 | a0002c0002t0001g0164 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.204-164C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76156440 | |||||||
| chr15:76156455 | G | A | 72 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(69): Show |
73 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.204-149G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76156455 | |||||||
| chr15:76156490 | A | T | 1 | a0001c0001t0002g0183 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.204-114A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 3/10 | chr15 | 76156490 | |||||||
| chr15:76156863 | G | A | 1 | a0002c0002t0001g0100 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.358+105G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76156863 | |||||||
| chr15:76156898 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.358+140C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76156898 | |||||||
| chr15:76156946 | T | C | 18 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0020 others(15): Show |
18 | HG01243.hp1 HG01243.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.358+188T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76156946 | |||||||
| chr15:76157042 | C | T | 28 | a0001c0001t0002g0002 a0001c0001t0002g0032 a0001c0001t0002g0043 others(25): Show |
29 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.358+284C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76157042 | |||||||
| chr15:76157177 | A | G | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.358+419A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76157177 | |||||||
| chr15:76157331 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.358+573C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76157331 | |||||||
| chr15:76157373 | G | A | 15 | a0001c0001t0001g0272 a0001c0001t0002g0004 a0001c0001t0002g0063 others(12): Show |
15 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(12): Show |
intron_variant | MODIFIER | c.358+615G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76157373 | |||||||
| chr15:76157385 | G | A | 1 | a0001c0001t0002g0167 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.358+627G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76157385 | |||||||
| chr15:76157464 | T | C | 1 | a0001c0001t0002g0184 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.358+706T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76157464 | |||||||
| chr15:76157578 | G | T | 1 | a0002c0002t0001g0016 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.358+820G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76157578 | |||||||
| chr15:76157580 | G | A | 1 | a0002c0002t0001g0197 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.358+822G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76157580 | |||||||
| chr15:76157851 | A | G | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.358+1093A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76157851 | |||||||
| chr15:76157881 | G | A | 1 | a0001c0001t0004g0254 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.358+1123G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76157881 | |||||||
| chr15:76157924 | G | C | 1 | a0002c0002t0001g0164 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.358+1166G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76157924 | |||||||
| chr15:76157998 | G | GTAAA | 27 | a0001c0001t0002g0002 a0001c0001t0002g0032 a0001c0001t0002g0043 others(24): Show |
28 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.358+1267_358+1270d others(6): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr15 | 76157998 | ||||||
| chr15:76157998 | GTAAATAA others(5): Show |
G | 1 | a0001c0001t0001g0247 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.358+1259_358+1270d others(14): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr15 | 76157998 | ||||||
| chr15:76158002 | A | G | 31 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(28): Show |
31 | HG01074.hp1 HG01167.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.358+1244A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76158002 | |||||||
| chr15:76158046 | T | C | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.358+1288T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76158046 | |||||||
| chr15:76158053 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.358+1295A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76158053 | |||||||
| chr15:76158120 | G | A | 1 | a0002c0002t0001g0164 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.358+1362G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76158120 | |||||||
| chr15:76158143 | G | A | 3 | a0002c0002t0001g0232 a0002c0002t0001g0233 a0002c0002t0001g0237 |
3 | NA18969.hp1 NA18974.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.358+1385G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76158143 | |||||||
| chr15:76158150 | A | G | 1 | a0002c0002t0001g0164 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.358+1392A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76158150 | |||||||
| chr15:76158502 | G | C | 1 | a0001c0001t0001g0079 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.359-1593G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76158502 | |||||||
| chr15:76158629 | ACAAT | A | 3 | a0001c0001t0002g0074 a0001c0001t0002g0106 a0001c0001t0002g0108 |
3 | HG01257.hp2 HG01516.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.359-1463_359-1460d others(6): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr15 | 76158629 | ||||||
| chr15:76158786 | T | C | 6 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0255 others(3): Show |
6 | HG02486.hp1 HG02922.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.359-1309T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76158786 | |||||||
| chr15:76158805 | C | T | 5 | a0001c0001t0001g0076 a0001c0001t0001g0135 a0001c0001t0001g0143 others(2): Show |
5 | HG01243.hp2 HG02145.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.359-1290C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76158805 | |||||||
| chr15:76159021 | TG | T | 46 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0060 others(43): Show |
47 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(44): Show |
intron_variant | MODIFIER | c.359-1066delG | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr15 | 76159021 | ||||||
| chr15:76159024 | G | T | 27 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(24): Show |
27 | HG01074.hp1 HG01167.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.359-1071G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76159024 | |||||||
| chr15:76159027 | G | C | 29 | a0001c0001t0002g0002 a0001c0001t0002g0032 a0001c0001t0002g0043 others(26): Show |
30 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.359-1068G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76159027 | |||||||
| chr15:76159070 | A | G | 1 | a0004c0005t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.359-1025A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76159070 | |||||||
| chr15:76159310 | C | A | 1 | a0004c0005t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.359-785C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76159310 | |||||||
| chr15:76159356 | C | G | 1 | a0001c0001t0001g0137 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.359-739C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76159356 | |||||||
| chr15:76159457 | T | C | 5 | a0001c0001t0001g0008 a0001c0001t0002g0001 a0001c0001t0003g0265 others(2): Show |
6 | HG02630.hp2 HG02809.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.359-638T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76159457 | |||||||
| chr15:76159476 | TCATCCCA | T | 3 | a0001c0001t0002g0001 a0001c0001t0003g0265 a0001c0001t0007g0252 |
4 | HG02630.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.359-617_359-611del others(7): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr15 | 76159476 | ||||||
| chr15:76159898 | C | T | 1 | a0002c0007t0001g0212 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.359-197C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76159898 | |||||||
| chr15:76159899 | T | G | 2 | a0001c0001t0001g0192 a0002c0007t0001g0212 |
2 | HG00621.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.359-196T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76159899 | |||||||
| chr15:76159921 | A | G | 2 | a0002c0002t0001g0127 a0002c0002t0001g0128 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.359-174A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76159921 | |||||||
| chr15:76159981 | G | A | 1 | a0004c0005t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.359-114G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 4/10 | chr15 | 76159981 | |||||||
| chr15:76160240 | T | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0135 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.432+72T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76160240 | |||||||
| chr15:76160332 | A | T | 1 | a0002c0007t0001g0212 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.432+164A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76160332 | |||||||
| chr15:76160467 | C | T | 1 | a0001c0001t0002g0041 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.432+299C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76160467 | |||||||
| chr15:76160560 | G | A | 6 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0255 others(3): Show |
6 | HG02486.hp1 HG02922.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.432+392G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76160560 | |||||||
| chr15:76160830 | A | C | 3 | a0001c0001t0001g0266 a0001c0001t0004g0005 a0001c0001t0004g0006 |
3 | HG02970.hp2 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.432+662A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76160830 | |||||||
| chr15:76160845 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.432+677C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76160845 | |||||||
| chr15:76160846 | G | A | 53 | a0001c0001t0001g0025 a0001c0001t0001g0038 a0001c0001t0001g0060 others(50): Show |
53 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.432+678G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76160846 | |||||||
| chr15:76160912 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.432+744C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76160912 | |||||||
| chr15:76161028 | C | T | 1 | a0001c0001t0002g0173 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.432+860C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76161028 | |||||||
| chr15:76161428 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.432+1260C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76161428 | |||||||
| chr15:76161450 | G | C | 1 | a0001c0001t0005g0186 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.432+1282G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76161450 | |||||||
| chr15:76161462 | G | GCT | 53 | a0001c0001t0001g0025 a0001c0001t0001g0038 a0001c0001t0001g0060 others(50): Show |
53 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.432+1312_432+1313d others(4): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 76161462 | ||||||
| chr15:76161475 | C | T | 5 | a0001c0001t0001g0234 a0001c0001t0002g0235 a0002c0002t0001g0232 others(2): Show |
5 | HG02155.hp2 NA18946.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.432+1307C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76161475 | |||||||
| chr15:76161537 | G | A | 6 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0255 others(3): Show |
6 | HG02486.hp1 HG02922.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.432+1369G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76161537 | |||||||
| chr15:76161557 | C | T | 1 | a0001c0001t0002g0173 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.432+1389C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76161557 | |||||||
| chr15:76161580 | G | A | 1 | a0002c0002t0002g0107 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.432+1412G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76161580 | |||||||
| chr15:76161779 | T | G | 2 | a0001c0001t0001g0008 a0004c0005t0001g0211 |
2 | HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.432+1611T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76161779 | |||||||
| chr15:76161815 | C | A | 1 | a0002c0002t0001g0016 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.432+1647C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76161815 | |||||||
| chr15:76161853 | C | G | 26 | a0001c0001t0002g0002 a0001c0001t0002g0027 a0001c0001t0002g0028 others(23): Show |
27 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.432+1685C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76161853 | |||||||
| chr15:76161994 | C | T | 52 | a0001c0001t0001g0025 a0001c0001t0001g0038 a0001c0001t0001g0060 others(49): Show |
52 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.432+1826C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76161994 | |||||||
| chr15:76162114 | G | A | 27 | a0001c0001t0002g0002 a0001c0001t0002g0027 a0001c0001t0002g0028 others(24): Show |
28 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.432+1946G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76162114 | |||||||
| chr15:76162215 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.432+2047G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76162215 | |||||||
| chr15:76162282 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.432+2114A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76162282 | |||||||
| chr15:76162297 | C | T | 4 | a0001c0001t0002g0070 a0001c0001t0002g0116 a0001c0001t0002g0210 others(1): Show |
4 | HG00609.hp2 HG00621.hp2 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.432+2129C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76162297 | |||||||
| chr15:76162321 | C | T | 27 | a0001c0001t0002g0002 a0001c0001t0002g0027 a0001c0001t0002g0028 others(24): Show |
28 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.432+2153C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76162321 | |||||||
| chr15:76162422 | T | C | 1 | a0001c0001t0002g0173 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.432+2254T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76162422 | |||||||
| chr15:76162446 | G | A | 1 | a0001c0001t0002g0054 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.432+2278G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76162446 | |||||||
| chr15:76162773 | G | A | 1 | a0002c0002t0001g0194 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.432+2605G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76162773 | |||||||
| chr15:76162824 | G | A | 1 | a0002c0002t0001g0016 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.432+2656G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76162824 | |||||||
| chr15:76162894 | G | T | 7 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0050 others(4): Show |
7 | HG00558.hp2 HG00609.hp1 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.432+2726G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76162894 | |||||||
| chr15:76162908 | G | A | 52 | a0001c0001t0001g0025 a0001c0001t0001g0038 a0001c0001t0001g0060 others(49): Show |
52 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.432+2740G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76162908 | |||||||
| chr15:76162977 | A | G | 2 | a0001c0001t0001g0008 a0004c0005t0001g0211 |
2 | HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.432+2809A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76162977 | |||||||
| chr15:76163002 | C | CCTGGGCC others(6): Show |
1 | a0001c0001t0004g0254 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.432+2835_432+2847d others(15): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 76163002 | ||||||
| chr15:76163184 | C | T | 1 | a0002c0002t0001g0146 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.432+3016C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76163184 | |||||||
| chr15:76163562 | T | G | 26 | a0001c0001t0002g0002 a0001c0001t0002g0027 a0001c0001t0002g0028 others(23): Show |
27 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.432+3394T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76163562 | |||||||
| chr15:76163593 | C | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0078 others(7): Show |
10 | HG00735.hp2 HG01106.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.432+3425C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76163593 | |||||||
| chr15:76163624 | G | A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0255 others(1): Show |
4 | HG02486.hp1 HG03209.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.432+3456G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76163624 | |||||||
| chr15:76163737 | G | A | 1 | a0001c0001t0002g0116 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.432+3569G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76163737 | |||||||
| chr15:76163843 | G | C | 11 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0078 others(8): Show |
11 | HG00735.hp2 HG01106.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.432+3675G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76163843 | |||||||
| chr15:76163923 | G | A | 2 | a0001c0001t0001g0008 a0004c0005t0001g0211 |
2 | HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.432+3755G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76163923 | |||||||
| chr15:76164110 | G | A | 18 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0060 others(15): Show |
18 | HG01109.hp1 HG01123.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.432+3942G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76164110 | |||||||
| chr15:76164444 | G | A | 1 | a0001c0001t0003g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.432+4276G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76164444 | |||||||
| chr15:76164503 | C | T | 14 | a0001c0001t0001g0093 a0001c0001t0001g0241 a0001c0001t0002g0065 others(11): Show |
14 | HG01074.hp1 HG01167.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.432+4335C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76164503 | |||||||
| chr15:76164508 | CCAATTTT others(1): Show |
C | 10 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0078 others(7): Show |
10 | HG00735.hp2 HG01106.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.432+4342_432+4349d others(10): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 76164508 | ||||||
| chr15:76164519 | TCTC | T | 18 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0060 others(15): Show |
18 | HG01109.hp1 HG01123.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.432+4355_432+4357d others(5): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 76164519 | ||||||
| chr15:76164556 | A | G | 1 | a0001c0001t0002g0082 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.432+4388A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76164556 | |||||||
| chr15:76164579 | T | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0060 others(19): Show |
23 | HG01109.hp1 HG01123.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.432+4411T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76164579 | |||||||
| chr15:76164805 | G | A | 1 | a0002c0002t0001g0163 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.432+4637G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76164805 | |||||||
| chr15:76164815 | C | G | 14 | a0001c0001t0001g0093 a0001c0001t0001g0241 a0001c0001t0002g0065 others(11): Show |
14 | HG01074.hp1 HG01167.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.432+4647C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76164815 | |||||||
| chr15:76164840 | TG | T | 8 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0255 others(5): Show |
8 | HG01243.hp1 HG01255.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.432+4674delG | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 76164840 | ||||||
| chr15:76164857 | A | C | 7 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0050 others(4): Show |
7 | HG00558.hp2 HG00609.hp1 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.432+4689A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76164857 | |||||||
| chr15:76164881 | G | A | 1 | a0001c0001t0002g0114 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.432+4713G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76164881 | |||||||
| chr15:76165050 | T | C | 21 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0060 others(18): Show |
22 | HG01109.hp1 HG01123.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.433-4766T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76165050 | |||||||
| chr15:76165076 | C | T | 14 | a0001c0001t0001g0093 a0001c0001t0001g0241 a0001c0001t0002g0065 others(11): Show |
14 | HG01074.hp1 HG01167.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.433-4740C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76165076 | |||||||
| chr15:76165145 | A | T | 1 | a0001c0001t0003g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.433-4671A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76165145 | |||||||
| chr15:76165297 | C | T | 40 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0076 others(37): Show |
41 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.433-4519C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76165297 | |||||||
| chr15:76165391 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.433-4425A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76165391 | |||||||
| chr15:76165632 | A | G | 3 | a0001c0001t0002g0001 a0001c0001t0003g0265 a0001c0001t0007g0252 |
4 | HG02630.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.433-4184A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76165632 | |||||||
| chr15:76165640 | G | T | 26 | a0001c0001t0002g0002 a0001c0001t0002g0027 a0001c0001t0002g0028 others(23): Show |
27 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.433-4176G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76165640 | |||||||
| chr15:76165699 | C | T | 16 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0060 others(13): Show |
16 | HG01109.hp1 HG01123.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.433-4117C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76165699 | |||||||
| chr15:76165733 | G | T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0266 a0001c0001t0004g0005 others(1): Show |
4 | HG02970.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.433-4083G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76165733 | |||||||
| chr15:76165791 | G | C | 1 | a0002c0002t0001g0127 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.433-4025G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76165791 | |||||||
| chr15:76165904 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.433-3912G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76165904 | |||||||
| chr15:76165938 | C | T | 1 | a0004c0005t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.433-3878C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76165938 | |||||||
| chr15:76166148 | G | T | 1 | a0001c0001t0003g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.433-3668G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76166148 | |||||||
| chr15:76166175 | C | T | 1 | a0001c0001t0003g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.433-3641C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76166175 | |||||||
| chr15:76166221 | G | C | 6 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0255 others(3): Show |
6 | HG02486.hp1 HG02922.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.433-3595G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76166221 | |||||||
| chr15:76166273 | G | A | 2 | a0001c0001t0002g0140 a0001c0001t0002g0245 |
2 | HG00738.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.433-3543G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76166273 | |||||||
| chr15:76166364 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.433-3452C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76166364 | |||||||
| chr15:76166568 | C | T | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.433-3248C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76166568 | |||||||
| chr15:76166588 | T | A | 17 | a0001c0001t0001g0038 a0001c0001t0001g0068 a0001c0001t0001g0093 others(14): Show |
17 | HG01074.hp1 HG01167.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.433-3228T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76166588 | |||||||
| chr15:76166608 | C | T | 20 | a0001c0001t0001g0272 a0001c0001t0002g0004 a0001c0001t0002g0063 others(17): Show |
20 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(17): Show |
intron_variant | MODIFIER | c.433-3208C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76166608 | |||||||
| chr15:76166890 | G | A | 15 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0060 others(12): Show |
15 | HG01109.hp1 HG01123.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.433-2926G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76166890 | |||||||
| chr15:76167261 | T | G | 19 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0060 others(16): Show |
20 | HG01109.hp1 HG01123.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.433-2555T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76167261 | |||||||
| chr15:76167323 | A | T | 17 | a0001c0001t0001g0076 a0001c0001t0001g0135 a0001c0001t0001g0229 others(14): Show |
17 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(14): Show |
intron_variant | MODIFIER | c.433-2493A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76167323 | |||||||
| chr15:76167467 | C | CA | 50 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0038 others(47): Show |
50 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.433-2332dupA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 76167467 | ||||||
| chr15:76167467 | CA | C | 16 | a0001c0001t0001g0143 a0001c0001t0001g0177 a0001c0001t0001g0244 others(13): Show |
17 | HG00099.hp1 HG00733.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.433-2332delA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 76167467 | ||||||
| chr15:76167810 | T | C | 3 | a0001c0001t0001g0266 a0001c0001t0004g0005 a0001c0001t0004g0006 |
3 | HG02970.hp2 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.433-2006T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76167810 | |||||||
| chr15:76167863 | T | C | 1 | a0004c0005t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.433-1953T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76167863 | |||||||
| chr15:76167866 | T | TA | 19 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0060 others(16): Show |
20 | HG01109.hp1 HG01123.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.433-1949dupA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 76167866 | ||||||
| chr15:76167921 | C | A | 1 | a0001c0001t0001g0172 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.433-1895C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76167921 | |||||||
| chr15:76167962 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.433-1854C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76167962 | |||||||
| chr15:76167964 | G | A | 6 | a0001c0001t0001g0269 a0002c0002t0001g0022 a0002c0002t0001g0024 others(3): Show |
6 | HG01243.hp2 HG02451.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.433-1852G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76167964 | |||||||
| chr15:76168065 | A | T | 1 | a0001c0001t0009g0091 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.433-1751A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76168065 | |||||||
| chr15:76168235 | G | A | 6 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0255 others(3): Show |
6 | HG02486.hp1 HG02922.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.433-1581G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76168235 | |||||||
| chr15:76168420 | C | T | 1 | a0002c0002t0012g0267 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.433-1396C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76168420 | |||||||
| chr15:76168504 | T | C | 16 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0060 others(13): Show |
16 | HG01109.hp1 HG01123.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.433-1312T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76168504 | |||||||
| chr15:76168521 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.433-1295G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76168521 | |||||||
| chr15:76168677 | C | T | 1 | a0002c0002t0001g0133 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.433-1139C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76168677 | |||||||
| chr15:76168838 | C | T | 15 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0060 others(12): Show |
15 | HG01109.hp1 HG01123.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.433-978C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76168838 | |||||||
| chr15:76168839 | A | G | 16 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0060 others(13): Show |
16 | HG01109.hp1 HG01123.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.433-977A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76168839 | |||||||
| chr15:76168881 | C | T | 1 | a0001c0001t0002g0182 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.433-935C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76168881 | |||||||
| chr15:76168892 | GA | G | 4 | a0001c0001t0001g0020 a0001c0001t0001g0266 a0001c0001t0004g0005 others(1): Show |
4 | HG02970.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.433-922delA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 76168892 | ||||||
| chr15:76168904 | G | A | 1 | a0002c0002t0001g0160 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.433-912G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76168904 | |||||||
| chr15:76168922 | T | G | 9 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0255 others(6): Show |
9 | HG01243.hp1 HG01255.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.433-894T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76168922 | |||||||
| chr15:76168958 | A | G | 1 | a0001c0001t0002g0108 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.433-858A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76168958 | |||||||
| chr15:76169056 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.433-760C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76169056 | |||||||
| chr15:76169101 | A | G | 1 | a0001c0001t0002g0054 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.433-715A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76169101 | |||||||
| chr15:76169139 | G | T | 3 | a0001c0001t0002g0152 a0001c0001t0002g0154 a0001c0001t0002g0191 |
3 | HG00558.hp1 HG02056.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.433-677G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76169139 | |||||||
| chr15:76169153 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.433-663G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76169153 | |||||||
| chr15:76169185 | G | C | 1 | a0001c0001t0003g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.433-631G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76169185 | |||||||
| chr15:76169218 | G | T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0266 a0001c0001t0004g0005 others(1): Show |
4 | HG02970.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.433-598G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76169218 | |||||||
| chr15:76169235 | A | T | 16 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0060 others(13): Show |
16 | HG01109.hp1 HG01123.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.433-581A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76169235 | |||||||
| chr15:76169315 | G | A | 4 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0165 others(1): Show |
4 | HG01074.hp1 HG01167.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.433-501G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76169315 | |||||||
| chr15:76169425 | G | A | 1 | a0004c0005t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.433-391G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76169425 | |||||||
| chr15:76169507 | T | A | 34 | a0001c0001t0001g0038 a0001c0001t0001g0068 a0001c0001t0001g0076 others(31): Show |
34 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(31): Show |
intron_variant | MODIFIER | c.433-309T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76169507 | |||||||
| chr15:76169508 | T | TG | 16 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0060 others(13): Show |
16 | HG01109.hp1 HG01123.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.433-307dupG | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 76169508 | ||||||
| chr15:76169531 | G | A | 3 | a0001c0001t0002g0062 a0001c0001t0002g0173 a0001c0001t0002g0213 |
3 | HG01109.hp2 HG02486.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.433-285G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76169531 | |||||||
| chr15:76169605 | A | G | 16 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0060 others(13): Show |
16 | HG01109.hp1 HG01123.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.433-211A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 5/10 | chr15 | 76169605 | |||||||
| chr15:76169922 | C | T | 15 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0060 others(12): Show |
15 | HG01109.hp1 HG01123.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.489+50C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 6/10 | chr15 | 76169922 | |||||||
| chr15:76169945 | A | G | 27 | a0001c0001t0001g0177 a0001c0001t0002g0002 a0001c0001t0002g0027 others(24): Show |
28 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.489+73A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 6/10 | chr15 | 76169945 | |||||||
| chr15:76170141 | GA | G | 33 | a0001c0001t0001g0038 a0001c0001t0001g0068 a0001c0001t0001g0076 others(30): Show |
33 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.489+273delA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 76170141 | ||||||
| chr15:76170205 | A | G | 1 | a0004c0005t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.489+333A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 6/10 | chr15 | 76170205 | |||||||
| chr15:76170213 | C | T | 1 | a0002c0002t0001g0164 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.489+341C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 6/10 | chr15 | 76170213 | |||||||
| chr15:76170234 | C | T | 33 | a0001c0001t0001g0038 a0001c0001t0001g0068 a0001c0001t0001g0076 others(30): Show |
33 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.489+362C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 6/10 | chr15 | 76170234 | |||||||
| chr15:76170336 | C | T | 266 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(263): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.489+464C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 6/10 | chr15 | 76170336 | |||||||
| chr15:76170533 | A | G | 1 | a0004c0005t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.490-460A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 6/10 | chr15 | 76170533 | |||||||
| chr15:76170677 | C | T | 6 | a0001c0001t0001g0269 a0002c0002t0001g0022 a0002c0002t0001g0024 others(3): Show |
6 | HG01243.hp2 HG02451.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-316C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 6/10 | chr15 | 76170677 | |||||||
| chr15:76170859 | C | A | 1 | a0004c0005t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.490-134C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 6/10 | chr15 | 76170859 | |||||||
| chr15:76170871 | G | A | 5 | a0001c0001t0001g0020 a0001c0001t0001g0266 a0001c0001t0004g0005 others(2): Show |
5 | HG02970.hp1 HG02970.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-122G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 6/10 | chr15 | 76170871 | |||||||
| chr15:76171147 | G | C | 2 | a0002c0002t0001g0170 a0002c0002t0001g0171 |
2 | HG01515.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.628+16G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76171147 | |||||||
| chr15:76171304 | T | C | 1 | a0002c0002t0001g0016 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.628+173T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76171304 | |||||||
| chr15:76171505 | C | T | 6 | a0001c0001t0001g0244 a0002c0002t0001g0094 a0002c0002t0001g0099 others(3): Show |
6 | NA18948.hp2 NA18968.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.628+374C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76171505 | |||||||
| chr15:76171678 | G | C | 1 | a0001c0001t0001g0188 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.628+547G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76171678 | |||||||
| chr15:76171861 | A | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0019 others(83): Show |
87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.628+730A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76171861 | |||||||
| chr15:76172039 | C | T | 31 | a0001c0001t0001g0177 a0001c0001t0002g0002 a0001c0001t0002g0027 others(28): Show |
32 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.628+908C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76172039 | |||||||
| chr15:76172134 | G | A | 1 | a0004c0005t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.628+1003G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76172134 | |||||||
| chr15:76172216 | C | T | 6 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0255 others(3): Show |
6 | HG02486.hp1 HG02922.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.628+1085C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76172216 | |||||||
| chr15:76172353 | C | T | 3 | a0001c0001t0001g0076 a0001c0001t0001g0135 a0001c0001t0001g0229 |
3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.628+1222C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76172353 | |||||||
| chr15:76172354 | G | A | 29 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0021 others(26): Show |
29 | HG00735.hp2 HG01106.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.628+1223G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76172354 | |||||||
| chr15:76172453 | T | G | 29 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0021 others(26): Show |
29 | HG00735.hp2 HG01106.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.628+1322T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76172453 | |||||||
| chr15:76172962 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.628+1831C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76172962 | |||||||
| chr15:76173009 | G | A | 1 | a0001c0001t0005g0084 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.628+1878G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76173009 | |||||||
| chr15:76173127 | G | A | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.628+1996G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76173127 | |||||||
| chr15:76173154 | G | A | 2 | a0001c0001t0002g0057 a0002c0002t0001g0208 |
2 | HG01243.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.628+2023G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76173154 | |||||||
| chr15:76173179 | C | T | 1 | a0002c0002t0001g0194 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.628+2048C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76173179 | |||||||
| chr15:76173245 | T | C | 1 | a0001c0001t0002g0165 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.628+2114T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76173245 | |||||||
| chr15:76173258 | G | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0257 |
2 | HG02280.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.628+2127G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76173258 | |||||||
| chr15:76173685 | C | T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0021 others(26): Show |
29 | HG00735.hp2 HG01106.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.629-1874C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76173685 | |||||||
| chr15:76173862 | G | A | 1 | a0001c0001t0002g0236 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.629-1697G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76173862 | |||||||
| chr15:76173926 | C | T | 2 | a0002c0002t0001g0127 a0002c0002t0001g0128 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.629-1633C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76173926 | |||||||
| chr15:76173942 | T | A | 1 | a0001c0001t0002g0104 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.629-1617T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76173942 | |||||||
| chr15:76173942 | T | TA | 16 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0060 others(13): Show |
16 | HG01109.hp1 HG01123.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.629-1603dupA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 76173942 | ||||||
| chr15:76173945 | A | AT | 6 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0255 others(3): Show |
6 | HG02486.hp1 HG02922.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.629-1614_629-1613i others(3): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76173945 | |||||||
| chr15:76173962 | C | G | 12 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0078 others(9): Show |
12 | HG00735.hp2 HG01106.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.629-1597C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76173962 | |||||||
| chr15:76174034 | C | A | 1 | a0001c0001t0001g0008 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.629-1525C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76174034 | |||||||
| chr15:76174238 | G | A | 83 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0019 others(80): Show |
84 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.629-1321G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76174238 | |||||||
| chr15:76174302 | G | A | 13 | a0001c0001t0001g0083 a0001c0001t0001g0109 a0001c0001t0001g0157 others(10): Show |
13 | HG00438.hp1 HG01099.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.629-1257G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76174302 | |||||||
| chr15:76174505 | C | T | 12 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0078 others(9): Show |
12 | HG00735.hp2 HG01106.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.629-1054C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76174505 | |||||||
| chr15:76174700 | C | T | 3 | a0001c0001t0002g0224 a0001c0001t0002g0226 a0002c0002t0001g0067 |
3 | HG01099.hp1 HG01516.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.629-859C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76174700 | |||||||
| chr15:76174721 | T | C | 33 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0021 others(30): Show |
34 | HG00735.hp2 HG01106.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.629-838T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76174721 | |||||||
| chr15:76174722 | A | G | 3 | a0001c0001t0001g0266 a0001c0001t0004g0005 a0001c0001t0004g0006 |
3 | HG02970.hp2 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.629-837A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76174722 | |||||||
| chr15:76174765 | A | G | 6 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0255 others(3): Show |
6 | HG02486.hp1 HG02922.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.629-794A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76174765 | |||||||
| chr15:76174842 | G | A | 9 | a0001c0001t0001g0098 a0001c0001t0001g0269 a0002c0002t0001g0022 others(6): Show |
9 | HG01243.hp2 HG02055.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.629-717G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76174842 | |||||||
| chr15:76174846 | C | T | 33 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0021 others(30): Show |
34 | HG00735.hp2 HG01106.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.629-713C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76174846 | |||||||
| chr15:76175096 | C | T | 10 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0255 others(7): Show |
11 | HG02486.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.629-463C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76175096 | |||||||
| chr15:76175129 | C | T | 1 | a0001c0001t0002g0106 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.629-430C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76175129 | |||||||
| chr15:76175307 | G | A | 1 | a0002c0002t0001g0164 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.629-252G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76175307 | |||||||
| chr15:76175435 | C | T | 1 | a0001c0001t0002g0193 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.629-124C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 7/10 | chr15 | 76175435 | |||||||
| chr15:76175984 | G | A | 1 | a0002c0002t0001g0120 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.744+310G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76175984 | |||||||
| chr15:76176081 | C | T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0266 a0001c0001t0004g0005 others(1): Show |
4 | HG02970.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.744+407C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76176081 | |||||||
| chr15:76176268 | G | A | 1 | a0002c0002t0001g0120 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.744+594G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76176268 | |||||||
| chr15:76176348 | G | C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0266 a0001c0001t0004g0005 others(1): Show |
4 | HG02970.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.744+674G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76176348 | |||||||
| chr15:76176435 | T | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0255 others(7): Show |
11 | HG02486.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.744+761T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76176435 | |||||||
| chr15:76176442 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.744+768C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76176442 | |||||||
| chr15:76176605 | C | T | 9 | a0001c0001t0001g0098 a0001c0001t0001g0269 a0002c0002t0001g0022 others(6): Show |
9 | HG01243.hp2 HG02055.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.744+931C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76176605 | |||||||
| chr15:76176683 | T | A | 31 | a0001c0001t0001g0177 a0001c0001t0002g0002 a0001c0001t0002g0027 others(28): Show |
32 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.744+1009T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76176683 | |||||||
| chr15:76176740 | G | A | 15 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0078 others(12): Show |
15 | HG00735.hp2 HG01106.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.744+1066G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76176740 | |||||||
| chr15:76176802 | G | T | 1 | a0001c0001t0003g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.744+1128G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76176802 | |||||||
| chr15:76176865 | T | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0255 others(7): Show |
11 | HG02486.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.744+1191T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76176865 | |||||||
| chr15:76176866 | G | A | 5 | a0001c0001t0002g0057 a0001c0001t0003g0014 a0001c0001t0008g0249 others(2): Show |
5 | HG01243.hp1 HG01255.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.744+1192G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76176866 | |||||||
| chr15:76176880 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0002g0041 |
2 | HG02055.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.744+1206C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76176880 | |||||||
| chr15:76176985 | G | C | 15 | a0001c0001t0001g0234 a0001c0001t0002g0030 a0001c0001t0002g0033 others(12): Show |
15 | HG00558.hp1 HG02056.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.744+1311G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76176985 | |||||||
| chr15:76177021 | G | A | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(11): Show |
15 | HG02486.hp1 HG02630.hp2 HG02809.hp1 others(12): Show |
intron_variant | MODIFIER | c.744+1347G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76177021 | |||||||
| chr15:76177114 | C | T | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.744+1440C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76177114 | |||||||
| chr15:76177180 | C | G | 1 | a0002c0002t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.744+1506C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76177180 | |||||||
| chr15:76177185 | T | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0255 others(7): Show |
11 | HG02486.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.744+1511T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76177185 | |||||||
| chr15:76177292 | A | G | 10 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0255 others(7): Show |
11 | HG02486.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.744+1618A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76177292 | |||||||
| chr15:76177312 | G | A | 6 | a0001c0001t0001g0102 a0001c0001t0001g0137 a0001c0001t0001g0153 others(3): Show |
6 | HG00735.hp2 HG01106.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.744+1638G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76177312 | |||||||
| chr15:76177341 | C | A | 1 | a0001c0001t0001g0038 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.744+1667C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76177341 | |||||||
| chr15:76177344 | G | A | 5 | a0002c0002t0001g0123 a0002c0002t0001g0180 a0002c0002t0001g0181 others(2): Show |
5 | HG00280.hp2 HG01069.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.744+1670G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76177344 | |||||||
| chr15:76177467 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.744+1793A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76177467 | |||||||
| chr15:76177567 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.744+1893C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76177567 | |||||||
| chr15:76177801 | C | T | 10 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0255 others(7): Show |
11 | HG02486.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.744+2127C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76177801 | |||||||
| chr15:76177810 | CAG | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0255 others(7): Show |
11 | HG02486.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.744+2137_744+2138d others(4): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76177810 | |||||||
| chr15:76178035 | G | GC | 6 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0081 others(3): Show |
6 | HG02886.hp1 HG02965.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.744+2366dupC | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 76178035 | ||||||
| chr15:76178253 | A | T | 1 | a0001c0001t0003g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.744+2579A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76178253 | |||||||
| chr15:76178268 | A | G | 1 | a0002c0002t0012g0267 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.744+2594A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76178268 | |||||||
| chr15:76178275 | G | A | 1 | a0001c0001t0002g0062 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.744+2601G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76178275 | |||||||
| chr15:76178294 | A | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0068 a0002c0002t0001g0175 |
3 | HG02559.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.744+2620A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76178294 | |||||||
| chr15:76178414 | C | T | 145 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0019 others(142): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.744+2740C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76178414 | |||||||
| chr15:76178442 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.744+2768A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76178442 | |||||||
| chr15:76178452 | G | A | 1 | a0001c0001t0002g0246 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.744+2778G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76178452 | |||||||
| chr15:76178469 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.744+2795A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76178469 | |||||||
| chr15:76178499 | G | A | 2 | a0001c0001t0001g0230 a0001c0001t0004g0253 |
2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.744+2825G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76178499 | |||||||
| chr15:76178587 | C | T | 65 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0089 others(62): Show |
66 | HG00099.hp1 HG00597.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.744+2913C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76178587 | |||||||
| chr15:76178616 | A | G | 23 | a0001c0001t0002g0004 a0001c0001t0002g0045 a0001c0001t0002g0063 others(20): Show |
23 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(20): Show |
intron_variant | MODIFIER | c.744+2942A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76178616 | |||||||
| chr15:76178639 | G | A | 1 | a0001c0001t0008g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.744+2965G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76178639 | |||||||
| chr15:76178780 | G | A | 5 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0037 others(2): Show |
5 | HG02155.hp1 NA18948.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+3106G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76178780 | |||||||
| chr15:76178892 | G | C | 91 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(88): Show |
91 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.744+3218G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76178892 | |||||||
| chr15:76178941 | A | T | 20 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0021 others(17): Show |
20 | HG00735.hp2 HG01106.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.744+3267A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76178941 | |||||||
| chr15:76178969 | C | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0260 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.744+3295C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76178969 | |||||||
| chr15:76178978 | G | A | 1 | a0001c0001t0008g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.744+3304G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76178978 | |||||||
| chr15:76179089 | TG | T | 31 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(28): Show |
31 | HG00438.hp1 HG01109.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.744+3417delG | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 76179089 | ||||||
| chr15:76179139 | G | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0260 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.744+3465G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76179139 | |||||||
| chr15:76179285 | G | A | 6 | a0001c0001t0001g0020 a0001c0001t0001g0068 a0001c0001t0001g0230 others(3): Show |
6 | HG02559.hp1 HG02970.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.744+3611G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76179285 | |||||||
| chr15:76179303 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.744+3629C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76179303 | |||||||
| chr15:76179355 | G | A | 4 | a0002c0002t0001g0123 a0002c0002t0001g0181 a0002c0002t0001g0225 others(1): Show |
4 | HG00280.hp2 HG01069.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.744+3681G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76179355 | |||||||
| chr15:76179437 | G | A | 1 | a0001c0001t0002g0182 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.744+3763G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76179437 | |||||||
| chr15:76179470 | G | C | 86 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(83): Show |
87 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.744+3796G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76179470 | |||||||
| chr15:76179625 | A | G | 114 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(111): Show |
116 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.744+3951A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76179625 | |||||||
| chr15:76179936 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0269 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.744+4262A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76179936 | |||||||
| chr15:76179952 | T | TAAAAC | 9 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0037 others(6): Show |
9 | HG02083.hp1 HG02155.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.744+4304_744+4308d others(7): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 76179952 | ||||||
| chr15:76179952 | T | TAAAACAA others(3): Show |
5 | a0001c0001t0001g0068 a0001c0001t0001g0230 a0001c0001t0001g0266 others(2): Show |
5 | HG02559.hp1 HG02970.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+4299_744+4308d others(12): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 76179952 | ||||||
| chr15:76179952 | TAAAAC | T | 4 | a0001c0001t0008g0249 a0002c0002t0001g0071 a0002c0002t0001g0133 others(1): Show |
4 | NA18978.hp2 NA18992.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.744+4304_744+4308d others(7): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 76179952 | ||||||
| chr15:76180116 | G | A | 4 | a0002c0002t0001g0067 a0002c0002t0001g0170 a0002c0002t0001g0171 others(1): Show |
4 | HG01346.hp1 HG01515.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.744+4442G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76180116 | |||||||
| chr15:76180205 | A | G | 1 | a0004c0005t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.744+4531A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76180205 | |||||||
| chr15:76180211 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0269 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.744+4537A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76180211 | |||||||
| chr15:76180310 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.744+4636A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76180310 | |||||||
| chr15:76180509 | C | T | 1 | a0002c0002t0001g0146 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.744+4835C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76180509 | |||||||
| chr15:76180510 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0135 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.744+4836G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76180510 | |||||||
| chr15:76180526 | A | C | 1 | a0002c0002t0001g0225 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.744+4852A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76180526 | |||||||
| chr15:76180543 | C | T | 1 | a0001c0001t0003g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.744+4869C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76180543 | |||||||
| chr15:76180555 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.744+4881C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76180555 | |||||||
| chr15:76180605 | AG | A | 28 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(25): Show |
28 | HG00438.hp1 HG01109.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.744+4932delG | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76180605 | |||||||
| chr15:76180606 | G | C | 236 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(233): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.744+4932G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76180606 | |||||||
| chr15:76180607 | C | CCT | 3 | a0002c0002t0001g0170 a0002c0002t0001g0171 a0002c0002t0001g0209 |
3 | HG01346.hp1 HG01515.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.744+4933_744+4934i others(4): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76180607 | |||||||
| chr15:76180607 | C | CTT | 110 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0038 others(107): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.744+4956_744+4957d others(4): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 76180607 | ||||||
| chr15:76180607 | C | CTTT | 87 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(84): Show |
88 | HG00280.hp2 HG00597.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.744+4955_744+4957d others(5): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 76180607 | ||||||
| chr15:76180607 | C | CTTTT | 17 | a0001c0001t0001g0003 a0001c0001t0001g0068 a0001c0001t0001g0078 others(14): Show |
17 | HG00621.hp1 HG00741.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.744+4954_744+4957d others(6): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 76180607 | ||||||
| chr15:76180607 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0004g0254 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.744+4947_744+4957d others(13): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 76180607 | ||||||
| chr15:76180608 | T | C | 28 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(25): Show |
28 | HG00438.hp1 HG01109.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.744+4934T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76180608 | |||||||
| chr15:76180660 | C | G | 1 | a0002c0002t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.744+4986C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76180660 | |||||||
| chr15:76180699 | C | T | 18 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(15): Show |
18 | HG00735.hp2 HG01106.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.744+5025C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76180699 | |||||||
| chr15:76180734 | T | C | 1 | a0001c0001t0001g0234 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.744+5060T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76180734 | |||||||
| chr15:76180806 | G | T | 1 | a0001c0001t0002g0176 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.744+5132G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76180806 | |||||||
| chr15:76180822 | C | A | 1 | a0001c0001t0001g0172 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.744+5148C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76180822 | |||||||
| chr15:76181035 | T | C | 39 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(36): Show |
39 | HG00438.hp1 HG01109.hp1 HG01123.hp1 others(36): Show |
intron_variant | MODIFIER | c.744+5361T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76181035 | |||||||
| chr15:76181265 | A | G | 86 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0089 others(83): Show |
87 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.744+5591A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76181265 | |||||||
| chr15:76181349 | G | C | 264 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(261): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.744+5675G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76181349 | |||||||
| chr15:76181614 | C | T | 56 | a0001c0001t0001g0177 a0001c0001t0001g0192 a0001c0001t0001g0244 others(53): Show |
56 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.744+5940C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76181614 | |||||||
| chr15:76181733 | G | C | 1 | a0001c0001t0002g0124 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.744+6059G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76181733 | |||||||
| chr15:76181756 | A | G | 2 | a0001c0001t0001g0098 a0002c0002t0001g0164 |
2 | HG01496.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.744+6082A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76181756 | |||||||
| chr15:76181759 | A | G | 3 | a0002c0002t0001g0022 a0002c0002t0001g0024 a0002c0002t0001g0268 |
3 | HG02451.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.744+6085A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76181759 | |||||||
| chr15:76181766 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0135 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.744+6092C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76181766 | |||||||
| chr15:76181841 | A | T | 23 | a0001c0001t0001g0020 a0001c0001t0001g0068 a0001c0001t0001g0230 others(20): Show |
23 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(20): Show |
intron_variant | MODIFIER | c.744+6167A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76181841 | |||||||
| chr15:76181876 | C | T | 30 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(27): Show |
30 | HG00438.hp1 HG01109.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.744+6202C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76181876 | |||||||
| chr15:76181885 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0269 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.744+6211A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76181885 | |||||||
| chr15:76181919 | T | G | 219 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(216): Show |
221 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.744+6245T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76181919 | |||||||
| chr15:76181969 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.744+6295G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76181969 | |||||||
| chr15:76181969 | G | T | 2 | a0002c0002t0001g0029 a0002c0002t0001g0040 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.744+6295G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76181969 | |||||||
| chr15:76182002 | C | A | 3 | a0001c0001t0002g0001 a0001c0001t0002g0263 a0001c0001t0007g0252 |
4 | HG02630.hp2 HG02809.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.744+6328C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76182002 | |||||||
| chr15:76182004 | T | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0269 a0001c0001t0002g0057 others(1): Show |
4 | HG01243.hp1 HG01243.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.744+6330T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76182004 | |||||||
| chr15:76182224 | T | C | 2 | a0002c0002t0001g0059 a0002c0002t0001g0100 |
2 | HG00140.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.744+6550T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76182224 | |||||||
| chr15:76182358 | C | T | 2 | a0001c0001t0001g0256 a0001c0001t0001g0258 |
2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.744+6684C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76182358 | |||||||
| chr15:76182386 | T | C | 264 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(261): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.744+6712T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76182386 | |||||||
| chr15:76182408 | G | A | 48 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0012 others(45): Show |
48 | HG00438.hp1 HG00735.hp2 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.744+6734G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76182408 | |||||||
| chr15:76182464 | G | A | 6 | a0001c0001t0001g0020 a0001c0001t0001g0068 a0001c0001t0001g0230 others(3): Show |
6 | HG02559.hp1 HG02970.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.744+6790G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76182464 | |||||||
| chr15:76182472 | TA | T | 16 | a0001c0001t0002g0004 a0001c0001t0002g0063 a0001c0001t0002g0064 others(13): Show |
16 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(13): Show |
intron_variant | MODIFIER | c.744+6807delA | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 76182472 | ||||||
| chr15:76182481 | AT | A | 8 | a0001c0001t0001g0020 a0001c0001t0001g0068 a0001c0001t0001g0230 others(5): Show |
8 | HG02559.hp1 HG02970.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.744+6808delT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76182481 | |||||||
| chr15:76182482 | T | A | 233 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(230): Show |
235 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.744+6808T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76182482 | |||||||
| chr15:76182501 | C | G | 55 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(52): Show |
55 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.744+6827C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76182501 | |||||||
| chr15:76182512 | C | T | 6 | a0001c0001t0001g0020 a0001c0001t0001g0068 a0001c0001t0001g0230 others(3): Show |
6 | HG02559.hp1 HG02970.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.744+6838C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76182512 | |||||||
| chr15:76182541 | G | A | 11 | a0001c0001t0001g0025 a0001c0001t0001g0060 a0001c0001t0001g0079 others(8): Show |
11 | HG01109.hp1 HG01123.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.744+6867G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76182541 | |||||||
| chr15:76182560 | C | T | 16 | a0001c0001t0002g0004 a0001c0001t0002g0063 a0001c0001t0002g0064 others(13): Show |
16 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(13): Show |
intron_variant | MODIFIER | c.744+6886C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76182560 | |||||||
| chr15:76182685 | T | C | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.744+7011T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76182685 | |||||||
| chr15:76182891 | C | T | 23 | a0001c0001t0001g0020 a0001c0001t0001g0068 a0001c0001t0001g0230 others(20): Show |
23 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(20): Show |
intron_variant | MODIFIER | c.744+7217C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76182891 | |||||||
| chr15:76183097 | T | C | 6 | a0001c0001t0001g0020 a0001c0001t0001g0068 a0001c0001t0001g0230 others(3): Show |
6 | HG02559.hp1 HG02970.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.744+7423T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76183097 | |||||||
| chr15:76183103 | C | CTTT | 6 | a0001c0001t0001g0089 a0001c0001t0002g0002 a0001c0001t0002g0051 others(3): Show |
7 | HG00733.hp1 HG01943.hp2 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.744+7457_744+7459d others(5): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 76183103 | ||||||
| chr15:76183103 | C | CTTTT | 33 | a0001c0001t0002g0027 a0001c0001t0002g0047 a0001c0001t0002g0050 others(30): Show |
33 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.744+7456_744+7459d others(6): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 76183103 | ||||||
| chr15:76183103 | C | CTTTTT | 25 | a0001c0001t0001g0017 a0001c0001t0001g0130 a0001c0001t0001g0264 others(22): Show |
25 | HG00621.hp2 HG00741.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.744+7455_744+7459d others(7): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 76183103 | ||||||
| chr15:76183103 | C | CTTTTTT | 15 | a0001c0001t0001g0018 a0001c0001t0001g0258 a0001c0001t0002g0043 others(12): Show |
15 | HG00609.hp2 HG01099.hp1 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.744+7454_744+7459d others(8): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 76183103 | ||||||
| chr15:76183103 | CT | C | 23 | a0001c0001t0001g0020 a0001c0001t0001g0076 a0001c0001t0001g0137 others(20): Show |
23 | HG00099.hp2 HG00280.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.744+7459delT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 76183103 | ||||||
| chr15:76183103 | CTT | C | 44 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(41): Show |
45 | HG00438.hp2 HG00597.hp2 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.744+7458_744+7459d others(4): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 76183103 | ||||||
| chr15:76183103 | CTTT | C | 56 | a0001c0001t0001g0192 a0001c0001t0001g0244 a0001c0001t0002g0235 others(53): Show |
56 | HG00280.hp2 HG00621.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.744+7457_744+7459d others(5): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 76183103 | ||||||
| chr15:76183103 | CTTTT | C | 5 | a0002c0002t0001g0067 a0002c0002t0001g0123 a0002c0002t0001g0144 others(2): Show |
5 | HG01515.hp1 HG01516.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+7456_744+7459d others(6): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 76183103 | ||||||
| chr15:76183103 | CTTTTTT | C | 12 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0081 others(9): Show |
12 | HG01243.hp1 HG01255.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.744+7454_744+7459d others(8): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 76183103 | ||||||
| chr15:76183103 | CTTTTTTT | C | 22 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0060 others(19): Show |
22 | HG00140.hp1 HG00438.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.744+7453_744+7459d others(9): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 76183103 | ||||||
| chr15:76183103 | CTTTTTTT others(6): Show |
C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0038 a0001c0001t0001g0269 others(1): Show |
4 | HG01243.hp2 HG02280.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.744+7447_744+7459d others(15): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 76183103 | ||||||
| chr15:76183147 | G | A | 2 | a0001c0001t0001g0038 a0004c0005t0001g0211 |
2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.744+7473G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76183147 | |||||||
| chr15:76183189 | C | G | 1 | a0001c0001t0001g0137 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.744+7515C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76183189 | |||||||
| chr15:76183241 | G | A | 16 | a0001c0001t0002g0004 a0001c0001t0002g0063 a0001c0001t0002g0064 others(13): Show |
16 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(13): Show |
intron_variant | MODIFIER | c.744+7567G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76183241 | |||||||
| chr15:76183590 | C | A | 86 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0038 others(83): Show |
87 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.744+7916C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76183590 | |||||||
| chr15:76183673 | C | A | 1 | a0002c0002t0001g0194 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.744+7999C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76183673 | |||||||
| chr15:76183920 | G | A | 6 | a0001c0001t0001g0020 a0001c0001t0001g0068 a0001c0001t0001g0230 others(3): Show |
6 | HG02559.hp1 HG02970.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.745-8048G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76183920 | |||||||
| chr15:76183956 | C | G | 1 | a0001c0001t0008g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.745-8012C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76183956 | |||||||
| chr15:76183989 | T | G | 1 | a0001c0001t0002g0236 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.745-7979T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76183989 | |||||||
| chr15:76184020 | G | A | 10 | a0001c0001t0001g0083 a0001c0001t0001g0109 a0001c0001t0001g0157 others(7): Show |
10 | HG00438.hp1 HG01175.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.745-7948G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76184020 | |||||||
| chr15:76184028 | G | A | 3 | a0001c0001t0001g0266 a0001c0001t0004g0005 a0001c0001t0004g0006 |
3 | HG02970.hp2 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.745-7940G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76184028 | |||||||
| chr15:76184125 | G | T | 25 | a0001c0001t0001g0020 a0001c0001t0001g0068 a0001c0001t0001g0230 others(22): Show |
25 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(22): Show |
intron_variant | MODIFIER | c.745-7843G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76184125 | |||||||
| chr15:76184207 | C | T | 1 | a0001c0001t0002g0136 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.745-7761C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76184207 | |||||||
| chr15:76184327 | G | A | 1 | a0001c0001t0001g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.745-7641G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76184327 | |||||||
| chr15:76184400 | A | G | 2 | a0001c0001t0001g0098 a0002c0002t0001g0164 |
2 | HG01496.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.745-7568A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76184400 | |||||||
| chr15:76184693 | A | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0269 a0001c0001t0002g0057 others(1): Show |
4 | HG01243.hp1 HG01243.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.745-7275A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76184693 | |||||||
| chr15:76184697 | G | A | 90 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0027 others(87): Show |
91 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.745-7271G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76184697 | |||||||
| chr15:76184710 | G | A | 6 | a0002c0002t0001g0022 a0002c0002t0001g0024 a0002c0002t0001g0174 others(3): Show |
6 | HG02451.hp1 HG02723.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.745-7258G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76184710 | |||||||
| chr15:76184717 | C | T | 3 | a0001c0001t0001g0038 a0001c0001t0004g0253 a0004c0005t0001g0211 |
3 | HG02280.hp2 HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.745-7251C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76184717 | |||||||
| chr15:76184814 | G | A | 90 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0027 others(87): Show |
91 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.745-7154G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76184814 | |||||||
| chr15:76184947 | C | A | 1 | a0001c0001t0001g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.745-7021C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76184947 | |||||||
| chr15:76184950 | G | T | 3 | a0001c0001t0001g0076 a0001c0001t0001g0135 a0001c0001t0001g0229 |
3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.745-7018G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76184950 | |||||||
| chr15:76184951 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.745-7017C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76184951 | |||||||
| chr15:76184980 | C | T | 1 | a0002c0002t0001g0040 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.745-6988C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76184980 | |||||||
| chr15:76184982 | G | A | 57 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(54): Show |
57 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.745-6986G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76184982 | |||||||
| chr15:76185041 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0135 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-6927G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76185041 | |||||||
| chr15:76185091 | T | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0068 others(3): Show |
6 | HG02559.hp1 HG02970.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.745-6877T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76185091 | |||||||
| chr15:76185222 | C | T | 6 | a0002c0002t0001g0022 a0002c0002t0001g0024 a0002c0002t0001g0174 others(3): Show |
6 | HG02451.hp1 HG02723.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.745-6746C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76185222 | |||||||
| chr15:76185546 | C | A | 264 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(261): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.745-6422C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76185546 | |||||||
| chr15:76185630 | C | G | 1 | a0002c0002t0001g0115 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.745-6338C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76185630 | |||||||
| chr15:76185721 | G | A | 93 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0068 others(90): Show |
94 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.745-6247G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76185721 | |||||||
| chr15:76185836 | C | T | 2 | a0002c0002t0001g0053 a0002c0002t0001g0087 |
2 | HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.745-6132C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76185836 | |||||||
| chr15:76185927 | A | T | 36 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(33): Show |
36 | HG00438.hp1 HG01109.hp1 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.745-6041A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76185927 | |||||||
| chr15:76185967 | A | G | 89 | a0001c0001t0001g0192 a0001c0001t0001g0244 a0001c0001t0002g0041 others(86): Show |
89 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.745-6001A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76185967 | |||||||
| chr15:76186081 | G | A | 3 | a0001c0001t0001g0076 a0001c0001t0001g0135 a0001c0001t0001g0229 |
3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.745-5887G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76186081 | |||||||
| chr15:76186159 | T | G | 89 | a0001c0001t0001g0192 a0001c0001t0001g0244 a0001c0001t0002g0041 others(86): Show |
89 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.745-5809T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76186159 | |||||||
| chr15:76186297 | G | C | 12 | a0001c0001t0001g0021 a0001c0001t0001g0078 a0001c0001t0001g0102 others(9): Show |
12 | HG00735.hp2 HG01106.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.745-5671G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76186297 | |||||||
| chr15:76186368 | C | T | 1 | a0004c0005t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.745-5600C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76186368 | |||||||
| chr15:76186393 | G | A | 1 | a0001c0001t0003g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.745-5575G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76186393 | |||||||
| chr15:76186498 | C | T | 1 | a0001c0001t0004g0254 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.745-5470C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76186498 | |||||||
| chr15:76186584 | C | T | 49 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(46): Show |
49 | HG00438.hp1 HG00735.hp2 HG01106.hp1 others(46): Show |
intron_variant | MODIFIER | c.745-5384C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76186584 | |||||||
| chr15:76186731 | A | G | 1 | a0001c0001t0001g0247 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.745-5237A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76186731 | |||||||
| chr15:76186749 | G | A | 149 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(146): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.745-5219G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76186749 | |||||||
| chr15:76186881 | C | G | 1 | a0001c0001t0002g0050 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.745-5087C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76186881 | |||||||
| chr15:76186950 | A | G | 13 | a0001c0001t0001g0021 a0001c0001t0001g0078 a0001c0001t0001g0102 others(10): Show |
13 | HG00735.hp2 HG01106.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.745-5018A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76186950 | |||||||
| chr15:76187003 | G | A | 87 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0027 others(84): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.745-4965G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76187003 | |||||||
| chr15:76187046 | C | T | 1 | a0002c0002t0001g0141 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.745-4922C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76187046 | |||||||
| chr15:76187068 | C | A | 5 | a0002c0002t0001g0022 a0002c0002t0001g0024 a0002c0002t0001g0174 others(2): Show |
5 | HG02451.hp1 HG02723.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.745-4900C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76187068 | |||||||
| chr15:76187119 | C | T | 1 | a0001c0001t0002g0124 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.745-4849C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76187119 | |||||||
| chr15:76187144 | C | CTGAA | 97 | a0001c0001t0001g0192 a0001c0001t0001g0244 a0001c0001t0002g0001 others(94): Show |
98 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.745-4809_745-4806d others(6): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 76187144 | ||||||
| chr15:76187325 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.745-4643C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76187325 | |||||||
| chr15:76187389 | A | G | 1 | a0001c0001t0001g0017 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.745-4579A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76187389 | |||||||
| chr15:76187450 | G | A | 3 | a0001c0001t0002g0001 a0001c0001t0002g0263 a0001c0001t0007g0252 |
4 | HG02630.hp2 HG02809.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-4518G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76187450 | |||||||
| chr15:76187555 | A | T | 264 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(261): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.745-4413A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76187555 | |||||||
| chr15:76187560 | G | T | 119 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0078 others(116): Show |
120 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.745-4408G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76187560 | |||||||
| chr15:76187583 | C | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0068 others(3): Show |
6 | HG02559.hp1 HG02970.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.745-4385C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76187583 | |||||||
| chr15:76187584 | G | A | 1 | a0002c0003t0001g0015 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.745-4384G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76187584 | |||||||
| chr15:76187595 | C | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0269 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.745-4373C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76187595 | |||||||
| chr15:76187753 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0269 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.745-4215C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76187753 | |||||||
| chr15:76187754 | C | T | 3 | a0001c0001t0002g0001 a0001c0001t0002g0263 a0001c0001t0007g0252 |
4 | HG02630.hp2 HG02809.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-4214C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76187754 | |||||||
| chr15:76187884 | C | T | 162 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(159): Show |
163 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.745-4084C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76187884 | |||||||
| chr15:76188011 | C | T | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.745-3957C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76188011 | |||||||
| chr15:76188086 | C | G | 137 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(134): Show |
138 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.745-3882C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76188086 | |||||||
| chr15:76188086 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.745-3882C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76188086 | |||||||
| chr15:76188167 | C | T | 9 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0068 others(6): Show |
10 | HG02559.hp1 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.745-3801C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76188167 | |||||||
| chr15:76188362 | C | T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0076 others(13): Show |
16 | HG00735.hp2 HG01106.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.745-3606C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76188362 | |||||||
| chr15:76188401 | G | A | 2 | a0002c0002t0001g0029 a0002c0002t0001g0040 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.745-3567G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76188401 | |||||||
| chr15:76188553 | A | C | 1 | a0001c0001t0002g0187 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.745-3415A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76188553 | |||||||
| chr15:76188563 | A | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0269 a0001c0001t0002g0057 |
3 | HG01243.hp2 HG01255.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.745-3405A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76188563 | |||||||
| chr15:76188584 | G | A | 156 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.745-3384G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76188584 | |||||||
| chr15:76188617 | A | G | 1 | a0002c0002t0001g0262 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.745-3351A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76188617 | |||||||
| chr15:76188631 | C | T | 93 | a0001c0001t0001g0192 a0001c0001t0001g0244 a0001c0001t0002g0001 others(90): Show |
94 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.745-3337C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76188631 | |||||||
| chr15:76188658 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0269 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.745-3310T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76188658 | |||||||
| chr15:76188754 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.745-3214G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76188754 | |||||||
| chr15:76188840 | G | A | 1 | a0001c0001t0004g0005 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.745-3128G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76188840 | |||||||
| chr15:76189061 | A | G | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.745-2907A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76189061 | |||||||
| chr15:76189075 | C | T | 97 | a0001c0001t0001g0192 a0001c0001t0001g0244 a0001c0001t0002g0001 others(94): Show |
98 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.745-2893C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76189075 | |||||||
| chr15:76189117 | A | G | 1 | a0001c0001t0002g0246 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.745-2851A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76189117 | |||||||
| chr15:76189257 | T | G | 269 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(266): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.745-2711T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76189257 | |||||||
| chr15:76189266 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.745-2702G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76189266 | |||||||
| chr15:76189273 | G | A | 1 | a0001c0001t0002g0104 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.745-2695G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76189273 | |||||||
| chr15:76189282 | AAGGGTAG others(69): Show |
A | 6 | a0002c0002t0001g0022 a0002c0002t0001g0024 a0002c0002t0001g0174 others(3): Show |
6 | HG02451.hp1 HG02723.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.745-2681_745-2606d others(78): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 76189282 | ||||||
| chr15:76189351 | G | GGGGA | 16 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0076 others(13): Show |
16 | HG00735.hp2 HG01106.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.745-2606_745-2603d others(6): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 76189351 | ||||||
| chr15:76189360 | G | A | 6 | a0002c0002t0001g0022 a0002c0002t0001g0024 a0002c0002t0001g0174 others(3): Show |
6 | HG02451.hp1 HG02723.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.745-2608G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76189360 | |||||||
| chr15:76189362 | G | A | 6 | a0002c0002t0001g0022 a0002c0002t0001g0024 a0002c0002t0001g0174 others(3): Show |
6 | HG02451.hp1 HG02723.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.745-2606G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76189362 | |||||||
| chr15:76189378 | A | G | 6 | a0002c0002t0001g0022 a0002c0002t0001g0024 a0002c0002t0001g0174 others(3): Show |
6 | HG02451.hp1 HG02723.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.745-2590A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76189378 | |||||||
| chr15:76189575 | A | T | 1 | a0001c0001t0008g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.745-2393A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76189575 | |||||||
| chr15:76189736 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.745-2232G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76189736 | |||||||
| chr15:76189748 | A | G | 1 | a0002c0002t0001g0046 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.745-2220A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76189748 | |||||||
| chr15:76189892 | C | T | 1 | a0001c0001t0008g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.745-2076C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76189892 | |||||||
| chr15:76190075 | T | A | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.745-1893T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76190075 | |||||||
| chr15:76190277 | A | G | 92 | a0001c0001t0001g0038 a0001c0001t0001g0192 a0001c0001t0002g0041 others(89): Show |
92 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.745-1691A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76190277 | |||||||
| chr15:76190290 | G | A | 2 | a0002c0002t0001g0029 a0002c0002t0001g0040 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.745-1678G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76190290 | |||||||
| chr15:76190308 | A | G | 6 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0068 others(3): Show |
6 | HG02559.hp1 HG02970.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.745-1660A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76190308 | |||||||
| chr15:76190618 | A | C | 5 | a0001c0001t0001g0038 a0001c0001t0004g0253 a0002c0002t0001g0029 others(2): Show |
5 | HG02280.hp2 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.745-1350A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76190618 | |||||||
| chr15:76190662 | T | A | 1 | a0002c0002t0001g0073 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.745-1306T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76190662 | |||||||
| chr15:76190719 | T | C | 7 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0111 others(4): Show |
7 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(4): Show |
intron_variant | MODIFIER | c.745-1249T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76190719 | |||||||
| chr15:76190861 | G | A | 3 | a0001c0001t0001g0076 a0001c0001t0001g0135 a0001c0001t0001g0229 |
3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.745-1107G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76190861 | |||||||
| chr15:76191001 | C | T | 71 | a0001c0001t0002g0002 a0001c0001t0002g0027 a0001c0001t0002g0028 others(68): Show |
72 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.745-967C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76191001 | |||||||
| chr15:76191126 | T | C | 6 | a0002c0002t0001g0022 a0002c0002t0001g0024 a0002c0002t0001g0174 others(3): Show |
6 | HG02451.hp1 HG02723.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.745-842T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76191126 | |||||||
| chr15:76191148 | A | C | 1 | a0001c0001t0002g0062 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.745-820A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76191148 | |||||||
| chr15:76191325 | A | G | 2 | a0001c0001t0004g0253 a0004c0005t0001g0211 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.745-643A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76191325 | |||||||
| chr15:76191447 | G | A | 1 | a0002c0003t0001g0015 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.745-521G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76191447 | |||||||
| chr15:76191520 | G | C | 1 | a0001c0001t0002g0063 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.745-448G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76191520 | |||||||
| chr15:76191789 | G | C | 265 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(262): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.745-179G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76191789 | |||||||
| chr15:76191904 | G | A | 1 | a0004c0005t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.745-64G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76191904 | |||||||
| chr15:76191928 | C | T | 4 | a0001c0001t0001g0130 a0001c0001t0001g0256 a0001c0001t0001g0258 others(1): Show |
4 | HG02145.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.745-40C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76191928 | |||||||
| chr15:76191954 | G | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0068 a0001c0001t0001g0266 others(2): Show |
5 | HG02559.hp1 HG02970.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.745-14G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 8/10 | chr15 | 76191954 | |||||||
| chr15:76192182 | C | T | 2 | a0001c0001t0002g0041 a0001c0001t0002g0050 |
2 | NA18968.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.934+25C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76192182 | |||||||
| chr15:76192218 | T | G | 6 | a0002c0002t0001g0022 a0002c0002t0001g0024 a0002c0002t0001g0174 others(3): Show |
6 | HG02451.hp1 HG02723.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.934+61T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76192218 | |||||||
| chr15:76192331 | A | G | 1 | a0002c0002t0001g0168 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.934+174A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76192331 | |||||||
| chr15:76192351 | T | A | 15 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0025 others(12): Show |
15 | HG01109.hp1 HG01123.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.934+194T>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76192351 | |||||||
| chr15:76192352 | A | G | 15 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0025 others(12): Show |
15 | HG01109.hp1 HG01123.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.934+195A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76192352 | |||||||
| chr15:76192354 | T | TGC | 15 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0025 others(12): Show |
15 | HG01109.hp1 HG01123.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.934+197_934+198ins others(2): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76192354 | |||||||
| chr15:76192355 | C | G | 8 | a0001c0001t0001g0018 a0001c0001t0001g0089 a0001c0001t0001g0130 others(5): Show |
8 | HG02145.hp2 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.934+198C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76192355 | |||||||
| chr15:76192355 | C | T | 15 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0025 others(12): Show |
15 | HG01109.hp1 HG01123.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.934+198C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76192355 | |||||||
| chr15:76192363 | C | T | 2 | a0002c0002t0001g0196 a0002c0002t0001g0238 |
2 | NA18971.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.934+206C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76192363 | |||||||
| chr15:76192413 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.934+256C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76192413 | |||||||
| chr15:76192489 | A | T | 38 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(35): Show |
38 | HG00438.hp1 HG00621.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.934+332A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76192489 | |||||||
| chr15:76192520 | G | A | 1 | a0001c0001t0002g0220 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.934+363G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76192520 | |||||||
| chr15:76192550 | C | T | 2 | a0002c0002t0001g0029 a0002c0002t0001g0040 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.934+393C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76192550 | |||||||
| chr15:76192606 | A | T | 54 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0012 others(51): Show |
54 | HG00438.hp1 HG00621.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.934+449A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76192606 | |||||||
| chr15:76192972 | C | A | 2 | a0002c0002t0001g0053 a0002c0002t0001g0087 |
2 | HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.934+815C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76192972 | |||||||
| chr15:76193195 | A | G | 52 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0012 others(49): Show |
52 | HG00438.hp1 HG00621.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.934+1038A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76193195 | |||||||
| chr15:76193208 | C | A | 1 | a0001c0001t0008g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.934+1051C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76193208 | |||||||
| chr15:76193239 | C | CT | 101 | a0001c0001t0001g0008 a0001c0001t0001g0076 a0001c0001t0001g0135 others(98): Show |
101 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.934+1091dupT | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr15 | 76193239 | ||||||
| chr15:76193242 | T | TC | 52 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0012 others(49): Show |
52 | HG00438.hp1 HG00621.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.934+1085_934+1086i others(3): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76193242 | |||||||
| chr15:76193480 | G | A | 1 | a0001c0001t0002g0226 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.934+1323G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76193480 | |||||||
| chr15:76193589 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0269 a0001c0001t0002g0057 |
3 | HG01243.hp2 HG01255.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.934+1432G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76193589 | |||||||
| chr15:76193625 | T | C | 160 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(157): Show |
160 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.934+1468T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76193625 | |||||||
| chr15:76193790 | C | T | 1 | a0002c0003t0001g0015 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.934+1633C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76193790 | |||||||
| chr15:76193872 | T | C | 1 | a0002c0002t0001g0016 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.934+1715T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76193872 | |||||||
| chr15:76194033 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0269 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.934+1876C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76194033 | |||||||
| chr15:76194041 | A | G | 162 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(159): Show |
162 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.934+1884A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76194041 | |||||||
| chr15:76194147 | C | T | 1 | a0002c0002t0001g0115 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.934+1990C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76194147 | |||||||
| chr15:76194441 | C | T | 1 | a0001c0001t0002g0032 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.934+2284C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76194441 | |||||||
| chr15:76194653 | G | A | 1 | a0004c0005t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.934+2496G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76194653 | |||||||
| chr15:76194689 | T | C | 160 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(157): Show |
160 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.934+2532T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76194689 | |||||||
| chr15:76194760 | T | C | 1 | a0002c0002t0001g0270 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.934+2603T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76194760 | |||||||
| chr15:76194883 | C | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0068 others(3): Show |
6 | HG02559.hp1 HG02970.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.934+2726C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76194883 | |||||||
| chr15:76194956 | C | A | 1 | a0001c0001t0001g0038 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.934+2799C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76194956 | |||||||
| chr15:76194956 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.934+2799C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76194956 | |||||||
| chr15:76195166 | G | C | 52 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0012 others(49): Show |
52 | HG00438.hp1 HG00621.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.934+3009G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76195166 | |||||||
| chr15:76195527 | C | T | 8 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0068 others(5): Show |
8 | HG02257.hp1 HG02559.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.934+3370C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76195527 | |||||||
| chr15:76195572 | C | G | 1 | a0002c0003t0001g0015 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.934+3415C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76195572 | |||||||
| chr15:76195699 | G | A | 6 | a0002c0002t0001g0022 a0002c0002t0001g0024 a0002c0002t0001g0174 others(3): Show |
6 | HG02451.hp1 HG02723.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.934+3542G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76195699 | |||||||
| chr15:76195764 | C | T | 1 | a0001c0001t0008g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.934+3607C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76195764 | |||||||
| chr15:76195833 | A | C | 264 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(261): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.934+3676A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76195833 | |||||||
| chr15:76195870 | A | G | 2 | a0002c0002t0001g0029 a0002c0002t0001g0040 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.934+3713A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76195870 | |||||||
| chr15:76195930 | C | A | 1 | a0001c0001t0004g0253 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.934+3773C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76195930 | |||||||
| chr15:76195985 | C | CAGG | 5 | a0001c0001t0001g0018 a0001c0001t0001g0089 a0001c0001t0001g0264 others(2): Show |
5 | HG01516.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.934+3841_934+3843d others(5): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr15 | 76195985 | ||||||
| chr15:76196280 | C | T | 83 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0027 others(80): Show |
84 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.934+4123C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76196280 | |||||||
| chr15:76196361 | C | A | 2 | a0001c0001t0001g0255 a0001c0001t0004g0248 |
2 | HG02486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.934+4204C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76196361 | |||||||
| chr15:76196448 | A | G | 1 | a0002c0002t0001g0270 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.934+4291A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76196448 | |||||||
| chr15:76196518 | C | T | 5 | a0001c0001t0002g0136 a0001c0001t0002g0200 a0001c0001t0002g0201 others(2): Show |
5 | HG02071.hp2 NA18959.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.934+4361C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76196518 | |||||||
| chr15:76196701 | T | G | 1 | a0001c0001t0002g0057 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.934+4544T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76196701 | |||||||
| chr15:76196765 | C | CTCCACAG others(9): Show |
1 | a0004c0005t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.934+4614_934+4615i others(18): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr15 | 76196765 | ||||||
| chr15:76196772 | A | G | 176 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(173): Show |
176 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.934+4615A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76196772 | |||||||
| chr15:76196865 | GCA | G | 38 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(35): Show |
38 | HG00438.hp1 HG00621.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.934+4709_934+4710d others(4): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76196865 | |||||||
| chr15:76196999 | A | T | 5 | a0002c0002t0001g0022 a0002c0002t0001g0024 a0002c0002t0001g0174 others(2): Show |
5 | HG02451.hp1 HG02723.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.934+4842A>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76196999 | |||||||
| chr15:76197021 | AC | A | 3 | a0001c0001t0002g0001 a0001c0001t0002g0263 a0001c0001t0007g0252 |
4 | HG02630.hp2 HG02809.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.934+4866delC | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr15 | 76197021 | ||||||
| chr15:76197064 | C | T | 2 | a0002c0002t0001g0164 a0002c0002t0001g0208 |
2 | HG01243.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.934+4907C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76197064 | |||||||
| chr15:76197079 | G | A | 38 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(35): Show |
38 | HG00438.hp1 HG00621.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.934+4922G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76197079 | |||||||
| chr15:76197224 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.935-4978C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76197224 | |||||||
| chr15:76197298 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.935-4904G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76197298 | |||||||
| chr15:76197572 | T | C | 20 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0021 others(17): Show |
20 | HG00735.hp2 HG01106.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.935-4630T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76197572 | |||||||
| chr15:76197576 | G | A | 172 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(169): Show |
172 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.935-4626G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76197576 | |||||||
| chr15:76197599 | T | C | 3 | a0001c0001t0001g0076 a0001c0001t0001g0135 a0001c0001t0001g0229 |
3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.935-4603T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76197599 | |||||||
| chr15:76197614 | A | G | 38 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(35): Show |
38 | HG00438.hp1 HG00621.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.935-4588A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76197614 | |||||||
| chr15:76197891 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.935-4311G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76197891 | |||||||
| chr15:76198206 | T | G | 94 | a0001c0001t0001g0255 a0001c0001t0002g0041 a0001c0001t0002g0050 others(91): Show |
94 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.935-3996T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76198206 | |||||||
| chr15:76198236 | C | T | 3 | a0002c0002t0001g0221 a0002c0002t0001g0222 a0002c0002t0001g0223 |
3 | HG01069.hp1 HG01106.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.935-3966C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76198236 | |||||||
| chr15:76198326 | G | T | 265 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(262): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.935-3876G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76198326 | |||||||
| chr15:76198381 | CGGG | C | 60 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(57): Show |
60 | HG00438.hp1 HG00597.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.935-3818_935-3816d others(5): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr15 | 76198381 | ||||||
| chr15:76198794 | C | G | 1 | a0002c0002t0001g0238 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.935-3408C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76198794 | |||||||
| chr15:76198865 | T | TGGCTCTC others(60): Show |
90 | a0001c0001t0001g0008 a0001c0001t0001g0076 a0001c0001t0001g0135 others(87): Show |
90 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.935-3336_935-3270d others(69): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr15 | 76198865 | ||||||
| chr15:76198880 | C | T | 2 | a0001c0001t0001g0261 a0002c0003t0001g0015 |
2 | HG02257.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.935-3322C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76198880 | |||||||
| chr15:76198881 | G | GCCTTAAA others(60): Show |
5 | a0002c0002t0001g0007 a0002c0002t0001g0053 a0002c0002t0001g0087 others(2): Show |
5 | HG01346.hp2 HG01884.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.935-3270_935-3269i others(69): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr15 | 76198881 | ||||||
| chr15:76199015 | C | T | 11 | a0001c0001t0001g0021 a0001c0001t0001g0078 a0001c0001t0001g0102 others(8): Show |
11 | HG00735.hp2 HG01106.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.935-3187C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76199015 | |||||||
| chr15:76199207 | G | A | 1 | a0002c0002t0001g0164 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.935-2995G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76199207 | |||||||
| chr15:76199480 | G | T | 1 | a0002c0002t0001g0225 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.935-2722G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76199480 | |||||||
| chr15:76199510 | G | A | 1 | a0001c0001t0002g0205 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.935-2692G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76199510 | |||||||
| chr15:76199540 | TG | T | 101 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0016 others(98): Show |
101 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.935-2659delG | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr15 | 76199540 | ||||||
| chr15:76199544 | T | C | 259 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(256): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.935-2658T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76199544 | |||||||
| chr15:76199548 | C | T | 3 | a0002c0002t0001g0170 a0002c0002t0001g0171 a0002c0002t0001g0209 |
3 | HG01346.hp1 HG01515.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.935-2654C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76199548 | |||||||
| chr15:76199569 | A | G | 1 | a0002c0002t0001g0198 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.935-2633A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76199569 | |||||||
| chr15:76199611 | A | G | 2 | a0002c0002t0001g0029 a0002c0002t0001g0040 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.935-2591A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76199611 | |||||||
| chr15:76199762 | G | GTCCCTCC others(1): Show |
258 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(255): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.935-2435_935-2428d others(10): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr15 | 76199762 | ||||||
| chr15:76199762 | G | GTCCCTCC others(5): Show |
1 | a0002c0003t0001g0015 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.935-2439_935-2428d others(14): Show |
TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr15 | 76199762 | ||||||
| chr15:76199858 | G | C | 3 | a0001c0001t0001g0076 a0001c0001t0001g0135 a0001c0001t0001g0229 |
3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.935-2344G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76199858 | |||||||
| chr15:76199996 | T | C | 12 | a0001c0001t0001g0083 a0001c0001t0001g0109 a0001c0001t0001g0157 others(9): Show |
12 | HG00438.hp1 HG00621.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.935-2206T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76199996 | |||||||
| chr15:76200001 | C | T | 6 | a0002c0002t0001g0022 a0002c0002t0001g0024 a0002c0002t0001g0174 others(3): Show |
6 | HG02451.hp1 HG02723.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.935-2201C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76200001 | |||||||
| chr15:76200054 | G | C | 6 | a0002c0002t0001g0022 a0002c0002t0001g0024 a0002c0002t0001g0174 others(3): Show |
6 | HG02451.hp1 HG02723.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.935-2148G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76200054 | |||||||
| chr15:76200061 | G | A | 1 | a0002c0002t0001g0215 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.935-2141G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76200061 | |||||||
| chr15:76200083 | G | A | 1 | a0002c0002t0001g0270 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.935-2119G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76200083 | |||||||
| chr15:76200124 | G | C | 9 | a0001c0001t0001g0018 a0001c0001t0001g0089 a0001c0001t0001g0130 others(6): Show |
9 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.935-2078G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76200124 | |||||||
| chr15:76200260 | T | C | 259 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(256): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.935-1942T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76200260 | |||||||
| chr15:76200371 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.935-1831C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76200371 | |||||||
| chr15:76200399 | A | G | 1 | a0001c0001t0001g0008 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.935-1803A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76200399 | |||||||
| chr15:76200423 | G | C | 14 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0038 others(11): Show |
14 | HG00735.hp2 HG01106.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.935-1779G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76200423 | |||||||
| chr15:76200461 | C | T | 1 | a0001c0001t0002g0063 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.935-1741C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76200461 | |||||||
| chr15:76200790 | T | C | 1 | a0001c0001t0002g0190 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.935-1412T>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76200790 | |||||||
| chr15:76200792 | G | T | 1 | a0001c0001t0008g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.935-1410G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76200792 | |||||||
| chr15:76200820 | C | A | 1 | a0002c0002t0001g0189 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.935-1382C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76200820 | |||||||
| chr15:76200928 | G | A | 2 | a0002c0002t0001g0029 a0002c0002t0001g0040 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.935-1274G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76200928 | |||||||
| chr15:76201185 | C | G | 1 | a0002c0002t0001g0072 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.935-1017C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76201185 | |||||||
| chr15:76201231 | T | G | 7 | a0002c0002t0001g0022 a0002c0002t0001g0024 a0002c0002t0001g0174 others(4): Show |
7 | HG02257.hp1 HG02451.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.935-971T>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76201231 | |||||||
| chr15:76201237 | C | A | 4 | a0002c0002t0001g0058 a0002c0002t0001g0072 a0002c0002t0001g0120 others(1): Show |
4 | HG02129.hp1 NA18940.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.935-965C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76201237 | |||||||
| chr15:76201304 | C | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0038 |
2 | HG02055.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.935-898C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76201304 | |||||||
| chr15:76201609 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.935-593C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76201609 | |||||||
| chr15:76201733 | C | T | 2 | a0002c0002t0001g0029 a0002c0002t0001g0040 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.935-469C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76201733 | |||||||
| chr15:76201950 | G | A | 3 | a0001c0001t0001g0076 a0001c0001t0001g0135 a0001c0001t0001g0229 |
3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.935-252G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76201950 | |||||||
| chr15:76201974 | C | G | 102 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0016 others(99): Show |
102 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.935-228C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76201974 | |||||||
| chr15:76202194 | C | A | 1 | a0001c0001t0001g0102 | 1 | HG02602.hp2 | splice_region_variant&intron_variant | LOW | c.935-8C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 9/10 | chr15 | 76202194 | |||||||
| chr15:76202304 | C | G | 3 | a0001c0001t0002g0001 a0001c0001t0002g0263 a0001c0001t0007g0252 |
4 | HG02630.hp2 HG02809.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.997+40C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 10/10 | chr15 | 76202304 | |||||||
| chr15:76202385 | G | T | 1 | a0002c0003t0001g0015 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.997+121G>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 10/10 | chr15 | 76202385 | |||||||
| chr15:76202534 | G | A | 95 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0016 others(92): Show |
95 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.997+270G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 10/10 | chr15 | 76202534 | |||||||
| chr15:76202663 | C | A | 103 | a0001c0001t0002g0044 a0002c0002t0001g0007 a0002c0002t0001g0011 others(100): Show |
103 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.997+399C>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 10/10 | chr15 | 76202663 | |||||||
| chr15:76202664 | C | T | 103 | a0001c0001t0002g0044 a0002c0002t0001g0007 a0002c0002t0001g0011 others(100): Show |
103 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.997+400C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 10/10 | chr15 | 76202664 | |||||||
| chr15:76202699 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0269 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.997+435G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 10/10 | chr15 | 76202699 | |||||||
| chr15:76202747 | C | T | 166 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(163): Show |
166 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.997+483C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 10/10 | chr15 | 76202747 | |||||||
| chr15:76202775 | C | T | 1 | a0001c0001t0002g0032 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.997+511C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 10/10 | chr15 | 76202775 | |||||||
| chr15:76202829 | G | A | 1 | a0001c0001t0002g0082 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.997+565G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 10/10 | chr15 | 76202829 | |||||||
| chr15:76202963 | A | G | 5 | a0001c0001t0001g0017 a0001c0001t0001g0068 a0001c0001t0001g0266 others(2): Show |
5 | HG02559.hp1 HG02970.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.997+699A>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 10/10 | chr15 | 76202963 | |||||||
| chr15:76202982 | G | C | 7 | a0002c0002t0001g0022 a0002c0002t0001g0024 a0002c0002t0001g0174 others(4): Show |
7 | HG02257.hp1 HG02451.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.997+718G>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 10/10 | chr15 | 76202982 | |||||||
| chr15:76203021 | C | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0269 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.998-720C>G | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 10/10 | chr15 | 76203021 | |||||||
| chr15:76203225 | A | C | 1 | a0001c0001t0004g0253 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.998-516A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 10/10 | chr15 | 76203225 | |||||||
| chr15:76203328 | A | C | 1 | a0001c0001t0002g0057 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.998-413A>C | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 10/10 | chr15 | 76203328 | |||||||
| chr15:76203623 | C | T | 1 | a0004c0005t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.998-118C>T | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 10/10 | chr15 | 76203623 | |||||||
| chr15:76203702 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0269 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.998-39G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 10/10 | chr15 | 76203702 | |||||||
| chr15:76203708 | G | A | 11 | a0002c0002t0001g0055 a0002c0002t0001g0113 a0002c0002t0001g0118 others(8): Show |
11 | HG00438.hp2 HG00733.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.998-33G>A | TMEM266 | ENSG00000169758.13 | transcript | ENST00000388942.9 | protein_coding | 10/10 | chr15 | 76203708 |