Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 90362 |
| ensemblid | ENSG00000169122.12 |
| hgncid | 28587 |
| symbol | FAM110B |
| name | family with sequence similarity 110 member B |
| refseq_nuc | NM_001377989.1 |
| refseq_prot | NP_001364918.1 |
| ensembl_nuc | ENST00000519262.6 |
| ensembl_prot | ENSP00000509301.1 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 57994523 |
| end | 58148784 |
| strand | + |
| ver | v1.2 |
| region | chr8:57994523-58148784 |
| region5000 | chr8:57989523-58153784 |
| regionname0 | FAM110B_chr8_57994523_58148784 |
| regionname5000 | FAM110B_chr8_57989523_58153784 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 370 | 298 | 88 | 54 | 118 | 12 | 24 | 90 | FAM110B_chr8_57989523_58153784 | FAM110B | MPTET others(365): Show |
chr8 | 57989523 | 58153784 |
| a0002 | 0/0 | 370 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | MPTET others(365): Show |
chr8 | 57989523 | 58153784 |
| a0003 | 0/0 | 370 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | MPTET others(365): Show |
chr8 | 57989523 | 58153784 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1110 | 298 | 88 | 54 | 118 | 12 | 24 | FAM110B_chr8_57989523_58153784 | FAM110B | ATGCC others(1105): Show |
chr8 | 57989523 | 58153784 | ||
| a0002c0002 | 0/0 | 1110 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | ATGCC others(1105): Show |
chr8 | 57989523 | 58153784 | ||
| a0003c0003 | 0/0 | 1110 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | ATGCC others(1105): Show |
chr8 | 57989523 | 58153784 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3349 | 72 | 11 | 13 | 35 | 5 | 7 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3344): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0002 | 1/0 | 3349 | 64 | 18 | 12 | 25 | 3 | 5 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3344): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0003 | 0/0 | 3349 | 59 | 26 | 4 | 25 | 1 | 3 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3344): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0004 | 0/0 | 3350 | 17 | 1 | 5 | 9 | 0 | 2 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3345): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0005 | 0/0 | 3350 | 15 | 3 | 2 | 9 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3345): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0006 | 0/0 | 3349 | 12 | 0 | 9 | 0 | 2 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3344): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0007 | 0/0 | 3348 | 9 | 8 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3343): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0008 | 0/0 | 3349 | 7 | 6 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3344): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0009 | 0/0 | 3350 | 7 | 2 | 1 | 3 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3345): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0010 | 0/0 | 3349 | 5 | 5 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3344): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0011 | 0/0 | 3349 | 3 | 0 | 2 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3344): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0012 | 0/0 | 3349 | 2 | 2 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3344): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0013 | 0/0 | 3349 | 2 | 0 | 0 | 2 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3344): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0014 | 0/0 | 3349 | 2 | 0 | 0 | 2 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3344): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0015 | 0/0 | 3348 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3343): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0017 | 0/0 | 3349 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3344): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0018 | 0/0 | 3349 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3344): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0019 | 0/0 | 3348 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3343): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0020 | 0/0 | 3350 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3345): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0021 | 0/0 | 3349 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3344): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0022 | 0/0 | 3338 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3333): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0023 | 0/0 | 3349 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3344): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0024 | 0/0 | 3348 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3343): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0025 | 0/0 | 3350 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3345): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0026 | 0/0 | 3349 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3344): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0027 | 0/0 | 3348 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3343): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0028 | 0/0 | 3350 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3345): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0029 | 0/0 | 3349 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3344): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0030 | 0/0 | 3348 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3343): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0031 | 0/0 | 3348 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3343): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0032 | 0/0 | 3349 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3344): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0033 | 0/0 | 3349 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3344): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0034 | 0/0 | 3349 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3344): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0035 | 0/0 | 3349 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3344): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0036 | 0/0 | 3349 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3344): Show |
chr8 | 57989523 | 58153784 |
| a0001c0001t0037 | 0/0 | 3349 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3344): Show |
chr8 | 57989523 | 58153784 |
| a0002c0002t0016 | 0/0 | 3348 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3343): Show |
chr8 | 57989523 | 58153784 |
| a0003c0003t0003 | 0/0 | 3349 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | ACTCT others(3344): Show |
chr8 | 57989523 | 58153784 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0256 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0053 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0006g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0006g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0006g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0006g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0006g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0006g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0006g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0006g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0006g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0006g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0006g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0006g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0007g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0007g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0007g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0007g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0007g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0007g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0007g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0007g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0007g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0008g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0008g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0008g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0008g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0008g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0008g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0008g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0009g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0009g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0009g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0009g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0009g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0009g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0009g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0010g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0010g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0010g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0010g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0010g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0011g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0011g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0011g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0012g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0012g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0013g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0013g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0014g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0014g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0015g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0017g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0018g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0019g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0020g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0021g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0022g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0023g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0024g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0025g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0026g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0027g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0028g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0029g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0030g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0031g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0032g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0033g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0034g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0035g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0036g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0037g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0002c0002t0016g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0003c0003t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0021 | g0248 | EUR | GBR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0109 | EUR | GBR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0126 | EUR | FIN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | FIN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00323 | hp1 | a0001 | c0001 | t0006 | g0246 | EUR | FIN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0156 | EUR | FIN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | CHS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00544 | hp2 | a0001 | c0001 | t0029 | g0276 | EAS | CHS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | CHS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | CHS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0188 | EAS | CHS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00609 | hp2 | a0001 | c0001 | t0014 | g0242 | EAS | CHS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | CHS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | CHS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0280 | EAS | CHS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0105 | EAS | CHS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0237 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0014 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00741 | hp1 | a0001 | c0001 | t0022 | g0174 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01069 | hp1 | a0001 | c0001 | t0036 | g0132 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01070 | hp1 | a0001 | c0001 | t0006 | g0219 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01081 | hp1 | a0001 | c0001 | t0006 | g0025 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01081 | hp2 | a0001 | c0001 | t0020 | g0033 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01109 | hp1 | a0001 | c0001 | t0007 | g0004 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0041 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01168 | hp2 | a0001 | c0001 | t0006 | g0245 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01175 | hp1 | a0001 | c0001 | t0011 | g0212 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01175 | hp2 | a0001 | c0001 | t0006 | g0113 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01192 | hp1 | a0001 | c0001 | t0031 | g0159 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0238 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01243 | hp2 | a0001 | c0001 | t0008 | g0169 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01255 | hp1 | a0001 | c0001 | t0006 | g0155 | AMR | CLM | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01255 | hp2 | a0001 | c0001 | t0006 | g0218 | AMR | CLM | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01261 | hp1 | a0001 | c0001 | t0011 | g0195 | AMR | CLM | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | CLM | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01433 | hp2 | a0001 | c0001 | t0009 | g0077 | AMR | CLM | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0194 | AMR | CLM | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0019 | AMR | CLM | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0042 | EUR | IBS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0250 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01884 | hp2 | a0001 | c0001 | t0024 | g0176 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01891 | hp1 | a0001 | c0001 | t0010 | g0160 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01891 | hp2 | a0001 | c0001 | t0007 | g0131 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01928 | hp1 | a0001 | c0001 | t0006 | g0116 | AMR | PEL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | PEL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | PEL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01934 | hp2 | a0001 | c0001 | t0006 | g0101 | AMR | PEL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0257 | AMR | PEL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01952 | hp1 | a0001 | c0001 | t0006 | g0052 | AMR | PEL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | PEL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0202 | AMR | PEL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0187 | AMR | PEL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PEL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PEL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | KHV | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02055 | hp1 | a0001 | c0001 | t0009 | g0168 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02055 | hp2 | a0001 | c0001 | t0007 | g0197 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0083 | EAS | KHV | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02080 | hp2 | a0001 | c0001 | t0033 | g0081 | EAS | KHV | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | KHV | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0189 | EAS | KHV | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | KHV | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | KHV | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | CDX | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CDX | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | CDX | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | CDX | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02257 | hp1 | a0001 | c0001 | t0027 | g0137 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0269 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02258 | hp1 | a0002 | c0002 | t0016 | g0166 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02258 | hp2 | a0001 | c0001 | t0015 | g0007 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0130 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0297 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02451 | hp2 | a0001 | c0001 | t0012 | g0148 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0299 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0271 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0151 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0141 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02622 | hp2 | a0001 | c0001 | t0010 | g0175 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0173 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02630 | hp2 | a0001 | c0001 | t0034 | g0244 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0291 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02683 | hp2 | a0001 | c0001 | t0006 | g0051 | SAS | PJL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0300 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0071 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0249 | SAS | PJL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | PJL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0247 | SAS | PJL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0270 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0296 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02886 | hp2 | a0001 | c0001 | t0009 | g0140 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0165 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0074 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02897 | hp1 | a0001 | c0001 | t0030 | g0035 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0164 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | ESN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0127 | AFR | ESN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | ESN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02965 | hp2 | a0001 | c0001 | t0010 | g0294 | AFR | ESN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | ESN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0161 | AFR | ESN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0298 | SAS | PJL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03041 | hp1 | a0001 | c0001 | t0010 | g0145 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03041 | hp2 | a0001 | c0001 | t0012 | g0150 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03098 | hp1 | a0001 | c0001 | t0008 | g0170 | AFR | MSL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03098 | hp2 | a0001 | c0001 | t0008 | g0265 | AFR | MSL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0143 | AFR | ESN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0289 | AFR | ESN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0231 | AFR | ESN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0133 | AFR | ESN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0134 | AFR | MSL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03209 | hp2 | a0001 | c0001 | t0010 | g0072 | AFR | MSL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0295 | AFR | MSL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0157 | AFR | MSL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03453 | hp2 | a0003 | c0003 | t0003 | g0264 | AFR | MSL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | MSL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0139 | AFR | MSL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0090 | AFR | MSL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03669 | hp1 | a0001 | c0001 | t0009 | g0064 | SAS | PJL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0125 | SAS | PJL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | STU | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03688 | hp2 | a0001 | c0001 | t0025 | g0009 | SAS | STU | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0026 | SAS | BEB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03831 | hp2 | a0001 | c0001 | t0032 | g0114 | SAS | BEB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0275 | SAS | BEB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03834 | hp2 | a0001 | c0001 | t0011 | g0228 | SAS | BEB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0263 | SAS | BEB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | BEB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03942 | hp1 | a0001 | c0001 | t0023 | g0085 | SAS | BEB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0057 | SAS | BEB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | STU | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0049 | SAS | STU | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0288 | AFR | YRI | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | YRI | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | YRI | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18940 | hp2 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18942 | hp1 | a0001 | c0001 | t0018 | g0215 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18948 | hp1 | a0001 | c0001 | t0019 | g0222 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18956 | hp1 | a0001 | c0001 | t0005 | g0225 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18959 | hp2 | a0001 | c0001 | t0037 | g0180 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0274 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18972 | hp2 | a0001 | c0001 | t0013 | g0177 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18975 | hp1 | a0001 | c0001 | t0005 | g0196 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18977 | hp2 | a0001 | c0001 | t0005 | g0093 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18979 | hp1 | a0001 | c0001 | t0005 | g0210 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18984 | hp2 | a0001 | c0001 | t0005 | g0058 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18989 | hp1 | a0001 | c0001 | t0013 | g0183 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18989 | hp2 | a0001 | c0001 | t0005 | g0061 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0279 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18992 | hp1 | a0001 | c0001 | t0028 | g0182 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19006 | hp2 | a0001 | c0001 | t0026 | g0021 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0268 | AFR | LWK | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | LWK | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0138 | AFR | LWK | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | LWK | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19060 | hp1 | a0001 | c0001 | t0014 | g0243 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19063 | hp2 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19064 | hp2 | a0001 | c0001 | t0009 | g0179 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19072 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19079 | hp1 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19079 | hp2 | a0001 | c0001 | t0009 | g0199 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19087 | hp1 | a0001 | c0001 | t0009 | g0205 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19091 | hp1 | a0001 | c0001 | t0017 | g0119 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0286 | AFR | YRI | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | YRI | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0129 | AFR | ASW | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ASW | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | TSI | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA20752 | hp2 | a0001 | c0001 | t0006 | g0220 | EUR | TSI | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0078 | EUR | TSI | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0234 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0075 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02559 | hp1 | a0001 | c0001 | t0035 | g0290 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0135 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | MSL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0144 | AFR | MSL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | USA | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0266 | AFR | USA | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0287 | AFR | USA | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0260 | AFR | USA | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | LWK | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA21309 | hp2 | a0001 | c0001 | t0008 | g0079 | AFR | LWK | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0256 | REF | REF | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0053 | REF | REF | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:58146669 | C | T | 1 | a0003 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.439C>T | p.His147Tyr | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 1234/3349 | 439/1113 | 147/370 | chr8 | 58146669 | |||
| chr8:58146870 | G | A | 1 | a0002 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.640G>A | p.Ala214Thr | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 1435/3349 | 640/1113 | 214/370 | chr8 | 58146870 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:57994553 | C | T | 1 | a0001c0001t0037 | 1 | NA18959.hp2 | 5_prime_UTR_variant | MODIFIER | c.-765C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/4 | 151678 | chr8 | 57994553 | ||||||
| chr8:57994567 | C | T | 1 | a0001c0001t0036 | 1 | HG01069.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-751C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/4 | chr8 | 57994567 | |||||||
| chr8:57994585 | G | T | 1 | a0001c0001t0035 | 1 | HG02559.hp1 | 5_prime_UTR_variant | MODIFIER | c.-733G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/4 | 151646 | chr8 | 57994585 | ||||||
| chr8:57994677 | A | C | 1 | a0001c0001t0014 | 2 | HG00609.hp2 NA19060.hp1 |
5_prime_UTR_variant | MODIFIER | c.-641A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/4 | 151554 | chr8 | 57994677 | ||||||
| chr8:57994757 | C | T | 1 | a0001c0001t0034 | 1 | HG02630.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-561C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/4 | chr8 | 57994757 | |||||||
| chr8:57994766 | G | T | 1 | a0001c0001t0033 | 1 | HG02080.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-552G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/4 | chr8 | 57994766 | |||||||
| chr8:58031651 | C | T | 1 | a0001c0001t0032 | 1 | HG03831.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-466C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/4 | chr8 | 58031651 | |||||||
| chr8:58075619 | C | G | 1 | a0001c0001t0031 | 1 | HG01192.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-329C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/4 | chr8 | 58075619 | |||||||
| chr8:58146023 | G | A | 1 | a0001c0001t0015 | 1 | HG02258.hp2 | 5_prime_UTR_variant | MODIFIER | c.-208G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 208 | chr8 | 58146023 | ||||||
| chr8:58146086 | A | T | 1 | a0001c0001t0030 | 1 | HG02897.hp1 | 5_prime_UTR_variant | MODIFIER | c.-145A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 145 | chr8 | 58146086 | ||||||
| chr8:58146090 | G | T | 1 | a0001c0001t0029 | 1 | HG00544.hp2 | 5_prime_UTR_variant | MODIFIER | c.-141G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 141 | chr8 | 58146090 | ||||||
| chr8:58147538 | C | A | 1 | a0001c0001t0034 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*195C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 195 | chr8 | 58147538 | ||||||
| chr8:58147541 | G | A | 1 | a0002c0002t0016 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*198G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 198 | chr8 | 58147541 | ||||||
| chr8:58147665 | G | A | 1 | a0001c0001t0017 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*322G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 322 | chr8 | 58147665 | ||||||
| chr8:58147716 | A | G | 12 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0012 others(9): Show |
99 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*373A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 373 | chr8 | 58147716 | ||||||
| chr8:58147813 | G | A | 1 | a0001c0001t0012 | 2 | HG02451.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*470G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 470 | chr8 | 58147813 | ||||||
| chr8:58147853 | T | A | 1 | a0001c0001t0014 | 2 | HG00609.hp2 NA19060.hp1 |
3_prime_UTR_variant | MODIFIER | c.*510T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 510 | chr8 | 58147853 | ||||||
| chr8:58148090 | T | C | 2 | a0001c0001t0018 a0001c0001t0019 |
2 | NA18942.hp1 NA18948.hp1 |
3_prime_UTR_variant | MODIFIER | c.*747T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 747 | chr8 | 58148090 | ||||||
| chr8:58148139 | TA | T | 30 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(27): Show |
212 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*809delA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 809 | INFO_REALIGN_3_PRIME | chr8 | 58148139 | |||||
| chr8:58148147 | A | T | 1 | a0001c0001t0025 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*804A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 804 | chr8 | 58148147 | ||||||
| chr8:58148166 | G | GT | 16 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(13): Show |
173 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*843dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 844 | INFO_REALIGN_3_PRIME | chr8 | 58148166 | |||||
| chr8:58148166 | G | GTT | 3 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0028 |
23 | HG00609.hp1 HG01243.hp1 HG01433.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*842_*843dupTT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 844 | INFO_REALIGN_3_PRIME | chr8 | 58148166 | |||||
| chr8:58148166 | G | T | 2 | a0001c0001t0021 a0001c0001t0030 |
2 | HG00099.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*823G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 823 | chr8 | 58148166 | ||||||
| chr8:58148166 | GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0022 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*834_*843delTTTTTT others(4): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 834 | INFO_REALIGN_3_PRIME | chr8 | 58148166 | |||||
| chr8:58148171 | T | TG | 1 | a0001c0001t0011 | 3 | HG01175.hp1 HG01261.hp1 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*828_*829insG | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 829 | chr8 | 58148171 | ||||||
| chr8:58148177 | T | TG | 4 | a0001c0001t0006 a0001c0001t0020 a0001c0001t0023 others(1): Show |
15 | HG00323.hp1 HG01070.hp1 HG01081.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*834_*835insG | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 835 | chr8 | 58148177 | ||||||
| chr8:58148242 | G | C | 1 | a0001c0001t0025 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*899G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 899 | chr8 | 58148242 | ||||||
| chr8:58148421 | A | G | 2 | a0001c0001t0008 a0001c0001t0030 |
8 | HG01243.hp2 HG02630.hp1 HG02886.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1078A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 1078 | chr8 | 58148421 | ||||||
| chr8:58148513 | T | C | 5 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0020 others(2): Show |
20 | HG00323.hp1 HG01070.hp1 HG01081.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1170T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 1170 | chr8 | 58148513 | ||||||
| chr8:58148524 | T | A | 1 | a0001c0001t0024 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1181T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 1181 | chr8 | 58148524 | ||||||
| chr8:58148542 | G | T | 2 | a0001c0001t0013 a0001c0001t0028 |
3 | NA18972.hp2 NA18989.hp1 NA18992.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1199G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 1199 | chr8 | 58148542 | ||||||
| chr8:58148671 | T | C | 1 | a0001c0001t0023 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1328T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 1328 | chr8 | 58148671 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:57994887 | G | A | 1 | a0001c0001t0002g0001 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-512+81G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57994887 | |||||||
| chr8:57994902 | G | T | 1 | a0001c0001t0007g0300 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-512+96G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57994902 | |||||||
| chr8:57994906 | G | T | 1 | a0001c0001t0003g0299 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-512+100G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57994906 | |||||||
| chr8:57995061 | C | T | 1 | a0001c0001t0007g0300 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-512+255C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57995061 | |||||||
| chr8:57995131 | C | CTGGAGCC others(5): Show |
1 | a0001c0001t0002g0298 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-512+333_-512+344d others(14): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 57995131 | ||||||
| chr8:57995141 | G | A | 1 | a0001c0001t0001g0002 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-512+335G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57995141 | |||||||
| chr8:57995258 | C | T | 1 | a0001c0001t0002g0297 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-512+452C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57995258 | |||||||
| chr8:57995313 | A | T | 1 | a0001c0001t0008g0296 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-512+507A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57995313 | |||||||
| chr8:57995411 | C | T | 2 | a0001c0001t0003g0295 a0001c0001t0010g0294 |
2 | HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-512+605C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57995411 | |||||||
| chr8:57995630 | G | A | 1 | a0001c0001t0004g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-512+824G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57995630 | |||||||
| chr8:57995871 | T | C | 1 | a0001c0001t0007g0004 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-512+1065T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57995871 | |||||||
| chr8:57995903 | A | G | 2 | a0001c0001t0002g0293 a0001c0001t0003g0292 |
2 | NA18944.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.-512+1097A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57995903 | |||||||
| chr8:57995967 | G | A | 1 | a0001c0001t0003g0005 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-512+1161G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57995967 | |||||||
| chr8:57996114 | A | T | 6 | a0001c0001t0002g0291 a0001c0001t0003g0286 a0001c0001t0003g0287 others(3): Show |
6 | HG02559.hp1 HG02647.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-512+1308A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57996114 | |||||||
| chr8:57996188 | C | T | 129 | a0001c0001t0001g0002 a0001c0001t0001g0172 a0001c0001t0001g0184 others(126): Show |
129 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.-512+1382C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57996188 | |||||||
| chr8:57996770 | A | C | 14 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0281 others(11): Show |
14 | HG00438.hp1 HG00544.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.-512+1964A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57996770 | |||||||
| chr8:57996868 | A | C | 7 | a0001c0001t0001g0267 a0001c0001t0002g0266 a0001c0001t0002g0268 others(4): Show |
7 | HG00733.hp1 HG02257.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-512+2062A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57996868 | |||||||
| chr8:57997818 | A | G | 1 | a0003c0003t0003g0264 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-512+3012A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57997818 | |||||||
| chr8:57998123 | T | G | 1 | a0001c0001t0001g0006 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-512+3317T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57998123 | |||||||
| chr8:57998211 | A | G | 1 | a0003c0003t0003g0264 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-512+3405A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57998211 | |||||||
| chr8:57998217 | A | G | 233 | a0001c0001t0001g0002 a0001c0001t0001g0073 a0001c0001t0001g0084 others(230): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.-512+3411A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57998217 | |||||||
| chr8:57998320 | G | C | 6 | a0001c0001t0001g0073 a0001c0001t0003g0071 a0001c0001t0003g0074 others(3): Show |
6 | HG01109.hp1 HG02486.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-512+3514G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57998320 | |||||||
| chr8:57998400 | G | A | 1 | a0001c0001t0003g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-512+3594G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57998400 | |||||||
| chr8:57998514 | C | T | 10 | a0001c0001t0001g0073 a0001c0001t0001g0158 a0001c0001t0003g0071 others(7): Show |
10 | HG01109.hp1 HG01192.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-512+3708C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57998514 | |||||||
| chr8:57998548 | G | T | 1 | a0001c0001t0002g0070 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-512+3742G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57998548 | |||||||
| chr8:57998762 | A | G | 1 | a0001c0001t0003g0156 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-512+3956A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57998762 | |||||||
| chr8:57998903 | A | T | 1 | a0001c0001t0002g0263 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-512+4097A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57998903 | |||||||
| chr8:57999047 | G | T | 1 | a0001c0001t0006g0155 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-512+4241G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57999047 | |||||||
| chr8:57999089 | G | A | 1 | a0001c0001t0010g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-512+4283G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57999089 | |||||||
| chr8:57999150 | A | C | 170 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0068 others(167): Show |
170 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.-512+4344A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57999150 | |||||||
| chr8:57999153 | A | G | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0004g0260 |
3 | HG01070.hp2 HG01071.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-512+4347A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57999153 | |||||||
| chr8:57999261 | G | A | 2 | a0001c0001t0002g0078 a0001c0001t0009g0077 |
2 | HG01433.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-512+4455G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57999261 | |||||||
| chr8:57999333 | T | C | 1 | a0001c0001t0008g0127 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-512+4527T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57999333 | |||||||
| chr8:57999374 | A | G | 215 | a0001c0001t0001g0002 a0001c0001t0001g0065 a0001c0001t0001g0073 others(212): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.-512+4568A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57999374 | |||||||
| chr8:57999403 | T | A | 1 | a0001c0001t0015g0007 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-512+4597T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57999403 | |||||||
| chr8:57999518 | A | AT | 7 | a0001c0001t0001g0154 a0001c0001t0002g0291 a0001c0001t0003g0286 others(4): Show |
7 | HG02559.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-512+4722dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 57999518 | ||||||
| chr8:57999518 | AT | A | 6 | a0001c0001t0001g0158 a0001c0001t0007g0004 a0001c0001t0007g0157 others(3): Show |
6 | HG01109.hp1 HG01192.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.-512+4722delT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 57999518 | ||||||
| chr8:57999554 | A | G | 3 | a0001c0001t0007g0004 a0001c0001t0008g0079 a0001c0001t0031g0159 |
3 | HG01109.hp1 HG01192.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-512+4748A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57999554 | |||||||
| chr8:57999673 | C | G | 1 | a0001c0001t0001g0259 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-512+4867C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57999673 | |||||||
| chr8:57999802 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-512+4996C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57999802 | |||||||
| chr8:58000229 | C | A | 2 | a0001c0001t0002g0128 a0001c0001t0005g0161 |
2 | HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-512+5423C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58000229 | |||||||
| chr8:58000236 | G | A | 10 | a0001c0001t0001g0008 a0001c0001t0002g0178 a0001c0001t0002g0181 others(7): Show |
10 | HG02080.hp2 NA18959.hp2 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.-512+5430G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58000236 | |||||||
| chr8:58000289 | A | G | 9 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0258 others(6): Show |
9 | HG00438.hp2 NA18948.hp2 NA18964.hp2 others(6): Show |
intron_variant | MODIFIER | c.-512+5483A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58000289 | |||||||
| chr8:58000376 | A | G | 3 | a0001c0001t0001g0124 a0001c0001t0002g0126 a0001c0001t0004g0125 |
3 | HG00280.hp1 HG02738.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-512+5570A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58000376 | |||||||
| chr8:58000393 | C | T | 2 | a0001c0001t0002g0123 a0001c0001t0003g0257 |
2 | HG01943.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.-512+5587C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58000393 | |||||||
| chr8:58000603 | T | C | 8 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0002g0082 others(5): Show |
8 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-512+5797T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58000603 | |||||||
| chr8:58000731 | G | A | 52 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0089 others(49): Show |
52 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.-512+5925G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58000731 | |||||||
| chr8:58000745 | C | T | 4 | a0001c0001t0004g0260 a0001c0001t0007g0090 a0001c0001t0024g0176 others(1): Show |
4 | HG01192.hp1 HG01884.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-512+5939C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58000745 | |||||||
| chr8:58001029 | C | A | 1 | a0001c0001t0027g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-512+6223C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58001029 | |||||||
| chr8:58001375 | GGT | G | 170 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(167): Show |
170 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.-512+6585_-512+658 others(6): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58001375 | ||||||
| chr8:58001422 | T | C | 5 | a0001c0001t0002g0082 a0001c0001t0002g0162 a0001c0001t0002g0163 others(2): Show |
5 | HG01891.hp2 HG02280.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.-512+6616T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58001422 | |||||||
| chr8:58001563 | C | T | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-512+6757C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58001563 | |||||||
| chr8:58001564 | G | A | 1 | a0001c0001t0002g0030 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-512+6758G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58001564 | |||||||
| chr8:58001665 | A | T | 1 | a0001c0001t0003g0122 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-512+6859A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58001665 | |||||||
| chr8:58001792 | G | T | 1 | a0003c0003t0003g0264 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-512+6986G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58001792 | |||||||
| chr8:58001804 | C | T | 1 | a0002c0002t0016g0166 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-512+6998C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58001804 | |||||||
| chr8:58002044 | C | CAG | 3 | a0001c0001t0002g0152 a0001c0001t0003g0151 a0001c0001t0027g0137 |
3 | HG02257.hp1 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-512+7248_-512+724 others(6): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58002044 | ||||||
| chr8:58002553 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-512+7747A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58002553 | |||||||
| chr8:58002562 | A | G | 5 | a0001c0001t0001g0158 a0001c0001t0004g0260 a0001c0001t0007g0090 others(2): Show |
5 | HG01192.hp1 HG01884.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-512+7756A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58002562 | |||||||
| chr8:58002580 | C | T | 1 | a0001c0001t0005g0196 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-512+7774C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58002580 | |||||||
| chr8:58002812 | A | C | 53 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0089 others(50): Show |
53 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.-512+8006A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58002812 | |||||||
| chr8:58002901 | G | A | 2 | a0001c0001t0001g0267 a0001c0001t0002g0266 |
2 | HG00733.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-512+8095G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58002901 | |||||||
| chr8:58002970 | T | A | 1 | a0001c0001t0002g0095 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-512+8164T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58002970 | |||||||
| chr8:58003244 | C | T | 1 | a0001c0001t0008g0296 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-512+8438C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58003244 | |||||||
| chr8:58003258 | G | A | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-512+8452G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58003258 | |||||||
| chr8:58003321 | G | A | 1 | a0001c0001t0012g0148 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-512+8515G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58003321 | |||||||
| chr8:58003381 | C | T | 3 | a0001c0001t0002g0152 a0001c0001t0003g0151 a0001c0001t0027g0137 |
3 | HG02257.hp1 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-512+8575C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58003381 | |||||||
| chr8:58003858 | C | T | 80 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0017 others(77): Show |
80 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-512+9052C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58003858 | |||||||
| chr8:58003887 | C | A | 1 | a0001c0001t0001g0060 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-512+9081C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58003887 | |||||||
| chr8:58003920 | C | T | 2 | a0001c0001t0013g0183 a0001c0001t0028g0182 |
2 | NA18989.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.-512+9114C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58003920 | |||||||
| chr8:58003980 | A | G | 3 | a0001c0001t0002g0167 a0001c0001t0007g0135 a0002c0002t0016g0166 |
3 | HG02258.hp1 HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-512+9174A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58003980 | |||||||
| chr8:58003981 | C | T | 8 | a0001c0001t0002g0186 a0001c0001t0003g0129 a0001c0001t0003g0133 others(5): Show |
8 | HG01069.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-512+9175C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58003981 | |||||||
| chr8:58004001 | A | G | 8 | a0001c0001t0001g0158 a0001c0001t0002g0167 a0001c0001t0004g0260 others(5): Show |
8 | HG01192.hp1 HG01884.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-512+9195A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58004001 | |||||||
| chr8:58004017 | G | A | 1 | a0001c0001t0002g0031 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-512+9211G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58004017 | |||||||
| chr8:58004059 | T | C | 1 | a0001c0001t0004g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-512+9253T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58004059 | |||||||
| chr8:58004154 | G | A | 8 | a0001c0001t0002g0186 a0001c0001t0003g0129 a0001c0001t0003g0133 others(5): Show |
8 | HG01069.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-512+9348G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58004154 | |||||||
| chr8:58004291 | A | C | 1 | a0001c0001t0001g0089 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-512+9485A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58004291 | |||||||
| chr8:58004436 | T | C | 1 | a0001c0001t0011g0228 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-512+9630T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58004436 | |||||||
| chr8:58004566 | G | A | 1 | a0001c0001t0004g0083 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-512+9760G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58004566 | |||||||
| chr8:58004774 | G | C | 175 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(172): Show |
175 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.-512+9968G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58004774 | |||||||
| chr8:58005126 | G | A | 5 | a0001c0001t0001g0158 a0001c0001t0004g0260 a0001c0001t0007g0090 others(2): Show |
5 | HG01192.hp1 HG01884.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-512+10320G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58005126 | |||||||
| chr8:58005146 | A | G | 1 | a0001c0001t0022g0174 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-512+10340A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58005146 | |||||||
| chr8:58005255 | G | A | 7 | a0001c0001t0001g0267 a0001c0001t0002g0136 a0001c0001t0002g0266 others(4): Show |
7 | HG00733.hp1 HG02257.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-512+10449G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58005255 | |||||||
| chr8:58005263 | G | A | 8 | a0001c0001t0002g0186 a0001c0001t0003g0129 a0001c0001t0003g0133 others(5): Show |
8 | HG01069.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-512+10457G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58005263 | |||||||
| chr8:58005311 | C | T | 1 | a0001c0001t0011g0195 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-512+10505C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58005311 | |||||||
| chr8:58005470 | T | C | 3 | a0001c0001t0002g0032 a0001c0001t0003g0034 a0001c0001t0020g0033 |
3 | HG00642.hp1 HG01074.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.-512+10664T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58005470 | |||||||
| chr8:58005505 | C | T | 1 | a0001c0001t0002g0121 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-512+10699C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58005505 | |||||||
| chr8:58005617 | A | T | 1 | a0001c0001t0002g0120 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-512+10811A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58005617 | |||||||
| chr8:58005637 | C | T | 5 | a0001c0001t0002g0082 a0001c0001t0002g0162 a0001c0001t0002g0163 others(2): Show |
5 | HG01891.hp2 HG02280.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.-512+10831C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58005637 | |||||||
| chr8:58005936 | T | C | 3 | a0001c0001t0002g0152 a0001c0001t0003g0151 a0001c0001t0027g0137 |
3 | HG02257.hp1 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-512+11130T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58005936 | |||||||
| chr8:58005976 | A | G | 1 | a0001c0001t0003g0122 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-512+11170A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58005976 | |||||||
| chr8:58006212 | T | C | 10 | a0001c0001t0002g0082 a0001c0001t0002g0162 a0001c0001t0002g0163 others(7): Show |
10 | HG01192.hp1 HG01891.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-512+11406T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006212 | |||||||
| chr8:58006525 | G | C | 1 | a0001c0001t0001g0200 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-512+11719G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006525 | |||||||
| chr8:58006532 | C | G | 45 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0089 others(42): Show |
45 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.-512+11726C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006532 | |||||||
| chr8:58006558 | C | T | 1 | a0002c0002t0016g0166 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-512+11752C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006558 | |||||||
| chr8:58006604 | A | AT | 9 | a0001c0001t0001g0029 a0001c0001t0001g0259 a0001c0001t0002g0162 others(6): Show |
9 | HG00408.hp2 HG01891.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-512+11813dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006604 | ||||||
| chr8:58006604 | AT | A | 18 | a0001c0001t0002g0186 a0001c0001t0002g0297 a0001c0001t0003g0129 others(15): Show |
18 | HG01069.hp1 HG01884.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.-512+11813delT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006604 | ||||||
| chr8:58006786 | A | G | 1 | a0001c0001t0001g0088 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-512+11980A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006786 | |||||||
| chr8:58006810 | C | T | 1 | a0001c0001t0004g0194 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-512+12004C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006810 | |||||||
| chr8:58006830 | C | T | 4 | a0001c0001t0001g0253 a0001c0001t0001g0258 a0001c0001t0002g0121 others(1): Show |
4 | HG00438.hp2 HG00621.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.-512+12024C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006830 | |||||||
| chr8:58006901 | G | GTA | 8 | a0001c0001t0002g0082 a0001c0001t0002g0147 a0001c0001t0002g0162 others(5): Show |
8 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-512+12117_-512+12 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | ||||||
| chr8:58006901 | G | GTATA | 8 | a0001c0001t0001g0172 a0001c0001t0001g0261 a0001c0001t0001g0262 others(5): Show |
8 | HG01070.hp2 HG01071.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-512+12115_-512+12 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | ||||||
| chr8:58006901 | G | GTATATAT others(3): Show |
1 | a0001c0001t0007g0135 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-512+12109_-512+12 others(16): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | ||||||
| chr8:58006901 | G | GTATATAT others(7): Show |
2 | a0001c0001t0002g0031 a0001c0001t0002g0128 |
2 | HG02004.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-512+12105_-512+12 others(20): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | ||||||
| chr8:58006901 | G | GTATATAT others(41): Show |
1 | a0001c0001t0003g0229 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-512+12109_-512+12 others(54): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | ||||||
| chr8:58006901 | G | GTATATAT others(9): Show |
15 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0253 others(12): Show |
15 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.-512+12103_-512+12 others(22): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | ||||||
| chr8:58006901 | G | GTATATAT others(11): Show |
24 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0110 others(21): Show |
24 | HG00099.hp2 HG00408.hp2 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.-512+12101_-512+12 others(24): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | ||||||
| chr8:58006901 | G | GTATATAT others(13): Show |
13 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0042 others(10): Show |
13 | HG00673.hp2 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.-512+12099_-512+12 others(26): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | ||||||
| chr8:58006901 | G | GTATATAT others(15): Show |
12 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0282 others(9): Show |
12 | HG00280.hp1 HG00544.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.-512+12097_-512+12 others(28): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | ||||||
| chr8:58006901 | G | GTATATAT others(17): Show |
9 | a0001c0001t0001g0098 a0001c0001t0001g0281 a0001c0001t0002g0099 others(6): Show |
9 | HG01952.hp2 HG02155.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(30): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | ||||||
| chr8:58006901 | G | GTATATAT others(19): Show |
2 | a0001c0001t0003g0151 a0001c0001t0007g0300 |
2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(32): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | ||||||
| chr8:58006901 | G | GTATATAT others(23): Show |
2 | a0001c0001t0001g0230 a0001c0001t0006g0155 |
2 | HG01255.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(36): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | ||||||
| chr8:58006901 | G | GTATATAT others(27): Show |
2 | a0001c0001t0001g0097 a0001c0001t0001g0185 |
2 | HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(40): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | ||||||
| chr8:58006901 | G | GTATATAT others(33): Show |
1 | a0001c0001t0001g0184 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(46): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | ||||||
| chr8:58006901 | GTATA | G | 3 | a0001c0001t0001g0252 a0001c0001t0003g0251 a0001c0001t0017g0119 |
3 | NA18949.hp2 NA18997.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-512+12115_-512+12 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | ||||||
| chr8:58006901 | GTATATAT others(5): Show |
G | 1 | a0001c0001t0003g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-512+12107_-512+12 others(18): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | ||||||
| chr8:58006919 | A | ATTTT | 38 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(35): Show |
38 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.-512+12114_-512+12 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006919 | ||||||
| chr8:58006919 | A | T | 3 | a0001c0001t0001g0065 a0001c0001t0005g0028 a0001c0001t0005g0061 |
3 | NA18989.hp2 NA19079.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-512+12113A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006919 | |||||||
| chr8:58006921 | A | ATTTT | 23 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0091 others(20): Show |
23 | HG00280.hp2 HG00741.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.-512+12116_-512+12 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006921 | ||||||
| chr8:58006921 | A | ATTTTT | 13 | a0001c0001t0001g0203 a0001c0001t0001g0207 a0001c0001t0001g0208 others(10): Show |
13 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(10): Show |
intron_variant | MODIFIER | c.-512+12116_-512+12 others(11): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006921 | ||||||
| chr8:58006921 | A | T | 42 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(39): Show |
42 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.-512+12115A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006921 | |||||||
| chr8:58006923 | A | ATATATAT others(49): Show |
1 | a0001c0001t0003g0096 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(62): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATATAT others(43): Show |
1 | a0001c0001t0007g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(56): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATATAT others(40): Show |
2 | a0001c0001t0013g0183 a0001c0001t0028g0182 |
2 | NA18989.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(53): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATATAT others(27): Show |
1 | a0001c0001t0003g0138 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(40): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATATAT others(33): Show |
1 | a0001c0001t0002g0181 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(46): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATATAT others(34): Show |
2 | a0001c0001t0002g0178 a0001c0001t0013g0177 |
2 | NA18972.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(47): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATATAT others(35): Show |
1 | a0001c0001t0003g0080 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(48): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATATAT others(22): Show |
1 | a0001c0001t0002g0012 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(35): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATATAT others(23): Show |
1 | a0001c0001t0010g0294 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(36): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATATAT others(30): Show |
1 | a0001c0001t0009g0179 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(43): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATATAT others(31): Show |
1 | a0001c0001t0001g0008 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(44): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATATAT others(21): Show |
2 | a0001c0001t0001g0006 a0001c0001t0005g0139 |
2 | HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(34): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATATAT others(27): Show |
1 | a0001c0001t0009g0140 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(40): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATATAT others(29): Show |
3 | a0001c0001t0009g0199 a0001c0001t0033g0081 a0001c0001t0037g0180 |
3 | HG02080.hp2 NA18959.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(42): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATATAT others(19): Show |
1 | a0001c0001t0003g0141 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(32): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATATAT others(25): Show |
1 | a0001c0001t0003g0142 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(38): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATATAT others(26): Show |
1 | a0001c0001t0001g0013 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(39): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATATAT others(27): Show |
1 | a0001c0001t0004g0014 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(40): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATATAT others(17): Show |
1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(30): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATATAT others(11): Show |
3 | a0001c0001t0001g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 |
3 | HG02486.hp2 HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(24): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATATAT others(11): Show |
2 | a0001c0001t0001g0088 a0001c0001t0002g0266 |
2 | HG06807.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(24): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATATAT others(12): Show |
3 | a0001c0001t0001g0267 a0001c0001t0004g0194 a0001c0001t0010g0160 |
3 | HG00733.hp1 HG01496.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(25): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATATAT others(8): Show |
1 | a0001c0001t0004g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(21): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATATAT others(9): Show |
4 | a0001c0001t0002g0066 a0001c0001t0003g0187 a0001c0001t0005g0058 others(1): Show |
4 | HG01978.hp2 NA18975.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(22): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATATAT others(11): Show |
8 | a0001c0001t0002g0136 a0001c0001t0002g0263 a0001c0001t0002g0268 others(5): Show |
8 | HG00609.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(24): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATATTT others(5): Show |
1 | a0001c0001t0007g0090 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(18): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATATTT others(7): Show |
1 | a0001c0001t0001g0158 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(20): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATATTT others(8): Show |
8 | a0001c0001t0001g0084 a0001c0001t0003g0171 a0001c0001t0003g0299 others(5): Show |
8 | HG02129.hp2 HG02145.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(21): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATATTT others(9): Show |
17 | a0001c0001t0001g0226 a0001c0001t0002g0011 a0001c0001t0002g0059 others(14): Show |
17 | HG00597.hp1 HG01928.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(22): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATTTTT others(9): Show |
1 | a0001c0001t0001g0089 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(22): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | ATATTTTT others(10): Show |
1 | a0001c0001t0011g0195 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(23): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | ||||||
| chr8:58006923 | A | T | 80 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0017 others(77): Show |
80 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-512+12117A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006923 | |||||||
| chr8:58006924 | T | TATATATA others(10): Show |
1 | a0001c0001t0003g0235 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(23): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006924 | |||||||
| chr8:58006924 | T | TATATATA others(14): Show |
1 | a0001c0001t0004g0062 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(27): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006924 | |||||||
| chr8:58006924 | T | TATATATA others(22): Show |
2 | a0001c0001t0002g0036 a0001c0001t0003g0198 |
2 | HG01433.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(35): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006924 | |||||||
| chr8:58006925 | T | G | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-512+12119T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006925 | |||||||
| chr8:58006995 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-512+12189C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006995 | |||||||
| chr8:58007039 | G | C | 1 | a0001c0001t0001g0046 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-512+12233G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58007039 | |||||||
| chr8:58007142 | T | C | 2 | a0001c0001t0004g0260 a0001c0001t0031g0159 |
2 | HG01192.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-512+12336T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58007142 | |||||||
| chr8:58007173 | G | A | 2 | a0001c0001t0004g0260 a0001c0001t0031g0159 |
2 | HG01192.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-512+12367G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58007173 | |||||||
| chr8:58007237 | G | T | 1 | a0001c0001t0003g0229 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-512+12431G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58007237 | |||||||
| chr8:58007469 | A | T | 82 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0017 others(79): Show |
82 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.-512+12663A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58007469 | |||||||
| chr8:58007642 | G | A | 1 | a0001c0001t0007g0300 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-512+12836G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58007642 | |||||||
| chr8:58007797 | T | C | 1 | a0001c0001t0002g0128 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-512+12991T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58007797 | |||||||
| chr8:58007809 | TTTTGTTA others(32): Show |
T | 1 | a0001c0001t0007g0135 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-512+13006_-512+13 others(45): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58007809 | ||||||
| chr8:58007828 | A | G | 1 | a0001c0001t0005g0271 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-512+13022A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58007828 | |||||||
| chr8:58007849 | T | A | 1 | a0001c0001t0007g0135 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-512+13043T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58007849 | |||||||
| chr8:58007884 | T | C | 4 | a0001c0001t0002g0030 a0001c0001t0002g0050 a0001c0001t0002g0070 others(1): Show |
4 | HG01074.hp2 HG01168.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-512+13078T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58007884 | |||||||
| chr8:58008126 | A | AT | 134 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0017 others(131): Show |
134 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.-512+13343dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58008126 | ||||||
| chr8:58008126 | A | ATT | 21 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0029 others(18): Show |
21 | HG00738.hp2 HG02080.hp2 HG02647.hp1 others(18): Show |
intron_variant | MODIFIER | c.-512+13342_-512+13 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58008126 | ||||||
| chr8:58008126 | AT | A | 10 | a0001c0001t0001g0172 a0001c0001t0001g0261 a0001c0001t0001g0281 others(7): Show |
10 | HG01070.hp2 HG01074.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.-512+13343delT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58008126 | ||||||
| chr8:58008189 | G | A | 9 | a0001c0001t0002g0186 a0001c0001t0003g0129 a0001c0001t0003g0133 others(6): Show |
9 | HG00323.hp1 HG01069.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-512+13383G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58008189 | |||||||
| chr8:58008198 | G | T | 1 | a0001c0001t0004g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-512+13392G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58008198 | |||||||
| chr8:58008320 | G | A | 5 | a0001c0001t0002g0167 a0001c0001t0004g0260 a0001c0001t0007g0135 others(2): Show |
5 | HG01192.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-512+13514G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58008320 | |||||||
| chr8:58008384 | C | T | 5 | a0001c0001t0001g0172 a0001c0001t0001g0261 a0001c0001t0001g0262 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-512+13578C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58008384 | |||||||
| chr8:58008385 | G | A | 13 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0002g0178 others(10): Show |
13 | HG00738.hp2 HG02080.hp2 NA18959.hp2 others(10): Show |
intron_variant | MODIFIER | c.-512+13579G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58008385 | |||||||
| chr8:58008548 | G | T | 5 | a0001c0001t0002g0082 a0001c0001t0002g0162 a0001c0001t0002g0163 others(2): Show |
5 | HG01891.hp2 HG02280.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.-512+13742G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58008548 | |||||||
| chr8:58008658 | T | C | 2 | a0001c0001t0007g0090 a0001c0001t0024g0176 |
2 | HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-512+13852T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58008658 | |||||||
| chr8:58008735 | G | A | 1 | a0001c0001t0004g0202 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-512+13929G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58008735 | |||||||
| chr8:58008774 | T | C | 1 | a0001c0001t0005g0247 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-512+13968T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58008774 | |||||||
| chr8:58008796 | T | C | 45 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0089 others(42): Show |
45 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.-512+13990T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58008796 | |||||||
| chr8:58008822 | G | A | 4 | a0001c0001t0003g0138 a0001c0001t0003g0141 a0001c0001t0005g0139 others(1): Show |
4 | HG02622.hp1 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-512+14016G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58008822 | |||||||
| chr8:58008974 | C | G | 1 | a0001c0001t0002g0193 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-512+14168C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58008974 | |||||||
| chr8:58009133 | G | A | 1 | a0001c0001t0003g0204 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-512+14327G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58009133 | |||||||
| chr8:58009153 | C | T | 2 | a0001c0001t0004g0260 a0001c0001t0031g0159 |
2 | HG01192.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-512+14347C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58009153 | |||||||
| chr8:58009271 | G | A | 5 | a0001c0001t0002g0167 a0001c0001t0004g0260 a0001c0001t0007g0135 others(2): Show |
5 | HG01192.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-512+14465G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58009271 | |||||||
| chr8:58009275 | T | C | 13 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0002g0178 others(10): Show |
13 | HG00738.hp2 HG02080.hp2 NA18959.hp2 others(10): Show |
intron_variant | MODIFIER | c.-512+14469T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58009275 | |||||||
| chr8:58009516 | T | C | 1 | a0001c0001t0008g0265 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-512+14710T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58009516 | |||||||
| chr8:58009521 | C | T | 8 | a0001c0001t0002g0186 a0001c0001t0003g0129 a0001c0001t0003g0133 others(5): Show |
8 | HG01069.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-512+14715C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58009521 | |||||||
| chr8:58009679 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-512+14873A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58009679 | |||||||
| chr8:58009724 | T | C | 1 | a0001c0001t0003g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-512+14918T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58009724 | |||||||
| chr8:58009738 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-512+14932C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58009738 | |||||||
| chr8:58009929 | C | T | 1 | a0001c0001t0002g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-512+15123C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58009929 | |||||||
| chr8:58009958 | C | T | 1 | a0001c0001t0030g0035 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-512+15152C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58009958 | |||||||
| chr8:58010183 | G | GT | 12 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0259 others(9): Show |
12 | HG00738.hp2 HG02080.hp2 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.-512+15394dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58010183 | ||||||
| chr8:58010300 | G | A | 1 | a0001c0001t0003g0255 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-512+15494G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58010300 | |||||||
| chr8:58010318 | G | A | 8 | a0001c0001t0002g0186 a0001c0001t0003g0129 a0001c0001t0003g0133 others(5): Show |
8 | HG01069.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-512+15512G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58010318 | |||||||
| chr8:58010668 | G | A | 13 | a0001c0001t0002g0167 a0001c0001t0002g0186 a0001c0001t0003g0129 others(10): Show |
13 | HG01069.hp1 HG01192.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-512+15862G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58010668 | |||||||
| chr8:58010673 | A | G | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-512+15867A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58010673 | |||||||
| chr8:58010855 | T | TTATGTGA others(316): Show |
1 | a0001c0001t0003g0134 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-512+16065_-512+16 others(329): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58010855 | ||||||
| chr8:58011096 | G | C | 2 | a0001c0001t0001g0149 a0001c0001t0001g0154 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-512+16290G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58011096 | |||||||
| chr8:58011382 | T | A | 6 | a0001c0001t0002g0082 a0001c0001t0002g0162 a0001c0001t0002g0163 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-512+16576T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58011382 | |||||||
| chr8:58011429 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0003g0289 |
2 | HG01993.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-512+16623C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58011429 | |||||||
| chr8:58011506 | A | G | 19 | a0001c0001t0001g0073 a0001c0001t0002g0167 a0001c0001t0002g0186 others(16): Show |
19 | HG01069.hp1 HG01192.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.-512+16700A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58011506 | |||||||
| chr8:58011635 | G | C | 103 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(100): Show |
103 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(100): Show |
intron_variant | MODIFIER | c.-512+16829G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58011635 | |||||||
| chr8:58011660 | A | T | 10 | a0001c0001t0001g0006 a0001c0001t0001g0158 a0001c0001t0002g0012 others(7): Show |
10 | HG02622.hp1 HG02818.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.-512+16854A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58011660 | |||||||
| chr8:58011700 | C | T | 8 | a0001c0001t0002g0186 a0001c0001t0003g0129 a0001c0001t0003g0133 others(5): Show |
8 | HG01069.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-512+16894C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58011700 | |||||||
| chr8:58012231 | A | G | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-512+17425A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58012231 | |||||||
| chr8:58012259 | A | AT | 15 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0029 others(12): Show |
15 | HG00738.hp2 HG02080.hp2 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.-512+17462dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58012259 | ||||||
| chr8:58012390 | G | A | 6 | a0001c0001t0001g0267 a0001c0001t0002g0136 a0001c0001t0002g0266 others(3): Show |
6 | HG00733.hp1 HG02257.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-512+17584G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58012390 | |||||||
| chr8:58012466 | T | A | 14 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0002g0178 others(11): Show |
14 | HG00738.hp2 HG02080.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.-512+17660T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58012466 | |||||||
| chr8:58012999 | C | T | 1 | a0001c0001t0008g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-512+18193C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58012999 | |||||||
| chr8:58013028 | G | A | 8 | a0001c0001t0002g0186 a0001c0001t0003g0129 a0001c0001t0003g0133 others(5): Show |
8 | HG01069.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-512+18222G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58013028 | |||||||
| chr8:58013184 | T | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0029 |
2 | NA18993.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-512+18378T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58013184 | |||||||
| chr8:58013216 | T | C | 12 | a0001c0001t0001g0006 a0001c0001t0001g0158 a0001c0001t0002g0012 others(9): Show |
12 | HG01884.hp2 HG02622.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.-511-18390T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58013216 | |||||||
| chr8:58013271 | G | A | 1 | a0001c0001t0030g0035 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-511-18335G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58013271 | |||||||
| chr8:58013568 | A | G | 3 | a0001c0001t0002g0152 a0001c0001t0003g0151 a0001c0001t0027g0137 |
3 | HG02257.hp1 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-511-18038A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58013568 | |||||||
| chr8:58013586 | A | T | 83 | a0001c0001t0001g0006 a0001c0001t0001g0073 a0001c0001t0001g0084 others(80): Show |
83 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.-511-18020A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58013586 | |||||||
| chr8:58013641 | C | G | 162 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(159): Show |
162 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.-511-17965C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58013641 | |||||||
| chr8:58013860 | T | A | 64 | a0001c0001t0001g0006 a0001c0001t0001g0084 a0001c0001t0001g0088 others(61): Show |
64 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.-511-17746T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58013860 | |||||||
| chr8:58013927 | T | A | 5 | a0001c0001t0002g0147 a0001c0001t0002g0167 a0001c0001t0004g0260 others(2): Show |
5 | HG02258.hp1 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-511-17679T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58013927 | |||||||
| chr8:58014028 | T | C | 2 | a0001c0001t0001g0158 a0001c0001t0031g0159 |
2 | HG01192.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-511-17578T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58014028 | |||||||
| chr8:58014048 | G | A | 1 | a0001c0001t0003g0198 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-511-17558G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58014048 | |||||||
| chr8:58014106 | G | A | 95 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0017 others(92): Show |
95 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.-511-17500G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58014106 | |||||||
| chr8:58014223 | G | A | 1 | a0001c0001t0003g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-511-17383G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58014223 | |||||||
| chr8:58014241 | G | A | 14 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0002g0178 others(11): Show |
14 | HG00738.hp2 HG02080.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.-511-17365G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58014241 | |||||||
| chr8:58014407 | C | T | 257 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(254): Show |
257 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.-511-17199C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58014407 | |||||||
| chr8:58014416 | C | T | 2 | a0001c0001t0003g0198 a0001c0001t0007g0300 |
2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-511-17190C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58014416 | |||||||
| chr8:58014545 | G | A | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-511-17061G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58014545 | |||||||
| chr8:58014630 | A | G | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-511-16976A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58014630 | |||||||
| chr8:58014674 | A | T | 1 | a0001c0001t0003g0075 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-511-16932A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58014674 | |||||||
| chr8:58014784 | C | T | 1 | a0001c0001t0003g0249 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-511-16822C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58014784 | |||||||
| chr8:58014812 | T | TATG | 90 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(87): Show |
90 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.-511-16792_-511-16 others(9): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58014812 | ||||||
| chr8:58014968 | C | G | 14 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0002g0178 others(11): Show |
14 | HG00738.hp2 HG02080.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.-511-16638C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58014968 | |||||||
| chr8:58015109 | A | T | 1 | a0001c0001t0022g0174 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-511-16497A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58015109 | |||||||
| chr8:58015158 | C | G | 9 | a0001c0001t0001g0006 a0001c0001t0002g0012 a0001c0001t0003g0138 others(6): Show |
9 | HG02622.hp1 HG02818.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-511-16448C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58015158 | |||||||
| chr8:58015720 | C | T | 14 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0002g0178 others(11): Show |
14 | HG00738.hp2 HG02080.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.-511-15886C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58015720 | |||||||
| chr8:58015844 | C | CA | 6 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0002g0241 others(3): Show |
6 | HG02129.hp2 HG02280.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-511-15746dupA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58015844 | ||||||
| chr8:58015844 | CA | C | 99 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(96): Show |
99 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.-511-15746delA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58015844 | ||||||
| chr8:58015875 | G | A | 4 | a0001c0001t0002g0167 a0001c0001t0004g0260 a0001c0001t0007g0135 others(1): Show |
4 | HG02258.hp1 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-511-15731G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58015875 | |||||||
| chr8:58016048 | C | T | 61 | a0001c0001t0001g0006 a0001c0001t0001g0084 a0001c0001t0001g0088 others(58): Show |
61 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.-511-15558C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58016048 | |||||||
| chr8:58016049 | G | A | 1 | a0001c0001t0005g0271 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-511-15557G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58016049 | |||||||
| chr8:58016090 | A | G | 14 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0002g0178 others(11): Show |
14 | HG00738.hp2 HG02080.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.-511-15516A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58016090 | |||||||
| chr8:58016182 | A | G | 4 | a0001c0001t0001g0045 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
4 | NA18950.hp2 NA18975.hp2 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.-511-15424A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58016182 | |||||||
| chr8:58016243 | A | G | 1 | a0001c0001t0008g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-511-15363A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58016243 | |||||||
| chr8:58016313 | C | G | 90 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(87): Show |
90 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.-511-15293C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58016313 | |||||||
| chr8:58016335 | C | T | 9 | a0001c0001t0001g0006 a0001c0001t0002g0012 a0001c0001t0003g0138 others(6): Show |
9 | HG02622.hp1 HG02818.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-511-15271C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58016335 | |||||||
| chr8:58016369 | C | T | 62 | a0001c0001t0001g0006 a0001c0001t0001g0084 a0001c0001t0001g0088 others(59): Show |
62 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.-511-15237C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58016369 | |||||||
| chr8:58016389 | G | C | 1 | a0001c0001t0003g0198 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-511-15217G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58016389 | |||||||
| chr8:58016448 | A | G | 14 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0002g0178 others(11): Show |
14 | HG00738.hp2 HG02080.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.-511-15158A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58016448 | |||||||
| chr8:58016478 | A | C | 5 | a0001c0001t0002g0082 a0001c0001t0002g0162 a0001c0001t0002g0163 others(2): Show |
5 | HG01891.hp2 HG02280.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.-511-15128A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58016478 | |||||||
| chr8:58016491 | T | A | 1 | a0001c0001t0004g0083 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-511-15115T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58016491 | |||||||
| chr8:58016867 | G | T | 1 | a0001c0001t0001g0088 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-511-14739G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58016867 | |||||||
| chr8:58016897 | G | T | 3 | a0001c0001t0003g0250 a0001c0001t0012g0148 a0001c0001t0012g0150 |
3 | HG01884.hp1 HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-511-14709G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58016897 | |||||||
| chr8:58017074 | G | A | 90 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(87): Show |
90 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.-511-14532G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58017074 | |||||||
| chr8:58017129 | G | A | 173 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(170): Show |
173 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.-511-14477G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58017129 | |||||||
| chr8:58017166 | T | C | 14 | a0001c0001t0002g0147 a0001c0001t0002g0167 a0001c0001t0002g0186 others(11): Show |
14 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-511-14440T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58017166 | |||||||
| chr8:58017230 | C | T | 4 | a0001c0001t0001g0201 a0001c0001t0003g0295 a0001c0001t0007g0004 others(1): Show |
4 | HG01109.hp1 HG01243.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-511-14376C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58017230 | |||||||
| chr8:58017231 | G | A | 13 | a0001c0001t0002g0147 a0001c0001t0002g0167 a0001c0001t0002g0186 others(10): Show |
13 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-511-14375G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58017231 | |||||||
| chr8:58017244 | C | G | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-511-14362C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58017244 | |||||||
| chr8:58017341 | A | G | 90 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(87): Show |
90 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.-511-14265A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58017341 | |||||||
| chr8:58017366 | G | T | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-511-14240G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58017366 | |||||||
| chr8:58017391 | A | C | 6 | a0001c0001t0001g0006 a0001c0001t0002g0012 a0001c0001t0003g0138 others(3): Show |
6 | HG02622.hp1 HG02818.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-511-14215A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58017391 | |||||||
| chr8:58017444 | A | G | 1 | a0001c0001t0003g0198 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-511-14162A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58017444 | |||||||
| chr8:58017624 | T | C | 1 | a0001c0001t0003g0231 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-511-13982T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58017624 | |||||||
| chr8:58017646 | C | G | 8 | a0001c0001t0001g0073 a0001c0001t0001g0158 a0001c0001t0003g0074 others(5): Show |
8 | HG01192.hp1 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-511-13960C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58017646 | |||||||
| chr8:58017945 | G | C | 3 | a0001c0001t0001g0172 a0001c0001t0001g0261 a0001c0001t0001g0262 |
3 | HG01070.hp2 HG01071.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-511-13661G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58017945 | |||||||
| chr8:58018114 | TCAAA | T | 17 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0073 others(14): Show |
17 | HG00738.hp2 HG02080.hp2 HG02165.hp1 others(14): Show |
intron_variant | MODIFIER | c.-511-13487_-511-13 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58018114 | ||||||
| chr8:58018284 | C | T | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-511-13322C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58018284 | |||||||
| chr8:58018288 | C | T | 76 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(73): Show |
76 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.-511-13318C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58018288 | |||||||
| chr8:58018809 | A | AATAG | 78 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0029 others(75): Show |
78 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.-511-12751_-511-12 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58018809 | ||||||
| chr8:58018809 | A | AATAGATA others(1): Show |
14 | a0001c0001t0001g0103 a0001c0001t0002g0001 a0001c0001t0002g0078 others(11): Show |
14 | HG00544.hp1 HG00741.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.-511-12755_-511-12 others(14): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58018809 | ||||||
| chr8:58018809 | AATAG | A | 71 | a0001c0001t0001g0006 a0001c0001t0001g0065 a0001c0001t0001g0067 others(68): Show |
71 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.-511-12751_-511-12 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58018809 | ||||||
| chr8:58018809 | AATAGATA others(1): Show |
A | 6 | a0001c0001t0002g0167 a0001c0001t0003g0141 a0001c0001t0003g0250 others(3): Show |
6 | HG01884.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-511-12755_-511-12 others(14): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58018809 | ||||||
| chr8:58019160 | C | CCCCATCT others(1): Show |
20 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0267 others(17): Show |
20 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.-511-12444_-511-12 others(14): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58019160 | ||||||
| chr8:58019264 | G | A | 6 | a0001c0001t0001g0267 a0001c0001t0002g0136 a0001c0001t0002g0266 others(3): Show |
6 | HG00733.hp1 HG02257.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-511-12342G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58019264 | |||||||
| chr8:58019315 | C | T | 55 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(52): Show |
55 | HG00438.hp1 HG00733.hp1 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.-511-12291C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58019315 | |||||||
| chr8:58019316 | G | A | 4 | a0001c0001t0002g0167 a0001c0001t0004g0010 a0001c0001t0007g0135 others(1): Show |
4 | HG02258.hp1 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-511-12290G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58019316 | |||||||
| chr8:58019336 | CA | C | 14 | a0001c0001t0001g0098 a0001c0001t0001g0158 a0001c0001t0001g0172 others(11): Show |
14 | HG01070.hp2 HG01071.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.-511-12246delA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58019336 | ||||||
| chr8:58019336 | CAA | C | 99 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(96): Show |
99 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.-511-12247_-511-12 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58019336 | ||||||
| chr8:58019336 | CAAA | C | 65 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0017 others(62): Show |
65 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.-511-12248_-511-12 others(9): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58019336 | ||||||
| chr8:58019349 | AAAAAAAA others(6): Show |
A | 7 | a0001c0001t0002g0186 a0001c0001t0003g0129 a0001c0001t0003g0133 others(4): Show |
7 | HG02896.hp1 HG02897.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.-511-12253_-511-12 others(19): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58019349 | ||||||
| chr8:58019354 | AAAAAAAG others(1): Show |
A | 8 | a0001c0001t0001g0006 a0001c0001t0002g0012 a0001c0001t0003g0138 others(5): Show |
8 | HG02622.hp1 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-511-12248_-511-12 others(14): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58019354 | ||||||
| chr8:58019355 | AAAAAAGG | A | 48 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0089 others(45): Show |
48 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.-511-12247_-511-12 others(13): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58019355 | ||||||
| chr8:58019356 | AAAAAGG | A | 15 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0002g0082 others(12): Show |
15 | HG00738.hp2 HG02129.hp2 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.-511-12246_-511-12 others(12): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58019356 | ||||||
| chr8:58019361 | G | A | 2 | a0001c0001t0003g0198 a0001c0001t0007g0300 |
2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-511-12245G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58019361 | |||||||
| chr8:58019362 | G | A | 2 | a0001c0001t0003g0198 a0001c0001t0007g0300 |
2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-511-12244G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58019362 | |||||||
| chr8:58019365 | A | G | 86 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(83): Show |
86 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.-511-12241A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58019365 | |||||||
| chr8:58019366 | G | A | 2 | a0001c0001t0007g0135 a0002c0002t0016g0166 |
2 | HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-511-12240G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58019366 | |||||||
| chr8:58019369 | A | G | 2 | a0001c0001t0007g0135 a0002c0002t0016g0166 |
2 | HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-511-12237A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58019369 | |||||||
| chr8:58019502 | T | C | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-511-12104T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58019502 | |||||||
| chr8:58019566 | A | C | 6 | a0001c0001t0001g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(3): Show |
6 | HG01884.hp1 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-511-12040A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58019566 | |||||||
| chr8:58019602 | G | A | 3 | a0001c0001t0001g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 |
3 | HG02486.hp2 HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-511-12004G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58019602 | |||||||
| chr8:58019619 | A | G | 3 | a0001c0001t0001g0027 a0001c0001t0001g0094 a0001c0001t0004g0026 |
3 | HG01192.hp2 HG01993.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-511-11987A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58019619 | |||||||
| chr8:58019728 | A | C | 270 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(267): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.-511-11878A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58019728 | |||||||
| chr8:58019987 | C | A | 3 | a0001c0001t0002g0167 a0001c0001t0007g0135 a0002c0002t0016g0166 |
3 | HG02258.hp1 HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-511-11619C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58019987 | |||||||
| chr8:58020065 | A | G | 1 | a0001c0001t0003g0055 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-511-11541A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58020065 | |||||||
| chr8:58020183 | C | T | 1 | a0001c0001t0005g0019 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-511-11423C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58020183 | |||||||
| chr8:58020213 | C | T | 3 | a0001c0001t0002g0167 a0001c0001t0007g0135 a0002c0002t0016g0166 |
3 | HG02258.hp1 HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-511-11393C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58020213 | |||||||
| chr8:58020394 | A | C | 2 | a0001c0001t0007g0090 a0001c0001t0024g0176 |
2 | HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-511-11212A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58020394 | |||||||
| chr8:58020606 | A | G | 1 | a0001c0001t0007g0144 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-511-11000A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58020606 | |||||||
| chr8:58020677 | A | T | 2 | a0001c0001t0007g0090 a0001c0001t0024g0176 |
2 | HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-511-10929A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58020677 | |||||||
| chr8:58020817 | A | T | 1 | a0001c0001t0003g0071 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-511-10789A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58020817 | |||||||
| chr8:58020866 | G | A | 2 | a0001c0001t0001g0211 a0001c0001t0003g0206 |
2 | HG00408.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-511-10740G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58020866 | |||||||
| chr8:58020908 | C | CA | 101 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(98): Show |
101 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(98): Show |
intron_variant | MODIFIER | c.-511-10698_-511-10 others(7): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58020908 | |||||||
| chr8:58020960 | C | T | 1 | a0001c0001t0002g0050 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-511-10646C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58020960 | |||||||
| chr8:58021040 | G | C | 1 | a0001c0001t0002g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-511-10566G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58021040 | |||||||
| chr8:58021061 | G | T | 2 | a0001c0001t0001g0054 a0001c0001t0021g0248 |
2 | HG00099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.-511-10545G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58021061 | |||||||
| chr8:58021164 | C | T | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-511-10442C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58021164 | |||||||
| chr8:58021292 | T | C | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-511-10314T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58021292 | |||||||
| chr8:58021469 | G | A | 6 | a0001c0001t0001g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(3): Show |
6 | HG01884.hp1 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-511-10137G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58021469 | |||||||
| chr8:58021488 | T | C | 2 | a0001c0001t0001g0115 a0001c0001t0003g0156 |
2 | HG00323.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-511-10118T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58021488 | |||||||
| chr8:58021902 | A | G | 78 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(75): Show |
78 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.-511-9704A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58021902 | |||||||
| chr8:58021959 | T | C | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-511-9647T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58021959 | |||||||
| chr8:58022004 | G | A | 3 | a0001c0001t0001g0002 a0001c0001t0002g0016 a0001c0001t0002g0153 |
3 | HG00741.hp2 HG01168.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.-511-9602G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58022004 | |||||||
| chr8:58022143 | A | G | 1 | a0001c0001t0002g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-511-9463A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58022143 | |||||||
| chr8:58022406 | G | A | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-511-9200G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58022406 | |||||||
| chr8:58022499 | T | C | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-511-9107T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58022499 | |||||||
| chr8:58022511 | A | G | 2 | a0001c0001t0007g0090 a0001c0001t0024g0176 |
2 | HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-511-9095A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58022511 | |||||||
| chr8:58022743 | G | C | 1 | a0001c0001t0003g0122 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-511-8863G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58022743 | |||||||
| chr8:58023171 | AATTTTT | A | 90 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(87): Show |
90 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.-511-8416_-511-841 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58023171 | ||||||
| chr8:58023383 | C | T | 6 | a0001c0001t0001g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(3): Show |
6 | HG01884.hp1 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-511-8223C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58023383 | |||||||
| chr8:58023512 | C | T | 77 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(74): Show |
77 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.-511-8094C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58023512 | |||||||
| chr8:58023542 | C | T | 1 | a0001c0001t0002g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-511-8064C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58023542 | |||||||
| chr8:58023620 | A | C | 77 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(74): Show |
77 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.-511-7986A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58023620 | |||||||
| chr8:58024158 | A | C | 8 | a0001c0001t0002g0011 a0001c0001t0002g0087 a0001c0001t0002g0273 others(5): Show |
8 | HG01928.hp2 HG01978.hp2 HG03834.hp1 others(5): Show |
intron_variant | MODIFIER | c.-511-7448A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58024158 | |||||||
| chr8:58024172 | C | CTTTTT | 64 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0084 others(61): Show |
64 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.-511-7423_-511-741 others(9): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58024172 | ||||||
| chr8:58024172 | C | CTTTTTT | 25 | a0001c0001t0001g0006 a0001c0001t0001g0158 a0001c0001t0002g0082 others(22): Show |
25 | HG01069.hp1 HG01261.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.-511-7424_-511-741 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58024172 | ||||||
| chr8:58024209 | G | A | 14 | a0001c0001t0002g0147 a0001c0001t0002g0167 a0001c0001t0002g0186 others(11): Show |
14 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-511-7397G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58024209 | |||||||
| chr8:58024700 | T | C | 10 | a0001c0001t0001g0006 a0001c0001t0001g0158 a0001c0001t0002g0012 others(7): Show |
10 | HG02622.hp1 HG02818.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.-511-6906T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58024700 | |||||||
| chr8:58024830 | G | T | 1 | a0001c0001t0002g0240 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-511-6776G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58024830 | |||||||
| chr8:58024882 | T | C | 2 | a0001c0001t0003g0198 a0001c0001t0007g0300 |
2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-511-6724T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58024882 | |||||||
| chr8:58024910 | A | G | 1 | a0001c0001t0007g0135 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-511-6696A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58024910 | |||||||
| chr8:58024966 | G | T | 8 | a0001c0001t0002g0186 a0001c0001t0003g0129 a0001c0001t0003g0133 others(5): Show |
8 | HG01069.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-511-6640G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58024966 | |||||||
| chr8:58024979 | C | G | 4 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0003g0005 others(1): Show |
4 | HG02145.hp1 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-511-6627C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58024979 | |||||||
| chr8:58025191 | T | C | 270 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(267): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.-511-6415T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58025191 | |||||||
| chr8:58025205 | A | G | 5 | a0001c0001t0002g0082 a0001c0001t0002g0162 a0001c0001t0002g0163 others(2): Show |
5 | HG01891.hp2 HG02280.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.-511-6401A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58025205 | |||||||
| chr8:58025329 | GAC | G | 9 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0104 others(6): Show |
9 | HG00438.hp2 HG00621.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.-511-6275_-511-627 others(6): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58025329 | ||||||
| chr8:58025331 | CAG | C | 3 | a0001c0001t0014g0242 a0001c0001t0014g0243 a0001c0001t0017g0119 |
3 | HG00609.hp2 NA19060.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-511-6274_-511-627 others(6): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58025331 | |||||||
| chr8:58025333 | G | T | 9 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0104 others(6): Show |
9 | HG00438.hp2 HG00621.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.-511-6273G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58025333 | |||||||
| chr8:58025366 | A | C | 1 | a0001c0001t0008g0170 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-511-6240A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58025366 | |||||||
| chr8:58025492 | C | A | 8 | a0001c0001t0002g0186 a0001c0001t0003g0129 a0001c0001t0003g0133 others(5): Show |
8 | HG01069.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-511-6114C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58025492 | |||||||
| chr8:58025583 | C | G | 14 | a0001c0001t0002g0147 a0001c0001t0002g0167 a0001c0001t0002g0186 others(11): Show |
14 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-511-6023C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58025583 | |||||||
| chr8:58025615 | G | A | 13 | a0001c0001t0002g0147 a0001c0001t0002g0167 a0001c0001t0002g0186 others(10): Show |
13 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-511-5991G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58025615 | |||||||
| chr8:58025710 | C | T | 2 | a0001c0001t0013g0183 a0001c0001t0028g0182 |
2 | NA18989.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.-511-5896C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58025710 | |||||||
| chr8:58025757 | T | G | 1 | a0001c0001t0010g0175 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-511-5849T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58025757 | |||||||
| chr8:58025782 | C | T | 13 | a0001c0001t0002g0147 a0001c0001t0002g0167 a0001c0001t0002g0186 others(10): Show |
13 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-511-5824C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58025782 | |||||||
| chr8:58025832 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-511-5774T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58025832 | |||||||
| chr8:58026112 | G | A | 9 | a0001c0001t0001g0006 a0001c0001t0002g0012 a0001c0001t0003g0138 others(6): Show |
9 | HG02622.hp1 HG02818.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-511-5494G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58026112 | |||||||
| chr8:58026223 | G | A | 76 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(73): Show |
76 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.-511-5383G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58026223 | |||||||
| chr8:58026286 | C | T | 1 | a0003c0003t0003g0264 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-511-5320C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58026286 | |||||||
| chr8:58026705 | C | T | 8 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0293 others(5): Show |
8 | HG01496.hp2 HG02027.hp1 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.-511-4901C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58026705 | |||||||
| chr8:58026894 | T | C | 1 | a0001c0001t0006g0246 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-511-4712T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58026894 | |||||||
| chr8:58026984 | T | TCTTGGAA | 91 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(88): Show |
91 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(88): Show |
intron_variant | MODIFIER | c.-511-4619_-511-461 others(11): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58026984 | ||||||
| chr8:58027102 | C | T | 77 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(74): Show |
77 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.-511-4504C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58027102 | |||||||
| chr8:58027240 | T | C | 20 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0002g0082 others(17): Show |
20 | HG00738.hp2 HG01891.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.-511-4366T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58027240 | |||||||
| chr8:58027423 | GT | G | 90 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(87): Show |
90 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.-511-4171delT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58027423 | ||||||
| chr8:58027509 | C | T | 1 | a0001c0001t0004g0232 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-511-4097C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58027509 | |||||||
| chr8:58027525 | A | T | 1 | a0001c0001t0003g0074 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-511-4081A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58027525 | |||||||
| chr8:58027739 | C | T | 1 | a0001c0001t0003g0106 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-511-3867C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58027739 | |||||||
| chr8:58027755 | G | A | 92 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(89): Show |
92 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.-511-3851G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58027755 | |||||||
| chr8:58027831 | G | T | 91 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(88): Show |
91 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(88): Show |
intron_variant | MODIFIER | c.-511-3775G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58027831 | |||||||
| chr8:58027993 | C | T | 91 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(88): Show |
91 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(88): Show |
intron_variant | MODIFIER | c.-511-3613C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58027993 | |||||||
| chr8:58028104 | C | T | 14 | a0001c0001t0002g0147 a0001c0001t0002g0167 a0001c0001t0002g0186 others(11): Show |
14 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-511-3502C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58028104 | |||||||
| chr8:58028244 | C | G | 8 | a0001c0001t0001g0073 a0001c0001t0003g0005 a0001c0001t0003g0074 others(5): Show |
8 | HG01192.hp1 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-511-3362C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58028244 | |||||||
| chr8:58028260 | C | T | 77 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(74): Show |
77 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.-511-3346C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58028260 | |||||||
| chr8:58028303 | C | T | 77 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(74): Show |
77 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.-511-3303C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58028303 | |||||||
| chr8:58028385 | C | T | 7 | a0001c0001t0001g0073 a0001c0001t0003g0005 a0001c0001t0003g0074 others(4): Show |
7 | HG01884.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-511-3221C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58028385 | |||||||
| chr8:58028571 | A | G | 1 | a0001c0001t0034g0244 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-511-3035A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58028571 | |||||||
| chr8:58028582 | T | C | 77 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(74): Show |
77 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.-511-3024T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58028582 | |||||||
| chr8:58028583 | T | C | 1 | a0001c0001t0002g0263 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-511-3023T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58028583 | |||||||
| chr8:58028644 | G | T | 1 | a0002c0002t0016g0166 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-511-2962G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58028644 | |||||||
| chr8:58028661 | T | C | 3 | a0001c0001t0001g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 |
3 | HG02486.hp2 HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-511-2945T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58028661 | |||||||
| chr8:58028737 | G | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0004g0014 |
3 | HG00738.hp2 NA20129.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-511-2869G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58028737 | |||||||
| chr8:58028755 | G | A | 1 | a0001c0001t0003g0229 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-511-2851G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58028755 | |||||||
| chr8:58028904 | C | T | 72 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0017 others(69): Show |
72 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.-511-2702C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58028904 | |||||||
| chr8:58029243 | G | T | 77 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(74): Show |
77 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.-511-2363G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58029243 | |||||||
| chr8:58029259 | A | C | 1 | a0001c0001t0001g0158 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-511-2347A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58029259 | |||||||
| chr8:58029328 | A | G | 1 | a0001c0001t0002g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-511-2278A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58029328 | |||||||
| chr8:58029451 | G | A | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-511-2155G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58029451 | |||||||
| chr8:58029538 | A | AT | 6 | a0001c0001t0001g0158 a0001c0001t0002g0293 a0001c0001t0003g0075 others(3): Show |
6 | HG00733.hp2 HG01243.hp1 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.-511-2058dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58029538 | ||||||
| chr8:58029538 | ATT | A | 8 | a0001c0001t0002g0186 a0001c0001t0003g0129 a0001c0001t0003g0133 others(5): Show |
8 | HG01069.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-511-2059_-511-205 others(6): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58029538 | ||||||
| chr8:58029562 | A | G | 14 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0002g0178 others(11): Show |
14 | HG00738.hp2 HG02080.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.-511-2044A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58029562 | |||||||
| chr8:58029588 | G | C | 2 | a0001c0001t0014g0242 a0001c0001t0014g0243 |
2 | HG00609.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-511-2018G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58029588 | |||||||
| chr8:58029673 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-511-1933A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58029673 | |||||||
| chr8:58029750 | A | T | 72 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0017 others(69): Show |
72 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.-511-1856A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58029750 | |||||||
| chr8:58029910 | A | C | 13 | a0001c0001t0002g0167 a0001c0001t0002g0186 a0001c0001t0003g0129 others(10): Show |
13 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-511-1696A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58029910 | |||||||
| chr8:58030034 | A | G | 14 | a0001c0001t0002g0147 a0001c0001t0002g0167 a0001c0001t0002g0186 others(11): Show |
14 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-511-1572A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58030034 | |||||||
| chr8:58030180 | G | T | 269 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(266): Show |
269 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.-511-1426G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58030180 | |||||||
| chr8:58030194 | A | G | 1 | a0001c0001t0003g0231 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-511-1412A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58030194 | |||||||
| chr8:58030261 | G | A | 91 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(88): Show |
91 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(88): Show |
intron_variant | MODIFIER | c.-511-1345G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58030261 | |||||||
| chr8:58030266 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0002g0012 |
2 | HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-511-1340G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58030266 | |||||||
| chr8:58030431 | A | G | 13 | a0001c0001t0002g0167 a0001c0001t0002g0186 a0001c0001t0003g0129 others(10): Show |
13 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-511-1175A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58030431 | |||||||
| chr8:58030479 | A | C | 1 | a0001c0001t0003g0108 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-511-1127A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58030479 | |||||||
| chr8:58030546 | GGCATAGA others(7): Show |
G | 78 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(75): Show |
78 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.-511-1058_-511-104 others(18): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58030546 | ||||||
| chr8:58030675 | A | C | 1 | a0001c0001t0003g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-511-931A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58030675 | |||||||
| chr8:58030791 | C | T | 14 | a0001c0001t0002g0147 a0001c0001t0002g0167 a0001c0001t0002g0186 others(11): Show |
14 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-511-815C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58030791 | |||||||
| chr8:58031045 | T | C | 2 | a0001c0001t0001g0226 a0001c0001t0005g0188 |
2 | HG00609.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-511-561T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58031045 | |||||||
| chr8:58031353 | A | C | 92 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(89): Show |
92 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.-511-253A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58031353 | |||||||
| chr8:58031451 | T | C | 1 | a0001c0001t0003g0295 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-511-155T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58031451 | |||||||
| chr8:58031484 | T | C | 92 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(89): Show |
92 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.-511-122T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58031484 | |||||||
| chr8:58031741 | G | A | 93 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(90): Show |
93 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(90): Show |
intron_variant | MODIFIER | c.-414+38G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58031741 | |||||||
| chr8:58031831 | C | G | 14 | a0001c0001t0002g0147 a0001c0001t0002g0167 a0001c0001t0002g0186 others(11): Show |
14 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-414+128C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58031831 | |||||||
| chr8:58032112 | C | T | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-414+409C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032112 | |||||||
| chr8:58032118 | C | T | 5 | a0001c0001t0002g0082 a0001c0001t0002g0162 a0001c0001t0002g0163 others(2): Show |
5 | HG01891.hp2 HG02280.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.-414+415C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032118 | |||||||
| chr8:58032130 | T | G | 5 | a0001c0001t0003g0129 a0001c0001t0003g0134 a0001c0001t0003g0164 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-414+427T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032130 | |||||||
| chr8:58032132 | C | T | 7 | a0001c0001t0002g0082 a0001c0001t0002g0162 a0001c0001t0002g0163 others(4): Show |
7 | HG01891.hp2 HG02280.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-414+429C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032132 | |||||||
| chr8:58032133 | G | A | 8 | a0001c0001t0002g0186 a0001c0001t0003g0129 a0001c0001t0003g0133 others(5): Show |
8 | HG01069.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-414+430G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032133 | |||||||
| chr8:58032305 | A | G | 8 | a0001c0001t0002g0186 a0001c0001t0003g0129 a0001c0001t0003g0133 others(5): Show |
8 | HG01069.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-414+602A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032305 | |||||||
| chr8:58032374 | G | T | 6 | a0001c0001t0001g0267 a0001c0001t0002g0136 a0001c0001t0002g0266 others(3): Show |
6 | HG00733.hp1 HG02257.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-414+671G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032374 | |||||||
| chr8:58032436 | T | G | 3 | a0001c0001t0002g0167 a0001c0001t0007g0135 a0002c0002t0016g0166 |
3 | HG02258.hp1 HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-414+733T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032436 | |||||||
| chr8:58032472 | C | T | 14 | a0001c0001t0002g0147 a0001c0001t0002g0167 a0001c0001t0002g0186 others(11): Show |
14 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-414+769C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032472 | |||||||
| chr8:58032487 | C | G | 14 | a0001c0001t0002g0147 a0001c0001t0002g0167 a0001c0001t0002g0186 others(11): Show |
14 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-414+784C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032487 | |||||||
| chr8:58032508 | C | G | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-414+805C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032508 | |||||||
| chr8:58032533 | C | A | 6 | a0001c0001t0001g0267 a0001c0001t0002g0136 a0001c0001t0002g0266 others(3): Show |
6 | HG00733.hp1 HG02257.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-414+830C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032533 | |||||||
| chr8:58032615 | G | A | 14 | a0001c0001t0002g0147 a0001c0001t0002g0167 a0001c0001t0002g0186 others(11): Show |
14 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-414+912G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032615 | |||||||
| chr8:58032664 | C | T | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-414+961C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032664 | |||||||
| chr8:58032841 | A | C | 5 | a0001c0001t0003g0080 a0001c0001t0009g0179 a0001c0001t0009g0199 others(2): Show |
5 | HG02080.hp2 NA18959.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.-414+1138A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032841 | |||||||
| chr8:58032878 | G | T | 7 | a0001c0001t0001g0073 a0001c0001t0003g0005 a0001c0001t0003g0074 others(4): Show |
7 | HG01884.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-414+1175G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032878 | |||||||
| chr8:58032937 | A | G | 74 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0043 others(71): Show |
74 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.-414+1234A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032937 | |||||||
| chr8:58033148 | G | A | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-414+1445G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58033148 | |||||||
| chr8:58033193 | G | A | 3 | a0001c0001t0002g0167 a0001c0001t0007g0135 a0002c0002t0016g0166 |
3 | HG02258.hp1 HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-414+1490G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58033193 | |||||||
| chr8:58033225 | C | T | 14 | a0001c0001t0002g0147 a0001c0001t0002g0167 a0001c0001t0002g0186 others(11): Show |
14 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-414+1522C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58033225 | |||||||
| chr8:58033291 | C | T | 70 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0043 others(67): Show |
70 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.-414+1588C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58033291 | |||||||
| chr8:58033418 | A | G | 1 | a0001c0001t0003g0229 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-414+1715A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58033418 | |||||||
| chr8:58033586 | C | T | 12 | a0001c0001t0001g0006 a0001c0001t0001g0158 a0001c0001t0002g0012 others(9): Show |
12 | HG01884.hp2 HG02622.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.-414+1883C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58033586 | |||||||
| chr8:58033587 | G | A | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-414+1884G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58033587 | |||||||
| chr8:58033666 | C | T | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-414+1963C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58033666 | |||||||
| chr8:58033688 | A | G | 100 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(97): Show |
100 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(97): Show |
intron_variant | MODIFIER | c.-414+1985A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58033688 | |||||||
| chr8:58033755 | TA | T | 10 | a0001c0001t0001g0253 a0001c0001t0001g0258 a0001c0001t0001g0267 others(7): Show |
10 | HG00438.hp2 HG00621.hp1 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.-414+2061delA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58033755 | ||||||
| chr8:58033833 | C | T | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-414+2130C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58033833 | |||||||
| chr8:58033851 | C | T | 74 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0017 others(71): Show |
74 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.-414+2148C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58033851 | |||||||
| chr8:58033911 | A | C | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-414+2208A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58033911 | |||||||
| chr8:58034091 | G | A | 44 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0089 others(41): Show |
44 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.-414+2388G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58034091 | |||||||
| chr8:58034125 | T | C | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-414+2422T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58034125 | |||||||
| chr8:58034132 | C | T | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-414+2429C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58034132 | |||||||
| chr8:58034143 | G | A | 3 | a0001c0001t0002g0167 a0001c0001t0007g0135 a0002c0002t0016g0166 |
3 | HG02258.hp1 HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-414+2440G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58034143 | |||||||
| chr8:58034249 | G | C | 1 | a0001c0001t0001g0038 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-414+2546G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58034249 | |||||||
| chr8:58034507 | A | T | 1 | a0001c0001t0002g0192 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-414+2804A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58034507 | |||||||
| chr8:58034584 | A | G | 1 | a0001c0001t0003g0204 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-414+2881A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58034584 | |||||||
| chr8:58034651 | G | T | 2 | a0001c0001t0002g0126 a0001c0001t0004g0125 |
2 | HG00280.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-414+2948G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58034651 | |||||||
| chr8:58034804 | G | C | 1 | a0001c0001t0002g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-414+3101G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58034804 | |||||||
| chr8:58034930 | T | C | 99 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(96): Show |
99 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(96): Show |
intron_variant | MODIFIER | c.-414+3227T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58034930 | |||||||
| chr8:58034959 | A | C | 19 | a0001c0001t0001g0006 a0001c0001t0001g0073 a0001c0001t0001g0158 others(16): Show |
19 | HG01884.hp1 HG01884.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.-414+3256A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58034959 | |||||||
| chr8:58034970 | C | T | 84 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(81): Show |
84 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(81): Show |
intron_variant | MODIFIER | c.-414+3267C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58034970 | |||||||
| chr8:58035191 | T | C | 1 | a0001c0001t0002g0193 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-414+3488T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58035191 | |||||||
| chr8:58035293 | G | A | 5 | a0001c0001t0001g0103 a0001c0001t0001g0230 a0001c0001t0003g0096 others(2): Show |
5 | HG00544.hp1 HG02027.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.-414+3590G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58035293 | |||||||
| chr8:58035344 | G | A | 7 | a0001c0001t0001g0073 a0001c0001t0003g0005 a0001c0001t0003g0074 others(4): Show |
7 | HG01884.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-414+3641G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58035344 | |||||||
| chr8:58035363 | A | G | 2 | a0001c0001t0003g0198 a0001c0001t0007g0300 |
2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-414+3660A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58035363 | |||||||
| chr8:58035394 | C | T | 1 | a0001c0001t0005g0196 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-414+3691C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58035394 | |||||||
| chr8:58035461 | T | C | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-414+3758T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58035461 | |||||||
| chr8:58035606 | G | A | 1 | a0001c0001t0030g0035 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-414+3903G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58035606 | |||||||
| chr8:58035624 | A | T | 89 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0043 others(86): Show |
89 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.-414+3921A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58035624 | |||||||
| chr8:58035771 | T | C | 45 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0089 others(42): Show |
45 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.-414+4068T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58035771 | |||||||
| chr8:58035996 | G | A | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-414+4293G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58035996 | |||||||
| chr8:58036063 | G | C | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-414+4360G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58036063 | |||||||
| chr8:58036395 | C | T | 4 | a0001c0001t0001g0203 a0001c0001t0001g0208 a0001c0001t0001g0209 others(1): Show |
4 | NA18960.hp2 NA18979.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.-414+4692C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58036395 | |||||||
| chr8:58036680 | C | T | 1 | a0001c0001t0009g0064 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-414+4977C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58036680 | |||||||
| chr8:58036707 | A | G | 92 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(89): Show |
92 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.-414+5004A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58036707 | |||||||
| chr8:58036954 | C | T | 7 | a0001c0001t0001g0038 a0001c0001t0002g0030 a0001c0001t0002g0032 others(4): Show |
7 | HG00642.hp1 HG01074.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.-414+5251C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58036954 | |||||||
| chr8:58037079 | A | G | 44 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0226 others(41): Show |
44 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.-414+5376A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037079 | |||||||
| chr8:58037132 | A | AT | 92 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(89): Show |
92 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.-414+5438dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58037132 | ||||||
| chr8:58037288 | C | G | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-414+5585C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037288 | |||||||
| chr8:58037306 | G | GGTTT | 91 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(88): Show |
91 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(88): Show |
intron_variant | MODIFIER | c.-414+5624_-414+562 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58037306 | ||||||
| chr8:58037306 | GGTTT | G | 7 | a0001c0001t0002g0146 a0001c0001t0002g0152 a0001c0001t0003g0151 others(4): Show |
7 | HG02257.hp1 HG02615.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-414+5624_-414+562 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58037306 | ||||||
| chr8:58037331 | T | G | 95 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0043 others(92): Show |
95 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.-414+5628T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037331 | |||||||
| chr8:58037344 | G | A | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-414+5641G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037344 | |||||||
| chr8:58037372 | G | A | 2 | a0001c0001t0002g0024 a0001c0001t0003g0280 |
2 | HG00621.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.-414+5669G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037372 | |||||||
| chr8:58037471 | C | CA | 46 | a0001c0001t0001g0022 a0001c0001t0001g0084 a0001c0001t0001g0088 others(43): Show |
46 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.-414+5779dupA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58037471 | ||||||
| chr8:58037473 | A | C | 1 | a0001c0001t0003g0288 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-414+5770A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037473 | |||||||
| chr8:58037479 | A | T | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-414+5776A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037479 | |||||||
| chr8:58037483 | T | A | 92 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(89): Show |
92 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.-414+5780T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037483 | |||||||
| chr8:58037510 | C | T | 74 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0017 others(71): Show |
74 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.-414+5807C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037510 | |||||||
| chr8:58037519 | C | T | 1 | a0001c0001t0002g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-414+5816C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037519 | |||||||
| chr8:58037711 | T | G | 4 | a0001c0001t0002g0162 a0001c0001t0002g0163 a0001c0001t0007g0130 others(1): Show |
4 | HG01891.hp2 HG02280.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-414+6008T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037711 | |||||||
| chr8:58037821 | C | A | 1 | a0001c0001t0007g0135 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-414+6118C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037821 | |||||||
| chr8:58037821 | C | T | 1 | a0001c0001t0002g0117 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-414+6118C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037821 | |||||||
| chr8:58037858 | G | A | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-414+6155G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037858 | |||||||
| chr8:58037871 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0029 |
2 | NA18993.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-414+6168A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037871 | |||||||
| chr8:58037902 | A | G | 92 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(89): Show |
92 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.-414+6199A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037902 | |||||||
| chr8:58038151 | T | C | 1 | a0001c0001t0004g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-414+6448T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58038151 | |||||||
| chr8:58038162 | A | G | 2 | a0001c0001t0001g0211 a0001c0001t0003g0206 |
2 | HG00408.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-414+6459A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58038162 | |||||||
| chr8:58038212 | T | C | 3 | a0001c0001t0001g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 |
3 | HG02486.hp2 HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-414+6509T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58038212 | |||||||
| chr8:58038305 | A | G | 92 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(89): Show |
92 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.-414+6602A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58038305 | |||||||
| chr8:58038596 | G | A | 6 | a0001c0001t0001g0084 a0001c0001t0002g0167 a0001c0001t0003g0198 others(3): Show |
6 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-414+6893G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58038596 | |||||||
| chr8:58038606 | G | A | 1 | a0001c0001t0002g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-414+6903G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58038606 | |||||||
| chr8:58038706 | C | T | 1 | a0002c0002t0016g0166 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-414+7003C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58038706 | |||||||
| chr8:58038755 | C | CA | 47 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(44): Show |
47 | HG00642.hp2 HG00738.hp2 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.-414+7065dupA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58038755 | ||||||
| chr8:58038782 | A | G | 1 | a0001c0001t0008g0169 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-414+7079A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58038782 | |||||||
| chr8:58038970 | C | T | 1 | a0003c0003t0003g0264 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-414+7267C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58038970 | |||||||
| chr8:58039174 | G | A | 1 | a0001c0001t0005g0188 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-414+7471G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58039174 | |||||||
| chr8:58039182 | T | A | 2 | a0001c0001t0002g0112 a0001c0001t0017g0119 |
2 | NA18952.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-414+7479T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58039182 | |||||||
| chr8:58039185 | C | T | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-414+7482C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58039185 | |||||||
| chr8:58039188 | G | T | 5 | a0001c0001t0002g0167 a0001c0001t0003g0198 a0001c0001t0007g0135 others(2): Show |
5 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-414+7485G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58039188 | |||||||
| chr8:58039359 | C | T | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-414+7656C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58039359 | |||||||
| chr8:58039532 | A | T | 50 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0089 others(47): Show |
50 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.-414+7829A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58039532 | |||||||
| chr8:58039670 | T | C | 92 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(89): Show |
92 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.-414+7967T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58039670 | |||||||
| chr8:58039833 | A | G | 1 | a0001c0001t0005g0019 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-414+8130A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58039833 | |||||||
| chr8:58039973 | T | A | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-414+8270T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58039973 | |||||||
| chr8:58039975 | A | G | 1 | a0001c0001t0005g0274 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-414+8272A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58039975 | |||||||
| chr8:58040009 | T | TA | 75 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0017 others(72): Show |
75 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.-414+8313dupA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58040009 | ||||||
| chr8:58040089 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-414+8386C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58040089 | |||||||
| chr8:58040164 | A | C | 48 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0089 others(45): Show |
48 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.-414+8461A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58040164 | |||||||
| chr8:58040232 | C | T | 14 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0002g0178 others(11): Show |
14 | HG00738.hp2 HG02080.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.-414+8529C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58040232 | |||||||
| chr8:58040366 | T | C | 51 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0089 others(48): Show |
51 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.-414+8663T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58040366 | |||||||
| chr8:58040367 | A | G | 263 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(260): Show |
263 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.-414+8664A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58040367 | |||||||
| chr8:58040549 | C | T | 1 | a0001c0001t0003g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-414+8846C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58040549 | |||||||
| chr8:58040569 | A | G | 70 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(67): Show |
70 | HG00733.hp1 HG00738.hp2 HG01099.hp1 others(67): Show |
intron_variant | MODIFIER | c.-414+8866A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58040569 | |||||||
| chr8:58040748 | A | G | 44 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0226 others(41): Show |
44 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.-414+9045A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58040748 | |||||||
| chr8:58040766 | T | TA | 7 | a0001c0001t0001g0073 a0001c0001t0003g0005 a0001c0001t0003g0074 others(4): Show |
7 | HG01884.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-414+9071dupA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58040766 | ||||||
| chr8:58040767 | A | T | 149 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0040 others(146): Show |
149 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.-414+9064A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58040767 | |||||||
| chr8:58040935 | C | CT | 89 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0042 others(86): Show |
89 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.-414+9255dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58040935 | ||||||
| chr8:58040935 | C | CTT | 7 | a0001c0001t0001g0104 a0001c0001t0001g0252 a0001c0001t0001g0258 others(4): Show |
7 | HG00438.hp2 HG02004.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.-414+9254_-414+925 others(6): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58040935 | ||||||
| chr8:58040935 | CT | C | 33 | a0001c0001t0001g0006 a0001c0001t0001g0073 a0001c0001t0001g0158 others(30): Show |
33 | HG01069.hp1 HG01099.hp2 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.-414+9255delT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58040935 | ||||||
| chr8:58040935 | CTT | C | 21 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0002g0082 others(18): Show |
21 | HG00738.hp2 HG01891.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.-414+9254_-414+925 others(6): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58040935 | ||||||
| chr8:58040935 | CTTTT | C | 46 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0089 others(43): Show |
46 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.-414+9252_-414+925 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58040935 | ||||||
| chr8:58041184 | C | T | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-414+9481C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58041184 | |||||||
| chr8:58041229 | C | T | 5 | a0001c0001t0002g0082 a0001c0001t0002g0162 a0001c0001t0002g0163 others(2): Show |
5 | HG01891.hp2 HG02280.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.-414+9526C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58041229 | |||||||
| chr8:58041320 | C | T | 48 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0089 others(45): Show |
48 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.-414+9617C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58041320 | |||||||
| chr8:58041365 | G | A | 5 | a0001c0001t0002g0082 a0001c0001t0002g0162 a0001c0001t0002g0163 others(2): Show |
5 | HG01891.hp2 HG02280.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.-414+9662G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58041365 | |||||||
| chr8:58041420 | T | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0017 others(71): Show |
74 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.-414+9717T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58041420 | |||||||
| chr8:58041448 | A | G | 1 | a0001c0001t0003g0204 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-414+9745A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58041448 | |||||||
| chr8:58041455 | G | A | 92 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(89): Show |
92 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.-414+9752G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58041455 | |||||||
| chr8:58041650 | A | G | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-414+9947A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58041650 | |||||||
| chr8:58041662 | T | G | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-414+9959T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58041662 | |||||||
| chr8:58041782 | T | G | 15 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0002g0178 others(12): Show |
15 | HG00738.hp2 HG02080.hp2 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.-414+10079T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58041782 | |||||||
| chr8:58042054 | T | C | 2 | a0001c0001t0003g0138 a0001c0001t0003g0141 |
2 | HG02622.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-414+10351T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58042054 | |||||||
| chr8:58042055 | A | T | 51 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0089 others(48): Show |
51 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.-414+10352A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58042055 | |||||||
| chr8:58042098 | G | T | 3 | a0001c0001t0002g0128 a0001c0001t0003g0143 a0001c0001t0007g0144 |
3 | HG03130.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-414+10395G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58042098 | |||||||
| chr8:58042104 | G | A | 92 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(89): Show |
92 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.-414+10401G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58042104 | |||||||
| chr8:58042354 | G | A | 5 | a0001c0001t0002g0082 a0001c0001t0002g0162 a0001c0001t0002g0163 others(2): Show |
5 | HG01891.hp2 HG02280.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.-414+10651G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58042354 | |||||||
| chr8:58042365 | G | A | 2 | a0001c0001t0007g0090 a0001c0001t0024g0176 |
2 | HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-414+10662G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58042365 | |||||||
| chr8:58042544 | A | G | 51 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0089 others(48): Show |
51 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.-414+10841A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58042544 | |||||||
| chr8:58042652 | A | G | 7 | a0001c0001t0001g0073 a0001c0001t0003g0005 a0001c0001t0003g0074 others(4): Show |
7 | HG01884.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-414+10949A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58042652 | |||||||
| chr8:58042903 | C | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | NA18953.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.-414+11200C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58042903 | |||||||
| chr8:58042978 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0004g0014 |
2 | HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-414+11275G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58042978 | |||||||
| chr8:58043090 | G | T | 14 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0104 others(11): Show |
14 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.-414+11387G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58043090 | |||||||
| chr8:58043100 | C | T | 1 | a0001c0001t0004g0232 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-414+11397C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58043100 | |||||||
| chr8:58043409 | T | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(161): Show |
164 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.-414+11706T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58043409 | |||||||
| chr8:58043512 | A | G | 15 | a0001c0001t0001g0073 a0001c0001t0002g0146 a0001c0001t0002g0152 others(12): Show |
15 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-414+11809A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58043512 | |||||||
| chr8:58043579 | G | C | 107 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(104): Show |
107 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-414+11876G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58043579 | |||||||
| chr8:58043738 | G | A | 26 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0060 others(23): Show |
26 | HG00597.hp2 HG01081.hp1 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.-414+12035G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58043738 | |||||||
| chr8:58043746 | T | G | 4 | a0001c0001t0003g0005 a0001c0001t0003g0250 a0001c0001t0012g0148 others(1): Show |
4 | HG01884.hp1 HG02451.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-414+12043T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58043746 | |||||||
| chr8:58043757 | A | G | 4 | a0001c0001t0003g0005 a0001c0001t0003g0250 a0001c0001t0012g0148 others(1): Show |
4 | HG01884.hp1 HG02451.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-414+12054A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58043757 | |||||||
| chr8:58043774 | T | G | 1 | a0001c0001t0007g0130 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-414+12071T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58043774 | |||||||
| chr8:58044103 | T | A | 1 | a0001c0001t0002g0190 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-414+12400T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58044103 | |||||||
| chr8:58044252 | C | T | 4 | a0001c0001t0001g0103 a0001c0001t0001g0230 a0001c0001t0003g0100 others(1): Show |
4 | HG00544.hp1 HG02027.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-414+12549C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58044252 | |||||||
| chr8:58044470 | A | G | 27 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0158 others(24): Show |
27 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.-414+12767A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58044470 | |||||||
| chr8:58044854 | T | C | 1 | a0001c0001t0005g0061 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-414+13151T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58044854 | |||||||
| chr8:58044914 | A | G | 35 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0073 others(32): Show |
35 | HG00738.hp2 HG01069.hp1 HG02080.hp2 others(32): Show |
intron_variant | MODIFIER | c.-414+13211A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58044914 | |||||||
| chr8:58044927 | C | T | 13 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0104 others(10): Show |
13 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.-414+13224C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58044927 | |||||||
| chr8:58045021 | T | G | 1 | a0001c0001t0003g0229 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-414+13318T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58045021 | |||||||
| chr8:58045028 | C | T | 45 | a0001c0001t0001g0006 a0001c0001t0001g0084 a0001c0001t0001g0089 others(42): Show |
45 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(42): Show |
intron_variant | MODIFIER | c.-414+13325C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58045028 | |||||||
| chr8:58045130 | A | C | 178 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(175): Show |
178 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.-414+13427A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58045130 | |||||||
| chr8:58045163 | G | A | 1 | a0001c0001t0002g0030 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-414+13460G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58045163 | |||||||
| chr8:58045297 | C | G | 1 | a0001c0001t0027g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-414+13594C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58045297 | |||||||
| chr8:58045336 | A | G | 1 | a0001c0001t0010g0175 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-414+13633A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58045336 | |||||||
| chr8:58045618 | A | G | 31 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0158 others(28): Show |
31 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.-414+13915A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58045618 | |||||||
| chr8:58045673 | G | A | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-414+13970G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58045673 | |||||||
| chr8:58046177 | A | G | 1 | a0001c0001t0005g0061 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-414+14474A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58046177 | |||||||
| chr8:58046428 | T | C | 31 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0158 others(28): Show |
31 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.-414+14725T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58046428 | |||||||
| chr8:58046551 | T | C | 4 | a0001c0001t0002g0147 a0001c0001t0003g0071 a0001c0001t0007g0157 others(1): Show |
4 | HG02055.hp2 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-414+14848T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58046551 | |||||||
| chr8:58046626 | C | G | 1 | a0003c0003t0003g0264 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-414+14923C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58046626 | |||||||
| chr8:58046748 | A | G | 4 | a0001c0001t0002g0147 a0001c0001t0003g0071 a0001c0001t0007g0157 others(1): Show |
4 | HG02055.hp2 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-414+15045A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58046748 | |||||||
| chr8:58046774 | G | A | 5 | a0001c0001t0002g0162 a0001c0001t0002g0163 a0001c0001t0007g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-414+15071G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58046774 | |||||||
| chr8:58047122 | T | G | 4 | a0001c0001t0002g0147 a0001c0001t0003g0071 a0001c0001t0007g0157 others(1): Show |
4 | HG02055.hp2 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-414+15419T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58047122 | |||||||
| chr8:58047200 | G | C | 5 | a0001c0001t0002g0162 a0001c0001t0002g0163 a0001c0001t0007g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-414+15497G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58047200 | |||||||
| chr8:58047288 | A | T | 2 | a0001c0001t0002g0167 a0001c0001t0003g0133 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-414+15585A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58047288 | |||||||
| chr8:58047335 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-414+15632C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58047335 | |||||||
| chr8:58047405 | A | G | 18 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(15): Show |
18 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.-414+15702A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58047405 | |||||||
| chr8:58047472 | A | G | 1 | a0001c0001t0004g0279 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-414+15769A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58047472 | |||||||
| chr8:58047481 | G | T | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-414+15778G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58047481 | |||||||
| chr8:58047590 | T | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0262 |
2 | HG01071.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-414+15887T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58047590 | |||||||
| chr8:58047591 | C | CCT | 49 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(46): Show |
49 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.-414+15931_-414+15 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | ||||||
| chr8:58047591 | C | CCTCT | 45 | a0001c0001t0001g0029 a0001c0001t0001g0065 a0001c0001t0001g0067 others(42): Show |
45 | HG00597.hp1 HG00621.hp1 HG01168.hp2 others(42): Show |
intron_variant | MODIFIER | c.-414+15929_-414+15 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | ||||||
| chr8:58047591 | C | CCTCTCT | 21 | a0001c0001t0001g0027 a0001c0001t0001g0094 a0001c0001t0001g0104 others(18): Show |
21 | HG00408.hp1 HG00673.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.-414+15927_-414+15 others(12): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | ||||||
| chr8:58047591 | C | CCTCTCTC others(1): Show |
6 | a0001c0001t0001g0259 a0001c0001t0001g0261 a0001c0001t0002g0095 others(3): Show |
6 | HG01070.hp2 HG01934.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-414+15925_-414+15 others(14): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | ||||||
| chr8:58047591 | C | CCTCTCTC others(3): Show |
4 | a0001c0001t0001g0097 a0001c0001t0003g0133 a0001c0001t0004g0026 others(1): Show |
4 | HG02886.hp2 HG03195.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.-414+15923_-414+15 others(16): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | ||||||
| chr8:58047591 | C | CCTCTCTC others(5): Show |
9 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0154 others(6): Show |
9 | HG00621.hp2 HG01243.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-414+15921_-414+15 others(18): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | ||||||
| chr8:58047591 | C | CCTCTCTC others(7): Show |
9 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0149 others(6): Show |
9 | HG00733.hp2 HG00741.hp1 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.-414+15919_-414+15 others(20): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | ||||||
| chr8:58047591 | C | CCTCTCTC others(9): Show |
5 | a0001c0001t0002g0082 a0001c0001t0002g0109 a0001c0001t0002g0297 others(2): Show |
5 | HG00099.hp2 HG02155.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-414+15917_-414+15 others(22): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | ||||||
| chr8:58047591 | C | CCTCTCTC others(11): Show |
12 | a0001c0001t0001g0102 a0001c0001t0001g0184 a0001c0001t0001g0252 others(9): Show |
12 | HG00673.hp2 HG00735.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-414+15915_-414+15 others(24): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | ||||||
| chr8:58047591 | C | CCTCTCTC others(13): Show |
8 | a0001c0001t0001g0185 a0001c0001t0001g0236 a0001c0001t0003g0076 others(5): Show |
8 | HG01109.hp2 HG01934.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.-414+15913_-414+15 others(26): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | ||||||
| chr8:58047591 | C | CCTCTCTC others(15): Show |
7 | a0001c0001t0001g0111 a0001c0001t0002g0120 a0001c0001t0002g0123 others(4): Show |
7 | HG01069.hp1 HG01175.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.-414+15911_-414+15 others(28): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | ||||||
| chr8:58047591 | C | CCTCTCTC others(17): Show |
15 | a0001c0001t0001g0040 a0001c0001t0001g0047 a0001c0001t0001g0110 others(12): Show |
15 | HG01433.hp1 HG01943.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.-414+15909_-414+15 others(30): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | ||||||
| chr8:58047591 | C | CCTCTCTC others(19): Show |
2 | a0001c0001t0001g0282 a0001c0001t0002g0037 |
2 | HG00642.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.-414+15907_-414+15 others(32): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | ||||||
| chr8:58047591 | C | CCTCTCTC others(21): Show |
9 | a0001c0001t0001g0046 a0001c0001t0001g0098 a0001c0001t0001g0103 others(6): Show |
9 | HG00280.hp1 HG00544.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.-414+15905_-414+15 others(34): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | ||||||
| chr8:58047591 | C | CCTCTCTC others(23): Show |
3 | a0001c0001t0002g0240 a0001c0001t0003g0255 a0001c0001t0007g0300 |
3 | HG00408.hp2 HG02717.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-414+15903_-414+15 others(36): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | ||||||
| chr8:58047591 | C | CCTCTCTC others(25): Show |
2 | a0001c0001t0003g0106 a0001c0001t0007g0135 |
2 | HG02129.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-414+15901_-414+15 others(38): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | ||||||
| chr8:58047591 | C | CCTCTCTC others(29): Show |
2 | a0001c0001t0002g0186 a0001c0001t0005g0271 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-414+15897_-414+15 others(42): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | ||||||
| chr8:58047591 | C | CTCTCTCT others(6): Show |
2 | a0001c0001t0001g0043 a0001c0001t0001g0262 |
2 | HG01071.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-414+15888_-414+15 others(19): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58047591 | |||||||
| chr8:58047591 | C | CTCTCTCT others(14): Show |
2 | a0001c0001t0001g0045 a0001c0001t0002g0239 |
2 | NA18975.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.-414+15888_-414+15 others(27): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58047591 | |||||||
| chr8:58047591 | C | CTCTCTCT others(22): Show |
1 | a0001c0001t0003g0100 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-414+15888_-414+15 others(35): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58047591 | |||||||
| chr8:58047591 | CCT | C | 34 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0060 others(31): Show |
34 | HG00280.hp2 HG00323.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.-414+15931_-414+15 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | ||||||
| chr8:58047591 | CCTCT | C | 3 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0031g0159 |
3 | HG01192.hp1 HG03017.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-414+15929_-414+15 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | ||||||
| chr8:58047591 | CCTCTCTC others(5): Show |
C | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-414+15921_-414+15 others(18): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | ||||||
| chr8:58047591 | CCTCTCTC others(7): Show |
C | 14 | a0001c0001t0001g0006 a0001c0001t0002g0012 a0001c0001t0002g0146 others(11): Show |
14 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-414+15919_-414+15 others(20): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | ||||||
| chr8:58047591 | CCTCTCTC others(9): Show |
C | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-414+15917_-414+15 others(22): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | ||||||
| chr8:58047673 | C | A | 1 | a0001c0001t0003g0005 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-414+15970C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58047673 | |||||||
| chr8:58047887 | A | G | 7 | a0001c0001t0001g0158 a0001c0001t0003g0138 a0001c0001t0003g0141 others(4): Show |
7 | HG02622.hp1 HG02886.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-414+16184A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58047887 | |||||||
| chr8:58047893 | T | A | 1 | a0001c0001t0003g0229 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-414+16190T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58047893 | |||||||
| chr8:58048427 | C | A | 1 | a0001c0001t0002g0117 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-414+16724C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58048427 | |||||||
| chr8:58048496 | C | G | 35 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0073 others(32): Show |
35 | HG00738.hp2 HG01069.hp1 HG02080.hp2 others(32): Show |
intron_variant | MODIFIER | c.-414+16793C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58048496 | |||||||
| chr8:58048583 | C | A | 1 | a0001c0001t0003g0288 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-414+16880C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58048583 | |||||||
| chr8:58048586 | T | C | 2 | a0001c0001t0003g0198 a0001c0001t0007g0300 |
2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-414+16883T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58048586 | |||||||
| chr8:58048617 | A | T | 7 | a0001c0001t0001g0158 a0001c0001t0003g0138 a0001c0001t0003g0141 others(4): Show |
7 | HG02622.hp1 HG02886.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-414+16914A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58048617 | |||||||
| chr8:58048814 | A | G | 1 | a0001c0001t0003g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-414+17111A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58048814 | |||||||
| chr8:58048841 | A | G | 35 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0073 others(32): Show |
35 | HG00738.hp2 HG01069.hp1 HG02080.hp2 others(32): Show |
intron_variant | MODIFIER | c.-414+17138A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58048841 | |||||||
| chr8:58048942 | T | C | 1 | a0001c0001t0008g0265 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-414+17239T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58048942 | |||||||
| chr8:58049162 | A | G | 71 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0043 others(68): Show |
71 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.-414+17459A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58049162 | |||||||
| chr8:58049186 | G | A | 6 | a0001c0001t0002g0146 a0001c0001t0008g0127 a0001c0001t0010g0072 others(3): Show |
6 | HG01891.hp1 HG02622.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-414+17483G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58049186 | |||||||
| chr8:58049347 | A | C | 1 | a0001c0001t0001g0029 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-414+17644A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58049347 | |||||||
| chr8:58049453 | G | A | 1 | a0001c0001t0013g0177 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-414+17750G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58049453 | |||||||
| chr8:58049553 | G | A | 2 | a0001c0001t0005g0139 a0001c0001t0010g0294 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-414+17850G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58049553 | |||||||
| chr8:58049573 | G | T | 1 | a0001c0001t0005g0247 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-414+17870G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58049573 | |||||||
| chr8:58049664 | C | T | 6 | a0001c0001t0001g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(3): Show |
6 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-414+17961C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58049664 | |||||||
| chr8:58049997 | A | G | 1 | a0001c0001t0002g0291 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-414+18294A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58049997 | |||||||
| chr8:58050054 | G | A | 18 | a0001c0001t0001g0073 a0001c0001t0002g0186 a0001c0001t0002g0297 others(15): Show |
18 | HG01069.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-414+18351G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050054 | |||||||
| chr8:58050162 | T | C | 7 | a0001c0001t0002g0082 a0001c0001t0002g0162 a0001c0001t0002g0163 others(4): Show |
7 | HG01891.hp2 HG02280.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.-414+18459T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050162 | |||||||
| chr8:58050183 | A | G | 11 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0027 others(8): Show |
11 | HG00621.hp2 HG00673.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.-414+18480A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050183 | |||||||
| chr8:58050210 | T | C | 4 | a0001c0001t0002g0147 a0001c0001t0003g0071 a0001c0001t0007g0157 others(1): Show |
4 | HG02055.hp2 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-414+18507T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050210 | |||||||
| chr8:58050211 | C | CT | 18 | a0001c0001t0001g0006 a0001c0001t0001g0184 a0001c0001t0001g0185 others(15): Show |
18 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.-414+18519dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58050211 | ||||||
| chr8:58050235 | T | C | 175 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(172): Show |
175 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.-414+18532T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050235 | |||||||
| chr8:58050289 | A | G | 3 | a0001c0001t0002g0128 a0001c0001t0003g0143 a0001c0001t0007g0144 |
3 | HG03130.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-414+18586A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050289 | |||||||
| chr8:58050343 | A | C | 3 | a0001c0001t0001g0089 a0001c0001t0004g0083 a0001c0001t0004g0189 |
3 | HG02056.hp1 HG02129.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-414+18640A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050343 | |||||||
| chr8:58050374 | T | A | 12 | a0001c0001t0001g0158 a0001c0001t0002g0082 a0001c0001t0002g0162 others(9): Show |
12 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-414+18671T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050374 | |||||||
| chr8:58050414 | T | G | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-414+18711T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050414 | |||||||
| chr8:58050434 | G | A | 14 | a0001c0001t0001g0006 a0001c0001t0002g0012 a0001c0001t0002g0146 others(11): Show |
14 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-414+18731G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050434 | |||||||
| chr8:58050478 | G | A | 77 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(74): Show |
77 | HG00733.hp1 HG00738.hp2 HG01069.hp1 others(74): Show |
intron_variant | MODIFIER | c.-414+18775G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050478 | |||||||
| chr8:58050521 | G | A | 1 | a0001c0001t0007g0004 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-414+18818G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050521 | |||||||
| chr8:58050525 | G | A | 18 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(15): Show |
18 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.-414+18822G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050525 | |||||||
| chr8:58050601 | C | T | 4 | a0001c0001t0003g0138 a0001c0001t0003g0141 a0001c0001t0005g0139 others(1): Show |
4 | HG02622.hp1 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-414+18898C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050601 | |||||||
| chr8:58050784 | C | T | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-414+19081C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050784 | |||||||
| chr8:58050901 | A | C | 85 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0043 others(82): Show |
85 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.-414+19198A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050901 | |||||||
| chr8:58051024 | A | G | 2 | a0001c0001t0001g0252 a0001c0001t0003g0251 |
2 | NA18949.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.-414+19321A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58051024 | |||||||
| chr8:58051154 | A | G | 1 | a0001c0001t0006g0246 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-414+19451A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58051154 | |||||||
| chr8:58051333 | C | A | 1 | a0001c0001t0008g0296 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-414+19630C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58051333 | |||||||
| chr8:58051365 | AC | A | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0217 others(2): Show |
5 | HG00597.hp2 NA18942.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.-414+19663delC | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58051365 | |||||||
| chr8:58051450 | C | G | 3 | a0001c0001t0002g0147 a0001c0001t0003g0071 a0001c0001t0007g0157 |
3 | HG02717.hp2 HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-414+19747C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58051450 | |||||||
| chr8:58051509 | T | C | 4 | a0001c0001t0002g0147 a0001c0001t0003g0071 a0001c0001t0007g0157 others(1): Show |
4 | HG02055.hp2 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-414+19806T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58051509 | |||||||
| chr8:58051604 | T | A | 1 | a0001c0001t0003g0204 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-414+19901T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58051604 | |||||||
| chr8:58051652 | A | G | 1 | a0001c0001t0002g0031 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-414+19949A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58051652 | |||||||
| chr8:58051803 | GA | G | 22 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(19): Show |
22 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.-414+20102delA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58051803 | ||||||
| chr8:58051859 | G | A | 2 | a0001c0001t0003g0198 a0001c0001t0007g0300 |
2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-414+20156G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58051859 | |||||||
| chr8:58051943 | G | T | 1 | a0001c0001t0001g0065 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-414+20240G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58051943 | |||||||
| chr8:58052008 | A | G | 1 | a0001c0001t0007g0090 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-414+20305A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052008 | |||||||
| chr8:58052093 | A | T | 3 | a0001c0001t0002g0128 a0001c0001t0003g0143 a0001c0001t0007g0144 |
3 | HG03130.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-414+20390A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052093 | |||||||
| chr8:58052157 | A | T | 22 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(19): Show |
22 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.-414+20454A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052157 | |||||||
| chr8:58052186 | C | G | 181 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(178): Show |
181 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.-414+20483C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052186 | |||||||
| chr8:58052204 | G | A | 2 | a0001c0001t0003g0198 a0001c0001t0007g0300 |
2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-414+20501G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052204 | |||||||
| chr8:58052217 | A | G | 22 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(19): Show |
22 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.-414+20514A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052217 | |||||||
| chr8:58052310 | A | G | 4 | a0001c0001t0001g0103 a0001c0001t0001g0230 a0001c0001t0003g0100 others(1): Show |
4 | HG00544.hp1 HG02027.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-414+20607A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052310 | |||||||
| chr8:58052387 | A | G | 2 | a0001c0001t0004g0041 a0001c0001t0006g0101 |
2 | HG01109.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.-414+20684A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052387 | |||||||
| chr8:58052493 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-414+20790C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052493 | |||||||
| chr8:58052494 | G | A | 3 | a0001c0001t0002g0147 a0001c0001t0003g0071 a0001c0001t0007g0157 |
3 | HG02717.hp2 HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-414+20791G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052494 | |||||||
| chr8:58052552 | G | A | 22 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(19): Show |
22 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.-414+20849G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052552 | |||||||
| chr8:58052661 | G | T | 2 | a0001c0001t0003g0142 a0001c0001t0009g0140 |
2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-414+20958G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052661 | |||||||
| chr8:58052772 | C | CT | 10 | a0001c0001t0001g0038 a0001c0001t0001g0054 a0001c0001t0002g0032 others(7): Show |
10 | HG00642.hp1 HG01081.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.-414+21100dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58052772 | ||||||
| chr8:58052772 | CT | C | 25 | a0001c0001t0001g0088 a0001c0001t0001g0094 a0001c0001t0001g0118 others(22): Show |
25 | HG00323.hp2 HG00597.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.-414+21100delT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58052772 | ||||||
| chr8:58052772 | CTT | C | 78 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0020 others(75): Show |
78 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.-414+21099_-414+21 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58052772 | ||||||
| chr8:58052772 | CTTT | C | 97 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(94): Show |
97 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.-414+21098_-414+21 others(9): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58052772 | ||||||
| chr8:58052772 | CTTTT | C | 16 | a0001c0001t0002g0186 a0001c0001t0002g0297 a0001c0001t0003g0074 others(13): Show |
16 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-414+21097_-414+21 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58052772 | ||||||
| chr8:58052772 | CTTTTTTT others(2): Show |
C | 22 | a0001c0001t0001g0089 a0001c0001t0001g0201 a0001c0001t0001g0267 others(19): Show |
22 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.-414+21092_-414+21 others(15): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58052772 | ||||||
| chr8:58052772 | CTTTTTTT others(3): Show |
C | 7 | a0001c0001t0002g0146 a0001c0001t0002g0152 a0001c0001t0002g0263 others(4): Show |
7 | HG01891.hp1 HG02257.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-414+21091_-414+21 others(16): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58052772 | ||||||
| chr8:58052772 | CTTTTTTT others(4): Show |
C | 9 | a0001c0001t0001g0006 a0001c0001t0002g0012 a0001c0001t0002g0153 others(6): Show |
9 | HG01168.hp1 HG01192.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.-414+21090_-414+21 others(17): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58052772 | ||||||
| chr8:58052772 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0002g0016 a0001c0001t0003g0005 |
2 | HG00741.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-414+21089_-414+21 others(18): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58052772 | ||||||
| chr8:58052911 | G | A | 3 | a0001c0001t0001g0149 a0001c0001t0001g0154 a0001c0001t0035g0290 |
3 | HG02559.hp1 HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-414+21208G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052911 | |||||||
| chr8:58052934 | C | T | 26 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(23): Show |
26 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.-414+21231C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052934 | |||||||
| chr8:58052937 | T | C | 26 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(23): Show |
26 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.-414+21234T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052937 | |||||||
| chr8:58052947 | G | A | 26 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(23): Show |
26 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.-414+21244G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052947 | |||||||
| chr8:58052949 | C | A | 2 | a0001c0001t0003g0198 a0001c0001t0007g0300 |
2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-414+21246C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052949 | |||||||
| chr8:58052952 | AT | A | 26 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(23): Show |
26 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.-414+21255delT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58052952 | ||||||
| chr8:58052975 | C | A | 26 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(23): Show |
26 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.-414+21272C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052975 | |||||||
| chr8:58053023 | G | C | 1 | a0001c0001t0012g0150 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-414+21320G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58053023 | |||||||
| chr8:58053028 | G | A | 3 | a0001c0001t0001g0089 a0001c0001t0004g0083 a0001c0001t0004g0189 |
3 | HG02056.hp1 HG02129.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-414+21325G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58053028 | |||||||
| chr8:58053162 | T | C | 1 | a0001c0001t0002g0193 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-414+21459T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58053162 | |||||||
| chr8:58053169 | C | G | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-414+21466C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58053169 | |||||||
| chr8:58053266 | G | T | 1 | a0001c0001t0001g0094 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-414+21563G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58053266 | |||||||
| chr8:58053436 | GAAGA | G | 18 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(15): Show |
18 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.-414+21739_-414+21 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58053436 | ||||||
| chr8:58053501 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-414+21798G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58053501 | |||||||
| chr8:58053663 | G | A | 5 | a0001c0001t0002g0059 a0001c0001t0002g0190 a0001c0001t0002g0191 others(2): Show |
5 | HG00597.hp1 NA18948.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-413-21872G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58053663 | |||||||
| chr8:58054186 | G | A | 1 | a0001c0001t0003g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-413-21349G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58054186 | |||||||
| chr8:58054216 | A | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0221 others(19): Show |
22 | HG00735.hp1 HG00738.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.-413-21319A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58054216 | |||||||
| chr8:58054287 | G | C | 1 | a0001c0001t0001g0184 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-413-21248G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58054287 | |||||||
| chr8:58054369 | C | G | 3 | a0001c0001t0002g0147 a0001c0001t0003g0071 a0001c0001t0007g0157 |
3 | HG02717.hp2 HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-413-21166C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58054369 | |||||||
| chr8:58054783 | A | G | 1 | a0001c0001t0002g0152 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-413-20752A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58054783 | |||||||
| chr8:58054792 | T | A | 3 | a0001c0001t0002g0147 a0001c0001t0003g0071 a0001c0001t0007g0157 |
3 | HG02717.hp2 HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-413-20743T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58054792 | |||||||
| chr8:58054793 | C | T | 3 | a0001c0001t0002g0147 a0001c0001t0003g0071 a0001c0001t0007g0157 |
3 | HG02717.hp2 HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-413-20742C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58054793 | |||||||
| chr8:58054881 | T | A | 1 | a0001c0001t0001g0065 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-413-20654T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58054881 | |||||||
| chr8:58054917 | C | CT | 79 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0043 others(76): Show |
79 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.-413-20609dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58054917 | ||||||
| chr8:58055012 | C | G | 3 | a0001c0001t0002g0146 a0001c0001t0008g0127 a0001c0001t0010g0160 |
3 | HG01891.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-413-20523C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58055012 | |||||||
| chr8:58055214 | G | A | 1 | a0001c0001t0002g0136 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-413-20321G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58055214 | |||||||
| chr8:58055323 | G | C | 3 | a0001c0001t0002g0128 a0001c0001t0003g0143 a0001c0001t0007g0144 |
3 | HG03130.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-413-20212G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58055323 | |||||||
| chr8:58055377 | C | T | 3 | a0001c0001t0002g0128 a0001c0001t0003g0143 a0001c0001t0007g0144 |
3 | HG03130.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-413-20158C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58055377 | |||||||
| chr8:58055483 | T | G | 1 | a0001c0001t0001g0200 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-413-20052T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58055483 | |||||||
| chr8:58055691 | A | G | 1 | a0001c0001t0022g0174 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-413-19844A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58055691 | |||||||
| chr8:58055739 | C | T | 4 | a0001c0001t0002g0147 a0001c0001t0003g0071 a0001c0001t0007g0157 others(1): Show |
4 | HG02055.hp2 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-413-19796C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58055739 | |||||||
| chr8:58055865 | C | T | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-413-19670C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58055865 | |||||||
| chr8:58055934 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-413-19601G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58055934 | |||||||
| chr8:58056008 | G | T | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-413-19527G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58056008 | |||||||
| chr8:58056303 | G | A | 1 | a0001c0001t0008g0173 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-413-19232G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58056303 | |||||||
| chr8:58056369 | T | A | 2 | a0001c0001t0006g0025 a0001c0001t0006g0218 |
2 | HG01081.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.-413-19166T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58056369 | |||||||
| chr8:58056374 | T | A | 2 | a0001c0001t0003g0142 a0001c0001t0009g0140 |
2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-413-19161T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58056374 | |||||||
| chr8:58056845 | TA | T | 12 | a0001c0001t0001g0158 a0001c0001t0002g0082 a0001c0001t0002g0162 others(9): Show |
12 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-413-18688delA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58056845 | ||||||
| chr8:58057133 | C | T | 2 | a0001c0001t0003g0071 a0001c0001t0007g0157 |
2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-413-18402C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58057133 | |||||||
| chr8:58057294 | A | G | 1 | a0001c0001t0006g0155 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-413-18241A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58057294 | |||||||
| chr8:58057357 | A | G | 1 | a0001c0001t0005g0247 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-413-18178A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58057357 | |||||||
| chr8:58057384 | G | A | 14 | a0001c0001t0001g0006 a0001c0001t0002g0012 a0001c0001t0002g0146 others(11): Show |
14 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-413-18151G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58057384 | |||||||
| chr8:58057389 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-413-18146C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58057389 | |||||||
| chr8:58057550 | C | G | 1 | a0001c0001t0005g0058 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-413-17985C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58057550 | |||||||
| chr8:58057770 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-413-17765A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58057770 | |||||||
| chr8:58057777 | G | T | 2 | a0001c0001t0003g0142 a0001c0001t0009g0140 |
2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-413-17758G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58057777 | |||||||
| chr8:58057779 | T | C | 2 | a0001c0001t0024g0176 a0001c0001t0031g0159 |
2 | HG01192.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.-413-17756T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58057779 | |||||||
| chr8:58057870 | G | A | 41 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0073 others(38): Show |
41 | HG00735.hp1 HG00738.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.-413-17665G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58057870 | |||||||
| chr8:58058004 | G | A | 26 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(23): Show |
26 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.-413-17531G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58058004 | |||||||
| chr8:58058132 | C | G | 1 | a0002c0002t0016g0166 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-413-17403C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58058132 | |||||||
| chr8:58058302 | T | C | 26 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(23): Show |
26 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.-413-17233T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58058302 | |||||||
| chr8:58058333 | A | AG | 82 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0038 others(79): Show |
82 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.-413-17200dupG | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58058333 | ||||||
| chr8:58058335 | G | GA | 95 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(92): Show |
95 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(92): Show |
intron_variant | MODIFIER | c.-413-17189dupA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58058335 | ||||||
| chr8:58058336 | A | G | 2 | a0001c0001t0001g0285 a0001c0001t0003g0233 |
2 | NA18970.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-413-17199A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58058336 | |||||||
| chr8:58058621 | C | T | 22 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(19): Show |
22 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.-413-16914C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58058621 | |||||||
| chr8:58058680 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-413-16855A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58058680 | |||||||
| chr8:58058807 | T | C | 3 | a0001c0001t0002g0147 a0001c0001t0003g0071 a0001c0001t0007g0157 |
3 | HG02717.hp2 HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-413-16728T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58058807 | |||||||
| chr8:58058897 | G | A | 1 | a0001c0001t0003g0234 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-413-16638G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58058897 | |||||||
| chr8:58059046 | T | C | 26 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(23): Show |
26 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.-413-16489T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58059046 | |||||||
| chr8:58059052 | T | G | 26 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(23): Show |
26 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.-413-16483T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58059052 | |||||||
| chr8:58059782 | T | G | 1 | a0001c0001t0002g0120 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-413-15753T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58059782 | |||||||
| chr8:58059926 | G | T | 15 | a0001c0001t0001g0006 a0001c0001t0002g0012 a0001c0001t0002g0146 others(12): Show |
15 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-413-15609G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58059926 | |||||||
| chr8:58059934 | G | A | 26 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(23): Show |
26 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.-413-15601G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58059934 | |||||||
| chr8:58059988 | A | C | 26 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(23): Show |
26 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.-413-15547A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58059988 | |||||||
| chr8:58060184 | G | A | 4 | a0001c0001t0002g0147 a0001c0001t0003g0071 a0001c0001t0007g0157 others(1): Show |
4 | HG02055.hp2 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-413-15351G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58060184 | |||||||
| chr8:58060203 | A | G | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-413-15332A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58060203 | |||||||
| chr8:58060446 | T | A | 1 | a0001c0001t0002g0066 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-413-15089T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58060446 | |||||||
| chr8:58060567 | A | G | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-413-14968A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58060567 | |||||||
| chr8:58060604 | C | A | 1 | a0001c0001t0007g0130 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-413-14931C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58060604 | |||||||
| chr8:58060662 | T | C | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-413-14873T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58060662 | |||||||
| chr8:58060738 | C | A | 41 | a0001c0001t0001g0006 a0001c0001t0001g0084 a0001c0001t0001g0089 others(38): Show |
41 | HG00733.hp1 HG01099.hp1 HG01192.hp1 others(38): Show |
intron_variant | MODIFIER | c.-413-14797C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58060738 | |||||||
| chr8:58060773 | C | A | 11 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0027 others(8): Show |
11 | HG00621.hp2 HG00673.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.-413-14762C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58060773 | |||||||
| chr8:58061013 | G | C | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-413-14522G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58061013 | |||||||
| chr8:58061024 | C | T | 3 | a0001c0001t0002g0147 a0001c0001t0003g0071 a0001c0001t0007g0157 |
3 | HG02717.hp2 HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-413-14511C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58061024 | |||||||
| chr8:58061102 | T | C | 1 | a0001c0001t0002g0018 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-413-14433T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58061102 | |||||||
| chr8:58061383 | A | G | 22 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(19): Show |
22 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.-413-14152A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58061383 | |||||||
| chr8:58061422 | AC | A | 8 | a0001c0001t0002g0146 a0001c0001t0002g0152 a0001c0001t0008g0127 others(5): Show |
8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-413-14112delC | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58061422 | |||||||
| chr8:58061424 | A | C | 22 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(19): Show |
22 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.-413-14111A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58061424 | |||||||
| chr8:58061668 | C | G | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-413-13867C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58061668 | |||||||
| chr8:58061702 | A | G | 2 | a0001c0001t0003g0071 a0001c0001t0007g0157 |
2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-413-13833A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58061702 | |||||||
| chr8:58061745 | C | A | 2 | a0001c0001t0003g0198 a0001c0001t0007g0300 |
2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-413-13790C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58061745 | |||||||
| chr8:58062038 | C | T | 15 | a0001c0001t0001g0006 a0001c0001t0002g0012 a0001c0001t0002g0146 others(12): Show |
15 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-413-13497C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58062038 | |||||||
| chr8:58062280 | A | G | 1 | a0001c0001t0006g0245 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-413-13255A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58062280 | |||||||
| chr8:58062497 | T | C | 1 | a0001c0001t0021g0248 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-413-13038T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58062497 | |||||||
| chr8:58062500 | A | G | 61 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(58): Show |
61 | HG00735.hp1 HG00738.hp2 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.-413-13035A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58062500 | |||||||
| chr8:58062704 | C | T | 1 | a0001c0001t0012g0150 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-413-12831C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58062704 | |||||||
| chr8:58062790 | T | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | NA18953.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.-413-12745T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58062790 | |||||||
| chr8:58063178 | G | A | 12 | a0001c0001t0001g0158 a0001c0001t0002g0082 a0001c0001t0002g0162 others(9): Show |
12 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-413-12357G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58063178 | |||||||
| chr8:58063194 | C | T | 20 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(17): Show |
20 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.-413-12341C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58063194 | |||||||
| chr8:58063214 | C | G | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-413-12321C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58063214 | |||||||
| chr8:58063469 | C | CCATT | 92 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0073 others(89): Show |
92 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(89): Show |
intron_variant | MODIFIER | c.-413-12066_-413-12 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58063469 | |||||||
| chr8:58063536 | G | A | 2 | a0001c0001t0003g0142 a0001c0001t0009g0140 |
2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-413-11999G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58063536 | |||||||
| chr8:58063589 | G | T | 94 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(91): Show |
94 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(91): Show |
intron_variant | MODIFIER | c.-413-11946G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58063589 | |||||||
| chr8:58063706 | G | T | 1 | a0001c0001t0002g0057 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-413-11829G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58063706 | |||||||
| chr8:58063751 | G | T | 3 | a0001c0001t0002g0147 a0001c0001t0003g0071 a0001c0001t0007g0157 |
3 | HG02717.hp2 HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-413-11784G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58063751 | |||||||
| chr8:58063790 | A | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0221 others(19): Show |
22 | HG00735.hp1 HG00738.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.-413-11745A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58063790 | |||||||
| chr8:58063855 | A | T | 20 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(17): Show |
20 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.-413-11680A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58063855 | |||||||
| chr8:58063945 | T | C | 18 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(15): Show |
18 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.-413-11590T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58063945 | |||||||
| chr8:58063948 | G | A | 12 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0104 others(9): Show |
12 | HG00438.hp2 HG00609.hp2 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.-413-11587G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58063948 | |||||||
| chr8:58064085 | C | T | 1 | a0001c0001t0002g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-413-11450C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58064085 | |||||||
| chr8:58064394 | CT | C | 61 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(58): Show |
61 | HG00735.hp1 HG00738.hp2 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.-413-11130delT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58064394 | ||||||
| chr8:58064460 | C | T | 98 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(95): Show |
98 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(95): Show |
intron_variant | MODIFIER | c.-413-11075C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58064460 | |||||||
| chr8:58064640 | A | G | 2 | a0001c0001t0002g0293 a0001c0001t0003g0223 |
2 | HG02027.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-413-10895A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58064640 | |||||||
| chr8:58064827 | G | A | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-413-10708G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58064827 | |||||||
| chr8:58064927 | G | A | 8 | a0001c0001t0002g0146 a0001c0001t0002g0152 a0001c0001t0008g0127 others(5): Show |
8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-413-10608G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58064927 | |||||||
| chr8:58065110 | T | A | 5 | a0001c0001t0003g0286 a0001c0001t0003g0287 a0001c0001t0003g0288 others(2): Show |
5 | HG02055.hp1 HG03139.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.-413-10425T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58065110 | |||||||
| chr8:58065269 | T | C | 20 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(17): Show |
20 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.-413-10266T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58065269 | |||||||
| chr8:58065350 | T | G | 1 | a0001c0001t0008g0265 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-413-10185T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58065350 | |||||||
| chr8:58065450 | G | A | 1 | a0001c0001t0036g0132 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-413-10085G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58065450 | |||||||
| chr8:58065763 | A | G | 61 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(58): Show |
61 | HG00735.hp1 HG00738.hp2 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.-413-9772A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58065763 | |||||||
| chr8:58065958 | A | G | 1 | a0001c0001t0002g0178 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-413-9577A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58065958 | |||||||
| chr8:58066011 | G | A | 20 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(17): Show |
20 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.-413-9524G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58066011 | |||||||
| chr8:58066246 | T | C | 130 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(127): Show |
130 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(127): Show |
intron_variant | MODIFIER | c.-413-9289T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58066246 | |||||||
| chr8:58066436 | G | C | 1 | a0001c0001t0003g0122 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-413-9099G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58066436 | |||||||
| chr8:58066591 | A | G | 5 | a0001c0001t0002g0186 a0001c0001t0003g0299 a0001c0001t0007g0135 others(2): Show |
5 | HG01069.hp1 HG02055.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-413-8944A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58066591 | |||||||
| chr8:58066594 | GGCACAAG others(2): Show |
G | 5 | a0001c0001t0002g0186 a0001c0001t0003g0299 a0001c0001t0007g0135 others(2): Show |
5 | HG01069.hp1 HG02055.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-413-8940_-413-893 others(13): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58066594 | |||||||
| chr8:58066633 | C | A | 20 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(17): Show |
20 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.-413-8902C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58066633 | |||||||
| chr8:58066668 | G | A | 15 | a0001c0001t0001g0158 a0001c0001t0002g0082 a0001c0001t0002g0162 others(12): Show |
15 | HG01884.hp2 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-413-8867G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58066668 | |||||||
| chr8:58066710 | C | T | 1 | a0001c0001t0002g0190 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-413-8825C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58066710 | |||||||
| chr8:58066734 | A | G | 20 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(17): Show |
20 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.-413-8801A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58066734 | |||||||
| chr8:58066821 | C | A | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-413-8714C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58066821 | |||||||
| chr8:58067014 | A | C | 16 | a0001c0001t0001g0158 a0001c0001t0002g0082 a0001c0001t0002g0162 others(13): Show |
16 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-413-8521A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58067014 | |||||||
| chr8:58067067 | T | C | 36 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0158 others(33): Show |
36 | HG00733.hp1 HG00741.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.-413-8468T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58067067 | |||||||
| chr8:58067087 | G | T | 1 | a0001c0001t0005g0188 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-413-8448G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58067087 | |||||||
| chr8:58067412 | T | C | 20 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(17): Show |
20 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.-413-8123T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58067412 | |||||||
| chr8:58067448 | T | C | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-413-8087T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58067448 | |||||||
| chr8:58067529 | G | A | 16 | a0001c0001t0001g0158 a0001c0001t0002g0082 a0001c0001t0002g0162 others(13): Show |
16 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-413-8006G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58067529 | |||||||
| chr8:58067586 | C | G | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-413-7949C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58067586 | |||||||
| chr8:58067758 | T | C | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-413-7777T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58067758 | |||||||
| chr8:58067932 | A | G | 7 | a0001c0001t0001g0060 a0001c0001t0001g0088 a0001c0001t0001g0252 others(4): Show |
7 | NA18953.hp1 NA18975.hp1 NA18984.hp2 others(4): Show |
intron_variant | MODIFIER | c.-413-7603A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58067932 | |||||||
| chr8:58068312 | T | A | 1 | a0001c0001t0015g0007 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-413-7223T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58068312 | |||||||
| chr8:58068376 | T | G | 1 | a0001c0001t0003g0129 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-413-7159T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58068376 | |||||||
| chr8:58068391 | T | G | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-413-7144T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58068391 | |||||||
| chr8:58068422 | A | G | 11 | a0001c0001t0002g0186 a0001c0001t0003g0129 a0001c0001t0003g0134 others(8): Show |
11 | HG01069.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-413-7113A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58068422 | |||||||
| chr8:58068598 | TA | T | 231 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(228): Show |
231 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.-413-6923delA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58068598 | ||||||
| chr8:58068622 | A | T | 30 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0158 others(27): Show |
30 | HG00733.hp1 HG00741.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.-413-6913A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58068622 | |||||||
| chr8:58068705 | C | A | 3 | a0001c0001t0001g0006 a0001c0001t0002g0012 a0001c0001t0004g0260 |
3 | HG02818.hp2 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-413-6830C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58068705 | |||||||
| chr8:58068721 | G | A | 20 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(17): Show |
20 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.-413-6814G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58068721 | |||||||
| chr8:58068815 | C | T | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-413-6720C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58068815 | |||||||
| chr8:58069131 | T | G | 10 | a0001c0001t0001g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 others(7): Show |
10 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-413-6404T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58069131 | |||||||
| chr8:58069177 | G | T | 1 | a0001c0001t0003g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-413-6358G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58069177 | |||||||
| chr8:58069347 | C | T | 2 | a0001c0001t0002g0167 a0001c0001t0003g0133 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-413-6188C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58069347 | |||||||
| chr8:58069350 | G | C | 14 | a0001c0001t0001g0006 a0001c0001t0002g0012 a0001c0001t0002g0146 others(11): Show |
14 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-413-6185G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58069350 | |||||||
| chr8:58069441 | G | T | 1 | a0001c0001t0001g0103 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-413-6094G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58069441 | |||||||
| chr8:58069483 | A | G | 2 | a0001c0001t0003g0198 a0001c0001t0007g0300 |
2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-413-6052A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58069483 | |||||||
| chr8:58069508 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-413-6027A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58069508 | |||||||
| chr8:58069562 | A | G | 13 | a0001c0001t0001g0065 a0001c0001t0001g0226 a0001c0001t0002g0011 others(10): Show |
13 | HG00609.hp1 HG00621.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.-413-5973A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58069562 | |||||||
| chr8:58069599 | C | G | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-413-5936C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58069599 | |||||||
| chr8:58069853 | A | T | 5 | a0001c0001t0002g0059 a0001c0001t0002g0190 a0001c0001t0002g0191 others(2): Show |
5 | HG00597.hp1 NA18948.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-413-5682A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58069853 | |||||||
| chr8:58069909 | G | A | 11 | a0001c0001t0001g0040 a0001c0001t0001g0098 a0001c0001t0001g0103 others(8): Show |
11 | HG00544.hp1 HG02027.hp2 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.-413-5626G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58069909 | |||||||
| chr8:58070036 | C | G | 1 | a0001c0001t0002g0016 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-413-5499C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58070036 | |||||||
| chr8:58070175 | C | T | 1 | a0001c0001t0002g0291 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-413-5360C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58070175 | |||||||
| chr8:58070309 | C | T | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-413-5226C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58070309 | |||||||
| chr8:58070393 | T | C | 8 | a0001c0001t0001g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 others(5): Show |
8 | HG00741.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-413-5142T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58070393 | |||||||
| chr8:58070432 | G | T | 17 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(14): Show |
17 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.-413-5103G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58070432 | |||||||
| chr8:58070765 | TA | T | 3 | a0001c0001t0002g0167 a0001c0001t0003g0133 a0001c0001t0004g0260 |
3 | HG02922.hp1 HG03195.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-413-4769delA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58070765 | |||||||
| chr8:58070968 | T | G | 2 | a0001c0001t0001g0267 a0001c0001t0002g0266 |
2 | HG00733.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-413-4567T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58070968 | |||||||
| chr8:58070975 | T | C | 15 | a0001c0001t0001g0006 a0001c0001t0002g0012 a0001c0001t0002g0146 others(12): Show |
15 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-413-4560T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58070975 | |||||||
| chr8:58071009 | C | G | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-413-4526C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58071009 | |||||||
| chr8:58071059 | G | A | 1 | a0001c0001t0003g0055 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-413-4476G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58071059 | |||||||
| chr8:58071298 | G | A | 2 | a0001c0001t0002g0167 a0001c0001t0003g0133 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-413-4237G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58071298 | |||||||
| chr8:58071417 | C | T | 94 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(91): Show |
94 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(91): Show |
intron_variant | MODIFIER | c.-413-4118C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58071417 | |||||||
| chr8:58071529 | T | C | 8 | a0001c0001t0001g0054 a0001c0001t0002g0095 a0001c0001t0002g0117 others(5): Show |
8 | HG00099.hp1 HG00323.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.-413-4006T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58071529 | |||||||
| chr8:58071746 | AT | A | 18 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(15): Show |
18 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.-413-3788delT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58071746 | |||||||
| chr8:58071748 | C | T | 3 | a0001c0001t0002g0297 a0001c0001t0003g0198 a0001c0001t0007g0300 |
3 | HG02280.hp2 HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-413-3787C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58071748 | |||||||
| chr8:58071879 | C | T | 2 | a0001c0001t0003g0071 a0001c0001t0007g0157 |
2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-413-3656C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58071879 | |||||||
| chr8:58071899 | C | T | 25 | a0001c0001t0001g0073 a0001c0001t0002g0082 a0001c0001t0002g0147 others(22): Show |
25 | HG01069.hp1 HG02055.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.-413-3636C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58071899 | |||||||
| chr8:58072099 | G | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0200 a0001c0001t0004g0202 |
3 | HG00280.hp2 HG01978.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-413-3436G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58072099 | |||||||
| chr8:58072105 | T | C | 28 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0020 others(25): Show |
28 | HG00280.hp2 HG00597.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.-413-3430T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58072105 | |||||||
| chr8:58072215 | A | G | 64 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0040 others(61): Show |
64 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.-413-3320A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58072215 | |||||||
| chr8:58072256 | G | A | 1 | a0001c0001t0003g0055 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-413-3279G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58072256 | |||||||
| chr8:58072287 | A | G | 12 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0104 others(9): Show |
12 | HG00438.hp2 HG00609.hp2 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.-413-3248A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58072287 | |||||||
| chr8:58072317 | A | C | 8 | a0001c0001t0001g0172 a0001c0001t0001g0184 a0001c0001t0001g0185 others(5): Show |
8 | HG01070.hp2 HG01071.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-413-3218A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58072317 | |||||||
| chr8:58072411 | C | T | 2 | a0001c0001t0001g0211 a0001c0001t0002g0147 |
2 | HG00408.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-413-3124C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58072411 | |||||||
| chr8:58072438 | T | A | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-413-3097T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58072438 | |||||||
| chr8:58072807 | C | T | 1 | a0001c0001t0001g0023 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-413-2728C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58072807 | |||||||
| chr8:58072866 | G | C | 1 | a0001c0001t0003g0292 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-413-2669G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58072866 | |||||||
| chr8:58072882 | A | G | 1 | a0001c0001t0001g0017 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-413-2653A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58072882 | |||||||
| chr8:58072902 | G | A | 3 | a0001c0001t0002g0167 a0001c0001t0003g0133 a0001c0001t0004g0260 |
3 | HG02922.hp1 HG03195.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-413-2633G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58072902 | |||||||
| chr8:58072909 | G | A | 1 | a0001c0001t0007g0090 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-413-2626G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58072909 | |||||||
| chr8:58072941 | T | C | 26 | a0001c0001t0001g0065 a0001c0001t0001g0226 a0001c0001t0002g0001 others(23): Show |
26 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.-413-2594T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58072941 | |||||||
| chr8:58073008 | A | G | 18 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(15): Show |
18 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.-413-2527A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58073008 | |||||||
| chr8:58073212 | T | G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0026g0021 |
3 | NA18993.hp2 NA18994.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.-413-2323T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58073212 | |||||||
| chr8:58073601 | C | G | 90 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(87): Show |
90 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(87): Show |
intron_variant | MODIFIER | c.-413-1934C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58073601 | |||||||
| chr8:58073608 | G | A | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-413-1927G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58073608 | |||||||
| chr8:58073636 | A | G | 21 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0060 others(18): Show |
21 | HG00597.hp2 HG00642.hp2 HG02738.hp2 others(18): Show |
intron_variant | MODIFIER | c.-413-1899A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58073636 | |||||||
| chr8:58073644 | C | G | 15 | a0001c0001t0001g0006 a0001c0001t0002g0012 a0001c0001t0002g0146 others(12): Show |
15 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-413-1891C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58073644 | |||||||
| chr8:58073808 | T | G | 119 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(116): Show |
119 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(116): Show |
intron_variant | MODIFIER | c.-413-1727T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58073808 | |||||||
| chr8:58073879 | C | A | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-413-1656C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58073879 | |||||||
| chr8:58073900 | G | A | 88 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0015 others(85): Show |
88 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(85): Show |
intron_variant | MODIFIER | c.-413-1635G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58073900 | |||||||
| chr8:58073988 | T | C | 18 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(15): Show |
18 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.-413-1547T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58073988 | |||||||
| chr8:58074044 | T | C | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-413-1491T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58074044 | |||||||
| chr8:58074082 | G | C | 105 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(102): Show |
105 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(102): Show |
intron_variant | MODIFIER | c.-413-1453G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58074082 | |||||||
| chr8:58074142 | A | G | 1 | a0001c0001t0015g0007 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-413-1393A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58074142 | |||||||
| chr8:58074263 | A | C | 28 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0172 others(25): Show |
28 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.-413-1272A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58074263 | |||||||
| chr8:58074272 | C | T | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-413-1263C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58074272 | |||||||
| chr8:58074319 | C | T | 2 | a0001c0001t0001g0201 a0001c0001t0008g0170 |
2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-413-1216C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58074319 | |||||||
| chr8:58074597 | T | C | 1 | a0001c0001t0009g0140 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-413-938T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58074597 | |||||||
| chr8:58074603 | G | A | 9 | a0001c0001t0001g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 others(6): Show |
9 | HG00597.hp1 HG00741.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.-413-932G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58074603 | |||||||
| chr8:58074692 | C | T | 28 | a0001c0001t0001g0006 a0001c0001t0001g0158 a0001c0001t0002g0012 others(25): Show |
28 | HG00741.hp1 HG01192.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.-413-843C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58074692 | |||||||
| chr8:58074957 | A | G | 2 | a0001c0001t0002g0297 a0001c0001t0024g0176 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.-413-578A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58074957 | |||||||
| chr8:58074979 | T | C | 1 | a0001c0001t0005g0093 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-413-556T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58074979 | |||||||
| chr8:58075265 | T | TTGTGTGT others(5): Show |
1 | a0001c0001t0002g0297 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-413-269_-413-268i others(14): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075265 | ||||||
| chr8:58075265 | T | TTGTGTGT others(7): Show |
9 | a0001c0001t0001g0084 a0001c0001t0001g0267 a0001c0001t0002g0057 others(6): Show |
9 | HG00733.hp1 HG01261.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.-413-269_-413-268i others(16): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075265 | ||||||
| chr8:58075265 | T | TTGTGTGT others(9): Show |
4 | a0001c0001t0001g0201 a0001c0001t0002g0268 a0001c0001t0008g0170 others(1): Show |
4 | HG02886.hp1 HG03098.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-413-269_-413-268i others(18): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075265 | ||||||
| chr8:58075265 | T | TTGTGTGT others(11): Show |
1 | a0001c0001t0004g0189 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-413-269_-413-268i others(20): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075265 | ||||||
| chr8:58075265 | T | TTGTGTGT others(13): Show |
1 | a0001c0001t0004g0083 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-413-269_-413-268i others(22): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075265 | ||||||
| chr8:58075265 | T | TTGTGTGT others(15): Show |
1 | a0001c0001t0002g0269 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-413-269_-413-268i others(24): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075265 | ||||||
| chr8:58075267 | T | G | 18 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(15): Show |
18 | HG00733.hp1 HG01261.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.-413-268T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58075267 | |||||||
| chr8:58075267 | T | TTGTGTGT others(5): Show |
1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-413-267_-413-266i others(14): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075267 | ||||||
| chr8:58075267 | T | TTGTGTGT others(11): Show |
1 | a0001c0001t0022g0174 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-413-267_-413-266i others(20): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075267 | ||||||
| chr8:58075267 | T | TTGTGTGT others(13): Show |
2 | a0001c0001t0001g0006 a0001c0001t0002g0012 |
2 | HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-413-267_-413-266i others(22): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075267 | ||||||
| chr8:58075269 | T | G | 22 | a0001c0001t0001g0006 a0001c0001t0001g0084 a0001c0001t0001g0089 others(19): Show |
22 | HG00733.hp1 HG00741.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.-413-266T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58075269 | |||||||
| chr8:58075269 | T | TTGTGTGT others(3): Show |
1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-413-265_-413-264i others(12): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075269 | ||||||
| chr8:58075269 | T | TTGTGTGT others(11): Show |
1 | a0001c0001t0002g0162 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-413-265_-413-264i others(20): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075269 | ||||||
| chr8:58075269 | T | TTGTGTGT others(13): Show |
5 | a0001c0001t0001g0172 a0001c0001t0001g0261 a0001c0001t0001g0262 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-413-265_-413-264i others(22): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075269 | ||||||
| chr8:58075271 | T | G | 44 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0015 others(41): Show |
44 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.-413-264T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58075271 | |||||||
| chr8:58075271 | T | TGTGTGTG others(16): Show |
1 | a0001c0001t0001g0184 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-413-264_-413-263i others(25): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58075271 | |||||||
| chr8:58075271 | T | TTGGTGTG others(14): Show |
1 | a0001c0001t0010g0145 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-413-263_-413-262i others(23): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075271 | ||||||
| chr8:58075271 | T | TTGGTGTG others(16): Show |
12 | a0001c0001t0002g0146 a0001c0001t0002g0152 a0001c0001t0003g0005 others(9): Show |
12 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-413-263_-413-262i others(25): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075271 | ||||||
| chr8:58075271 | T | TTGGTGTG others(18): Show |
1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-413-263_-413-262i others(27): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075271 | ||||||
| chr8:58075271 | T | TTGTGTGT others(11): Show |
3 | a0001c0001t0002g0163 a0001c0001t0002g0291 a0001c0001t0007g0090 |
3 | HG02647.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-413-263_-413-262i others(20): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075271 | ||||||
| chr8:58075271 | T | TTGTGTGT others(13): Show |
2 | a0001c0001t0005g0271 a0001c0001t0007g0131 |
2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-413-263_-413-262i others(22): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075271 | ||||||
| chr8:58075271 | T | TTGTGTGT others(15): Show |
1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-413-263_-413-262i others(24): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075271 | ||||||
| chr8:58075271 | T | TTGTGTGT others(21): Show |
1 | a0001c0001t0001g0185 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-413-263_-413-262i others(30): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075271 | ||||||
| chr8:58075273 | T | G | 79 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(76): Show |
79 | HG00673.hp2 HG00733.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.-413-262T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58075273 | |||||||
| chr8:58075273 | T | TTGTGTGT others(11): Show |
2 | a0001c0001t0001g0158 a0001c0001t0007g0130 |
2 | HG02280.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-413-261_-413-260i others(20): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075273 | ||||||
| chr8:58075275 | T | G | 89 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(86): Show |
89 | HG00621.hp2 HG00673.hp2 HG00733.hp1 others(86): Show |
intron_variant | MODIFIER | c.-413-260T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58075275 | |||||||
| chr8:58075275 | T | TTG | 12 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0104 others(9): Show |
12 | HG00438.hp2 HG00609.hp2 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.-413-240_-413-239d others(4): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075275 | ||||||
| chr8:58075275 | T | TTGTGTGT others(19): Show |
1 | a0001c0001t0002g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-413-239_-413-238i others(28): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075275 | ||||||
| chr8:58075275 | T | TTTTTTGT others(17): Show |
1 | a0001c0001t0003g0133 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-413-259_-413-258i others(26): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075275 | ||||||
| chr8:58075277 | G | T | 41 | a0001c0001t0001g0027 a0001c0001t0001g0045 a0001c0001t0001g0073 others(38): Show |
41 | HG00408.hp2 HG01069.hp1 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.-413-258G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58075277 | |||||||
| chr8:58075317 | T | C | 18 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(15): Show |
18 | HG00733.hp1 HG01261.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.-413-218T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58075317 | |||||||
| chr8:58075479 | G | C | 1 | a0001c0001t0001g0102 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-413-56G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58075479 | |||||||
| chr8:58075505 | A | G | 8 | a0001c0001t0001g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 others(5): Show |
8 | HG00741.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-413-30A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58075505 | |||||||
| chr8:58075661 | G | A | 18 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(15): Show |
18 | HG00733.hp1 HG01261.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.-325+38G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58075661 | |||||||
| chr8:58075751 | A | G | 1 | a0001c0001t0002g0291 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-325+128A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58075751 | |||||||
| chr8:58075825 | C | T | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-325+202C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58075825 | |||||||
| chr8:58075911 | T | C | 1 | a0001c0001t0011g0212 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-325+288T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58075911 | |||||||
| chr8:58076232 | T | G | 1 | a0001c0001t0002g0070 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-325+609T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58076232 | |||||||
| chr8:58076345 | C | T | 14 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0152 others(11): Show |
14 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-325+722C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58076345 | |||||||
| chr8:58076474 | G | A | 8 | a0001c0001t0001g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 others(5): Show |
8 | HG00741.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-325+851G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58076474 | |||||||
| chr8:58076554 | C | T | 1 | a0001c0001t0003g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-325+931C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58076554 | |||||||
| chr8:58076829 | A | G | 1 | a0001c0001t0003g0224 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-325+1206A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58076829 | |||||||
| chr8:58076924 | A | G | 18 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(15): Show |
18 | HG00733.hp1 HG01261.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.-325+1301A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58076924 | |||||||
| chr8:58077062 | C | T | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-325+1439C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58077062 | |||||||
| chr8:58077067 | C | T | 5 | a0001c0001t0002g0059 a0001c0001t0002g0190 a0001c0001t0002g0191 others(2): Show |
5 | HG00597.hp1 NA18948.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-325+1444C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58077067 | |||||||
| chr8:58077145 | C | T | 1 | a0001c0001t0006g0051 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-325+1522C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58077145 | |||||||
| chr8:58077441 | G | C | 8 | a0001c0001t0001g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 others(5): Show |
8 | HG00741.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-325+1818G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58077441 | |||||||
| chr8:58077462 | G | A | 2 | a0001c0001t0003g0295 a0001c0001t0030g0035 |
2 | HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-325+1839G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58077462 | |||||||
| chr8:58077505 | T | C | 1 | a0001c0001t0004g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-325+1882T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58077505 | |||||||
| chr8:58077508 | A | T | 6 | a0001c0001t0002g0146 a0001c0001t0008g0127 a0001c0001t0010g0072 others(3): Show |
6 | HG01891.hp1 HG02622.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-325+1885A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58077508 | |||||||
| chr8:58077553 | GACTGGGA others(4): Show |
G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0026g0021 |
3 | NA18993.hp2 NA18994.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.-325+1931_-325+194 others(15): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58077553 | |||||||
| chr8:58077567 | G | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0026g0021 |
3 | NA18993.hp2 NA18994.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.-325+1944G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58077567 | |||||||
| chr8:58077785 | A | G | 1 | a0001c0001t0011g0212 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-325+2162A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58077785 | |||||||
| chr8:58077801 | A | G | 8 | a0001c0001t0001g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 others(5): Show |
8 | HG00741.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-325+2178A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58077801 | |||||||
| chr8:58077828 | A | G | 3 | a0001c0001t0002g0167 a0001c0001t0003g0133 a0001c0001t0024g0176 |
3 | HG01884.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+2205A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58077828 | |||||||
| chr8:58077845 | A | G | 18 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(15): Show |
18 | HG00733.hp1 HG01261.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.-325+2222A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58077845 | |||||||
| chr8:58077929 | G | A | 1 | a0001c0001t0009g0179 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-325+2306G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58077929 | |||||||
| chr8:58078099 | T | A | 1 | a0001c0001t0001g0277 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-325+2476T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58078099 | |||||||
| chr8:58078133 | T | G | 1 | a0001c0001t0008g0169 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-325+2510T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58078133 | |||||||
| chr8:58078135 | C | T | 18 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(15): Show |
18 | HG00733.hp1 HG01261.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.-325+2512C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58078135 | |||||||
| chr8:58078169 | A | G | 7 | a0001c0001t0001g0027 a0001c0001t0001g0094 a0001c0001t0001g0227 others(4): Show |
7 | HG00621.hp2 HG00673.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.-325+2546A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58078169 | |||||||
| chr8:58078547 | C | CT | 41 | a0001c0001t0001g0027 a0001c0001t0001g0047 a0001c0001t0001g0073 others(38): Show |
41 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.-325+2945dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58078547 | ||||||
| chr8:58078547 | C | CTT | 32 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0015 others(29): Show |
32 | HG00738.hp2 HG01070.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.-325+2944_-325+294 others(6): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58078547 | ||||||
| chr8:58078547 | C | CTTT | 15 | a0001c0001t0001g0089 a0001c0001t0001g0201 a0001c0001t0001g0221 others(12): Show |
15 | HG00733.hp1 HG00735.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.-325+2943_-325+294 others(7): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58078547 | ||||||
| chr8:58078589 | C | T | 1 | a0001c0001t0002g0297 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-325+2966C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58078589 | |||||||
| chr8:58078644 | A | G | 130 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(127): Show |
130 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(127): Show |
intron_variant | MODIFIER | c.-325+3021A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58078644 | |||||||
| chr8:58078750 | C | T | 1 | a0001c0001t0002g0297 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-325+3127C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58078750 | |||||||
| chr8:58078752 | A | G | 19 | a0001c0001t0001g0006 a0001c0001t0001g0158 a0001c0001t0001g0172 others(16): Show |
19 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-325+3129A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58078752 | |||||||
| chr8:58078774 | T | C | 13 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0152 others(10): Show |
13 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-325+3151T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58078774 | |||||||
| chr8:58078839 | C | T | 2 | a0001c0001t0002g0167 a0001c0001t0003g0133 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+3216C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58078839 | |||||||
| chr8:58078846 | G | A | 15 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0104 others(12): Show |
15 | HG00438.hp2 HG00609.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.-325+3223G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58078846 | |||||||
| chr8:58078997 | C | T | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-325+3374C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58078997 | |||||||
| chr8:58078998 | G | A | 13 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0152 others(10): Show |
13 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-325+3375G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58078998 | |||||||
| chr8:58079013 | TGGTCCTC others(10): Show |
T | 5 | a0001c0001t0001g0172 a0001c0001t0001g0261 a0001c0001t0001g0262 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+3394_-325+341 others(21): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58079013 | ||||||
| chr8:58079234 | C | T | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+3611C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079234 | |||||||
| chr8:58079285 | G | A | 36 | a0001c0001t0001g0006 a0001c0001t0001g0158 a0001c0001t0001g0172 others(33): Show |
36 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.-325+3662G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079285 | |||||||
| chr8:58079372 | T | G | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-325+3749T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079372 | |||||||
| chr8:58079401 | A | G | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-325+3778A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079401 | |||||||
| chr8:58079464 | A | G | 1 | a0001c0001t0009g0064 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-325+3841A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079464 | |||||||
| chr8:58079488 | A | G | 7 | a0001c0001t0001g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 others(4): Show |
7 | HG01891.hp2 HG02280.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-325+3865A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079488 | |||||||
| chr8:58079515 | G | A | 1 | a0001c0001t0004g0194 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-325+3892G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079515 | |||||||
| chr8:58079563 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-325+3940G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079563 | |||||||
| chr8:58079583 | C | G | 1 | a0001c0001t0002g0297 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-325+3960C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079583 | |||||||
| chr8:58079622 | A | T | 4 | a0001c0001t0003g0005 a0001c0001t0003g0250 a0001c0001t0012g0148 others(1): Show |
4 | HG01884.hp1 HG02451.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-325+3999A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079622 | |||||||
| chr8:58079629 | A | T | 1 | a0001c0001t0008g0296 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-325+4006A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079629 | |||||||
| chr8:58079673 | C | T | 6 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0002g0057 others(3): Show |
6 | HG02056.hp1 HG02129.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-325+4050C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079673 | |||||||
| chr8:58079782 | TA | T | 13 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0152 others(10): Show |
13 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-325+4170delA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58079782 | ||||||
| chr8:58079816 | T | G | 1 | a0001c0001t0001g0277 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-325+4193T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079816 | |||||||
| chr8:58079846 | G | A | 42 | a0001c0001t0001g0006 a0001c0001t0001g0084 a0001c0001t0001g0089 others(39): Show |
42 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.-325+4223G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079846 | |||||||
| chr8:58079922 | C | T | 6 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0002g0057 others(3): Show |
6 | HG02056.hp1 HG02129.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-325+4299C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079922 | |||||||
| chr8:58080005 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-325+4382G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58080005 | |||||||
| chr8:58080137 | G | C | 2 | a0001c0001t0002g0167 a0001c0001t0003g0133 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+4514G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58080137 | |||||||
| chr8:58080150 | A | C | 1 | a0001c0001t0028g0182 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-325+4527A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58080150 | |||||||
| chr8:58080478 | G | C | 115 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(112): Show |
115 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.-325+4855G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58080478 | |||||||
| chr8:58080731 | G | A | 19 | a0001c0001t0001g0006 a0001c0001t0001g0158 a0001c0001t0001g0172 others(16): Show |
19 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-325+5108G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58080731 | |||||||
| chr8:58081115 | A | T | 19 | a0001c0001t0001g0006 a0001c0001t0001g0158 a0001c0001t0001g0172 others(16): Show |
19 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-325+5492A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58081115 | |||||||
| chr8:58081307 | T | C | 5 | a0001c0001t0001g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(2): Show |
5 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+5684T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58081307 | |||||||
| chr8:58081381 | A | G | 13 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0152 others(10): Show |
13 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-325+5758A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58081381 | |||||||
| chr8:58081486 | C | T | 6 | a0001c0001t0002g0146 a0001c0001t0008g0127 a0001c0001t0010g0072 others(3): Show |
6 | HG01891.hp1 HG02622.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-325+5863C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58081486 | |||||||
| chr8:58081529 | A | C | 5 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0002g0057 others(2): Show |
5 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+5906A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58081529 | |||||||
| chr8:58081669 | C | A | 1 | a0001c0001t0002g0152 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-325+6046C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58081669 | |||||||
| chr8:58081696 | G | A | 1 | a0001c0001t0003g0156 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-325+6073G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58081696 | |||||||
| chr8:58081704 | C | T | 25 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0015 others(22): Show |
25 | HG00735.hp1 HG00738.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.-325+6081C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58081704 | |||||||
| chr8:58081709 | T | A | 6 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0002g0057 others(3): Show |
6 | HG02056.hp1 HG02129.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-325+6086T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58081709 | |||||||
| chr8:58081751 | A | T | 1 | a0001c0001t0008g0265 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-325+6128A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58081751 | |||||||
| chr8:58081952 | A | C | 1 | a0001c0001t0004g0202 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-325+6329A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58081952 | |||||||
| chr8:58082072 | A | G | 1 | a0001c0001t0004g0194 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-325+6449A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58082072 | |||||||
| chr8:58082152 | T | A | 2 | a0001c0001t0002g0123 a0001c0001t0003g0257 |
2 | HG01943.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.-325+6529T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58082152 | |||||||
| chr8:58082226 | A | G | 6 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0002g0057 others(3): Show |
6 | HG02056.hp1 HG02129.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-325+6603A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58082226 | |||||||
| chr8:58082280 | G | A | 2 | a0001c0001t0003g0071 a0001c0001t0007g0157 |
2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-325+6657G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58082280 | |||||||
| chr8:58082355 | C | T | 32 | a0001c0001t0001g0027 a0001c0001t0001g0073 a0001c0001t0001g0094 others(29): Show |
32 | HG00621.hp2 HG00673.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.-325+6732C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58082355 | |||||||
| chr8:58082583 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-325+6960C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58082583 | |||||||
| chr8:58082597 | C | T | 1 | a0001c0001t0007g0131 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-325+6974C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58082597 | |||||||
| chr8:58082775 | C | T | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+7152C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58082775 | |||||||
| chr8:58082818 | G | A | 1 | a0001c0001t0011g0212 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-325+7195G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58082818 | |||||||
| chr8:58082824 | C | T | 32 | a0001c0001t0001g0027 a0001c0001t0001g0073 a0001c0001t0001g0094 others(29): Show |
32 | HG00621.hp2 HG00673.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.-325+7201C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58082824 | |||||||
| chr8:58082842 | T | TTG | 19 | a0001c0001t0001g0006 a0001c0001t0001g0158 a0001c0001t0001g0172 others(16): Show |
19 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-325+7220_-325+722 others(6): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58082842 | ||||||
| chr8:58082847 | G | GT | 34 | a0001c0001t0001g0027 a0001c0001t0001g0073 a0001c0001t0001g0094 others(31): Show |
34 | HG00621.hp2 HG00673.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.-325+7238dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58082847 | ||||||
| chr8:58082847 | G | GTT | 14 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0152 others(11): Show |
14 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-325+7237_-325+723 others(6): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58082847 | ||||||
| chr8:58082847 | G | T | 19 | a0001c0001t0001g0006 a0001c0001t0001g0158 a0001c0001t0001g0172 others(16): Show |
19 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-325+7224G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58082847 | |||||||
| chr8:58082847 | GT | G | 28 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0201 others(25): Show |
28 | HG00609.hp1 HG00733.hp1 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.-325+7238delT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58082847 | ||||||
| chr8:58082914 | C | T | 2 | a0001c0001t0003g0164 a0001c0001t0003g0165 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-325+7291C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58082914 | |||||||
| chr8:58082915 | G | A | 1 | a0001c0001t0002g0297 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-325+7292G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58082915 | |||||||
| chr8:58083012 | T | TA | 20 | a0001c0001t0001g0006 a0001c0001t0001g0158 a0001c0001t0001g0172 others(17): Show |
20 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.-325+7406dupA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58083012 | ||||||
| chr8:58083012 | TA | T | 23 | a0001c0001t0001g0038 a0001c0001t0001g0042 a0001c0001t0002g0146 others(20): Show |
23 | HG00323.hp2 HG01081.hp1 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.-325+7406delA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58083012 | ||||||
| chr8:58083108 | A | G | 5 | a0001c0001t0003g0286 a0001c0001t0003g0287 a0001c0001t0003g0288 others(2): Show |
5 | HG02055.hp1 HG03139.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+7485A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58083108 | |||||||
| chr8:58083215 | G | A | 19 | a0001c0001t0001g0006 a0001c0001t0001g0158 a0001c0001t0001g0172 others(16): Show |
19 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-325+7592G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58083215 | |||||||
| chr8:58083629 | G | C | 1 | a0001c0001t0008g0296 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-325+8006G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58083629 | |||||||
| chr8:58083773 | G | C | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+8150G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58083773 | |||||||
| chr8:58083826 | G | T | 5 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0002g0057 others(2): Show |
5 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+8203G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58083826 | |||||||
| chr8:58083976 | G | A | 1 | a0001c0001t0011g0195 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-325+8353G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58083976 | |||||||
| chr8:58084393 | C | CT | 6 | a0001c0001t0002g0039 a0001c0001t0003g0142 a0001c0001t0003g0280 others(3): Show |
6 | HG00609.hp2 HG00673.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-325+8785dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58084393 | ||||||
| chr8:58084393 | CTT | C | 24 | a0001c0001t0001g0006 a0001c0001t0001g0084 a0001c0001t0001g0089 others(21): Show |
24 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.-325+8784_-325+878 others(6): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58084393 | ||||||
| chr8:58084475 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-325+8852C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58084475 | |||||||
| chr8:58084543 | C | T | 25 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0015 others(22): Show |
25 | HG00735.hp1 HG00738.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.-325+8920C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58084543 | |||||||
| chr8:58084590 | A | G | 14 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0152 others(11): Show |
14 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-325+8967A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58084590 | |||||||
| chr8:58084644 | G | A | 5 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0002g0057 others(2): Show |
5 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+9021G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58084644 | |||||||
| chr8:58084724 | G | A | 73 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0073 others(70): Show |
73 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.-325+9101G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58084724 | |||||||
| chr8:58084772 | G | GT | 19 | a0001c0001t0001g0006 a0001c0001t0001g0158 a0001c0001t0001g0172 others(16): Show |
19 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-325+9151dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58084772 | ||||||
| chr8:58084844 | A | G | 2 | a0001c0001t0002g0297 a0001c0001t0003g0076 |
2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-325+9221A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58084844 | |||||||
| chr8:58084926 | G | A | 73 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0073 others(70): Show |
73 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.-325+9303G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58084926 | |||||||
| chr8:58085063 | G | A | 5 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0002g0057 others(2): Show |
5 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+9440G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58085063 | |||||||
| chr8:58085147 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-325+9524G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58085147 | |||||||
| chr8:58085179 | A | T | 1 | a0001c0001t0009g0199 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-325+9556A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58085179 | |||||||
| chr8:58085289 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-325+9666G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58085289 | |||||||
| chr8:58085461 | C | T | 5 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0002g0057 others(2): Show |
5 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+9838C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58085461 | |||||||
| chr8:58085462 | G | A | 6 | a0001c0001t0001g0267 a0001c0001t0002g0136 a0001c0001t0002g0266 others(3): Show |
6 | HG00733.hp1 HG02257.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-325+9839G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58085462 | |||||||
| chr8:58085794 | G | A | 36 | a0001c0001t0001g0006 a0001c0001t0001g0158 a0001c0001t0001g0172 others(33): Show |
36 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.-325+10171G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58085794 | |||||||
| chr8:58085811 | A | T | 1 | a0001c0001t0004g0279 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-325+10188A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58085811 | |||||||
| chr8:58085838 | C | T | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-325+10215C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58085838 | |||||||
| chr8:58086116 | C | G | 5 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0002g0057 others(2): Show |
5 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+10493C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086116 | |||||||
| chr8:58086281 | A | T | 16 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0152 others(13): Show |
16 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.-325+10658A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086281 | |||||||
| chr8:58086425 | T | C | 5 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0002g0057 others(2): Show |
5 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+10802T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086425 | |||||||
| chr8:58086550 | G | T | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-325+10927G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086550 | |||||||
| chr8:58086563 | A | C | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+10940A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086563 | |||||||
| chr8:58086595 | A | G | 73 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0073 others(70): Show |
73 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.-325+10972A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086595 | |||||||
| chr8:58086596 | C | T | 1 | a0001c0001t0002g0037 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-325+10973C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086596 | |||||||
| chr8:58086617 | C | T | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+10994C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086617 | |||||||
| chr8:58086772 | C | T | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+11149C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086772 | |||||||
| chr8:58086834 | C | A | 2 | a0001c0001t0003g0142 a0001c0001t0009g0140 |
2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-325+11211C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086834 | |||||||
| chr8:58086882 | G | A | 4 | a0001c0001t0003g0299 a0001c0001t0007g0135 a0001c0001t0007g0197 others(1): Show |
4 | HG01069.hp1 HG02055.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-325+11259G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086882 | |||||||
| chr8:58086966 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-325+11343T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086966 | |||||||
| chr8:58086981 | G | A | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-325+11358G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086981 | |||||||
| chr8:58086989 | G | A | 2 | a0001c0001t0002g0167 a0001c0001t0003g0133 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+11366G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086989 | |||||||
| chr8:58086999 | C | T | 5 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0002g0057 others(2): Show |
5 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+11376C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086999 | |||||||
| chr8:58087099 | G | A | 1 | a0001c0001t0002g0263 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-325+11476G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58087099 | |||||||
| chr8:58087115 | C | T | 3 | a0001c0001t0001g0015 a0001c0001t0006g0025 a0001c0001t0006g0218 |
3 | HG01081.hp1 HG01255.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.-325+11492C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58087115 | |||||||
| chr8:58087149 | A | C | 1 | a0001c0001t0003g0122 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-325+11526A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58087149 | |||||||
| chr8:58087381 | G | A | 32 | a0001c0001t0001g0027 a0001c0001t0001g0073 a0001c0001t0001g0094 others(29): Show |
32 | HG00621.hp2 HG00673.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.-325+11758G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58087381 | |||||||
| chr8:58087405 | T | C | 5 | a0001c0001t0001g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(2): Show |
5 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+11782T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58087405 | |||||||
| chr8:58087556 | A | G | 41 | a0001c0001t0001g0006 a0001c0001t0001g0084 a0001c0001t0001g0089 others(38): Show |
41 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.-325+11933A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58087556 | |||||||
| chr8:58087630 | T | C | 2 | a0001c0001t0006g0219 a0001c0001t0006g0220 |
2 | HG01070.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-325+12007T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58087630 | |||||||
| chr8:58088119 | T | C | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+12496T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58088119 | |||||||
| chr8:58088147 | C | T | 5 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0002g0057 others(2): Show |
5 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+12524C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58088147 | |||||||
| chr8:58088617 | T | C | 1 | a0001c0001t0011g0228 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-325+12994T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58088617 | |||||||
| chr8:58088643 | G | A | 6 | a0001c0001t0001g0040 a0001c0001t0001g0098 a0001c0001t0001g0282 others(3): Show |
6 | HG02155.hp2 HG02165.hp2 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+13020G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58088643 | |||||||
| chr8:58088671 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
2 | NA18944.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-325+13048A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58088671 | |||||||
| chr8:58088690 | G | T | 1 | a0001c0001t0003g0204 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-325+13067G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58088690 | |||||||
| chr8:58088926 | A | G | 3 | a0001c0001t0001g0149 a0001c0001t0001g0154 a0001c0001t0035g0290 |
3 | HG02559.hp1 HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-325+13303A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58088926 | |||||||
| chr8:58088936 | C | T | 1 | a0001c0001t0002g0193 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-325+13313C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58088936 | |||||||
| chr8:58088938 | T | C | 13 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0104 others(10): Show |
13 | HG00438.hp2 HG00609.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.-325+13315T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58088938 | |||||||
| chr8:58089053 | G | A | 115 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(112): Show |
115 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.-325+13430G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58089053 | |||||||
| chr8:58089061 | T | C | 5 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0002g0057 others(2): Show |
5 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+13438T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58089061 | |||||||
| chr8:58089141 | A | G | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+13518A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58089141 | |||||||
| chr8:58089186 | G | A | 5 | a0001c0001t0001g0172 a0001c0001t0001g0261 a0001c0001t0001g0262 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+13563G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58089186 | |||||||
| chr8:58089262 | A | G | 1 | a0001c0001t0002g0270 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-325+13639A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58089262 | |||||||
| chr8:58089384 | G | A | 1 | a0001c0001t0004g0125 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-325+13761G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58089384 | |||||||
| chr8:58089493 | C | T | 3 | a0001c0001t0002g0128 a0001c0001t0003g0143 a0001c0001t0007g0144 |
3 | HG03130.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-325+13870C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58089493 | |||||||
| chr8:58089816 | A | G | 1 | a0001c0001t0002g0001 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-325+14193A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58089816 | |||||||
| chr8:58089870 | T | A | 1 | a0001c0001t0008g0169 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-325+14247T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58089870 | |||||||
| chr8:58089914 | A | G | 2 | a0001c0001t0003g0198 a0001c0001t0007g0300 |
2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-325+14291A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58089914 | |||||||
| chr8:58089999 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-325+14376T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58089999 | |||||||
| chr8:58090191 | G | T | 27 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0015 others(24): Show |
27 | HG00735.hp1 HG00738.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.-325+14568G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58090191 | |||||||
| chr8:58090497 | A | G | 5 | a0001c0001t0001g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(2): Show |
5 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+14874A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58090497 | |||||||
| chr8:58090560 | A | T | 1 | a0001c0001t0002g0266 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-325+14937A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58090560 | |||||||
| chr8:58090620 | A | G | 62 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(59): Show |
62 | HG00735.hp1 HG00738.hp2 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.-325+14997A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58090620 | |||||||
| chr8:58090976 | A | G | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+15353A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58090976 | |||||||
| chr8:58091022 | A | G | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-325+15399A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58091022 | |||||||
| chr8:58091156 | A | T | 1 | a0001c0001t0003g0224 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-325+15533A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58091156 | |||||||
| chr8:58091164 | A | C | 6 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0252 others(3): Show |
6 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+15541A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58091164 | |||||||
| chr8:58091191 | C | G | 1 | a0001c0001t0006g0220 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-325+15568C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58091191 | |||||||
| chr8:58091387 | C | T | 21 | a0001c0001t0001g0027 a0001c0001t0001g0094 a0001c0001t0001g0158 others(18): Show |
21 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.-325+15764C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58091387 | |||||||
| chr8:58091417 | C | T | 3 | a0001c0001t0002g0128 a0001c0001t0003g0143 a0001c0001t0007g0144 |
3 | HG03130.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-325+15794C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58091417 | |||||||
| chr8:58091443 | C | T | 9 | a0001c0001t0003g0138 a0001c0001t0003g0141 a0001c0001t0003g0286 others(6): Show |
9 | HG02055.hp1 HG02622.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.-325+15820C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58091443 | |||||||
| chr8:58091444 | G | A | 3 | a0001c0001t0009g0199 a0001c0001t0033g0081 a0001c0001t0037g0180 |
3 | HG02080.hp2 NA18959.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-325+15821G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58091444 | |||||||
| chr8:58091514 | C | A | 1 | a0001c0001t0003g0229 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-325+15891C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58091514 | |||||||
| chr8:58091646 | A | G | 2 | a0001c0001t0002g0167 a0001c0001t0003g0133 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+16023A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58091646 | |||||||
| chr8:58091675 | C | G | 6 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0252 others(3): Show |
6 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+16052C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58091675 | |||||||
| chr8:58091710 | G | A | 2 | a0001c0001t0002g0167 a0001c0001t0003g0133 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+16087G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58091710 | |||||||
| chr8:58091819 | T | C | 9 | a0001c0001t0002g0186 a0001c0001t0003g0129 a0001c0001t0003g0134 others(6): Show |
9 | HG01069.hp1 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-325+16196T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58091819 | |||||||
| chr8:58091853 | C | G | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+16230C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58091853 | |||||||
| chr8:58092188 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-325+16565G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58092188 | |||||||
| chr8:58092235 | A | G | 6 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0252 others(3): Show |
6 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+16612A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58092235 | |||||||
| chr8:58092298 | G | T | 6 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0252 others(3): Show |
6 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+16675G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58092298 | |||||||
| chr8:58092406 | C | A | 39 | a0001c0001t0001g0027 a0001c0001t0001g0094 a0001c0001t0001g0158 others(36): Show |
39 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.-325+16783C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58092406 | |||||||
| chr8:58092776 | C | T | 1 | a0001c0001t0003g0138 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-325+17153C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58092776 | |||||||
| chr8:58092880 | C | G | 1 | a0001c0001t0003g0234 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-325+17257C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58092880 | |||||||
| chr8:58093098 | G | A | 1 | a0001c0001t0008g0173 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-325+17475G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58093098 | |||||||
| chr8:58093156 | G | A | 1 | a0001c0001t0003g0299 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-325+17533G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58093156 | |||||||
| chr8:58093301 | G | A | 1 | a0001c0001t0004g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-325+17678G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58093301 | |||||||
| chr8:58093309 | C | A | 1 | a0001c0001t0004g0279 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-325+17686C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58093309 | |||||||
| chr8:58093348 | G | A | 15 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0152 others(12): Show |
15 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-325+17725G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58093348 | |||||||
| chr8:58093529 | G | A | 2 | a0001c0001t0003g0198 a0001c0001t0007g0300 |
2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-325+17906G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58093529 | |||||||
| chr8:58093584 | T | C | 6 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0252 others(3): Show |
6 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+17961T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58093584 | |||||||
| chr8:58093601 | G | A | 1 | a0002c0002t0016g0166 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-325+17978G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58093601 | |||||||
| chr8:58093645 | C | G | 1 | a0001c0001t0003g0100 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-325+18022C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58093645 | |||||||
| chr8:58093967 | C | T | 1 | a0001c0001t0002g0039 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-325+18344C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58093967 | |||||||
| chr8:58094027 | T | A | 24 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0252 others(21): Show |
24 | HG01884.hp1 HG01891.hp1 HG02056.hp1 others(21): Show |
intron_variant | MODIFIER | c.-325+18404T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094027 | |||||||
| chr8:58094068 | G | A | 4 | a0001c0001t0002g0082 a0001c0001t0004g0063 a0001c0001t0004g0279 others(1): Show |
4 | HG02735.hp2 HG03453.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.-325+18445G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094068 | |||||||
| chr8:58094111 | T | C | 2 | a0001c0001t0002g0167 a0001c0001t0003g0133 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+18488T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094111 | |||||||
| chr8:58094349 | A | C | 2 | a0001c0001t0002g0167 a0001c0001t0003g0133 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+18726A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094349 | |||||||
| chr8:58094433 | A | C | 1 | a0001c0001t0003g0249 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-325+18810A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094433 | |||||||
| chr8:58094607 | T | C | 1 | a0001c0001t0004g0189 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-325+18984T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094607 | |||||||
| chr8:58094609 | G | A | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-325+18986G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094609 | |||||||
| chr8:58094616 | A | T | 3 | a0001c0001t0001g0253 a0001c0001t0001g0258 a0001c0001t0002g0121 |
3 | HG00438.hp2 HG03688.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.-325+18993A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094616 | |||||||
| chr8:58094628 | A | G | 1 | a0001c0001t0003g0204 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-325+19005A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094628 | |||||||
| chr8:58094637 | C | T | 24 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0252 others(21): Show |
24 | HG01884.hp1 HG01891.hp1 HG02056.hp1 others(21): Show |
intron_variant | MODIFIER | c.-325+19014C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094637 | |||||||
| chr8:58094644 | G | A | 1 | a0001c0001t0011g0228 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-325+19021G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094644 | |||||||
| chr8:58094652 | A | G | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+19029A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094652 | |||||||
| chr8:58094728 | C | T | 1 | a0001c0001t0001g0252 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-325+19105C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094728 | |||||||
| chr8:58094729 | G | A | 23 | a0001c0001t0001g0027 a0001c0001t0001g0094 a0001c0001t0001g0158 others(20): Show |
23 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.-325+19106G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094729 | |||||||
| chr8:58094757 | T | G | 71 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0084 others(68): Show |
71 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.-325+19134T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094757 | |||||||
| chr8:58094824 | G | A | 1 | a0001c0001t0023g0085 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-325+19201G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094824 | |||||||
| chr8:58094839 | T | C | 2 | a0001c0001t0002g0167 a0001c0001t0003g0133 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+19216T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094839 | |||||||
| chr8:58094882 | T | C | 6 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0252 others(3): Show |
6 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+19259T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094882 | |||||||
| chr8:58094954 | G | A | 8 | a0001c0001t0001g0027 a0001c0001t0001g0094 a0001c0001t0001g0201 others(5): Show |
8 | HG00621.hp2 HG00673.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.-325+19331G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094954 | |||||||
| chr8:58094962 | C | T | 6 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0252 others(3): Show |
6 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+19339C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094962 | |||||||
| chr8:58095035 | G | A | 2 | a0001c0001t0006g0219 a0001c0001t0006g0220 |
2 | HG01070.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-325+19412G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58095035 | |||||||
| chr8:58095092 | G | A | 1 | a0001c0001t0003g0071 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-325+19469G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58095092 | |||||||
| chr8:58095190 | C | T | 21 | a0001c0001t0001g0027 a0001c0001t0001g0094 a0001c0001t0001g0158 others(18): Show |
21 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.-325+19567C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58095190 | |||||||
| chr8:58095231 | G | A | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+19608G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58095231 | |||||||
| chr8:58095296 | G | A | 1 | a0001c0001t0003g0299 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-325+19673G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58095296 | |||||||
| chr8:58095704 | G | T | 2 | a0001c0001t0001g0042 a0001c0001t0002g0048 |
2 | HG01517.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-325+20081G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58095704 | |||||||
| chr8:58095811 | G | A | 1 | a0001c0001t0002g0291 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-325+20188G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58095811 | |||||||
| chr8:58095823 | C | T | 6 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0252 others(3): Show |
6 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+20200C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58095823 | |||||||
| chr8:58095917 | A | G | 6 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0252 others(3): Show |
6 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+20294A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58095917 | |||||||
| chr8:58095931 | T | G | 6 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0252 others(3): Show |
6 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+20308T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58095931 | |||||||
| chr8:58096040 | T | C | 1 | a0001c0001t0002g0031 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-325+20417T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58096040 | |||||||
| chr8:58096236 | C | T | 6 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0252 others(3): Show |
6 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+20613C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58096236 | |||||||
| chr8:58096300 | C | T | 13 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0104 others(10): Show |
13 | HG00438.hp2 HG00609.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.-325+20677C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58096300 | |||||||
| chr8:58096301 | G | A | 15 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0152 others(12): Show |
15 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-325+20678G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58096301 | |||||||
| chr8:58096466 | G | A | 9 | a0001c0001t0001g0027 a0001c0001t0001g0094 a0001c0001t0001g0201 others(6): Show |
9 | HG00621.hp2 HG00673.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.-325+20843G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58096466 | |||||||
| chr8:58096475 | C | T | 1 | a0001c0001t0008g0169 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-325+20852C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58096475 | |||||||
| chr8:58096501 | C | A | 12 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0104 others(9): Show |
12 | HG00438.hp2 HG00609.hp2 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.-325+20878C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58096501 | |||||||
| chr8:58096519 | T | C | 1 | a0001c0001t0003g0107 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-325+20896T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58096519 | |||||||
| chr8:58096684 | T | C | 6 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0252 others(3): Show |
6 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+21061T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58096684 | |||||||
| chr8:58096787 | T | G | 3 | a0001c0001t0003g0076 a0001c0001t0007g0157 a0001c0001t0031g0159 |
3 | HG01192.hp1 HG02647.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-325+21164T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58096787 | |||||||
| chr8:58096819 | A | G | 15 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0152 others(12): Show |
15 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-325+21196A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58096819 | |||||||
| chr8:58096937 | G | T | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+21314G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58096937 | |||||||
| chr8:58096948 | G | A | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+21325G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58096948 | |||||||
| chr8:58097000 | G | T | 1 | a0001c0001t0006g0246 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-325+21377G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58097000 | |||||||
| chr8:58097143 | A | G | 1 | a0001c0001t0001g0203 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-325+21520A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58097143 | |||||||
| chr8:58097190 | A | G | 25 | a0001c0001t0001g0065 a0001c0001t0001g0226 a0001c0001t0002g0001 others(22): Show |
25 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.-325+21567A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58097190 | |||||||
| chr8:58097303 | C | G | 1 | a0003c0003t0003g0264 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-325+21680C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58097303 | |||||||
| chr8:58097307 | G | T | 21 | a0001c0001t0001g0027 a0001c0001t0001g0094 a0001c0001t0001g0158 others(18): Show |
21 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.-325+21684G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58097307 | |||||||
| chr8:58097441 | A | G | 6 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0252 others(3): Show |
6 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+21818A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58097441 | |||||||
| chr8:58097592 | T | G | 71 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0084 others(68): Show |
71 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.-325+21969T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58097592 | |||||||
| chr8:58097624 | G | A | 8 | a0001c0001t0001g0027 a0001c0001t0001g0094 a0001c0001t0001g0201 others(5): Show |
8 | HG00621.hp2 HG00673.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.-325+22001G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58097624 | |||||||
| chr8:58097686 | C | T | 4 | a0001c0001t0001g0089 a0001c0001t0001g0252 a0001c0001t0004g0083 others(1): Show |
4 | HG02056.hp1 HG02129.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.-325+22063C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58097686 | |||||||
| chr8:58097819 | C | T | 1 | a0003c0003t0003g0264 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-325+22196C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58097819 | |||||||
| chr8:58097953 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-325+22330C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58097953 | |||||||
| chr8:58097954 | G | A | 3 | a0001c0001t0001g0002 a0001c0001t0002g0016 a0001c0001t0002g0153 |
3 | HG00741.hp2 HG01168.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.-325+22331G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58097954 | |||||||
| chr8:58097981 | G | A | 45 | a0001c0001t0001g0027 a0001c0001t0001g0084 a0001c0001t0001g0089 others(42): Show |
45 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.-325+22358G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58097981 | |||||||
| chr8:58097998 | C | T | 115 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0027 others(112): Show |
115 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.-325+22375C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58097998 | |||||||
| chr8:58098126 | G | T | 1 | a0001c0001t0001g0084 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-325+22503G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58098126 | |||||||
| chr8:58098172 | C | G | 1 | a0001c0001t0001g0203 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-325+22549C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58098172 | |||||||
| chr8:58098267 | G | A | 26 | a0001c0001t0001g0006 a0001c0001t0001g0172 a0001c0001t0001g0184 others(23): Show |
26 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.-325+22644G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58098267 | |||||||
| chr8:58098284 | T | C | 1 | a0001c0001t0003g0092 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-325+22661T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58098284 | |||||||
| chr8:58098315 | G | A | 2 | a0001c0001t0002g0167 a0001c0001t0003g0133 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+22692G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58098315 | |||||||
| chr8:58098361 | T | C | 71 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0084 others(68): Show |
71 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.-325+22738T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58098361 | |||||||
| chr8:58098602 | C | T | 1 | a0001c0001t0002g0297 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-325+22979C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58098602 | |||||||
| chr8:58098760 | A | G | 115 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0027 others(112): Show |
115 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.-325+23137A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58098760 | |||||||
| chr8:58098808 | G | A | 1 | a0001c0001t0005g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-325+23185G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58098808 | |||||||
| chr8:58098816 | C | T | 14 | a0001c0001t0002g0082 a0001c0001t0002g0186 a0001c0001t0003g0129 others(11): Show |
14 | HG01069.hp1 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-325+23193C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58098816 | |||||||
| chr8:58098846 | C | T | 1 | a0001c0001t0008g0296 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-325+23223C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58098846 | |||||||
| chr8:58099049 | C | T | 5 | a0001c0001t0001g0089 a0001c0001t0001g0252 a0001c0001t0002g0057 others(2): Show |
5 | HG02056.hp1 HG02129.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-325+23426C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58099049 | |||||||
| chr8:58099142 | A | G | 1 | a0001c0001t0005g0247 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-325+23519A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58099142 | |||||||
| chr8:58099727 | CTG | C | 32 | a0001c0001t0001g0015 a0001c0001t0001g0073 a0001c0001t0001g0221 others(29): Show |
32 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.-325+24108_-325+24 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58099727 | ||||||
| chr8:58099769 | T | C | 26 | a0001c0001t0001g0006 a0001c0001t0001g0172 a0001c0001t0001g0184 others(23): Show |
26 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.-325+24146T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58099769 | |||||||
| chr8:58099804 | A | G | 5 | a0001c0001t0001g0089 a0001c0001t0001g0252 a0001c0001t0002g0057 others(2): Show |
5 | HG02056.hp1 HG02129.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-325+24181A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58099804 | |||||||
| chr8:58099922 | T | C | 1 | a0001c0001t0003g0071 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-325+24299T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58099922 | |||||||
| chr8:58099935 | C | T | 3 | a0001c0001t0002g0167 a0001c0001t0003g0071 a0001c0001t0003g0133 |
3 | HG02717.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+24312C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58099935 | |||||||
| chr8:58100231 | C | G | 15 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0152 others(12): Show |
15 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-325+24608C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58100231 | |||||||
| chr8:58100252 | GA | G | 95 | a0001c0001t0001g0015 a0001c0001t0001g0067 a0001c0001t0001g0068 others(92): Show |
95 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.-325+24643delA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58100252 | ||||||
| chr8:58100321 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-325+24698C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58100321 | |||||||
| chr8:58100640 | A | G | 1 | a0001c0001t0003g0133 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-325+25017A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58100640 | |||||||
| chr8:58100699 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-325+25076T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58100699 | |||||||
| chr8:58100746 | T | G | 1 | a0001c0001t0021g0248 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-325+25123T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58100746 | |||||||
| chr8:58100942 | A | G | 43 | a0001c0001t0001g0027 a0001c0001t0001g0089 a0001c0001t0001g0094 others(40): Show |
43 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.-325+25319A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58100942 | |||||||
| chr8:58101077 | T | C | 1 | a0001c0001t0003g0092 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-325+25454T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58101077 | |||||||
| chr8:58101093 | C | T | 1 | a0001c0001t0002g0181 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-325+25470C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58101093 | |||||||
| chr8:58101099 | C | A | 1 | a0001c0001t0003g0005 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-325+25476C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58101099 | |||||||
| chr8:58101134 | G | A | 2 | a0001c0001t0002g0167 a0001c0001t0003g0133 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+25511G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58101134 | |||||||
| chr8:58101301 | T | C | 5 | a0001c0001t0001g0089 a0001c0001t0001g0252 a0001c0001t0002g0057 others(2): Show |
5 | HG02056.hp1 HG02129.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-325+25678T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58101301 | |||||||
| chr8:58101303 | G | C | 1 | a0001c0001t0008g0170 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-325+25680G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58101303 | |||||||
| chr8:58101408 | C | G | 8 | a0001c0001t0002g0146 a0001c0001t0003g0164 a0001c0001t0003g0165 others(5): Show |
8 | HG01891.hp1 HG02622.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-325+25785C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58101408 | |||||||
| chr8:58101461 | C | G | 20 | a0001c0001t0001g0027 a0001c0001t0001g0094 a0001c0001t0001g0158 others(17): Show |
20 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.-325+25838C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58101461 | |||||||
| chr8:58101545 | C | T | 1 | a0001c0001t0027g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-325+25922C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58101545 | |||||||
| chr8:58101550 | A | G | 2 | a0001c0001t0002g0167 a0001c0001t0003g0133 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+25927A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58101550 | |||||||
| chr8:58101781 | A | G | 25 | a0001c0001t0001g0065 a0001c0001t0001g0226 a0001c0001t0002g0001 others(22): Show |
25 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.-325+26158A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58101781 | |||||||
| chr8:58101881 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-325+26258G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58101881 | |||||||
| chr8:58102028 | A | G | 1 | a0001c0001t0006g0220 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-325+26405A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58102028 | |||||||
| chr8:58102032 | G | A | 11 | a0001c0001t0001g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 others(8): Show |
11 | HG00741.hp1 HG01891.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-325+26409G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58102032 | |||||||
| chr8:58102184 | C | G | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-325+26561C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58102184 | |||||||
| chr8:58102318 | G | T | 2 | a0001c0001t0005g0139 a0001c0001t0010g0294 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-325+26695G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58102318 | |||||||
| chr8:58102505 | C | T | 1 | a0001c0001t0006g0025 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-325+26882C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58102505 | |||||||
| chr8:58102512 | C | T | 1 | a0001c0001t0002g0193 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-325+26889C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58102512 | |||||||
| chr8:58102534 | C | T | 51 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0073 others(48): Show |
51 | HG00621.hp2 HG00673.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.-325+26911C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58102534 | |||||||
| chr8:58102587 | C | T | 1 | a0001c0001t0003g0129 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-325+26964C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58102587 | |||||||
| chr8:58102638 | C | T | 26 | a0001c0001t0001g0006 a0001c0001t0001g0172 a0001c0001t0001g0184 others(23): Show |
26 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.-325+27015C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58102638 | |||||||
| chr8:58102701 | C | A | 1 | a0001c0001t0004g0083 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-325+27078C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58102701 | |||||||
| chr8:58102944 | C | T | 46 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0172 others(43): Show |
46 | HG00735.hp1 HG01069.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.-325+27321C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58102944 | |||||||
| chr8:58103002 | G | GA | 57 | a0001c0001t0001g0017 a0001c0001t0001g0022 a0001c0001t0001g0023 others(54): Show |
57 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.-325+27401dupA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58103002 | ||||||
| chr8:58103002 | G | GAA | 6 | a0001c0001t0001g0089 a0001c0001t0001g0201 a0001c0001t0001g0252 others(3): Show |
6 | HG02056.hp1 HG03942.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+27400_-325+27 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58103002 | ||||||
| chr8:58103002 | GA | G | 23 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0060 others(20): Show |
23 | HG00408.hp1 HG00597.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.-325+27401delA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58103002 | ||||||
| chr8:58103002 | GAA | G | 13 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0152 others(10): Show |
13 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-325+27400_-325+27 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58103002 | ||||||
| chr8:58103002 | GAAAAAAA others(1): Show |
G | 62 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0067 others(59): Show |
62 | HG00438.hp2 HG00609.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.-325+27394_-325+27 others(14): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58103002 | ||||||
| chr8:58103002 | GAAAAAAA others(2): Show |
G | 9 | a0001c0001t0002g0186 a0001c0001t0003g0129 a0001c0001t0003g0134 others(6): Show |
9 | HG01069.hp1 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-325+27393_-325+27 others(15): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58103002 | ||||||
| chr8:58103218 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-325+27595G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58103218 | |||||||
| chr8:58103321 | C | T | 1 | a0001c0001t0001g0281 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-325+27698C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58103321 | |||||||
| chr8:58103360 | C | T | 15 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0152 others(12): Show |
15 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-325+27737C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58103360 | |||||||
| chr8:58103375 | A | G | 20 | a0001c0001t0001g0027 a0001c0001t0001g0094 a0001c0001t0001g0158 others(17): Show |
20 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.-325+27752A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58103375 | |||||||
| chr8:58103580 | G | A | 3 | a0001c0001t0002g0082 a0001c0001t0004g0063 a0001c0001t0004g0279 |
3 | HG02735.hp2 NA18990.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.-325+27957G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58103580 | |||||||
| chr8:58103755 | C | G | 8 | a0001c0001t0001g0027 a0001c0001t0001g0094 a0001c0001t0001g0201 others(5): Show |
8 | HG00621.hp2 HG00673.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.-325+28132C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58103755 | |||||||
| chr8:58103819 | C | CT | 14 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0104 others(11): Show |
14 | HG00438.hp2 HG00609.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.-325+28203dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58103819 | ||||||
| chr8:58104179 | G | A | 5 | a0001c0001t0001g0089 a0001c0001t0001g0252 a0001c0001t0002g0057 others(2): Show |
5 | HG02056.hp1 HG02129.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-325+28556G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58104179 | |||||||
| chr8:58104189 | G | T | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+28566G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58104189 | |||||||
| chr8:58104480 | T | G | 5 | a0001c0001t0001g0089 a0001c0001t0001g0252 a0001c0001t0002g0057 others(2): Show |
5 | HG02056.hp1 HG02129.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-325+28857T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58104480 | |||||||
| chr8:58104512 | A | G | 3 | a0001c0001t0003g0142 a0001c0001t0009g0140 a0001c0001t0022g0174 |
3 | HG00741.hp1 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-325+28889A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58104512 | |||||||
| chr8:58104749 | C | T | 2 | a0001c0001t0002g0167 a0001c0001t0003g0133 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+29126C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58104749 | |||||||
| chr8:58104915 | C | T | 259 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(256): Show |
259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.-325+29292C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58104915 | |||||||
| chr8:58104958 | A | G | 20 | a0001c0001t0001g0027 a0001c0001t0001g0094 a0001c0001t0001g0158 others(17): Show |
20 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.-325+29335A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58104958 | |||||||
| chr8:58104962 | G | GA | 109 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0027 others(106): Show |
109 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(106): Show |
intron_variant | MODIFIER | c.-325+29354dupA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58104962 | ||||||
| chr8:58104962 | G | GAA | 6 | a0001c0001t0001g0089 a0001c0001t0001g0252 a0001c0001t0002g0057 others(3): Show |
6 | HG02056.hp1 HG02129.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-325+29353_-325+29 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58104962 | ||||||
| chr8:58104999 | C | CT | 9 | a0001c0001t0001g0073 a0001c0001t0002g0152 a0001c0001t0003g0074 others(6): Show |
9 | HG01943.hp1 HG02145.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-325+29390dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58104999 | ||||||
| chr8:58104999 | CT | C | 8 | a0001c0001t0001g0089 a0001c0001t0001g0252 a0001c0001t0002g0057 others(5): Show |
8 | HG01070.hp1 HG02056.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.-325+29390delT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58104999 | ||||||
| chr8:58105556 | A | AT | 115 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(112): Show |
115 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.-325+29963dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58105556 | ||||||
| chr8:58105556 | A | ATT | 13 | a0001c0001t0001g0043 a0001c0001t0001g0230 a0001c0001t0002g0152 others(10): Show |
13 | HG01071.hp2 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.-325+29962_-325+29 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58105556 | ||||||
| chr8:58105556 | ATT | A | 9 | a0001c0001t0002g0167 a0001c0001t0002g0297 a0001c0001t0003g0071 others(6): Show |
9 | HG01433.hp2 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-325+29962_-325+29 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58105556 | ||||||
| chr8:58105556 | ATTT | A | 17 | a0001c0001t0001g0068 a0001c0001t0001g0073 a0001c0001t0001g0104 others(14): Show |
17 | HG00438.hp2 HG00609.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.-325+29961_-325+29 others(9): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58105556 | ||||||
| chr8:58105556 | ATTTT | A | 24 | a0001c0001t0001g0015 a0001c0001t0001g0067 a0001c0001t0001g0253 others(21): Show |
24 | HG01070.hp1 HG01081.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.-325+29960_-325+29 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58105556 | ||||||
| chr8:58105556 | ATTTTTTT | A | 13 | a0001c0001t0002g0186 a0001c0001t0003g0129 a0001c0001t0003g0134 others(10): Show |
13 | HG00741.hp1 HG01069.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-325+29957_-325+29 others(13): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58105556 | ||||||
| chr8:58105556 | ATTTTTTT others(1): Show |
A | 12 | a0001c0001t0001g0006 a0001c0001t0001g0172 a0001c0001t0001g0184 others(9): Show |
12 | HG01070.hp2 HG01071.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-325+29956_-325+29 others(14): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58105556 | ||||||
| chr8:58105816 | C | T | 1 | a0001c0001t0025g0009 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-325+30193C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58105816 | |||||||
| chr8:58105850 | A | G | 114 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0027 others(111): Show |
114 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(111): Show |
intron_variant | MODIFIER | c.-325+30227A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58105850 | |||||||
| chr8:58105949 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-325+30326C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58105949 | |||||||
| chr8:58106015 | A | T | 2 | a0001c0001t0002g0167 a0001c0001t0003g0133 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+30392A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58106015 | |||||||
| chr8:58106078 | C | T | 5 | a0001c0001t0001g0089 a0001c0001t0001g0252 a0001c0001t0002g0057 others(2): Show |
5 | HG02056.hp1 HG02129.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-325+30455C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58106078 | |||||||
| chr8:58106085 | T | C | 26 | a0001c0001t0001g0006 a0001c0001t0001g0172 a0001c0001t0001g0184 others(23): Show |
26 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.-325+30462T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58106085 | |||||||
| chr8:58106093 | A | G | 15 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0152 others(12): Show |
15 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-325+30470A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58106093 | |||||||
| chr8:58106115 | G | A | 5 | a0001c0001t0001g0089 a0001c0001t0001g0252 a0001c0001t0002g0057 others(2): Show |
5 | HG02056.hp1 HG02129.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-325+30492G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58106115 | |||||||
| chr8:58106147 | G | A | 5 | a0001c0001t0001g0089 a0001c0001t0001g0252 a0001c0001t0002g0057 others(2): Show |
5 | HG02056.hp1 HG02129.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-325+30524G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58106147 | |||||||
| chr8:58106409 | A | G | 1 | a0001c0001t0002g0037 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-325+30786A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58106409 | |||||||
| chr8:58106565 | A | G | 1 | a0001c0001t0002g0117 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-325+30942A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58106565 | |||||||
| chr8:58106625 | G | A | 1 | a0001c0001t0003g0133 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-325+31002G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58106625 | |||||||
| chr8:58106641 | T | G | 5 | a0001c0001t0001g0089 a0001c0001t0001g0252 a0001c0001t0002g0057 others(2): Show |
5 | HG02056.hp1 HG02129.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-325+31018T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58106641 | |||||||
| chr8:58106650 | A | G | 2 | a0001c0001t0001g0236 a0001c0001t0003g0251 |
2 | HG02080.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.-325+31027A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58106650 | |||||||
| chr8:58106674 | AAGGAGTT others(3): Show |
A | 1 | a0001c0001t0001g0203 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-325+31054_-325+31 others(16): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58106674 | ||||||
| chr8:58106832 | A | C | 1 | a0001c0001t0003g0133 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-325+31209A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58106832 | |||||||
| chr8:58106991 | G | A | 4 | a0001c0001t0001g0060 a0001c0001t0001g0149 a0001c0001t0001g0154 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-325+31368G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58106991 | |||||||
| chr8:58107013 | C | A | 47 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0094 others(44): Show |
47 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.-325+31390C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58107013 | |||||||
| chr8:58107077 | T | TA | 50 | a0001c0001t0001g0015 a0001c0001t0001g0067 a0001c0001t0001g0068 others(47): Show |
50 | HG00438.hp2 HG00609.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.-325+31465dupA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58107077 | ||||||
| chr8:58107077 | TA | T | 18 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0152 others(15): Show |
18 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-325+31465delA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58107077 | ||||||
| chr8:58107111 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-325+31488C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58107111 | |||||||
| chr8:58107221 | A | G | 1 | a0001c0001t0004g0202 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-325+31598A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58107221 | |||||||
| chr8:58107340 | G | T | 110 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0027 others(107): Show |
110 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(107): Show |
intron_variant | MODIFIER | c.-325+31717G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58107340 | |||||||
| chr8:58107409 | C | G | 1 | a0001c0001t0002g0269 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-325+31786C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58107409 | |||||||
| chr8:58107535 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-325+31912G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58107535 | |||||||
| chr8:58107610 | G | A | 114 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0027 others(111): Show |
114 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(111): Show |
intron_variant | MODIFIER | c.-325+31987G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58107610 | |||||||
| chr8:58107709 | G | T | 49 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0094 others(46): Show |
49 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.-325+32086G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58107709 | |||||||
| chr8:58107846 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-325+32223C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58107846 | |||||||
| chr8:58107862 | G | A | 2 | a0001c0001t0002g0167 a0001c0001t0003g0133 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+32239G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58107862 | |||||||
| chr8:58108003 | G | A | 2 | a0001c0001t0002g0167 a0001c0001t0003g0133 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+32380G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58108003 | |||||||
| chr8:58108009 | A | G | 1 | a0001c0001t0003g0049 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-325+32386A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58108009 | |||||||
| chr8:58108017 | T | A | 1 | a0001c0001t0005g0247 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-325+32394T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58108017 | |||||||
| chr8:58108232 | G | A | 1 | a0001c0001t0003g0234 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-325+32609G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58108232 | |||||||
| chr8:58108542 | C | T | 8 | a0001c0001t0001g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 others(5): Show |
8 | HG01891.hp2 HG02280.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-325+32919C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58108542 | |||||||
| chr8:58108770 | G | A | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-325+33147G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58108770 | |||||||
| chr8:58108847 | C | T | 27 | a0001c0001t0001g0006 a0001c0001t0001g0172 a0001c0001t0001g0184 others(24): Show |
27 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.-325+33224C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58108847 | |||||||
| chr8:58108889 | G | T | 36 | a0001c0001t0001g0015 a0001c0001t0001g0073 a0001c0001t0001g0089 others(33): Show |
36 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.-325+33266G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58108889 | |||||||
| chr8:58108963 | T | A | 2 | a0001c0001t0003g0198 a0001c0001t0007g0300 |
2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-325+33340T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58108963 | |||||||
| chr8:58109089 | G | A | 98 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0027 others(95): Show |
98 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.-325+33466G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58109089 | |||||||
| chr8:58109108 | C | T | 1 | a0001c0001t0008g0296 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-325+33485C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58109108 | |||||||
| chr8:58109218 | A | G | 11 | a0001c0001t0001g0040 a0001c0001t0001g0098 a0001c0001t0001g0103 others(8): Show |
11 | HG00544.hp1 HG02027.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.-325+33595A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58109218 | |||||||
| chr8:58109286 | G | A | 21 | a0001c0001t0001g0015 a0001c0001t0001g0221 a0001c0001t0001g0285 others(18): Show |
21 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.-325+33663G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58109286 | |||||||
| chr8:58109763 | G | A | 5 | a0001c0001t0001g0038 a0001c0001t0002g0032 a0001c0001t0003g0034 others(2): Show |
5 | HG00642.hp1 HG01074.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.-325+34140G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58109763 | |||||||
| chr8:58109957 | G | A | 20 | a0001c0001t0001g0027 a0001c0001t0001g0094 a0001c0001t0001g0158 others(17): Show |
20 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.-325+34334G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58109957 | |||||||
| chr8:58110062 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-325+34439A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58110062 | |||||||
| chr8:58110136 | A | C | 1 | a0001c0001t0010g0294 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-325+34513A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58110136 | |||||||
| chr8:58110265 | G | T | 2 | a0001c0001t0007g0135 a0001c0001t0007g0197 |
2 | HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-325+34642G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58110265 | |||||||
| chr8:58110453 | C | G | 1 | a0001c0001t0003g0249 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-325+34830C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58110453 | |||||||
| chr8:58110679 | A | G | 1 | a0001c0001t0006g0245 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-325+35056A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58110679 | |||||||
| chr8:58110810 | T | C | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-324-35097T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58110810 | |||||||
| chr8:58110925 | C | G | 21 | a0001c0001t0001g0015 a0001c0001t0001g0221 a0001c0001t0001g0285 others(18): Show |
21 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.-324-34982C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58110925 | |||||||
| chr8:58111099 | G | A | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-324-34808G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58111099 | |||||||
| chr8:58111163 | C | G | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-324-34744C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58111163 | |||||||
| chr8:58111190 | C | T | 1 | a0001c0001t0026g0021 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-324-34717C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58111190 | |||||||
| chr8:58111280 | G | A | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-324-34627G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58111280 | |||||||
| chr8:58111369 | G | A | 1 | a0001c0001t0002g0239 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-324-34538G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58111369 | |||||||
| chr8:58111410 | G | A | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-324-34497G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58111410 | |||||||
| chr8:58111538 | A | C | 1 | a0001c0001t0002g0001 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-324-34369A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58111538 | |||||||
| chr8:58111644 | A | G | 1 | a0001c0001t0002g0048 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-324-34263A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58111644 | |||||||
| chr8:58111751 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-324-34156C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58111751 | |||||||
| chr8:58111771 | T | C | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-324-34136T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58111771 | |||||||
| chr8:58111922 | G | C | 2 | a0001c0001t0002g0167 a0001c0001t0003g0133 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-324-33985G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58111922 | |||||||
| chr8:58112027 | T | G | 1 | a0001c0001t0002g0121 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-324-33880T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58112027 | |||||||
| chr8:58112154 | T | C | 115 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0027 others(112): Show |
115 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.-324-33753T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58112154 | |||||||
| chr8:58112213 | C | T | 1 | a0001c0001t0002g0297 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-324-33694C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58112213 | |||||||
| chr8:58112244 | G | A | 21 | a0001c0001t0001g0015 a0001c0001t0001g0221 a0001c0001t0001g0285 others(18): Show |
21 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.-324-33663G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58112244 | |||||||
| chr8:58112278 | A | C | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-324-33629A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58112278 | |||||||
| chr8:58112279 | A | T | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-324-33628A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58112279 | |||||||
| chr8:58112281 | A | G | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-324-33626A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58112281 | |||||||
| chr8:58112282 | T | G | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-324-33625T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58112282 | |||||||
| chr8:58112299 | A | G | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-324-33608A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58112299 | |||||||
| chr8:58112433 | G | A | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-324-33474G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58112433 | |||||||
| chr8:58112555 | T | C | 22 | a0001c0001t0001g0027 a0001c0001t0001g0094 a0001c0001t0001g0158 others(19): Show |
22 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.-324-33352T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58112555 | |||||||
| chr8:58112756 | G | A | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-324-33151G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58112756 | |||||||
| chr8:58112837 | G | A | 2 | a0001c0001t0002g0167 a0001c0001t0003g0133 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-324-33070G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58112837 | |||||||
| chr8:58112885 | C | A | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-324-33022C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58112885 | |||||||
| chr8:58113088 | TG | T | 96 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0027 others(93): Show |
96 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.-324-32810delG | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58113088 | ||||||
| chr8:58113502 | C | T | 1 | a0001c0001t0005g0274 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-324-32405C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58113502 | |||||||
| chr8:58113636 | A | G | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-324-32271A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58113636 | |||||||
| chr8:58113759 | C | T | 36 | a0001c0001t0001g0015 a0001c0001t0001g0073 a0001c0001t0001g0089 others(33): Show |
36 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.-324-32148C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58113759 | |||||||
| chr8:58113880 | A | G | 4 | a0001c0001t0002g0031 a0001c0001t0002g0036 a0001c0001t0002g0126 others(1): Show |
4 | HG00280.hp1 HG01433.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.-324-32027A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58113880 | |||||||
| chr8:58113935 | G | A | 3 | a0001c0001t0001g0253 a0001c0001t0001g0258 a0001c0001t0002g0121 |
3 | HG00438.hp2 HG03688.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.-324-31972G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58113935 | |||||||
| chr8:58113961 | A | T | 3 | a0001c0001t0002g0128 a0001c0001t0003g0143 a0001c0001t0007g0144 |
3 | HG03130.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-324-31946A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58113961 | |||||||
| chr8:58114283 | C | T | 34 | a0001c0001t0001g0027 a0001c0001t0001g0067 a0001c0001t0001g0068 others(31): Show |
34 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.-324-31624C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58114283 | |||||||
| chr8:58114301 | A | G | 2 | a0001c0001t0001g0006 a0001c0001t0002g0012 |
2 | HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-324-31606A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58114301 | |||||||
| chr8:58114383 | G | A | 37 | a0001c0001t0001g0015 a0001c0001t0001g0073 a0001c0001t0001g0089 others(34): Show |
37 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.-324-31524G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58114383 | |||||||
| chr8:58114578 | C | T | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-324-31329C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58114578 | |||||||
| chr8:58114615 | G | A | 5 | a0001c0001t0001g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(2): Show |
5 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-324-31292G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58114615 | |||||||
| chr8:58114706 | G | A | 3 | a0001c0001t0003g0142 a0001c0001t0009g0140 a0001c0001t0022g0174 |
3 | HG00741.hp1 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-324-31201G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58114706 | |||||||
| chr8:58114709 | A | G | 1 | a0002c0002t0016g0166 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-324-31198A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58114709 | |||||||
| chr8:58114797 | G | T | 1 | a0001c0001t0002g0057 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-324-31110G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58114797 | |||||||
| chr8:58114919 | G | A | 2 | a0001c0001t0002g0126 a0001c0001t0004g0125 |
2 | HG00280.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-324-30988G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58114919 | |||||||
| chr8:58115007 | GTT | G | 16 | a0001c0001t0001g0172 a0001c0001t0001g0184 a0001c0001t0001g0185 others(13): Show |
16 | HG00733.hp2 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.-324-30887_-324-30 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58115007 | ||||||
| chr8:58115007 | GTTT | G | 102 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0027 others(99): Show |
102 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(99): Show |
intron_variant | MODIFIER | c.-324-30888_-324-30 others(9): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58115007 | ||||||
| chr8:58115294 | T | C | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-324-30613T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58115294 | |||||||
| chr8:58115361 | A | G | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-324-30546A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58115361 | |||||||
| chr8:58115379 | A | AT | 47 | a0001c0001t0001g0006 a0001c0001t0001g0073 a0001c0001t0001g0158 others(44): Show |
47 | HG00733.hp2 HG00741.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.-324-30520dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58115379 | ||||||
| chr8:58115493 | AG | A | 6 | a0001c0001t0002g0291 a0001c0001t0003g0142 a0001c0001t0007g0090 others(3): Show |
6 | HG01891.hp2 HG02280.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-324-30413delG | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58115493 | |||||||
| chr8:58115672 | C | A | 42 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0046 others(39): Show |
42 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.-324-30235C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58115672 | |||||||
| chr8:58115755 | G | T | 1 | a0001c0001t0010g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-324-30152G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58115755 | |||||||
| chr8:58115822 | C | G | 1 | a0001c0001t0008g0265 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-324-30085C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58115822 | |||||||
| chr8:58115974 | C | G | 4 | a0001c0001t0001g0038 a0001c0001t0003g0034 a0001c0001t0006g0051 others(1): Show |
4 | HG01074.hp1 HG01081.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.-324-29933C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58115974 | |||||||
| chr8:58116035 | T | C | 3 | a0001c0001t0004g0260 a0001c0001t0005g0139 a0001c0001t0010g0294 |
3 | HG02965.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-324-29872T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58116035 | |||||||
| chr8:58116092 | G | A | 24 | a0001c0001t0001g0015 a0001c0001t0001g0089 a0001c0001t0001g0221 others(21): Show |
24 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.-324-29815G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58116092 | |||||||
| chr8:58116104 | A | G | 1 | a0001c0001t0004g0279 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-324-29803A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58116104 | |||||||
| chr8:58116112 | A | G | 2 | a0001c0001t0002g0297 a0001c0001t0031g0159 |
2 | HG01192.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-324-29795A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58116112 | |||||||
| chr8:58116135 | A | G | 5 | a0001c0001t0001g0285 a0001c0001t0002g0059 a0001c0001t0002g0190 others(2): Show |
5 | NA18948.hp2 NA18970.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-324-29772A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58116135 | |||||||
| chr8:58116179 | A | G | 24 | a0001c0001t0001g0015 a0001c0001t0001g0089 a0001c0001t0001g0221 others(21): Show |
24 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.-324-29728A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58116179 | |||||||
| chr8:58116257 | T | C | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-324-29650T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58116257 | |||||||
| chr8:58116301 | G | A | 66 | a0001c0001t0001g0015 a0001c0001t0001g0040 a0001c0001t0001g0045 others(63): Show |
66 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.-324-29606G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58116301 | |||||||
| chr8:58116627 | G | A | 42 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0046 others(39): Show |
42 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.-324-29280G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58116627 | |||||||
| chr8:58116840 | G | A | 1 | a0001c0001t0004g0279 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-324-29067G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58116840 | |||||||
| chr8:58116939 | A | G | 2 | a0001c0001t0007g0135 a0001c0001t0007g0197 |
2 | HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-324-28968A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58116939 | |||||||
| chr8:58117035 | G | A | 2 | a0001c0001t0002g0167 a0001c0001t0003g0133 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-324-28872G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58117035 | |||||||
| chr8:58117047 | G | A | 1 | a0001c0001t0007g0131 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-324-28860G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58117047 | |||||||
| chr8:58117076 | T | A | 48 | a0001c0001t0001g0073 a0001c0001t0001g0158 a0001c0001t0001g0172 others(45): Show |
48 | HG00733.hp2 HG00741.hp1 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.-324-28831T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58117076 | |||||||
| chr8:58117164 | G | A | 118 | a0001c0001t0001g0015 a0001c0001t0001g0040 a0001c0001t0001g0045 others(115): Show |
118 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.-324-28743G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58117164 | |||||||
| chr8:58117310 | T | G | 5 | a0001c0001t0001g0172 a0001c0001t0001g0261 a0001c0001t0001g0262 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-324-28597T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58117310 | |||||||
| chr8:58117524 | T | C | 3 | a0001c0001t0004g0260 a0001c0001t0005g0139 a0001c0001t0010g0294 |
3 | HG02965.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-324-28383T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58117524 | |||||||
| chr8:58117566 | G | A | 2 | a0001c0001t0002g0297 a0001c0001t0031g0159 |
2 | HG01192.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-324-28341G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58117566 | |||||||
| chr8:58117705 | C | T | 42 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0046 others(39): Show |
42 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.-324-28202C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58117705 | |||||||
| chr8:58117734 | C | T | 5 | a0001c0001t0001g0047 a0001c0001t0001g0111 a0001c0001t0001g0118 others(2): Show |
5 | NA18942.hp2 NA18950.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.-324-28173C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58117734 | |||||||
| chr8:58118011 | C | A | 2 | a0001c0001t0002g0297 a0001c0001t0031g0159 |
2 | HG01192.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-324-27896C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58118011 | |||||||
| chr8:58118018 | A | G | 24 | a0001c0001t0001g0073 a0001c0001t0001g0158 a0001c0001t0002g0128 others(21): Show |
24 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.-324-27889A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58118018 | |||||||
| chr8:58118204 | T | C | 157 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0027 others(154): Show |
157 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(154): Show |
intron_variant | MODIFIER | c.-324-27703T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58118204 | |||||||
| chr8:58118339 | T | A | 30 | a0001c0001t0001g0015 a0001c0001t0001g0089 a0001c0001t0001g0221 others(27): Show |
30 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.-324-27568T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58118339 | |||||||
| chr8:58118443 | G | A | 35 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0094 others(32): Show |
35 | HG00621.hp2 HG00673.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.-324-27464G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58118443 | |||||||
| chr8:58118537 | T | C | 2 | a0001c0001t0001g0149 a0001c0001t0001g0154 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-324-27370T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58118537 | |||||||
| chr8:58118553 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-324-27354A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58118553 | |||||||
| chr8:58118646 | G | T | 8 | a0001c0001t0001g0089 a0001c0001t0001g0252 a0001c0001t0003g0295 others(5): Show |
8 | HG01109.hp1 HG01243.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.-324-27261G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58118646 | |||||||
| chr8:58118663 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-324-27244C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58118663 | |||||||
| chr8:58118881 | C | T | 1 | a0001c0001t0011g0212 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-324-27026C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58118881 | |||||||
| chr8:58118934 | C | T | 29 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0094 others(26): Show |
29 | HG00621.hp2 HG00673.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.-324-26973C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58118934 | |||||||
| chr8:58119148 | C | A | 1 | a0001c0001t0004g0202 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-324-26759C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58119148 | |||||||
| chr8:58119163 | T | C | 1 | a0001c0001t0008g0170 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-324-26744T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58119163 | |||||||
| chr8:58119336 | G | A | 16 | a0001c0001t0001g0047 a0001c0001t0001g0098 a0001c0001t0001g0110 others(13): Show |
16 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(13): Show |
intron_variant | MODIFIER | c.-324-26571G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58119336 | |||||||
| chr8:58119397 | C | T | 1 | a0001c0001t0003g0292 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-324-26510C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58119397 | |||||||
| chr8:58119488 | A | G | 3 | a0001c0001t0007g0090 a0001c0001t0007g0130 a0001c0001t0007g0131 |
3 | HG01891.hp2 HG02280.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-324-26419A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58119488 | |||||||
| chr8:58119812 | G | A | 30 | a0001c0001t0001g0015 a0001c0001t0001g0089 a0001c0001t0001g0221 others(27): Show |
30 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.-324-26095G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58119812 | |||||||
| chr8:58119902 | T | G | 2 | a0001c0001t0002g0024 a0001c0001t0003g0280 |
2 | HG00621.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.-324-26005T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58119902 | |||||||
| chr8:58119996 | G | A | 2 | a0001c0001t0002g0162 a0001c0001t0002g0163 |
2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-324-25911G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58119996 | |||||||
| chr8:58120013 | C | T | 121 | a0001c0001t0001g0015 a0001c0001t0001g0040 a0001c0001t0001g0045 others(118): Show |
121 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.-324-25894C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58120013 | |||||||
| chr8:58120042 | C | T | 42 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0046 others(39): Show |
42 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.-324-25865C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58120042 | |||||||
| chr8:58120112 | A | G | 1 | a0001c0001t0002g0059 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-324-25795A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58120112 | |||||||
| chr8:58120324 | A | G | 2 | a0001c0001t0002g0167 a0001c0001t0003g0133 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-324-25583A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58120324 | |||||||
| chr8:58120390 | TC | T | 6 | a0001c0001t0002g0291 a0001c0001t0003g0142 a0001c0001t0007g0090 others(3): Show |
6 | HG01891.hp2 HG02280.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-324-25515delC | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58120390 | ||||||
| chr8:58120444 | G | A | 1 | a0001c0001t0006g0113 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-324-25463G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58120444 | |||||||
| chr8:58120457 | A | G | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-324-25450A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58120457 | |||||||
| chr8:58120621 | G | C | 72 | a0001c0001t0001g0015 a0001c0001t0001g0040 a0001c0001t0001g0045 others(69): Show |
72 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.-324-25286G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58120621 | |||||||
| chr8:58120656 | G | A | 2 | a0001c0001t0002g0167 a0001c0001t0003g0133 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-324-25251G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58120656 | |||||||
| chr8:58120662 | G | T | 4 | a0001c0001t0003g0129 a0001c0001t0003g0134 a0001c0001t0005g0161 others(1): Show |
4 | HG02559.hp1 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-324-25245G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58120662 | |||||||
| chr8:58120741 | A | C | 29 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0094 others(26): Show |
29 | HG00621.hp2 HG00673.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.-324-25166A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58120741 | |||||||
| chr8:58120833 | C | T | 121 | a0001c0001t0001g0015 a0001c0001t0001g0040 a0001c0001t0001g0045 others(118): Show |
121 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.-324-25074C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58120833 | |||||||
| chr8:58120914 | G | A | 1 | a0001c0001t0003g0156 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-324-24993G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58120914 | |||||||
| chr8:58121167 | G | A | 1 | a0001c0001t0007g0004 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-324-24740G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58121167 | |||||||
| chr8:58121183 | G | A | 44 | a0001c0001t0001g0073 a0001c0001t0001g0158 a0001c0001t0001g0172 others(41): Show |
44 | HG00733.hp2 HG00741.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.-324-24724G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58121183 | |||||||
| chr8:58121284 | A | G | 30 | a0001c0001t0001g0015 a0001c0001t0001g0089 a0001c0001t0001g0221 others(27): Show |
30 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.-324-24623A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58121284 | |||||||
| chr8:58121364 | C | T | 1 | a0001c0001t0002g0192 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-324-24543C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58121364 | |||||||
| chr8:58121433 | A | G | 2 | a0001c0001t0003g0295 a0001c0001t0030g0035 |
2 | HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-324-24474A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58121433 | |||||||
| chr8:58121629 | A | G | 157 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0027 others(154): Show |
157 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(154): Show |
intron_variant | MODIFIER | c.-324-24278A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58121629 | |||||||
| chr8:58121704 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-324-24203G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58121704 | |||||||
| chr8:58121706 | C | T | 1 | a0001c0001t0021g0248 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-324-24201C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58121706 | |||||||
| chr8:58121805 | C | T | 28 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0094 others(25): Show |
28 | HG00621.hp2 HG00673.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.-324-24102C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58121805 | |||||||
| chr8:58121910 | G | A | 3 | a0001c0001t0004g0260 a0001c0001t0005g0139 a0001c0001t0010g0294 |
3 | HG02965.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-324-23997G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58121910 | |||||||
| chr8:58122069 | T | A | 3 | a0001c0001t0004g0260 a0001c0001t0005g0139 a0001c0001t0010g0294 |
3 | HG02965.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-324-23838T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58122069 | |||||||
| chr8:58122093 | G | C | 1 | a0001c0001t0003g0049 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-324-23814G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58122093 | |||||||
| chr8:58122343 | G | A | 1 | a0001c0001t0007g0135 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-324-23564G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58122343 | |||||||
| chr8:58122446 | T | C | 43 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0046 others(40): Show |
43 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.-324-23461T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58122446 | |||||||
| chr8:58123140 | G | A | 8 | a0001c0001t0001g0089 a0001c0001t0001g0252 a0001c0001t0003g0295 others(5): Show |
8 | HG01109.hp1 HG01243.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.-324-22767G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58123140 | |||||||
| chr8:58123300 | G | A | 3 | a0001c0001t0001g0102 a0001c0001t0001g0267 a0001c0001t0005g0238 |
3 | HG00733.hp1 HG00735.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.-324-22607G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58123300 | |||||||
| chr8:58123840 | C | T | 1 | a0001c0001t0003g0133 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-324-22067C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58123840 | |||||||
| chr8:58123918 | G | A | 1 | a0001c0001t0002g0059 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-324-21989G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58123918 | |||||||
| chr8:58124011 | C | A | 72 | a0001c0001t0001g0015 a0001c0001t0001g0040 a0001c0001t0001g0045 others(69): Show |
72 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.-324-21896C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58124011 | |||||||
| chr8:58124069 | G | C | 1 | a0001c0001t0002g0297 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-324-21838G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58124069 | |||||||
| chr8:58124134 | A | G | 2 | a0001c0001t0003g0142 a0001c0001t0009g0140 |
2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-324-21773A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58124134 | |||||||
| chr8:58124309 | C | T | 3 | a0001c0001t0004g0260 a0001c0001t0005g0139 a0001c0001t0010g0294 |
3 | HG02965.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-324-21598C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58124309 | |||||||
| chr8:58124359 | G | C | 104 | a0001c0001t0001g0015 a0001c0001t0001g0040 a0001c0001t0001g0045 others(101): Show |
104 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.-324-21548G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58124359 | |||||||
| chr8:58124476 | C | T | 1 | a0001c0001t0002g0082 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-324-21431C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58124476 | |||||||
| chr8:58124588 | A | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0118 |
2 | NA18942.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.-324-21319A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58124588 | |||||||
| chr8:58124629 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-324-21278T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58124629 | |||||||
| chr8:58124658 | T | A | 1 | a0001c0001t0001g0042 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-324-21249T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58124658 | |||||||
| chr8:58124728 | C | T | 3 | a0001c0001t0001g0015 a0001c0001t0006g0025 a0001c0001t0006g0218 |
3 | HG01081.hp1 HG01255.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.-324-21179C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58124728 | |||||||
| chr8:58124764 | A | G | 244 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(241): Show |
244 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.-324-21143A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58124764 | |||||||
| chr8:58124824 | G | A | 16 | a0001c0001t0001g0172 a0001c0001t0001g0184 a0001c0001t0001g0185 others(13): Show |
16 | HG00733.hp2 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.-324-21083G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58124824 | |||||||
| chr8:58124891 | G | A | 45 | a0001c0001t0001g0073 a0001c0001t0001g0158 a0001c0001t0001g0172 others(42): Show |
45 | HG00733.hp2 HG00741.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.-324-21016G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58124891 | |||||||
| chr8:58124952 | A | T | 1 | a0001c0001t0002g0057 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-324-20955A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58124952 | |||||||
| chr8:58125213 | T | A | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-324-20694T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58125213 | |||||||
| chr8:58125305 | G | A | 1 | a0001c0001t0007g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-324-20602G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58125305 | |||||||
| chr8:58125397 | C | A | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-324-20510C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58125397 | |||||||
| chr8:58125430 | G | A | 1 | a0001c0001t0036g0132 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-324-20477G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58125430 | |||||||
| chr8:58125460 | G | A | 1 | a0001c0001t0002g0087 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-324-20447G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58125460 | |||||||
| chr8:58125574 | T | C | 1 | a0002c0002t0016g0166 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-324-20333T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58125574 | |||||||
| chr8:58125712 | C | T | 9 | a0001c0001t0001g0089 a0001c0001t0001g0252 a0001c0001t0003g0295 others(6): Show |
9 | HG01109.hp1 HG01243.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.-324-20195C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58125712 | |||||||
| chr8:58125743 | T | G | 1 | a0001c0001t0003g0100 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-324-20164T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58125743 | |||||||
| chr8:58125808 | G | C | 154 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0027 others(151): Show |
154 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(151): Show |
intron_variant | MODIFIER | c.-324-20099G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58125808 | |||||||
| chr8:58125902 | G | A | 1 | a0001c0001t0003g0080 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-324-20005G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58125902 | |||||||
| chr8:58125917 | CTA | C | 149 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0027 others(146): Show |
149 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.-324-19986_-324-19 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58125917 | ||||||
| chr8:58126236 | CT | C | 21 | a0001c0001t0001g0015 a0001c0001t0001g0221 a0001c0001t0002g0078 others(18): Show |
21 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.-324-19667delT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58126236 | ||||||
| chr8:58126438 | G | C | 1 | a0001c0001t0003g0107 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-324-19469G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58126438 | |||||||
| chr8:58126738 | A | G | 1 | a0001c0001t0001g0088 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-324-19169A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58126738 | |||||||
| chr8:58126793 | G | A | 1 | a0001c0001t0004g0232 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-324-19114G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58126793 | |||||||
| chr8:58126888 | A | C | 1 | a0001c0001t0005g0196 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-324-19019A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58126888 | |||||||
| chr8:58127496 | GCTT | G | 75 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0073 others(72): Show |
75 | HG00621.hp2 HG00673.hp1 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.-324-18404_-324-18 others(9): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58127496 | ||||||
| chr8:58128035 | G | A | 6 | a0001c0001t0002g0291 a0001c0001t0003g0142 a0001c0001t0007g0090 others(3): Show |
6 | HG01891.hp2 HG02280.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-324-17872G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58128035 | |||||||
| chr8:58128464 | C | T | 7 | a0001c0001t0001g0201 a0001c0001t0002g0291 a0001c0001t0003g0142 others(4): Show |
7 | HG01891.hp2 HG02280.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-324-17443C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58128464 | |||||||
| chr8:58128777 | A | G | 29 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0094 others(26): Show |
29 | HG00621.hp2 HG00673.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.-324-17130A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58128777 | |||||||
| chr8:58128915 | C | G | 75 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0073 others(72): Show |
75 | HG00621.hp2 HG00673.hp1 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.-324-16992C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58128915 | |||||||
| chr8:58129017 | C | T | 19 | a0001c0001t0001g0015 a0001c0001t0001g0221 a0001c0001t0002g0078 others(16): Show |
19 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-324-16890C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58129017 | |||||||
| chr8:58129025 | G | C | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-324-16882G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58129025 | |||||||
| chr8:58129463 | C | T | 1 | a0001c0001t0011g0212 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-324-16444C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58129463 | |||||||
| chr8:58129464 | G | A | 1 | a0001c0001t0007g0300 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-324-16443G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58129464 | |||||||
| chr8:58129499 | T | C | 1 | a0001c0001t0005g0028 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-324-16408T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58129499 | |||||||
| chr8:58129559 | G | C | 1 | a0001c0001t0008g0296 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-324-16348G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58129559 | |||||||
| chr8:58129720 | T | C | 1 | a0001c0001t0003g0295 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-324-16187T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58129720 | |||||||
| chr8:58129803 | G | A | 1 | a0001c0001t0003g0249 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-324-16104G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58129803 | |||||||
| chr8:58129893 | C | G | 1 | a0001c0001t0001g0201 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-324-16014C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58129893 | |||||||
| chr8:58129976 | G | A | 1 | a0001c0001t0007g0130 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-324-15931G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58129976 | |||||||
| chr8:58130011 | A | G | 1 | a0001c0001t0002g0240 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-324-15896A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58130011 | |||||||
| chr8:58130096 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-324-15811C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58130096 | |||||||
| chr8:58130197 | A | G | 48 | a0001c0001t0001g0089 a0001c0001t0001g0158 a0001c0001t0001g0172 others(45): Show |
48 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.-324-15710A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58130197 | |||||||
| chr8:58130504 | T | C | 1 | a0001c0001t0007g0300 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-324-15403T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58130504 | |||||||
| chr8:58130571 | A | G | 21 | a0001c0001t0001g0158 a0001c0001t0001g0201 a0001c0001t0002g0128 others(18): Show |
21 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-324-15336A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58130571 | |||||||
| chr8:58130639 | C | T | 1 | a0001c0001t0007g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-324-15268C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58130639 | |||||||
| chr8:58130741 | A | ATC | 141 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0045 others(138): Show |
141 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.-324-15164_-324-15 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58130741 | ||||||
| chr8:58130784 | C | T | 15 | a0001c0001t0001g0172 a0001c0001t0001g0261 a0001c0001t0001g0262 others(12): Show |
15 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.-324-15123C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58130784 | |||||||
| chr8:58130818 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-324-15089C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58130818 | |||||||
| chr8:58130870 | G | A | 12 | a0001c0001t0003g0076 a0001c0001t0003g0138 a0001c0001t0003g0141 others(9): Show |
12 | HG01261.hp1 HG01496.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.-324-15037G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58130870 | |||||||
| chr8:58130928 | G | A | 7 | a0001c0001t0001g0027 a0001c0001t0001g0094 a0001c0001t0001g0227 others(4): Show |
7 | HG00621.hp2 HG00673.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.-324-14979G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58130928 | |||||||
| chr8:58130930 | G | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0056 others(3): Show |
6 | HG00738.hp1 HG02056.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.-324-14977G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58130930 | |||||||
| chr8:58131361 | T | C | 1 | a0001c0001t0007g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-324-14546T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58131361 | |||||||
| chr8:58131433 | G | C | 1 | a0001c0001t0007g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-324-14474G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58131433 | |||||||
| chr8:58131443 | T | G | 27 | a0001c0001t0001g0089 a0001c0001t0001g0172 a0001c0001t0001g0252 others(24): Show |
27 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.-324-14464T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58131443 | |||||||
| chr8:58131480 | G | A | 69 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0067 others(66): Show |
69 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.-324-14427G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58131480 | |||||||
| chr8:58131531 | A | G | 1 | a0001c0001t0007g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-324-14376A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58131531 | |||||||
| chr8:58131533 | C | A | 7 | a0001c0001t0001g0027 a0001c0001t0001g0094 a0001c0001t0001g0227 others(4): Show |
7 | HG00621.hp2 HG00673.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.-324-14374C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58131533 | |||||||
| chr8:58131608 | A | C | 8 | a0001c0001t0001g0089 a0001c0001t0001g0252 a0001c0001t0002g0136 others(5): Show |
8 | HG01109.hp1 HG01243.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.-324-14299A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58131608 | |||||||
| chr8:58131878 | C | G | 5 | a0001c0001t0001g0038 a0001c0001t0003g0034 a0001c0001t0006g0051 others(2): Show |
5 | HG00323.hp1 HG01074.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.-324-14029C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58131878 | |||||||
| chr8:58131932 | A | C | 1 | a0001c0001t0003g0198 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-324-13975A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58131932 | |||||||
| chr8:58131951 | G | A | 2 | a0001c0001t0001g0201 a0001c0001t0007g0300 |
2 | HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-324-13956G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58131951 | |||||||
| chr8:58132121 | C | CCAAA | 161 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0027 others(158): Show |
161 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(158): Show |
intron_variant | MODIFIER | c.-324-13785_-324-13 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58132121 | ||||||
| chr8:58132151 | T | C | 1 | a0001c0001t0007g0300 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-324-13756T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58132151 | |||||||
| chr8:58132159 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-324-13748A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58132159 | |||||||
| chr8:58132278 | G | A | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-324-13629G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58132278 | |||||||
| chr8:58132312 | C | T | 1 | a0001c0001t0022g0174 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-324-13595C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58132312 | |||||||
| chr8:58132397 | A | AT | 67 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0067 others(64): Show |
67 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.-324-13499dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58132397 | ||||||
| chr8:58132642 | A | G | 3 | a0001c0001t0007g0090 a0001c0001t0007g0130 a0001c0001t0007g0131 |
3 | HG01891.hp2 HG02280.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-324-13265A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58132642 | |||||||
| chr8:58132780 | C | T | 3 | a0001c0001t0002g0030 a0001c0001t0002g0032 a0001c0001t0002g0087 |
3 | HG00642.hp1 HG01074.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.-324-13127C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58132780 | |||||||
| chr8:58132950 | A | G | 69 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0067 others(66): Show |
69 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.-324-12957A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58132950 | |||||||
| chr8:58132988 | G | A | 8 | a0001c0001t0001g0089 a0001c0001t0001g0252 a0001c0001t0002g0136 others(5): Show |
8 | HG01109.hp1 HG01243.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.-324-12919G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58132988 | |||||||
| chr8:58133132 | T | TGATCAGA others(313): Show |
1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-324-12760_-324-12 others(326): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58133132 | ||||||
| chr8:58133205 | G | GT | 117 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0027 others(114): Show |
117 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.-324-12688dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58133205 | ||||||
| chr8:58133205 | G | GTT | 6 | a0001c0001t0002g0297 a0001c0001t0003g0129 a0001c0001t0003g0134 others(3): Show |
6 | HG01192.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-324-12689_-324-12 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58133205 | ||||||
| chr8:58133391 | C | T | 39 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0067 others(36): Show |
39 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.-324-12516C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58133391 | |||||||
| chr8:58133392 | G | A | 1 | a0001c0001t0010g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-324-12515G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58133392 | |||||||
| chr8:58133440 | G | A | 1 | a0001c0001t0003g0187 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-324-12467G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58133440 | |||||||
| chr8:58133469 | G | T | 27 | a0001c0001t0001g0073 a0001c0001t0001g0172 a0001c0001t0001g0201 others(24): Show |
27 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.-324-12438G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58133469 | |||||||
| chr8:58133487 | C | T | 1 | a0001c0001t0007g0004 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-324-12420C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58133487 | |||||||
| chr8:58133492 | A | G | 1 | a0001c0001t0003g0075 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-324-12415A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58133492 | |||||||
| chr8:58133504 | AG | A | 3 | a0001c0001t0001g0253 a0001c0001t0001g0258 a0001c0001t0002g0121 |
3 | HG00438.hp2 HG03688.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.-324-12401delG | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58133504 | ||||||
| chr8:58133630 | C | T | 1 | a0001c0001t0007g0300 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-324-12277C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58133630 | |||||||
| chr8:58133657 | C | T | 1 | a0001c0001t0002g0126 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-324-12250C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58133657 | |||||||
| chr8:58133710 | GCCTGT | G | 72 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0067 others(69): Show |
72 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.-324-12196_-324-12 others(11): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58133710 | |||||||
| chr8:58133718 | T | A | 72 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0067 others(69): Show |
72 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.-324-12189T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58133718 | |||||||
| chr8:58133733 | C | T | 1 | a0001c0001t0003g0299 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-324-12174C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58133733 | |||||||
| chr8:58133758 | C | T | 1 | a0001c0001t0002g0136 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-324-12149C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58133758 | |||||||
| chr8:58133932 | A | G | 8 | a0001c0001t0001g0089 a0001c0001t0001g0252 a0001c0001t0002g0136 others(5): Show |
8 | HG01109.hp1 HG01243.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.-324-11975A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58133932 | |||||||
| chr8:58134082 | ATTAT | A | 20 | a0001c0001t0001g0015 a0001c0001t0001g0221 a0001c0001t0002g0078 others(17): Show |
20 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.-324-11820_-324-11 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58134082 | ||||||
| chr8:58134234 | A | G | 1 | a0001c0001t0002g0136 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-324-11673A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58134234 | |||||||
| chr8:58134307 | C | A | 1 | a0001c0001t0007g0300 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-324-11600C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58134307 | |||||||
| chr8:58134313 | C | T | 2 | a0001c0001t0003g0235 a0001c0001t0017g0119 |
2 | NA18952.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-324-11594C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58134313 | |||||||
| chr8:58134503 | G | C | 4 | a0001c0001t0002g0117 a0001c0001t0002g0266 a0001c0001t0002g0268 others(1): Show |
4 | HG02257.hp2 HG03486.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-324-11404G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58134503 | |||||||
| chr8:58134617 | C | T | 1 | a0001c0001t0008g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-324-11290C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58134617 | |||||||
| chr8:58134753 | C | T | 119 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0045 others(116): Show |
119 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.-324-11154C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58134753 | |||||||
| chr8:58134896 | T | C | 3 | a0001c0001t0001g0115 a0001c0001t0002g0016 a0001c0001t0002g0153 |
3 | HG00741.hp2 HG01168.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.-324-11011T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58134896 | |||||||
| chr8:58135137 | T | G | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-324-10770T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58135137 | |||||||
| chr8:58135143 | G | T | 1 | a0001c0001t0009g0064 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-324-10764G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58135143 | |||||||
| chr8:58135720 | C | T | 5 | a0001c0001t0001g0038 a0001c0001t0003g0034 a0001c0001t0006g0051 others(2): Show |
5 | HG00323.hp1 HG01074.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.-324-10187C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58135720 | |||||||
| chr8:58135811 | G | A | 1 | a0001c0001t0003g0257 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-324-10096G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58135811 | |||||||
| chr8:58135815 | G | A | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-324-10092G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58135815 | |||||||
| chr8:58135858 | G | A | 1 | a0001c0001t0002g0239 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-324-10049G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58135858 | |||||||
| chr8:58136003 | CT | C | 8 | a0001c0001t0001g0282 a0001c0001t0002g0018 a0001c0001t0002g0120 others(5): Show |
8 | HG00741.hp1 HG01175.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.-324-9878delT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58136003 | ||||||
| chr8:58136003 | CTT | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0017 others(124): Show |
127 | HG00280.hp1 HG00280.hp2 HG00621.hp2 others(124): Show |
intron_variant | MODIFIER | c.-324-9879_-324-987 others(6): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58136003 | ||||||
| chr8:58136003 | CTTT | C | 123 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0015 others(120): Show |
123 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.-324-9880_-324-987 others(7): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58136003 | ||||||
| chr8:58136003 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0002g0057 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-324-9892_-324-987 others(19): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58136003 | ||||||
| chr8:58136159 | G | A | 2 | a0001c0001t0004g0189 a0001c0001t0017g0119 |
2 | HG02129.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-324-9748G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58136159 | |||||||
| chr8:58136529 | C | A | 1 | a0001c0001t0002g0030 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-324-9378C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58136529 | |||||||
| chr8:58136595 | T | C | 1 | a0001c0001t0003g0080 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-324-9312T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58136595 | |||||||
| chr8:58136642 | G | C | 18 | a0001c0001t0002g0012 a0001c0001t0002g0146 a0001c0001t0002g0186 others(15): Show |
18 | HG00733.hp2 HG01069.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.-324-9265G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58136642 | |||||||
| chr8:58136781 | G | A | 267 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(264): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.-324-9126G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58136781 | |||||||
| chr8:58137073 | T | C | 1 | a0001c0001t0001g0201 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-324-8834T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58137073 | |||||||
| chr8:58137102 | A | C | 6 | a0001c0001t0002g0057 a0001c0001t0007g0135 a0001c0001t0007g0157 others(3): Show |
6 | HG01884.hp2 HG02055.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-324-8805A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58137102 | |||||||
| chr8:58137116 | A | G | 1 | a0003c0003t0003g0264 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-324-8791A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58137116 | |||||||
| chr8:58137144 | G | A | 2 | a0001c0001t0005g0161 a0001c0001t0035g0290 |
2 | HG02559.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-324-8763G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58137144 | |||||||
| chr8:58137247 | C | G | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-324-8660C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58137247 | |||||||
| chr8:58137334 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-324-8573C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58137334 | |||||||
| chr8:58137504 | G | T | 1 | a0001c0001t0005g0196 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-324-8403G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58137504 | |||||||
| chr8:58137517 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-324-8390G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58137517 | |||||||
| chr8:58137803 | T | A | 1 | a0001c0001t0003g0299 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-324-8104T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58137803 | |||||||
| chr8:58137962 | G | C | 1 | a0001c0001t0005g0247 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-324-7945G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58137962 | |||||||
| chr8:58138044 | G | A | 4 | a0001c0001t0002g0117 a0001c0001t0002g0266 a0001c0001t0002g0268 others(1): Show |
4 | HG02257.hp2 HG03486.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-324-7863G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58138044 | |||||||
| chr8:58138350 | G | A | 42 | a0001c0001t0001g0038 a0001c0001t0001g0149 a0001c0001t0001g0154 others(39): Show |
42 | HG00323.hp1 HG00323.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.-324-7557G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58138350 | |||||||
| chr8:58138366 | G | A | 41 | a0001c0001t0001g0038 a0001c0001t0001g0149 a0001c0001t0001g0154 others(38): Show |
41 | HG00323.hp1 HG00323.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.-324-7541G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58138366 | |||||||
| chr8:58138684 | T | C | 1 | a0001c0001t0002g0070 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-324-7223T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58138684 | |||||||
| chr8:58139053 | T | G | 2 | a0001c0001t0001g0207 a0001c0001t0006g0245 |
2 | HG01099.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.-324-6854T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58139053 | |||||||
| chr8:58139150 | C | T | 20 | a0001c0001t0001g0073 a0001c0001t0001g0201 a0001c0001t0002g0152 others(17): Show |
20 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.-324-6757C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58139150 | |||||||
| chr8:58139708 | A | C | 73 | a0001c0001t0001g0226 a0001c0001t0002g0001 a0001c0001t0002g0011 others(70): Show |
73 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.-324-6199A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58139708 | |||||||
| chr8:58139755 | C | T | 10 | a0001c0001t0006g0025 a0001c0001t0006g0051 a0001c0001t0006g0155 others(7): Show |
10 | HG00323.hp1 HG01070.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.-324-6152C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58139755 | |||||||
| chr8:58139930 | A | AAAT | 5 | a0001c0001t0002g0121 a0001c0001t0008g0127 a0001c0001t0011g0195 others(2): Show |
5 | HG01175.hp1 HG01261.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-324-5959_-324-595 others(7): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58139930 | ||||||
| chr8:58140038 | A | C | 1 | a0001c0001t0003g0231 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-324-5869A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58140038 | |||||||
| chr8:58140410 | G | A | 1 | a0001c0001t0002g0239 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-324-5497G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58140410 | |||||||
| chr8:58140733 | C | T | 158 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(155): Show |
158 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.-324-5174C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58140733 | |||||||
| chr8:58140745 | G | T | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-324-5162G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58140745 | |||||||
| chr8:58141019 | T | C | 15 | a0001c0001t0001g0282 a0001c0001t0003g0034 a0001c0001t0003g0055 others(12): Show |
15 | HG00323.hp2 HG01074.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.-324-4888T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58141019 | |||||||
| chr8:58141141 | T | C | 113 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(110): Show |
113 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.-324-4766T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58141141 | |||||||
| chr8:58141349 | C | A | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-324-4558C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58141349 | |||||||
| chr8:58141515 | A | G | 1 | a0001c0001t0004g0010 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-324-4392A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58141515 | |||||||
| chr8:58141584 | C | T | 7 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(4): Show |
7 | HG00738.hp1 HG01993.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.-324-4323C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58141584 | |||||||
| chr8:58141778 | G | A | 1 | a0001c0001t0022g0174 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-324-4129G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58141778 | |||||||
| chr8:58141816 | G | A | 7 | a0001c0001t0007g0090 a0001c0001t0007g0130 a0001c0001t0007g0131 others(4): Show |
7 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-324-4091G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58141816 | |||||||
| chr8:58141935 | G | A | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-324-3972G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58141935 | |||||||
| chr8:58142001 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-324-3906A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58142001 | |||||||
| chr8:58142308 | G | A | 1 | a0001c0001t0003g0080 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-324-3599G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58142308 | |||||||
| chr8:58142309 | A | T | 1 | a0001c0001t0007g0144 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-324-3598A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58142309 | |||||||
| chr8:58142325 | G | A | 1 | a0001c0001t0007g0004 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-324-3582G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58142325 | |||||||
| chr8:58142492 | T | G | 8 | a0001c0001t0001g0073 a0001c0001t0001g0172 a0001c0001t0001g0201 others(5): Show |
8 | HG01070.hp2 HG01071.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-324-3415T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58142492 | |||||||
| chr8:58142557 | C | T | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-324-3350C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58142557 | |||||||
| chr8:58142559 | T | C | 167 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(164): Show |
167 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.-324-3348T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58142559 | |||||||
| chr8:58142646 | C | T | 1 | a0001c0001t0005g0196 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-324-3261C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58142646 | |||||||
| chr8:58142661 | T | G | 1 | a0001c0001t0001g0013 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-324-3246T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58142661 | |||||||
| chr8:58142662 | T | A | 1 | a0001c0001t0001g0013 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-324-3245T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58142662 | |||||||
| chr8:58142744 | C | T | 11 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0104 others(8): Show |
11 | HG00408.hp2 HG00673.hp1 NA18940.hp2 others(8): Show |
intron_variant | MODIFIER | c.-324-3163C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58142744 | |||||||
| chr8:58142787 | A | G | 1 | a0001c0001t0019g0222 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-324-3120A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58142787 | |||||||
| chr8:58142898 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-324-3009G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58142898 | |||||||
| chr8:58143038 | A | AGT | 114 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(111): Show |
114 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.-324-2868_-324-286 others(6): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58143038 | ||||||
| chr8:58143041 | C | T | 1 | a0001c0001t0003g0129 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-324-2866C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58143041 | |||||||
| chr8:58143358 | C | A | 1 | a0001c0001t0002g0128 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-324-2549C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58143358 | |||||||
| chr8:58143378 | C | G | 1 | a0001c0001t0022g0174 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-324-2529C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58143378 | |||||||
| chr8:58143381 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-324-2526C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58143381 | |||||||
| chr8:58143543 | A | T | 8 | a0001c0001t0001g0073 a0001c0001t0001g0172 a0001c0001t0001g0201 others(5): Show |
8 | HG01070.hp2 HG01071.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-324-2364A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58143543 | |||||||
| chr8:58143611 | A | G | 1 | a0001c0001t0007g0300 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-324-2296A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58143611 | |||||||
| chr8:58143883 | T | G | 1 | a0001c0001t0002g0001 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-324-2024T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58143883 | |||||||
| chr8:58143908 | T | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(91): Show |
94 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.-324-1999T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58143908 | |||||||
| chr8:58144106 | G | C | 4 | a0001c0001t0007g0090 a0001c0001t0007g0130 a0001c0001t0007g0131 others(1): Show |
4 | HG01891.hp2 HG02280.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-324-1801G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58144106 | |||||||
| chr8:58144169 | T | A | 6 | a0001c0001t0002g0057 a0001c0001t0008g0079 a0001c0001t0008g0127 others(3): Show |
6 | HG01243.hp2 HG02886.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-324-1738T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58144169 | |||||||
| chr8:58144224 | G | T | 1 | a0001c0001t0007g0300 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-324-1683G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58144224 | |||||||
| chr8:58144239 | G | A | 1 | a0001c0001t0002g0298 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-324-1668G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58144239 | |||||||
| chr8:58144275 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-324-1632T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58144275 | |||||||
| chr8:58144400 | G | A | 1 | a0002c0002t0016g0166 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-324-1507G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58144400 | |||||||
| chr8:58144567 | G | A | 1 | a0001c0001t0002g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-324-1340G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58144567 | |||||||
| chr8:58144607 | T | G | 1 | a0001c0001t0030g0035 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-324-1300T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58144607 | |||||||
| chr8:58144670 | T | C | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-324-1237T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58144670 | |||||||
| chr8:58144682 | G | T | 16 | a0001c0001t0002g0037 a0001c0001t0002g0117 a0001c0001t0002g0128 others(13): Show |
16 | HG00642.hp2 HG01099.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.-324-1225G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58144682 | |||||||
| chr8:58144824 | G | T | 1 | a0001c0001t0011g0212 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-324-1083G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58144824 | |||||||
| chr8:58144854 | T | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(95): Show |
98 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.-324-1053T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58144854 | |||||||
| chr8:58145018 | G | A | 1 | a0002c0002t0016g0166 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-324-889G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58145018 | |||||||
| chr8:58145023 | G | T | 2 | a0001c0001t0006g0025 a0001c0001t0006g0218 |
2 | HG01081.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.-324-884G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58145023 | |||||||
| chr8:58145063 | G | T | 2 | a0001c0001t0003g0164 a0001c0001t0003g0165 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-324-844G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58145063 | |||||||
| chr8:58145070 | G | A | 5 | a0001c0001t0007g0004 a0001c0001t0007g0300 a0001c0001t0022g0174 others(2): Show |
5 | HG00741.hp1 HG01109.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.-324-837G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58145070 | |||||||
| chr8:58145144 | T | G | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-324-763T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58145144 | |||||||
| chr8:58145315 | G | GT | 8 | a0001c0001t0003g0005 a0001c0001t0003g0284 a0001c0001t0004g0062 others(5): Show |
8 | HG01978.hp1 HG02055.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-324-576dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58145315 | ||||||
| chr8:58145315 | GT | G | 40 | a0001c0001t0001g0282 a0001c0001t0003g0034 a0001c0001t0003g0055 others(37): Show |
40 | HG00323.hp1 HG00323.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.-324-576delT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58145315 | ||||||
| chr8:58145328 | T | C | 1 | a0001c0001t0003g0237 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-324-579T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58145328 | |||||||
| chr8:58145459 | A | C | 35 | a0001c0001t0001g0282 a0001c0001t0003g0034 a0001c0001t0003g0055 others(32): Show |
35 | HG00323.hp1 HG00323.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.-324-448A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58145459 | |||||||
| chr8:58145489 | G | A | 1 | a0001c0001t0003g0133 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-324-418G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58145489 | |||||||
| chr8:58145885 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-324-22G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58145885 |