Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 317662 |
|---|---|
| ensemblid | ENSG00000138286.15 |
| hgncid | 29162 |
| symbol | FAM149B1 |
| name | family with sequence similarity 149 member B1 |
| refseq_nuc | NM_173348.2 |
| refseq_prot | NP_775483.1 |
| ensembl_nuc | ENST00000242505.11 |
| ensembl_prot | ENSP00000242505.6 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 73168119 |
| end | 73244504 |
| strand | + |
| ver | v1.2 |
| region | chr10:73168119-73244504 |
| region5000 | chr10:73163119-73249504 |
| regionname0 | FAM149B1_chr10_73168119_73244504 |
| regionname5000 | FAM149B1_chr10_73163119_73249504 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 582 | 124 | 51 | 18 | 41 | 0 | 14 | 32 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0002 | 0/0 | 582 | 70 | 4 | 4 | 54 | 0 | 8 | 37 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0003 | 0/0 | 577 | 35 | 17 | 2 | 16 | 0 | 0 | 13 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0004 | 0/0 | 582 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0005 | 0/0 | 582 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0006 | 0/0 | 582 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0007 | 0/0 | 582 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0008 | 0/0 | 577 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0009 | 0/0 | 577 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0010 | 0/0 | 577 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1749 | 124 | 51 | 18 | 41 | 0 | 14 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| c0002 | 0/0 | 1749 | 69 | 4 | 4 | 53 | 0 | 8 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| c0003 | 0/0 | 1734 | 35 | 17 | 2 | 16 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| c0004 | 0/0 | 1749 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| c0005 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| c0006 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| c0007 | 0/0 | 1734 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| c0008 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| c0009 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| c0010 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| c0011 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3707 | 117 | 34 | 13 | 56 | 0 | 14 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| t0002 | 0/0 | 3704 | 63 | 3 | 5 | 47 | 0 | 8 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| t0003 | 0/0 | 3710 | 13 | 11 | 2 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| t0004 | 0/0 | 3708 | 7 | 7 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| t0005 | 0/0 | 3704 | 5 | 4 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| t0006 | 0/0 | 3710 | 3 | 2 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| t0007 | 0/0 | 3707 | 3 | 3 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| t0008 | 0/0 | 3704 | 3 | 2 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| t0009 | 0/0 | 3717 | 2 | 2 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| t0010 | 0/0 | 3705 | 2 | 0 | 2 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| t0011 | 0/0 | 3704 | 2 | 0 | 0 | 2 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| t0012 | 0/0 | 3704 | 2 | 1 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| t0013 | 0/0 | 3716 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| t0014 | 0/0 | 3710 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| t0015 | 0/0 | 3710 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| t0016 | 0/0 | 3707 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| t0017 | 0/0 | 3704 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| t0018 | 0/0 | 3707 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| t0019 | 0/0 | 3707 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| t0020 | 0/0 | 3707 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| t0021 | 0/0 | 3707 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| t0022 | 0/0 | 3707 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| t0023 | 0/0 | 3704 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| t0024 | 0/0 | 3704 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| t0025 | 0/0 | 3704 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| t0026 | 0/0 | 3704 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1749 | 124 | 51 | 18 | 41 | 0 | 14 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0002c0002 | 0/0 | 1749 | 69 | 4 | 4 | 53 | 0 | 8 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0002c0009 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0003c0003 | 0/0 | 1734 | 35 | 17 | 2 | 16 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0004c0010 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0005c0004 | 0/0 | 1749 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0006c0006 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0007c0011 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0008c0008 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0009c0007 | 0/0 | 1734 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0010c0005 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5455 | 90 | 24 | 12 | 40 | 0 | 14 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0001c0001t0002 | 0/0 | 5452 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0001c0001t0003 | 0/0 | 5458 | 13 | 11 | 2 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0001c0001t0004 | 0/0 | 5456 | 7 | 7 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0001c0001t0006 | 0/0 | 5458 | 3 | 2 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0001c0001t0007 | 0/0 | 5455 | 3 | 3 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0001c0001t0009 | 0/0 | 5465 | 2 | 2 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0001c0001t0010 | 0/0 | 5453 | 2 | 0 | 2 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0001c0001t0015 | 0/0 | 5458 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0001c0001t0019 | 0/0 | 5455 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0001c0001t0021 | 0/0 | 5455 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0002c0002t0002 | 0/0 | 5452 | 61 | 3 | 4 | 46 | 0 | 8 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0002c0002t0011 | 0/0 | 5452 | 2 | 0 | 0 | 2 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0002c0002t0016 | 0/0 | 5455 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0002c0002t0022 | 0/0 | 5455 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0002c0002t0023 | 0/0 | 5452 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0002c0002t0024 | 0/0 | 5452 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0002c0002t0025 | 0/0 | 5452 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0002c0002t0026 | 0/0 | 5452 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0002c0009t0002 | 0/0 | 5452 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0003c0003t0001 | 0/0 | 5440 | 25 | 10 | 0 | 15 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0003c0003t0005 | 0/0 | 5437 | 4 | 3 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0003c0003t0008 | 0/0 | 5437 | 2 | 2 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0003c0003t0012 | 0/0 | 5437 | 2 | 1 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0003c0003t0013 | 0/0 | 5449 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0003c0003t0018 | 0/0 | 5440 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0004c0010t0001 | 0/0 | 5455 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0005c0004t0001 | 0/0 | 5455 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0006c0006t0014 | 0/0 | 5458 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0007c0011t0020 | 0/0 | 5455 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0008c0008t0005 | 0/0 | 5437 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0009c0007t0008 | 0/0 | 5437 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| a0010c0005t0017 | 0/0 | 5437 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | copy fasta | chr10 | 73163119 | 73249504 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0006g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0007g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0007g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0009g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0009g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0010g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0010g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0015g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0019g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0001c0001t0021g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0011g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0011g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0016g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0022g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0023g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0024g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0025g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0002t0026g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0002c0009t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0005g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0008g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0008g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0012g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0012g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0013g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0003c0003t0018g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0004c0010t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0005c0004t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0006c0006t0014g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0007c0011t0020g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0008c0008t0005g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0009c0007t0008g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| a0010c0005t0017g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0070 | EAS | CHS | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG00408 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | CHS | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG00423 | hp1 | a0002 | c0002 | t0026 | g0073 | EAS | CHS | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0041 | EAS | CHS | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0081 | EAS | CHS | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG00558 | hp1 | a0003 | c0003 | t0001 | g0175 | EAS | CHS | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG00558 | hp2 | a0002 | c0009 | t0002 | g0064 | EAS | CHS | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0053 | EAS | CHS | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0032 | EAS | CHS | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG00621 | hp1 | a0003 | c0003 | t0001 | g0143 | EAS | CHS | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0088 | EAS | CHS | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG00642 | hp1 | a0009 | c0007 | t0008 | g0008 | AMR | PUR | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG00642 | hp2 | a0001 | c0001 | t0010 | g0111 | AMR | PUR | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0060 | EAS | CHS | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG00733 | hp1 | a0005 | c0004 | t0001 | g0144 | AMR | PUR | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG00733 | hp2 | a0002 | c0002 | t0002 | g0049 | AMR | PUR | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0231 | AMR | PUR | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG01069 | hp1 | a0001 | c0001 | t0010 | g0190 | AMR | PUR | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG01069 | hp2 | a0001 | c0001 | t0021 | g0192 | AMR | PUR | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG01074 | hp2 | a0003 | c0003 | t0012 | g0087 | AMR | PUR | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0021 | AMR | PUR | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0230 | AMR | PUR | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG01256 | hp1 | a0002 | c0002 | t0002 | g0047 | AMR | CLM | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0024 | AMR | CLM | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG01346 | hp2 | a0003 | c0003 | t0005 | g0006 | AMR | CLM | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0080 | AFR | ACB | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0223 | AFR | ACB | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PEL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | KHV | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02040 | hp2 | a0004 | c0010 | t0001 | g0166 | EAS | KHV | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02055 | hp1 | a0002 | c0002 | t0002 | g0048 | AFR | ACB | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0039 | EAS | KHV | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0029 | EAS | KHV | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | KHV | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0065 | EAS | KHV | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0224 | AFR | ACB | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0118 | AFR | ACB | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0038 | EAS | CDX | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CDX | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02257 | hp1 | a0003 | c0003 | t0012 | g0005 | AFR | ACB | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02257 | hp2 | a0003 | c0003 | t0018 | g0199 | AFR | ACB | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02258 | hp1 | a0003 | c0003 | t0001 | g0122 | AFR | ACB | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0228 | AFR | ACB | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02451 | hp1 | a0001 | c0001 | t0007 | g0078 | AFR | ACB | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02451 | hp2 | a0003 | c0003 | t0001 | g0107 | AFR | ACB | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0045 | EAS | KHV | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0018 | SAS | PJL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02615 | hp2 | a0007 | c0011 | t0020 | g0215 | AFR | GWD | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0135 | AFR | GWD | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02630 | hp1 | a0003 | c0003 | t0001 | g0123 | AFR | GWD | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02630 | hp2 | a0001 | c0001 | t0019 | g0202 | AFR | GWD | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | GWD | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0225 | AFR | GWD | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0030 | SAS | PJL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0194 | AFR | GWD | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02809 | hp1 | a0003 | c0003 | t0008 | g0003 | AFR | GWD | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0222 | AFR | GWD | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02896 | hp2 | a0001 | c0001 | t0009 | g0221 | AFR | GWD | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02897 | hp1 | a0001 | c0001 | t0009 | g0220 | AFR | GWD | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0216 | AFR | ESN | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02965 | hp1 | a0003 | c0003 | t0001 | g0124 | AFR | ESN | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02965 | hp2 | a0003 | c0003 | t0005 | g0084 | AFR | ESN | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02976 | hp2 | a0003 | c0003 | t0001 | g0126 | AFR | ESN | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03098 | hp1 | a0006 | c0006 | t0014 | g0096 | AFR | MSL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0022 | AFR | MSL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0119 | AFR | ESN | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03209 | hp1 | a0003 | c0003 | t0001 | g0125 | AFR | MSL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0108 | AFR | MSL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03225 | hp1 | a0003 | c0003 | t0001 | g0127 | AFR | MSL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03225 | hp2 | a0002 | c0002 | t0023 | g0086 | AFR | MSL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0023 | SAS | PJL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0233 | AFR | MSL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03453 | hp2 | a0008 | c0008 | t0005 | g0085 | AFR | MSL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0219 | AFR | MSL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0020 | SAS | PJL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0031 | SAS | PJL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0162 | AFR | ESN | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0218 | AFR | ESN | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03579 | hp1 | a0003 | c0003 | t0001 | g0128 | AFR | MSL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03579 | hp2 | a0003 | c0003 | t0005 | g0083 | AFR | MSL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | STU | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0046 | SAS | STU | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0015 | SAS | BEB | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | STU | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0076 | SAS | STU | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | STU | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | YRI | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0057 | EAS | CHB | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHB | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0079 | AFR | YRI | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | YRI | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18949 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0054 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18963 | hp2 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18964 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0050 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18968 | hp1 | a0003 | c0003 | t0001 | g0090 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18968 | hp2 | a0002 | c0002 | t0024 | g0012 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18971 | hp1 | a0002 | c0002 | t0011 | g0056 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18981 | hp2 | a0003 | c0003 | t0001 | g0091 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18992 | hp2 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18993 | hp2 | a0002 | c0002 | t0022 | g0052 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18998 | hp2 | a0003 | c0003 | t0001 | g0089 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19001 | hp1 | a0003 | c0003 | t0001 | g0102 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19003 | hp1 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19003 | hp2 | a0002 | c0002 | t0002 | g0062 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19005 | hp1 | a0003 | c0003 | t0001 | g0093 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19006 | hp1 | a0002 | c0002 | t0002 | g0051 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19006 | hp2 | a0003 | c0003 | t0001 | g0095 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19030 | hp1 | a0003 | c0003 | t0001 | g0121 | AFR | LWK | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | LWK | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0131 | AFR | LWK | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19043 | hp2 | a0010 | c0005 | t0017 | g0007 | AFR | LWK | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19054 | hp2 | a0003 | c0003 | t0001 | g0101 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19056 | hp1 | a0003 | c0003 | t0001 | g0094 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19057 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19057 | hp2 | a0001 | c0001 | t0006 | g0174 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19060 | hp2 | a0003 | c0003 | t0001 | g0193 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19066 | hp2 | a0002 | c0002 | t0025 | g0033 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19074 | hp1 | a0003 | c0003 | t0001 | g0183 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19075 | hp1 | a0002 | c0002 | t0016 | g0017 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19077 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19077 | hp2 | a0002 | c0002 | t0011 | g0058 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19078 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19083 | hp2 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19085 | hp1 | a0003 | c0003 | t0013 | g0186 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA20129 | hp1 | a0003 | c0003 | t0008 | g0004 | AFR | ASW | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA20129 | hp2 | a0003 | c0003 | t0005 | g0025 | AFR | ASW | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0227 | AFR | ACB | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02559 | hp1 | a0003 | c0003 | t0001 | g0112 | AFR | ACB | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0229 | AFR | ACB | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03471 | hp1 | a0001 | c0001 | t0015 | g0214 | AFR | MSL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | USA | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | USA | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | USA | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | USA | FAM149B1_chr10_73163119_73249504 | FAM149B1 | chr10 | 73163119 | 73249504 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:73168308
|
T | TGAG | 3 | a0001a0002a0006 | 19 | HG00735.hp1 HG01243.hp1 HG01891.hp1 others(16): Show |
start_lost&disruptive_inframe_insertion | HIGH | c.-2_1dupGGA | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/14 | 223/5455 | 2/1749 | 1/582 | INFO_REALIGN_3_PRIME | chr10 | 73168308 | ||
| chr10:73168308
|
T | TGAGGAGG others(2): Show |
2 | a0001a0003 | 3 | HG02896.hp2 HG02897.hp1 NA19085.hp1 |
start_lost&disruptive_inframe_insertion | HIGH | c.-8_1dupGGAGGAGGA | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/14 | 223/5455 | 2/1749 | 1/582 | INFO_REALIGN_3_PRIME | chr10 | 73168308 | ||
| chr10:73177962
|
C | T | 1 | a0004 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.269C>T | p.Ser90Phe | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/14 | 490/5455 | 269/1749 | 90/582 | chr10 | 73177962 | ||
| chr10:73210388
|
T | C | 1 | a0005 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.848T>C | p.Val283Ala | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/14 | 1069/5455 | 848/1749 | 283/582 | chr10 | 73210388 | ||
| chr10:73230466
|
T | G | 1 | a0010 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.1068T>G | p.Asp356Glu | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/14 | 1289/5455 | 1068/1749 | 356/582 | chr10 | 73230466 | ||
| chr10:73230514
|
G | C | 1 | a0006 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.1116G>C | p.Met372Ile | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/14 | 1337/5455 | 1116/1749 | 372/582 | chr10 | 73230514 | ||
| chr10:73233156
|
G | C | 1 | a0009 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.1345G>C | p.Ala449Pro | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 10/14 | 1566/5455 | 1345/1749 | 449/582 | chr10 | 73233156 | ||
| chr10:73239327
|
C | T | 1 | a0007 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.1618C>T | p.Arg540Cys | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 13/14 | 1839/5455 | 1618/1749 | 540/582 | chr10 | 73239327 | ||
| chr10:73239330
|
C | T | 1 | a0008 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.1621C>T | p.Arg541Cys | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 13/14 | 1842/5455 | 1621/1749 | 541/582 | chr10 | 73239330 | ||
| chr10:73240981
|
G | A | 5 | a0002a0003a0008others(2): Show | 108 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(105): Show |
missense_variant | MODERATE | c.1711G>A | p.Gly571Arg | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 14/14 | 1932/5455 | 1711/1749 | 571/582 | chr10 | 73240981 | ||
| chr10:73240983
|
AGGCAGAC others(8): Show |
A | 4 | a0003a0008a0009others(1): Show | 38 | HG00408.hp2 HG00558.hp1 HG00621.hp1 others(35): Show |
conservative_inframe_deletion | MODERATE | c.1714_1728delGGCAGA others(9): Show |
p.Gly572_Ser576del | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 14/14 | 1935/5455 | 1714/1749 | 572/582 | chr10 | 73240983 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:73177858
|
C | T | 1 | a0007c0011 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.165C>T | p.Ile55Ile | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/14 | 386/5455 | 165/1749 | 55/582 | chr10 | 73177858 | ||
| chr10:73228091
|
C | T | 1 | a0002c0009 | 1 | HG00558.hp2 | synonymous_variant | LOW | c.930C>T | p.Pro310Pro | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 8/14 | 1151/5455 | 930/1749 | 310/582 | chr10 | 73228091 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:73168123
|
C | G | 1 | a0002c0002t0026 | 1 | HG00423.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-217C>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/14 | chr10 | 73168123 | ||||||
| chr10:73241057
|
G | GA | 2 | a0001c0001t0004a0001c0001t0009 | 9 | HG02145.hp2 HG02622.hp1 HG02717.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*39dupA | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 14/14 | 40 | INFO_REALIGN_3_PRIME | chr10 | 73241057 | ||||
| chr10:73241138
|
G | C | 1 | a0010c0005t0017 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*119G>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 14/14 | 119 | chr10 | 73241138 | |||||
| chr10:73241179
|
A | G | 16 | a0001c0001t0002a0002c0002t0002a0002c0002t0011others(13): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*160A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 14/14 | 160 | chr10 | 73241179 | |||||
| chr10:73241395
|
A | G | 2 | a0001c0001t0003a0001c0001t0007 | 16 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*376A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 14/14 | 376 | chr10 | 73241395 | |||||
| chr10:73241555
|
G | T | 1 | a0002c0002t0025 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*536G>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 14/14 | 536 | chr10 | 73241555 | |||||
| chr10:73241744
|
G | T | 1 | a0002c0002t0024 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*725G>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 14/14 | 725 | chr10 | 73241744 | |||||
| chr10:73241927
|
T | C | 1 | a0002c0002t0011 | 2 | NA18971.hp1 NA19077.hp2 |
3_prime_UTR_variant | MODIFIER | c.*908T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 14/14 | 908 | chr10 | 73241927 | |||||
| chr10:73242015
|
A | G | 1 | a0001c0001t0015 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*996A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 14/14 | 996 | chr10 | 73242015 | |||||
| chr10:73242237
|
T | C | 9 | a0001c0001t0002a0002c0002t0002a0002c0002t0011others(6): Show | 70 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*1218T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 14/14 | 1218 | chr10 | 73242237 | |||||
| chr10:73242294
|
A | G | 1 | a0001c0001t0021 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1275A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 14/14 | 1275 | chr10 | 73242294 | |||||
| chr10:73242413
|
TAA | T | 15 | a0001c0001t0002a0002c0002t0002a0002c0002t0011others(12): Show | 81 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1396_*1397delAA | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 14/14 | 1396 | INFO_REALIGN_3_PRIME | chr10 | 73242413 | ||||
| chr10:73242419
|
A | G | 19 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(16): Show | 99 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*1400A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 14/14 | 1400 | chr10 | 73242419 | |||||
| chr10:73242521
|
G | A | 15 | a0001c0001t0002a0002c0002t0002a0002c0002t0011others(12): Show | 81 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1502G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 14/14 | 1502 | chr10 | 73242521 | |||||
| chr10:73242558
|
CT | C | 15 | a0001c0001t0002a0002c0002t0002a0002c0002t0011others(12): Show | 81 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1542delT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 14/14 | 1542 | INFO_REALIGN_3_PRIME | chr10 | 73242558 | ||||
| chr10:73242706
|
G | A | 1 | a0002c0002t0023 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1687G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 14/14 | 1687 | chr10 | 73242706 | |||||
| chr10:73243197
|
G | A | 1 | a0003c0003t0012 | 2 | HG01074.hp2 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2178G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 14/14 | 2178 | chr10 | 73243197 | |||||
| chr10:73243288
|
G | C | 3 | a0003c0003t0005a0003c0003t0012a0008c0008t0005 | 7 | HG01074.hp2 HG01346.hp2 HG02257.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2269G>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 14/14 | 2269 | chr10 | 73243288 | |||||
| chr10:73243335
|
C | T | 19 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(16): Show | 99 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*2316C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 14/14 | 2316 | chr10 | 73243335 | |||||
| chr10:73243437
|
C | T | 1 | a0001c0001t0019 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2418C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 14/14 | 2418 | chr10 | 73243437 | |||||
| chr10:73243440
|
C | G | 1 | a0006c0006t0014 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2421C>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 14/14 | 2421 | chr10 | 73243440 | |||||
| chr10:73243463
|
T | G | 1 | a0003c0003t0018 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2444T>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 14/14 | 2444 | chr10 | 73243463 | |||||
| chr10:73244011
|
TTC | T | 1 | a0001c0001t0010 | 2 | HG00642.hp2 HG01069.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2994_*2995delCT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 14/14 | 2994 | INFO_REALIGN_3_PRIME | chr10 | 73244011 | ||||
| chr10:73244218
|
G | A | 1 | a0003c0003t0018 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3199G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 14/14 | 3199 | chr10 | 73244218 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:73168497
|
C | T | 1 | a0001c0001t0003g0233 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.47+111C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73168497 | ||||||
| chr10:73168559
|
AG | A | 86 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0007g0078others(83): Show | 86 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.47+176delG | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 73168559 | |||||
| chr10:73168713
|
C | T | 1 | a0002c0002t0002g0088 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.47+327C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73168713 | ||||||
| chr10:73168918
|
C | G | 6 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0229others(3): Show | 6 | HG00735.hp1 HG01243.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.47+532C>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73168918 | ||||||
| chr10:73169084
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.47+698C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73169084 | ||||||
| chr10:73169151
|
T | A | 8 | a0001c0001t0001g0092a0003c0003t0001g0001a0003c0003t0001g0089others(5): Show | 10 | HG00408.hp2 NA18964.hp2 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.47+765T>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73169151 | ||||||
| chr10:73169156
|
A | T | 8 | a0001c0001t0001g0092a0003c0003t0001g0001a0003c0003t0001g0089others(5): Show | 10 | HG00408.hp2 NA18964.hp2 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.47+770A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73169156 | ||||||
| chr10:73169159
|
CA | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0092a0001c0001t0001g0103others(112): Show | 118 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.47+790delA | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 73169159 | |||||
| chr10:73169159
|
CAA | C | 8 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(5): Show | 8 | HG02280.hp2 HG02486.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.47+789_47+790delAA | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 73169159 | |||||
| chr10:73169159
|
CAAAAA | C | 101 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(98): Show | 101 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.47+786_47+790delAA others(3): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 73169159 | |||||
| chr10:73169281
|
C | G | 1 | a0003c0003t0012g0087 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.47+895C>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73169281 | ||||||
| chr10:73169459
|
C | CT | 18 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0222others(15): Show | 18 | HG00735.hp1 HG01243.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.47+1088dupT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 73169459 | |||||
| chr10:73169610
|
C | T | 2 | a0001c0001t0001g0207a0001c0001t0001g0226 | 2 | HG00423.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.47+1224C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73169610 | ||||||
| chr10:73169633
|
A | T | 1 | a0003c0003t0008g0003 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.47+1247A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73169633 | ||||||
| chr10:73169634
|
A | T | 88 | a0001c0001t0001g0044a0001c0001t0001g0205a0001c0001t0001g0206others(85): Show | 88 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.47+1248A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73169634 | ||||||
| chr10:73169635
|
T | A | 1 | a0001c0001t0001g0103 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.47+1249T>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73169635 | ||||||
| chr10:73169702
|
G | A | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02602.hp2 HG03017.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.47+1316G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73169702 | ||||||
| chr10:73169951
|
T | TTATTAAT others(23): Show |
103 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(100): Show | 103 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.47+1584_47+1585ins others(30): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 73169951 | |||||
| chr10:73170012
|
T | C | 1 | a0003c0003t0001g0107 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.47+1626T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73170012 | ||||||
| chr10:73170012
|
T | TA | 7 | a0003c0003t0005g0006a0003c0003t0008g0003a0003c0003t0008g0004others(4): Show | 7 | HG00642.hp1 HG01074.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.47+1627dupA | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 73170012 | |||||
| chr10:73170039
|
TATTTA | T | 15 | a0001c0001t0001g0002a0001c0001t0001g0203a0001c0001t0001g0204others(12): Show | 16 | HG00642.hp1 HG01074.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.47+1659_47+1663del others(5): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 73170039 | |||||
| chr10:73170052
|
A | T | 1 | a0006c0006t0014g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.47+1666A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73170052 | ||||||
| chr10:73170431
|
G | A | 18 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0222others(15): Show | 18 | HG00735.hp1 HG01243.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.47+2045G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73170431 | ||||||
| chr10:73170448
|
G | T | 1 | a0001c0001t0001g0106 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.47+2062G>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73170448 | ||||||
| chr10:73170518
|
A | G | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.47+2132A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73170518 | ||||||
| chr10:73170524
|
A | AAAAAT | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.47+2141_47+2145dup others(5): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 73170524 | |||||
| chr10:73170600
|
G | A | 1 | a0001c0001t0004g0108 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.47+2214G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73170600 | ||||||
| chr10:73170720
|
T | C | 6 | a0003c0003t0005g0006a0003c0003t0005g0083a0003c0003t0005g0084others(3): Show | 6 | HG01074.hp2 HG01346.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.47+2334T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73170720 | ||||||
| chr10:73170826
|
A | G | 1 | a0006c0006t0014g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.47+2440A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73170826 | ||||||
| chr10:73170975
|
AT | A | 94 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(91): Show | 94 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.47+2603delT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 73170975 | |||||
| chr10:73171311
|
G | A | 4 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(1): Show | 4 | HG02132.hp1 NA18968.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+2925G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73171311 | ||||||
| chr10:73171466
|
G | T | 20 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0222others(17): Show | 20 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.47+3080G>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73171466 | ||||||
| chr10:73171577
|
C | CAGTTAAC others(1): Show |
2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | HG00438.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.48-3108_48-3101dup others(8): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 73171577 | |||||
| chr10:73171630
|
CT | C | 96 | a0001c0001t0001g0044a0001c0001t0001g0110a0001c0001t0001g0208others(93): Show | 96 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.48-3041delT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 73171630 | |||||
| chr10:73171630
|
CTT | C | 10 | a0002c0002t0002g0013a0002c0002t0002g0014a0002c0002t0002g0015others(7): Show | 10 | HG01081.hp1 HG02602.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.48-3042_48-3041del others(2): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 73171630 | |||||
| chr10:73171634
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.48-3053T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73171634 | ||||||
| chr10:73171754
|
G | A | 1 | a0001c0001t0004g0108 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.48-2933G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73171754 | ||||||
| chr10:73171795
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.48-2892A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73171795 | ||||||
| chr10:73171874
|
T | C | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.48-2813T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73171874 | ||||||
| chr10:73171972
|
C | T | 1 | a0003c0003t0018g0199 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.48-2715C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73171972 | ||||||
| chr10:73171973
|
G | A | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.48-2714G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73171973 | ||||||
| chr10:73172092
|
G | GTTA | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.48-2593_48-2591dup others(3): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 73172092 | |||||
| chr10:73172103
|
G | A | 1 | a0003c0003t0001g0112 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.48-2584G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73172103 | ||||||
| chr10:73172192
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.48-2495T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73172192 | ||||||
| chr10:73172223
|
T | C | 21 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0222others(18): Show | 21 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.48-2464T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73172223 | ||||||
| chr10:73172224
|
G | C | 72 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(69): Show | 72 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.48-2463G>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73172224 | ||||||
| chr10:73172234
|
C | T | 83 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(80): Show | 83 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.48-2453C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73172234 | ||||||
| chr10:73172428
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.48-2259C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73172428 | ||||||
| chr10:73172519
|
C | T | 83 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(80): Show | 83 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.48-2168C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73172519 | ||||||
| chr10:73172565
|
G | T | 83 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(80): Show | 83 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.48-2122G>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73172565 | ||||||
| chr10:73172655
|
T | C | 5 | a0001c0001t0001g0103a0001c0001t0001g0114a0001c0001t0001g0115others(2): Show | 5 | NA18747.hp2 NA18942.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.48-2032T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73172655 | ||||||
| chr10:73172663
|
C | T | 1 | a0001c0001t0007g0080 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.48-2024C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73172663 | ||||||
| chr10:73172696
|
C | T | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.48-1991C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73172696 | ||||||
| chr10:73172878
|
A | G | 2 | a0009c0007t0008g0008a0010c0005t0017g0007 | 2 | HG00642.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.48-1809A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73172878 | ||||||
| chr10:73172918
|
C | T | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.48-1769C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73172918 | ||||||
| chr10:73172940
|
CA | C | 102 | a0001c0001t0001g0044a0001c0001t0001g0113a0001c0001t0001g0117others(99): Show | 102 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.48-1733delA | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 73172940 | |||||
| chr10:73173001
|
C | G | 1 | a0006c0006t0014g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.48-1686C>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73173001 | ||||||
| chr10:73173384
|
A | G | 83 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(80): Show | 83 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.48-1303A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73173384 | ||||||
| chr10:73173431
|
T | TAGAG | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.48-1254_48-1253ins others(4): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 73173431 | |||||
| chr10:73173444
|
C | A | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.48-1243C>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73173444 | ||||||
| chr10:73173540
|
T | C | 2 | a0001c0001t0004g0118a0001c0001t0004g0119 | 2 | HG02145.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.48-1147T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73173540 | ||||||
| chr10:73173559
|
A | G | 1 | a0006c0006t0014g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.48-1128A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73173559 | ||||||
| chr10:73173913
|
A | C | 1 | a0003c0003t0018g0199 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.48-774A>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73173913 | ||||||
| chr10:73174425
|
TAAC | T | 3 | a0003c0003t0005g0006a0003c0003t0012g0005a0003c0003t0012g0087 | 3 | HG01074.hp2 HG01346.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.48-258_48-256delAA others(1): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 73174425 | |||||
| chr10:73174556
|
T | C | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.48-131T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73174556 | ||||||
| chr10:73174684
|
C | T | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
splice_region_variant&intron_variant | LOW | c.48-3C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | chr10 | 73174684 | ||||||
| chr10:73174912
|
T | C | 1 | a0002c0002t0023g0086 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.152+121T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73174912 | ||||||
| chr10:73175015
|
G | A | 20 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0222others(17): Show | 20 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.152+224G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73175015 | ||||||
| chr10:73175043
|
AAAAC | A | 83 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(80): Show | 83 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.152+266_152+269del others(4): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 73175043 | |||||
| chr10:73175103
|
A | G | 20 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0222others(17): Show | 20 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.152+312A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73175103 | ||||||
| chr10:73175280
|
A | G | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.152+489A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73175280 | ||||||
| chr10:73175426
|
T | C | 1 | a0003c0003t0005g0025 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.152+635T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73175426 | ||||||
| chr10:73175452
|
G | A | 4 | a0001c0001t0001g0110a0001c0001t0001g0120a0001c0001t0001g0205others(1): Show | 4 | NA18973.hp2 NA19002.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+661G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73175452 | ||||||
| chr10:73175546
|
C | G | 6 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0229others(3): Show | 6 | HG00735.hp1 HG01243.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.152+755C>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73175546 | ||||||
| chr10:73175580
|
G | A | 1 | a0006c0006t0014g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.152+789G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73175580 | ||||||
| chr10:73175633
|
G | A | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.152+842G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73175633 | ||||||
| chr10:73175669
|
CA | C | 104 | a0001c0001t0001g0044a0001c0001t0001g0197a0001c0001t0002g0059others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.152+895delA | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 73175669 | |||||
| chr10:73175682
|
A | G | 1 | a0001c0001t0003g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.152+891A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73175682 | ||||||
| chr10:73175699
|
CAT | C | 72 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(69): Show | 72 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.152+910_152+911del others(2): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 73175699 | |||||
| chr10:73175705
|
T | C | 3 | a0001c0001t0007g0078a0001c0001t0007g0079a0001c0001t0007g0080 | 3 | HG01884.hp1 HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.152+914T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73175705 | ||||||
| chr10:73175933
|
G | A | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.152+1142G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73175933 | ||||||
| chr10:73175964
|
G | C | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.152+1173G>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73175964 | ||||||
| chr10:73176122
|
G | A | 1 | a0002c0002t0023g0086 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.152+1331G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73176122 | ||||||
| chr10:73176271
|
G | A | 3 | a0003c0003t0005g0083a0003c0003t0005g0084a0008c0008t0005g0085 | 3 | HG02965.hp2 HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.152+1480G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73176271 | ||||||
| chr10:73176277
|
T | C | 9 | a0003c0003t0001g0112a0003c0003t0001g0121a0003c0003t0001g0122others(6): Show | 9 | HG02258.hp1 HG02559.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.152+1486T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73176277 | ||||||
| chr10:73176336
|
C | T | 1 | a0001c0001t0001g0196 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.153-1510C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73176336 | ||||||
| chr10:73176401
|
C | A | 1 | a0002c0002t0002g0013 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.153-1445C>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73176401 | ||||||
| chr10:73176552
|
T | A | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.153-1294T>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73176552 | ||||||
| chr10:73176764
|
T | C | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.153-1082T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73176764 | ||||||
| chr10:73176932
|
C | T | 1 | a0007c0011t0020g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.153-914C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73176932 | ||||||
| chr10:73176934
|
G | A | 1 | a0002c0002t0002g0026 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.153-912G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73176934 | ||||||
| chr10:73176950
|
C | A | 1 | a0001c0001t0001g0129 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.153-896C>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73176950 | ||||||
| chr10:73176975
|
C | G | 1 | a0001c0001t0001g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.153-871C>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73176975 | ||||||
| chr10:73177012
|
C | T | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.153-834C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73177012 | ||||||
| chr10:73177038
|
CA | C | 3 | a0003c0003t0005g0006a0003c0003t0012g0005a0003c0003t0012g0087 | 3 | HG01074.hp2 HG01346.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.153-804delA | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 73177038 | |||||
| chr10:73177135
|
C | T | 84 | a0001c0001t0001g0044a0001c0001t0001g0195a0001c0001t0002g0059others(81): Show | 84 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.153-711C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73177135 | ||||||
| chr10:73177140
|
G | A | 1 | a0006c0006t0014g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.153-706G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73177140 | ||||||
| chr10:73177510
|
G | T | 1 | a0002c0002t0023g0086 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.153-336G>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73177510 | ||||||
| chr10:73177528
|
C | T | 1 | a0001c0001t0004g0194 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.153-318C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73177528 | ||||||
| chr10:73177552
|
C | T | 1 | a0003c0003t0008g0004 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.153-294C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73177552 | ||||||
| chr10:73177574
|
C | CAAAA | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.153-265_153-262dup others(4): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 73177574 | |||||
| chr10:73177673
|
A | G | 1 | a0003c0003t0001g0193 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.153-173A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73177673 | ||||||
| chr10:73177722
|
T | A | 1 | a0001c0001t0003g0227 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.153-124T>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73177722 | ||||||
| chr10:73177738
|
T | TACACATA others(49): Show |
20 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0222others(17): Show | 20 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.153-102_153-101ins others(56): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 73177738 | |||||
| chr10:73177748
|
A | T | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.153-98A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 2/13 | chr10 | 73177748 | ||||||
| chr10:73177984
|
T | C | 1 | a0001c0001t0003g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.282+9T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73177984 | ||||||
| chr10:73178281
|
T | C | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.282+306T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73178281 | ||||||
| chr10:73178349
|
G | A | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.282+374G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73178349 | ||||||
| chr10:73178380
|
A | T | 3 | a0001c0001t0001g0109a0001c0001t0010g0111a0001c0001t0021g0192 | 3 | HG00642.hp2 HG01069.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.282+405A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73178380 | ||||||
| chr10:73178386
|
G | C | 83 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(80): Show | 83 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.282+411G>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73178386 | ||||||
| chr10:73178388
|
G | C | 19 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0223others(16): Show | 19 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.282+413G>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73178388 | ||||||
| chr10:73178489
|
C | CAA | 82 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0224others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.282+526_282+527dup others(2): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73178489 | |||||
| chr10:73178489
|
C | CAAA | 21 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0222others(18): Show | 21 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.282+525_282+527dup others(3): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73178489 | |||||
| chr10:73178968
|
G | GT | 3 | a0002c0002t0002g0077a0003c0003t0008g0004a0003c0003t0012g0005 | 3 | HG02257.hp1 NA18949.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.282+999dupT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73178968 | |||||
| chr10:73178975
|
G | T | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.282+1000G>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73178975 | ||||||
| chr10:73179110
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.282+1135G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73179110 | ||||||
| chr10:73179241
|
G | A | 2 | a0003c0003t0008g0003a0003c0003t0008g0004 | 2 | HG02809.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.282+1266G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73179241 | ||||||
| chr10:73179422
|
T | TTCTG | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.282+1451_282+1454d others(6): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73179422 | |||||
| chr10:73179549
|
G | T | 21 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0222others(18): Show | 21 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.282+1574G>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73179549 | ||||||
| chr10:73179671
|
G | A | 1 | a0006c0006t0014g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.282+1696G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73179671 | ||||||
| chr10:73179842
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+1867A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73179842 | ||||||
| chr10:73179969
|
C | A | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.282+1994C>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73179969 | ||||||
| chr10:73180016
|
G | A | 1 | a0002c0002t0002g0030 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.282+2041G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73180016 | ||||||
| chr10:73180323
|
T | C | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.282+2348T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73180323 | ||||||
| chr10:73180520
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.282+2545G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73180520 | ||||||
| chr10:73180620
|
A | G | 2 | a0002c0002t0002g0021a0002c0002t0002g0022 | 2 | HG01081.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.282+2645A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73180620 | ||||||
| chr10:73180826
|
G | A | 1 | a0003c0003t0001g0089 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.282+2851G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73180826 | ||||||
| chr10:73180929
|
T | G | 1 | a0001c0001t0003g0217 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.282+2954T>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73180929 | ||||||
| chr10:73180930
|
A | G | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.282+2955A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73180930 | ||||||
| chr10:73181009
|
C | CT | 5 | a0001c0001t0001g0106a0001c0001t0001g0191a0001c0001t0001g0226others(2): Show | 5 | HG01346.hp2 HG02602.hp2 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.282+3049dupT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73181009 | |||||
| chr10:73181009
|
CT | C | 22 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0222others(19): Show | 22 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.282+3049delT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73181009 | |||||
| chr10:73181069
|
C | T | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.282+3094C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73181069 | ||||||
| chr10:73181182
|
A | T | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.282+3207A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73181182 | ||||||
| chr10:73181311
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.282+3336T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73181311 | ||||||
| chr10:73181357
|
T | C | 1 | a0006c0006t0014g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.282+3382T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73181357 | ||||||
| chr10:73181422
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3447T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73181422 | ||||||
| chr10:73181524
|
A | C | 1 | a0001c0001t0001g0226 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.282+3549A>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73181524 | ||||||
| chr10:73181941
|
G | A | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.282+3966G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73181941 | ||||||
| chr10:73181948
|
T | A | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.282+3973T>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73181948 | ||||||
| chr10:73181952
|
T | C | 4 | a0003c0003t0008g0003a0003c0003t0008g0004a0009c0007t0008g0008others(1): Show | 4 | HG00642.hp1 HG02809.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+3977T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73181952 | ||||||
| chr10:73182211
|
C | CTT | 76 | a0001c0001t0001g0044a0001c0001t0001g0191a0001c0001t0002g0059others(73): Show | 76 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.282+4256_282+4257d others(4): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73182211 | |||||
| chr10:73182211
|
C | CTTT | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0022others(3): Show | 6 | HG03098.hp2 HG03490.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.282+4255_282+4257d others(5): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73182211 | |||||
| chr10:73182211
|
CT | C | 5 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(2): Show | 5 | HG02523.hp1 HG02897.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.282+4257delT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73182211 | |||||
| chr10:73182211
|
CTT | C | 19 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0222others(16): Show | 19 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.282+4256_282+4257d others(4): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73182211 | |||||
| chr10:73182233
|
A | T | 83 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(80): Show | 83 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.282+4258A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73182233 | ||||||
| chr10:73182264
|
G | A | 2 | a0001c0001t0004g0118a0001c0001t0004g0119 | 2 | HG02145.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.282+4289G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73182264 | ||||||
| chr10:73182735
|
C | T | 1 | a0001c0001t0010g0190 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.282+4760C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73182735 | ||||||
| chr10:73182820
|
C | T | 233 | a0001c0001t0001g0002a0001c0001t0001g0044a0001c0001t0001g0092others(230): Show | 236 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.282+4845C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73182820 | ||||||
| chr10:73182841
|
C | T | 21 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0222others(18): Show | 21 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.282+4866C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73182841 | ||||||
| chr10:73182874
|
G | T | 82 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.282+4899G>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73182874 | ||||||
| chr10:73182970
|
C | G | 1 | a0001c0001t0001g0189 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.282+4995C>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73182970 | ||||||
| chr10:73182978
|
G | A | 1 | a0007c0011t0020g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.282+5003G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73182978 | ||||||
| chr10:73183116
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.282+5141C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73183116 | ||||||
| chr10:73183117
|
G | T | 1 | a0001c0001t0001g0189 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.282+5142G>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73183117 | ||||||
| chr10:73183118
|
A | T | 1 | a0001c0001t0001g0189 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.282+5143A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73183118 | ||||||
| chr10:73183129
|
T | C | 1 | a0001c0001t0001g0114 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.282+5154T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73183129 | ||||||
| chr10:73183165
|
G | C | 1 | a0006c0006t0014g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.282+5190G>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73183165 | ||||||
| chr10:73183276
|
T | G | 1 | a0001c0001t0001g0105 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.282+5301T>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73183276 | ||||||
| chr10:73183379
|
T | C | 1 | a0003c0003t0005g0025 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.282+5404T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73183379 | ||||||
| chr10:73183809
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.282+5834C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73183809 | ||||||
| chr10:73184059
|
C | T | 2 | a0001c0001t0009g0220a0001c0001t0009g0221 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.282+6084C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73184059 | ||||||
| chr10:73184109
|
C | T | 1 | a0001c0001t0003g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.282+6134C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73184109 | ||||||
| chr10:73184164
|
T | G | 29 | a0001c0001t0001g0044a0002c0002t0002g0009a0002c0002t0002g0010others(26): Show | 29 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.282+6189T>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73184164 | ||||||
| chr10:73184471
|
A | G | 83 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(80): Show | 83 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.282+6496A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73184471 | ||||||
| chr10:73184674
|
C | T | 21 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0222others(18): Show | 21 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.282+6699C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73184674 | ||||||
| chr10:73184678
|
G | A | 20 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0222others(17): Show | 20 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.282+6703G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73184678 | ||||||
| chr10:73185016
|
G | A | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.282+7041G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73185016 | ||||||
| chr10:73185017
|
A | G | 20 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0222others(17): Show | 20 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.282+7042A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73185017 | ||||||
| chr10:73185166
|
G | A | 20 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(17): Show | 20 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.282+7191G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73185166 | ||||||
| chr10:73185433
|
C | G | 1 | a0008c0008t0005g0085 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.283-7123C>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73185433 | ||||||
| chr10:73185624
|
T | G | 1 | a0001c0001t0001g0044 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.283-6932T>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73185624 | ||||||
| chr10:73185783
|
G | T | 3 | a0001c0001t0007g0078a0001c0001t0007g0079a0001c0001t0007g0080 | 3 | HG01884.hp1 HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.283-6773G>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73185783 | ||||||
| chr10:73185816
|
A | G | 1 | a0002c0002t0023g0086 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.283-6740A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73185816 | ||||||
| chr10:73185946
|
A | T | 1 | a0003c0003t0008g0003 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.283-6610A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73185946 | ||||||
| chr10:73185981
|
T | C | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.283-6575T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73185981 | ||||||
| chr10:73186012
|
G | C | 1 | a0006c0006t0014g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.283-6544G>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73186012 | ||||||
| chr10:73186163
|
C | T | 2 | a0003c0003t0008g0003a0003c0003t0008g0004 | 2 | HG02809.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.283-6393C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73186163 | ||||||
| chr10:73186364
|
A | C | 4 | a0003c0003t0008g0003a0003c0003t0008g0004a0009c0007t0008g0008others(1): Show | 4 | HG00642.hp1 HG02809.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-6192A>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73186364 | ||||||
| chr10:73186631
|
A | C | 1 | a0002c0002t0023g0086 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.283-5925A>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73186631 | ||||||
| chr10:73186686
|
G | A | 83 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(80): Show | 83 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.283-5870G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73186686 | ||||||
| chr10:73187110
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.283-5446A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73187110 | ||||||
| chr10:73187302
|
A | G | 1 | a0002c0002t0026g0073 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.283-5254A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73187302 | ||||||
| chr10:73187304
|
T | A | 1 | a0002c0002t0026g0073 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.283-5252T>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73187304 | ||||||
| chr10:73187391
|
T | C | 1 | a0003c0003t0001g0090 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.283-5165T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73187391 | ||||||
| chr10:73187391
|
T | TA | 26 | a0001c0001t0001g0097a0001c0001t0001g0106a0001c0001t0001g0132others(23): Show | 26 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.283-5141dupA | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73187391 | |||||
| chr10:73187391
|
TA | T | 30 | a0001c0001t0001g0113a0001c0001t0001g0116a0001c0001t0001g0130others(27): Show | 32 | HG00408.hp2 HG00544.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.283-5141delA | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73187391 | |||||
| chr10:73187392
|
A | T | 1 | a0003c0003t0001g0090 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.283-5164A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73187392 | ||||||
| chr10:73187393
|
A | T | 1 | a0003c0003t0001g0102 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.283-5163A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73187393 | ||||||
| chr10:73187678
|
G | C | 1 | a0003c0003t0001g0123 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.283-4878G>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73187678 | ||||||
| chr10:73187690
|
T | C | 1 | a0003c0003t0008g0003 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.283-4866T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73187690 | ||||||
| chr10:73187705
|
G | T | 2 | a0002c0002t0002g0031a0002c0002t0002g0049 | 2 | HG00733.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.283-4851G>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73187705 | ||||||
| chr10:73187714
|
A | G | 1 | a0003c0003t0013g0186 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.283-4842A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73187714 | ||||||
| chr10:73188314
|
G | A | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.283-4242G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73188314 | ||||||
| chr10:73188348
|
A | G | 1 | a0003c0003t0013g0186 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.283-4208A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73188348 | ||||||
| chr10:73188583
|
G | A | 1 | a0001c0001t0019g0202 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.283-3973G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73188583 | ||||||
| chr10:73188733
|
GA | G | 14 | a0002c0002t0002g0009a0002c0002t0002g0014a0002c0002t0002g0050others(11): Show | 14 | HG00609.hp1 HG00621.hp2 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.283-3812delA | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73188733 | |||||
| chr10:73188741
|
AAAAGGAA others(10): Show |
A | 1 | a0002c0002t0023g0086 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.283-3812_283-3796d others(19): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73188741 | |||||
| chr10:73188742
|
A | AAGG | 25 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0015others(22): Show | 25 | HG00544.hp1 HG00609.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.283-3813_283-3812i others(5): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73188742 | |||||
| chr10:73188742
|
A | AAGGAAGG | 29 | a0002c0002t0002g0010a0002c0002t0002g0011a0002c0002t0002g0013others(26): Show | 29 | HG00558.hp2 HG01261.hp1 HG02040.hp1 others(26): Show |
intron_variant | MODIFIER | c.283-3813_283-3812i others(9): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73188742 | |||||
| chr10:73188742
|
A | AAGGAAGG others(4): Show |
13 | a0002c0002t0002g0030a0002c0002t0002g0041a0002c0002t0002g0042others(10): Show | 13 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(10): Show |
intron_variant | MODIFIER | c.283-3813_283-3812i others(13): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73188742 | |||||
| chr10:73188742
|
A | AAGGAAGG others(8): Show |
1 | a0002c0002t0002g0072 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.283-3813_283-3812i others(17): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73188742 | |||||
| chr10:73188744
|
A | G | 13 | a0002c0002t0002g0030a0002c0002t0002g0041a0002c0002t0002g0042others(10): Show | 13 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(10): Show |
intron_variant | MODIFIER | c.283-3812A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73188744 | ||||||
| chr10:73188748
|
A | G | 29 | a0002c0002t0002g0010a0002c0002t0002g0011a0002c0002t0002g0013others(26): Show | 29 | HG00558.hp2 HG01261.hp1 HG02040.hp1 others(26): Show |
intron_variant | MODIFIER | c.283-3808A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73188748 | ||||||
| chr10:73188752
|
A | G | 25 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0015others(22): Show | 25 | HG00544.hp1 HG00609.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.283-3804A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73188752 | ||||||
| chr10:73188756
|
G | A | 71 | a0001c0001t0001g0044a0001c0001t0001g0211a0001c0001t0001g0212others(68): Show | 71 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.283-3800G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73188756 | ||||||
| chr10:73188756
|
G | GGGAA | 12 | a0001c0001t0001g0104a0001c0001t0001g0134a0001c0001t0001g0176others(9): Show | 12 | HG00558.hp1 HG01256.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.283-3747_283-3744d others(6): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73188756 | |||||
| chr10:73188756
|
G | GGGAAGGA others(1): Show |
6 | a0001c0001t0001g0105a0001c0001t0001g0130a0001c0001t0001g0181others(3): Show | 6 | HG02615.hp2 HG02809.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.283-3751_283-3744d others(10): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73188756 | |||||
| chr10:73188756
|
G | GGGAAGGA others(5): Show |
1 | a0001c0001t0001g0208 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.283-3755_283-3744d others(14): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73188756 | |||||
| chr10:73188756
|
GGGAA | G | 41 | a0001c0001t0001g0002a0001c0001t0001g0092a0001c0001t0001g0099others(38): Show | 42 | HG00438.hp1 HG00544.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.283-3747_283-3744d others(6): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73188756 | |||||
| chr10:73188756
|
GGGAAGGA others(1): Show |
G | 36 | a0001c0001t0001g0098a0001c0001t0001g0109a0001c0001t0001g0117others(33): Show | 38 | HG00408.hp2 HG00423.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.283-3751_283-3744d others(10): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73188756 | |||||
| chr10:73188756
|
GGGAAGGA others(5): Show |
G | 3 | a0001c0001t0001g0132a0003c0003t0001g0124a0003c0003t0001g0125 | 3 | HG02523.hp1 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.283-3755_283-3744d others(14): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73188756 | |||||
| chr10:73188756
|
GGGAAGGA others(9): Show |
G | 3 | a0001c0001t0001g0100a0001c0001t0001g0182a0001c0001t0001g0189 | 3 | NA18953.hp2 NA18970.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.283-3759_283-3744d others(18): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73188756 | |||||
| chr10:73188756
|
GGGAAGGA others(13): Show |
G | 16 | a0001c0001t0003g0217a0001c0001t0003g0224a0001c0001t0003g0225others(13): Show | 16 | HG00735.hp1 HG01243.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.283-3763_283-3744d others(22): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73188756 | |||||
| chr10:73188756
|
GGGAAGGA others(17): Show |
G | 4 | a0001c0001t0003g0218a0001c0001t0003g0222a0001c0001t0003g0223others(1): Show | 4 | HG01884.hp1 HG01891.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-3767_283-3744d others(26): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73188756 | |||||
| chr10:73188760
|
A | G | 3 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213 | 3 | HG02280.hp2 HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.283-3796A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73188760 | ||||||
| chr10:73188764
|
A | G | 1 | a0010c0005t0017g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.283-3792A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73188764 | ||||||
| chr10:73188772
|
A | G | 1 | a0002c0002t0023g0086 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.283-3784A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73188772 | ||||||
| chr10:73188788
|
A | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0182a0001c0001t0001g0189 | 3 | NA18953.hp2 NA18970.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.283-3768A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73188788 | ||||||
| chr10:73188944
|
A | C | 3 | a0002c0002t0002g0054a0002c0002t0002g0069a0002c0002t0016g0017 | 3 | NA18952.hp2 NA19057.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.283-3612A>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73188944 | ||||||
| chr10:73189341
|
C | A | 1 | a0008c0008t0005g0085 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.283-3215C>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73189341 | ||||||
| chr10:73189414
|
G | C | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.283-3142G>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73189414 | ||||||
| chr10:73189942
|
T | G | 6 | a0002c0002t0002g0050a0002c0002t0002g0051a0002c0002t0002g0055others(3): Show | 6 | NA18941.hp2 NA18949.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.283-2614T>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73189942 | ||||||
| chr10:73190241
|
AT | A | 23 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0222others(20): Show | 23 | HG00642.hp1 HG00735.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.283-2300delT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73190241 | |||||
| chr10:73190348
|
A | T | 1 | a0001c0001t0001g0136 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.283-2208A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73190348 | ||||||
| chr10:73190351
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.283-2205G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73190351 | ||||||
| chr10:73190352
|
G | C | 1 | a0001c0001t0001g0136 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.283-2204G>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73190352 | ||||||
| chr10:73190353
|
C | A | 1 | a0001c0001t0001g0136 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.283-2203C>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73190353 | ||||||
| chr10:73190357
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.283-2199C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73190357 | ||||||
| chr10:73190358
|
C | G | 1 | a0001c0001t0001g0136 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.283-2198C>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73190358 | ||||||
| chr10:73190361
|
A | T | 1 | a0001c0001t0001g0136 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.283-2195A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73190361 | ||||||
| chr10:73190362
|
A | G | 1 | a0001c0001t0001g0136 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.283-2194A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73190362 | ||||||
| chr10:73190363
|
G | T | 1 | a0001c0001t0001g0136 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.283-2193G>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73190363 | ||||||
| chr10:73190378
|
A | T | 63 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(60): Show | 63 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.283-2178A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73190378 | ||||||
| chr10:73190460
|
A | G | 7 | a0001c0001t0001g0002a0001c0001t0001g0109a0001c0001t0001g0203others(4): Show | 8 | HG00642.hp2 HG01069.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.283-2096A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73190460 | ||||||
| chr10:73190548
|
G | A | 73 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(70): Show | 73 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.283-2008G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73190548 | ||||||
| chr10:73190721
|
C | CT | 21 | a0001c0001t0001g0191a0001c0001t0003g0217a0001c0001t0003g0218others(18): Show | 21 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.283-1818dupT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73190721 | |||||
| chr10:73190721
|
CT | C | 76 | a0001c0001t0001g0044a0001c0001t0001g0161a0001c0001t0002g0059others(73): Show | 76 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.283-1818delT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73190721 | |||||
| chr10:73190771
|
A | G | 1 | a0002c0002t0026g0073 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.283-1785A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73190771 | ||||||
| chr10:73190780
|
A | C | 72 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(69): Show | 72 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.283-1776A>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73190780 | ||||||
| chr10:73191104
|
G | A | 1 | a0002c0002t0002g0021 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.283-1452G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73191104 | ||||||
| chr10:73191173
|
T | A | 3 | a0001c0001t0001g0100a0001c0001t0001g0182a0001c0001t0001g0189 | 3 | NA18953.hp2 NA18970.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.283-1383T>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73191173 | ||||||
| chr10:73191271
|
T | C | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.283-1285T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73191271 | ||||||
| chr10:73191283
|
C | T | 1 | a0001c0001t0003g0218 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.283-1273C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73191283 | ||||||
| chr10:73191322
|
T | C | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.283-1234T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73191322 | ||||||
| chr10:73191336
|
C | CT | 11 | a0001c0001t0001g0099a0001c0001t0003g0222a0001c0001t0003g0224others(8): Show | 11 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.283-1203dupT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73191336 | |||||
| chr10:73191413
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.283-1143C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73191413 | ||||||
| chr10:73191460
|
T | C | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.283-1096T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73191460 | ||||||
| chr10:73191731
|
G | A | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.283-825G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73191731 | ||||||
| chr10:73191869
|
T | C | 4 | a0001c0001t0001g0110a0001c0001t0001g0120a0001c0001t0001g0196others(1): Show | 4 | NA18973.hp1 NA19002.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-687T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73191869 | ||||||
| chr10:73191919
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.283-637A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73191919 | ||||||
| chr10:73192100
|
A | G | 1 | a0001c0001t0015g0214 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.283-456A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73192100 | ||||||
| chr10:73192198
|
C | A | 20 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0222others(17): Show | 20 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.283-358C>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73192198 | ||||||
| chr10:73192199
|
C | CT | 28 | a0001c0001t0001g0106a0001c0001t0001g0110a0001c0001t0001g0116others(25): Show | 28 | HG00438.hp1 HG00544.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.283-331dupT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73192199 | |||||
| chr10:73192199
|
CT | C | 57 | a0001c0001t0001g0002a0001c0001t0001g0133a0001c0001t0001g0203others(54): Show | 60 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.283-331delT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73192199 | |||||
| chr10:73192199
|
CTT | C | 62 | a0001c0001t0001g0044a0001c0001t0001g0113a0001c0001t0001g0130others(59): Show | 62 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.283-332_283-331del others(2): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73192199 | |||||
| chr10:73192199
|
CTTT | C | 6 | a0003c0003t0005g0006a0003c0003t0005g0083a0003c0003t0005g0084others(3): Show | 6 | HG00642.hp1 HG01074.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-333_283-331del others(3): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 73192199 | |||||
| chr10:73192388
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.283-168C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | chr10 | 73192388 | ||||||
| chr10:73193282
|
T | A | 73 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(70): Show | 73 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.426-195T>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 4/13 | chr10 | 73193282 | ||||||
| chr10:73193296
|
ATTC | A | 104 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.426-179_426-177del others(3): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 73193296 | |||||
| chr10:73193654
|
C | G | 72 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(69): Show | 72 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.542+61C>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73193654 | ||||||
| chr10:73193705
|
A | T | 1 | a0001c0001t0001g0136 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.542+112A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73193705 | ||||||
| chr10:73194171
|
G | A | 83 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(80): Show | 83 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.542+578G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73194171 | ||||||
| chr10:73194363
|
A | C | 1 | a0003c0003t0018g0199 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.542+770A>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73194363 | ||||||
| chr10:73194374
|
G | A | 31 | a0001c0001t0001g0113a0001c0001t0001g0130a0001c0001t0001g0208others(28): Show | 33 | HG00408.hp2 HG02257.hp2 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.542+781G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73194374 | ||||||
| chr10:73194435
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.542+842C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73194435 | ||||||
| chr10:73194662
|
C | CT | 134 | a0001c0001t0001g0044a0001c0001t0001g0113a0001c0001t0001g0130others(131): Show | 136 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.542+1079dupT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73194662 | |||||
| chr10:73194680
|
CT | C | 4 | a0001c0001t0001g0099a0001c0001t0001g0137a0001c0001t0001g0141others(1): Show | 4 | NA18964.hp1 NA18971.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.542+1096delT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73194680 | |||||
| chr10:73194701
|
G | C | 31 | a0001c0001t0001g0113a0001c0001t0001g0130a0001c0001t0001g0208others(28): Show | 33 | HG00408.hp2 HG02257.hp2 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.542+1108G>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73194701 | ||||||
| chr10:73194772
|
C | T | 79 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(76): Show | 79 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.542+1179C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73194772 | ||||||
| chr10:73194777
|
A | T | 1 | a0003c0003t0001g0123 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.542+1184A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73194777 | ||||||
| chr10:73194827
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.542+1234G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73194827 | ||||||
| chr10:73194941
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.542+1348T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73194941 | ||||||
| chr10:73194966
|
G | T | 1 | a0003c0003t0012g0087 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.542+1373G>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73194966 | ||||||
| chr10:73194989
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.542+1396T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73194989 | ||||||
| chr10:73195047
|
A | G | 1 | a0002c0002t0002g0031 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.542+1454A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73195047 | ||||||
| chr10:73195057
|
A | G | 5 | a0003c0003t0005g0006a0003c0003t0005g0083a0003c0003t0005g0084others(2): Show | 5 | HG01074.hp2 HG01346.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.542+1464A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73195057 | ||||||
| chr10:73195346
|
C | T | 2 | a0009c0007t0008g0008a0010c0005t0017g0007 | 2 | HG00642.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.542+1753C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73195346 | ||||||
| chr10:73195358
|
G | A | 29 | a0001c0001t0001g0113a0001c0001t0001g0130a0001c0001t0001g0208others(26): Show | 31 | HG00408.hp2 HG02257.hp2 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.542+1765G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73195358 | ||||||
| chr10:73195696
|
C | G | 1 | a0001c0001t0001g0195 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.542+2103C>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73195696 | ||||||
| chr10:73195829
|
T | A | 4 | a0001c0001t0004g0131a0001c0001t0004g0162a0001c0001t0004g0194others(1): Show | 4 | HG02451.hp2 HG02717.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.542+2236T>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73195829 | ||||||
| chr10:73196134
|
G | C | 1 | a0006c0006t0014g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.542+2541G>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73196134 | ||||||
| chr10:73196189
|
AACTTTAA others(25): Show |
A | 1 | a0002c0002t0002g0029 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.542+2611_542+2642d others(34): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73196189 | |||||
| chr10:73196465
|
G | C | 2 | a0002c0002t0002g0031a0002c0002t0002g0049 | 2 | HG00733.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.542+2872G>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73196465 | ||||||
| chr10:73196525
|
G | C | 5 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0163others(2): Show | 5 | HG00639.hp1 HG01243.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.542+2932G>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73196525 | ||||||
| chr10:73196628
|
A | C | 1 | a0001c0001t0001g0208 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.542+3035A>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73196628 | ||||||
| chr10:73196954
|
G | C | 1 | a0001c0001t0015g0214 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.542+3361G>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73196954 | ||||||
| chr10:73197081
|
G | A | 101 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(98): Show | 101 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.542+3488G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73197081 | ||||||
| chr10:73197192
|
T | TG | 101 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(98): Show | 101 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.542+3602dupG | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73197192 | |||||
| chr10:73197213
|
G | T | 1 | a0007c0011t0020g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.542+3620G>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73197213 | ||||||
| chr10:73197357
|
G | A | 2 | a0001c0001t0009g0220a0001c0001t0009g0221 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.542+3764G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73197357 | ||||||
| chr10:73197421
|
G | C | 4 | a0003c0003t0005g0025a0003c0003t0005g0083a0003c0003t0005g0084others(1): Show | 4 | HG02965.hp2 HG03453.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.542+3828G>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73197421 | ||||||
| chr10:73197446
|
G | GT | 101 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(98): Show | 101 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.542+3853_542+3854i others(3): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73197446 | ||||||
| chr10:73197508
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.542+3915G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73197508 | ||||||
| chr10:73197528
|
A | G | 101 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(98): Show | 101 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.542+3935A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73197528 | ||||||
| chr10:73197541
|
G | A | 1 | a0006c0006t0014g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.542+3948G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73197541 | ||||||
| chr10:73197785
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.542+4192C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73197785 | ||||||
| chr10:73197968
|
C | T | 1 | a0007c0011t0020g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.542+4375C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73197968 | ||||||
| chr10:73198138
|
G | A | 101 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(98): Show | 101 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.542+4545G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73198138 | ||||||
| chr10:73198203
|
A | T | 2 | a0001c0001t0001g0209a0001c0001t0015g0214 | 2 | HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.542+4610A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73198203 | ||||||
| chr10:73198540
|
C | T | 1 | a0003c0003t0008g0003 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.542+4947C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73198540 | ||||||
| chr10:73198665
|
C | G | 1 | a0001c0001t0001g0154 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.542+5072C>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73198665 | ||||||
| chr10:73198673
|
T | C | 3 | a0001c0001t0001g0098a0001c0001t0001g0191a0001c0001t0001g0206 | 3 | NA18973.hp2 NA18978.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.542+5080T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73198673 | ||||||
| chr10:73198737
|
G | A | 1 | a0003c0003t0008g0003 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.542+5144G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73198737 | ||||||
| chr10:73198746
|
A | G | 1 | a0001c0001t0003g0218 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.542+5153A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73198746 | ||||||
| chr10:73198754
|
G | A | 101 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(98): Show | 101 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.542+5161G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73198754 | ||||||
| chr10:73198764
|
C | G | 1 | a0006c0006t0014g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.542+5171C>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73198764 | ||||||
| chr10:73198837
|
T | C | 1 | a0010c0005t0017g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.542+5244T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73198837 | ||||||
| chr10:73198859
|
G | A | 1 | a0003c0003t0018g0199 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.542+5266G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73198859 | ||||||
| chr10:73198905
|
T | A | 1 | a0003c0003t0001g0123 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.542+5312T>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73198905 | ||||||
| chr10:73198951
|
C | T | 1 | a0003c0003t0005g0006 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.542+5358C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73198951 | ||||||
| chr10:73198958
|
G | T | 1 | a0003c0003t0005g0006 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.542+5365G>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73198958 | ||||||
| chr10:73199197
|
T | TTTG | 109 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0098others(106): Show | 110 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.542+5641_542+5643d others(5): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73199197 | |||||
| chr10:73199197
|
T | TTTGTTG | 65 | a0001c0001t0001g0044a0001c0001t0001g0113a0001c0001t0001g0115others(62): Show | 65 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.542+5638_542+5643d others(8): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73199197 | |||||
| chr10:73199197
|
T | TTTGTTGT others(2): Show |
8 | a0001c0001t0004g0131a0001c0001t0004g0162a0002c0002t0002g0015others(5): Show | 8 | HG00673.hp2 HG00733.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.542+5635_542+5643d others(11): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73199197 | |||||
| chr10:73199197
|
T | TTTGTTGT others(5): Show |
2 | a0001c0001t0001g0142a0002c0002t0002g0031 | 2 | HG03491.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.542+5632_542+5643d others(14): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73199197 | |||||
| chr10:73199343
|
G | A | 11 | a0003c0003t0005g0006a0003c0003t0005g0025a0003c0003t0005g0083others(8): Show | 11 | HG00642.hp1 HG01074.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.542+5750G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73199343 | ||||||
| chr10:73199344
|
A | C | 21 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(18): Show | 21 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(18): Show |
intron_variant | MODIFIER | c.542+5751A>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73199344 | ||||||
| chr10:73199444
|
C | T | 3 | a0001c0001t0001g0098a0001c0001t0001g0191a0001c0001t0001g0206 | 3 | NA18973.hp2 NA18978.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.542+5851C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73199444 | ||||||
| chr10:73199464
|
T | C | 101 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(98): Show | 101 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.542+5871T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73199464 | ||||||
| chr10:73199486
|
A | G | 100 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(97): Show | 100 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.542+5893A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73199486 | ||||||
| chr10:73199984
|
T | G | 18 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0222others(15): Show | 18 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.542+6391T>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73199984 | ||||||
| chr10:73200054
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.542+6461C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73200054 | ||||||
| chr10:73200459
|
C | A | 1 | a0008c0008t0005g0085 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.542+6866C>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73200459 | ||||||
| chr10:73200766
|
G | A | 101 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(98): Show | 101 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.542+7173G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73200766 | ||||||
| chr10:73200997
|
CT | C | 16 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0222others(13): Show | 16 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.542+7406delT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73200997 | |||||
| chr10:73201101
|
A | G | 1 | a0006c0006t0014g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.542+7508A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73201101 | ||||||
| chr10:73201240
|
A | G | 2 | a0001c0001t0001g0113a0001c0001t0001g0130 | 2 | HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.543-7379A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73201240 | ||||||
| chr10:73201259
|
G | A | 1 | a0003c0003t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.543-7360G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73201259 | ||||||
| chr10:73201275
|
CA | C | 16 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0222others(13): Show | 16 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.543-7343delA | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73201275 | ||||||
| chr10:73201338
|
C | T | 1 | a0002c0002t0002g0042 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.543-7281C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73201338 | ||||||
| chr10:73201546
|
C | G | 1 | a0007c0011t0020g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.543-7073C>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73201546 | ||||||
| chr10:73201817
|
T | G | 1 | a0007c0011t0020g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.543-6802T>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73201817 | ||||||
| chr10:73201847
|
CT | C | 2 | a0003c0003t0001g0124a0003c0003t0001g0126 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.543-6771delT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73201847 | ||||||
| chr10:73201904
|
C | T | 101 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(98): Show | 101 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.543-6715C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73201904 | ||||||
| chr10:73201979
|
A | T | 101 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(98): Show | 101 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.543-6640A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73201979 | ||||||
| chr10:73202001
|
C | T | 11 | a0003c0003t0001g0001a0003c0003t0001g0089a0003c0003t0001g0090others(8): Show | 13 | HG00408.hp2 NA18964.hp2 NA18968.hp1 others(10): Show |
intron_variant | MODIFIER | c.543-6618C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73202001 | ||||||
| chr10:73202294
|
T | TAGC | 101 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(98): Show | 101 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.543-6323_543-6322i others(5): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73202294 | |||||
| chr10:73202309
|
A | G | 1 | a0003c0003t0005g0084 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.543-6310A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73202309 | ||||||
| chr10:73202348
|
A | T | 3 | a0001c0001t0001g0134a0001c0001t0001g0180a0001c0001t0001g0181 | 3 | HG02809.hp2 HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.543-6271A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73202348 | ||||||
| chr10:73202370
|
T | G | 1 | a0003c0003t0013g0186 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.543-6249T>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73202370 | ||||||
| chr10:73202456
|
CT | C | 102 | a0001c0001t0001g0044a0001c0001t0001g0211a0001c0001t0002g0059others(99): Show | 102 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.543-6151delT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73202456 | |||||
| chr10:73202643
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.543-5976C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73202643 | ||||||
| chr10:73202769
|
C | A | 1 | a0006c0006t0014g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.543-5850C>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73202769 | ||||||
| chr10:73203102
|
C | T | 1 | a0001c0001t0003g0218 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.543-5517C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73203102 | ||||||
| chr10:73203216
|
C | G | 101 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(98): Show | 101 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.543-5403C>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73203216 | ||||||
| chr10:73203282
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.543-5337T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73203282 | ||||||
| chr10:73203444
|
A | G | 2 | a0002c0002t0002g0031a0002c0002t0002g0049 | 2 | HG00733.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.543-5175A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73203444 | ||||||
| chr10:73203453
|
T | G | 1 | a0001c0001t0001g0149 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.543-5166T>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73203453 | ||||||
| chr10:73203512
|
A | G | 2 | a0001c0001t0001g0149a0001c0001t0001g0179 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.543-5107A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73203512 | ||||||
| chr10:73203643
|
A | ATT | 5 | a0002c0002t0002g0027a0002c0002t0002g0032a0002c0002t0002g0062others(2): Show | 5 | HG00609.hp2 HG02965.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.543-4963_543-4962d others(4): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73203643 | |||||
| chr10:73203643
|
A | ATTT | 85 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(82): Show | 85 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.543-4964_543-4962d others(5): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73203643 | |||||
| chr10:73203643
|
A | ATTTT | 11 | a0001c0001t0003g0225a0001c0001t0003g0227a0001c0001t0003g0228others(8): Show | 11 | HG00735.hp1 HG01243.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.543-4965_543-4962d others(6): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73203643 | |||||
| chr10:73203889
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.543-4730C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73203889 | ||||||
| chr10:73204212
|
C | T | 1 | a0006c0006t0014g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.543-4407C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73204212 | ||||||
| chr10:73204282
|
G | A | 1 | a0003c0003t0005g0006 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.543-4337G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73204282 | ||||||
| chr10:73204616
|
A | G | 16 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0222others(13): Show | 16 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.543-4003A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73204616 | ||||||
| chr10:73204676
|
C | G | 1 | a0002c0002t0002g0032 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.543-3943C>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73204676 | ||||||
| chr10:73204771
|
C | CT | 26 | a0001c0001t0001g0148a0001c0001t0001g0187a0001c0001t0001g0191others(23): Show | 26 | HG00639.hp2 HG00735.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.543-3824dupT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204771 | |||||
| chr10:73204771
|
CT | C | 8 | a0001c0001t0001g0120a0001c0001t0010g0111a0001c0001t0021g0192others(5): Show | 8 | HG00621.hp1 HG00642.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.543-3824delT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204771 | |||||
| chr10:73204801
|
G | T | 1 | a0002c0002t0002g0032 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.543-3818G>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73204801 | ||||||
| chr10:73204808
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.543-3811C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73204808 | ||||||
| chr10:73204878
|
C | T | 1 | a0006c0006t0014g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.543-3741C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73204878 | ||||||
| chr10:73204944
|
A | AT | 6 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0178others(3): Show | 6 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(3): Show |
intron_variant | MODIFIER | c.543-3623dupT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204944 | |||||
| chr10:73204944
|
A | ATTTT | 7 | a0001c0001t0001g0105a0001c0001t0001g0140a0001c0001t0001g0145others(4): Show | 7 | HG00639.hp1 HG01243.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.543-3626_543-3623d others(6): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204944 | |||||
| chr10:73204944
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0165 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.543-3633_543-3623d others(13): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204944 | |||||
| chr10:73204944
|
A | ATTTTTTT others(5): Show |
1 | a0001c0001t0001g0160 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.543-3634_543-3623d others(14): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204944 | |||||
| chr10:73204944
|
AT | A | 14 | a0001c0001t0001g0103a0001c0001t0001g0116a0001c0001t0001g0134others(11): Show | 14 | HG00673.hp1 HG01069.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.543-3623delT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204944 | |||||
| chr10:73204944
|
ATT | A | 6 | a0001c0001t0001g0110a0001c0001t0001g0114a0001c0001t0001g0185others(3): Show | 6 | HG01346.hp2 HG03209.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.543-3624_543-3623d others(4): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204944 | |||||
| chr10:73204944
|
ATTTTT | A | 5 | a0001c0001t0001g0130a0001c0001t0003g0217a0002c0002t0002g0049others(2): Show | 5 | HG00733.hp2 HG01074.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.543-3627_543-3623d others(7): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204944 | |||||
| chr10:73204944
|
ATTTTTTT | A | 7 | a0001c0001t0002g0059a0002c0002t0002g0015a0002c0002t0002g0018others(4): Show | 7 | HG01978.hp2 HG02602.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.543-3629_543-3623d others(9): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204944 | |||||
| chr10:73204944
|
ATTTTTTT others(3): Show |
A | 3 | a0001c0001t0001g0176a0002c0002t0002g0048a0002c0002t0002g0051 | 3 | HG02055.hp1 HG04199.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.543-3632_543-3623d others(12): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204944 | |||||
| chr10:73204944
|
ATTTTTTT others(4): Show |
A | 34 | a0001c0001t0001g0044a0001c0001t0001g0147a0002c0002t0002g0010others(31): Show | 34 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.543-3633_543-3623d others(13): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204944 | |||||
| chr10:73204944
|
ATTTTTTT others(5): Show |
A | 26 | a0002c0002t0002g0009a0002c0002t0002g0013a0002c0002t0002g0014others(23): Show | 26 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.543-3634_543-3623d others(14): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204944 | |||||
| chr10:73204944
|
ATTTTTTT others(6): Show |
A | 4 | a0001c0001t0010g0111a0002c0002t0002g0016a0002c0002t0002g0027others(1): Show | 4 | HG00642.hp2 NA18942.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.543-3635_543-3623d others(15): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204944 | |||||
| chr10:73204944
|
ATTTTTTT others(7): Show |
A | 5 | a0003c0003t0001g0112a0003c0003t0001g0121a0003c0003t0001g0125others(2): Show | 5 | HG02559.hp1 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.543-3636_543-3623d others(16): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204944 | |||||
| chr10:73204944
|
ATTTTTTT others(8): Show |
A | 8 | a0001c0001t0001g0092a0001c0001t0001g0109a0001c0001t0001g0161others(5): Show | 8 | HG00558.hp1 HG01433.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.543-3637_543-3623d others(17): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204944 | |||||
| chr10:73204944
|
ATTTTTTT others(9): Show |
A | 3 | a0001c0001t0001g0208a0001c0001t0015g0214a0001c0001t0021g0192 | 3 | HG01069.hp2 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.543-3638_543-3623d others(18): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204944 | |||||
| chr10:73204944
|
ATTTTTTT others(10): Show |
A | 7 | a0001c0001t0001g0150a0001c0001t0001g0169a0001c0001t0001g0209others(4): Show | 7 | HG01261.hp2 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.543-3639_543-3623d others(19): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204944 | |||||
| chr10:73204944
|
ATTTTTTT others(11): Show |
A | 5 | a0001c0001t0001g0117a0001c0001t0001g0157a0001c0001t0004g0194others(2): Show | 5 | HG00735.hp2 HG02257.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.543-3640_543-3623d others(20): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204944 | |||||
| chr10:73204944
|
ATTTTTTT others(12): Show |
A | 13 | a0001c0001t0001g0153a0001c0001t0001g0168a0001c0001t0003g0229others(10): Show | 15 | HG00408.hp2 HG01243.hp1 HG02155.hp2 others(12): Show |
intron_variant | MODIFIER | c.543-3641_543-3623d others(21): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204944 | |||||
| chr10:73204944
|
ATTTTTTT others(13): Show |
A | 6 | a0001c0001t0001g0164a0001c0001t0003g0218a0001c0001t0003g0227others(3): Show | 6 | HG00735.hp1 HG02040.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.543-3642_543-3623d others(22): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204944 | |||||
| chr10:73204944
|
ATTTTTTT others(14): Show |
A | 12 | a0001c0001t0001g0133a0001c0001t0001g0163a0001c0001t0003g0223others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.543-3643_543-3623d others(23): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204944 | |||||
| chr10:73204944
|
ATTTTTTT others(15): Show |
A | 3 | a0001c0001t0001g0137a0001c0001t0003g0233a0001c0001t0004g0135 | 3 | HG02622.hp1 HG03453.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.543-3644_543-3623d others(24): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204944 | |||||
| chr10:73204944
|
ATTTTTTT others(16): Show |
A | 7 | a0001c0001t0001g0100a0001c0001t0001g0129a0001c0001t0001g0188others(4): Show | 7 | HG01346.hp1 HG01978.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.543-3645_543-3623d others(25): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204944 | |||||
| chr10:73204944
|
ATTTTTTT others(17): Show |
A | 5 | a0001c0001t0001g0113a0001c0001t0001g0120a0001c0001t0001g0205others(2): Show | 5 | HG02257.hp1 HG03471.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.543-3646_543-3623d others(26): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204944 | |||||
| chr10:73204944
|
ATTTTTTT others(18): Show |
A | 2 | a0001c0001t0001g0179a0009c0007t0008g0008 | 2 | HG00642.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.543-3647_543-3623d others(27): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204944 | |||||
| chr10:73204944
|
ATTTTTTT others(19): Show |
A | 1 | a0001c0001t0001g0138 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.543-3648_543-3623d others(28): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204944 | |||||
| chr10:73204944
|
ATTTTTTT others(20): Show |
A | 1 | a0001c0001t0001g0156 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.543-3649_543-3623d others(29): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204944 | |||||
| chr10:73204944
|
ATTTTTTT others(21): Show |
A | 2 | a0001c0001t0001g0148a0003c0003t0001g0107 | 2 | HG02451.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.543-3650_543-3623d others(30): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204944 | |||||
| chr10:73204944
|
ATTTTTTT others(23): Show |
A | 4 | a0001c0001t0001g0191a0001c0001t0001g0196a0001c0001t0001g0206others(1): Show | 4 | HG03225.hp2 NA18973.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.543-3652_543-3623d others(32): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204944 | |||||
| chr10:73204944
|
ATTTTTTT others(26): Show |
A | 1 | a0002c0002t0002g0035 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.543-3655_543-3623d others(35): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73204944 | |||||
| chr10:73204996
|
T | A | 3 | a0001c0001t0001g0109a0001c0001t0010g0111a0001c0001t0021g0192 | 3 | HG00642.hp2 HG01069.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.543-3623T>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73204996 | ||||||
| chr10:73205093
|
G | T | 7 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(4): Show | 7 | HG02280.hp2 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.543-3526G>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73205093 | ||||||
| chr10:73205113
|
A | G | 18 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0222others(15): Show | 18 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.543-3506A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73205113 | ||||||
| chr10:73205334
|
CCA | C | 101 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(98): Show | 101 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.543-3271_543-3270d others(4): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73205334 | |||||
| chr10:73205447
|
T | C | 1 | a0007c0011t0020g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.543-3172T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73205447 | ||||||
| chr10:73205475
|
C | T | 2 | a0002c0002t0002g0021a0002c0002t0002g0022 | 2 | HG01081.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.543-3144C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73205475 | ||||||
| chr10:73205615
|
G | A | 1 | a0002c0002t0002g0060 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.543-3004G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73205615 | ||||||
| chr10:73205639
|
C | T | 1 | a0003c0003t0005g0006 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.543-2980C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73205639 | ||||||
| chr10:73205708
|
T | C | 101 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(98): Show | 101 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.543-2911T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73205708 | ||||||
| chr10:73205783
|
A | C | 1 | a0007c0011t0020g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.543-2836A>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73205783 | ||||||
| chr10:73206057
|
A | G | 101 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(98): Show | 101 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.543-2562A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73206057 | ||||||
| chr10:73206138
|
A | G | 101 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(98): Show | 101 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.543-2481A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73206138 | ||||||
| chr10:73206205
|
A | G | 101 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(98): Show | 101 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.543-2414A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73206205 | ||||||
| chr10:73206359
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.543-2260G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73206359 | ||||||
| chr10:73206511
|
C | A | 1 | a0001c0001t0002g0059 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.543-2108C>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73206511 | ||||||
| chr10:73206588
|
A | G | 1 | a0010c0005t0017g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.543-2031A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73206588 | ||||||
| chr10:73206856
|
G | A | 101 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(98): Show | 101 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.543-1763G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73206856 | ||||||
| chr10:73206915
|
A | G | 2 | a0001c0001t0001g0167a0001c0001t0001g0172 | 2 | NA18986.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.543-1704A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73206915 | ||||||
| chr10:73206918
|
AAAAC | A | 102 | a0001c0001t0001g0044a0001c0001t0001g0147a0001c0001t0002g0059others(99): Show | 102 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.543-1677_543-1674d others(6): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 73206918 | |||||
| chr10:73207006
|
A | C | 83 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(80): Show | 83 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.543-1613A>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73207006 | ||||||
| chr10:73207050
|
G | C | 1 | a0001c0001t0001g0150 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.543-1569G>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73207050 | ||||||
| chr10:73207109
|
C | T | 1 | a0003c0003t0001g0123 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.543-1510C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73207109 | ||||||
| chr10:73207301
|
T | C | 2 | a0001c0001t0001g0104a0001c0001t0001g0176 | 2 | HG03017.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.543-1318T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73207301 | ||||||
| chr10:73207333
|
A | G | 101 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(98): Show | 101 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.543-1286A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73207333 | ||||||
| chr10:73207362
|
G | A | 3 | a0002c0002t0002g0026a0002c0002t0002g0070a0002c0009t0002g0064 | 3 | HG00408.hp1 HG00558.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.543-1257G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73207362 | ||||||
| chr10:73207489
|
G | A | 16 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0222others(13): Show | 16 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.543-1130G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73207489 | ||||||
| chr10:73207836
|
G | C | 1 | a0006c0006t0014g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.543-783G>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73207836 | ||||||
| chr10:73208001
|
T | G | 2 | a0002c0002t0002g0014a0002c0002t0002g0016 | 2 | NA19068.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.543-618T>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73208001 | ||||||
| chr10:73208024
|
C | T | 3 | a0003c0003t0005g0006a0003c0003t0012g0005a0003c0003t0012g0087 | 3 | HG01074.hp2 HG01346.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.543-595C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73208024 | ||||||
| chr10:73208192
|
C | T | 1 | a0006c0006t0014g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.543-427C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73208192 | ||||||
| chr10:73208508
|
G | A | 5 | a0001c0001t0001g0155a0003c0003t0005g0025a0003c0003t0005g0083others(2): Show | 5 | HG02698.hp2 HG02965.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.543-111G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | chr10 | 73208508 | ||||||
| chr10:73208806
|
A | C | 72 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(69): Show | 72 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.710+20A>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 6/13 | chr10 | 73208806 | ||||||
| chr10:73209050
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.710+264G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 6/13 | chr10 | 73209050 | ||||||
| chr10:73209319
|
G | A | 7 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(4): Show | 7 | HG02280.hp2 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.710+533G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 6/13 | chr10 | 73209319 | ||||||
| chr10:73209320
|
T | C | 101 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(98): Show | 101 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.710+534T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 6/13 | chr10 | 73209320 | ||||||
| chr10:73209355
|
A | G | 1 | a0001c0001t0003g0224 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.710+569A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 6/13 | chr10 | 73209355 | ||||||
| chr10:73209490
|
C | A | 3 | a0001c0001t0001g0138a0001c0001t0001g0151a0001c0001t0001g0159 | 3 | HG02055.hp2 HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.710+704C>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 6/13 | chr10 | 73209490 | ||||||
| chr10:73209576
|
A | G | 1 | a0002c0002t0024g0012 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.711-675A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 6/13 | chr10 | 73209576 | ||||||
| chr10:73209778
|
T | C | 4 | a0001c0001t0004g0118a0001c0001t0004g0119a0001c0001t0009g0220others(1): Show | 4 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.711-473T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 6/13 | chr10 | 73209778 | ||||||
| chr10:73209817
|
T | C | 101 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(98): Show | 101 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.711-434T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 6/13 | chr10 | 73209817 | ||||||
| chr10:73209880
|
AT | A | 127 | a0001c0001t0001g0044a0001c0001t0001g0113a0001c0001t0001g0130others(124): Show | 129 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.711-361delT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 73209880 | |||||
| chr10:73209899
|
AT | A | 83 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(80): Show | 83 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.711-345delT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 73209899 | |||||
| chr10:73210095
|
T | C | 16 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0222others(13): Show | 16 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.711-156T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 6/13 | chr10 | 73210095 | ||||||
| chr10:73210581
|
T | C | 1 | a0006c0006t0014g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.898+143T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73210581 | ||||||
| chr10:73210715
|
C | T | 1 | a0006c0006t0014g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.898+277C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73210715 | ||||||
| chr10:73211027
|
T | A | 101 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(98): Show | 101 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.898+589T>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73211027 | ||||||
| chr10:73211402
|
A | G | 1 | a0002c0002t0023g0086 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.898+964A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73211402 | ||||||
| chr10:73211421
|
T | C | 1 | a0003c0003t0001g0091 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.898+983T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73211421 | ||||||
| chr10:73211456
|
C | G | 1 | a0008c0008t0005g0085 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.898+1018C>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73211456 | ||||||
| chr10:73211559
|
G | A | 2 | a0006c0006t0014g0096a0007c0011t0020g0215 | 2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.898+1121G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73211559 | ||||||
| chr10:73211757
|
C | T | 1 | a0006c0006t0014g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.898+1319C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73211757 | ||||||
| chr10:73211933
|
A | C | 101 | a0001c0001t0001g0044a0001c0001t0002g0059a0001c0001t0003g0217others(98): Show | 101 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.898+1495A>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73211933 | ||||||
| chr10:73212248
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.898+1810G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73212248 | ||||||
| chr10:73212530
|
C | T | 1 | a0001c0001t0019g0202 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.898+2092C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73212530 | ||||||
| chr10:73212771
|
G | A | 1 | a0002c0002t0002g0013 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.898+2333G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73212771 | ||||||
| chr10:73212777
|
C | CAT | 83 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(80): Show | 83 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.898+2340_898+2341d others(4): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 73212777 | |||||
| chr10:73212861
|
G | C | 4 | a0001c0001t0001g0044a0002c0002t0002g0030a0002c0002t0002g0046others(1): Show | 4 | HG02698.hp1 HG03688.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.898+2423G>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73212861 | ||||||
| chr10:73212865
|
T | TTCTCTCT others(5): Show |
83 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(80): Show | 83 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.898+2429_898+2440d others(14): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 73212865 | |||||
| chr10:73213000
|
G | A | 1 | a0002c0002t0002g0072 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.898+2562G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73213000 | ||||||
| chr10:73213047
|
A | G | 1 | a0001c0001t0001g0142 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.898+2609A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73213047 | ||||||
| chr10:73213148
|
G | A | 1 | a0002c0002t0002g0041 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.898+2710G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73213148 | ||||||
| chr10:73213897
|
A | C | 83 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(80): Show | 83 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.898+3459A>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73213897 | ||||||
| chr10:73214025
|
G | C | 1 | a0001c0001t0001g0130 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.898+3587G>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73214025 | ||||||
| chr10:73214197
|
C | T | 1 | a0001c0001t0004g0108 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.898+3759C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73214197 | ||||||
| chr10:73214198
|
G | T | 1 | a0001c0001t0001g0176 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.898+3760G>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73214198 | ||||||
| chr10:73214322
|
T | C | 1 | a0001c0001t0004g0131 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.898+3884T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73214322 | ||||||
| chr10:73214409
|
T | C | 1 | a0010c0005t0017g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.898+3971T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73214409 | ||||||
| chr10:73214642
|
G | A | 4 | a0003c0003t0008g0003a0003c0003t0008g0004a0009c0007t0008g0008others(1): Show | 4 | HG00642.hp1 HG02809.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.898+4204G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73214642 | ||||||
| chr10:73214802
|
TG | T | 84 | a0001c0001t0001g0044a0001c0001t0001g0152a0001c0001t0002g0059others(81): Show | 84 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.898+4366delG | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 73214802 | |||||
| chr10:73215004
|
G | T | 1 | a0001c0001t0001g0116 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.898+4566G>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73215004 | ||||||
| chr10:73215082
|
G | A | 3 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213 | 3 | HG02280.hp2 HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.898+4644G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73215082 | ||||||
| chr10:73215171
|
C | A | 1 | a0003c0003t0008g0004 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.898+4733C>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73215171 | ||||||
| chr10:73215236
|
G | T | 6 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(3): Show | 6 | HG02622.hp2 HG02897.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.898+4798G>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73215236 | ||||||
| chr10:73215298
|
G | T | 128 | a0001c0001t0001g0044a0001c0001t0001g0113a0001c0001t0001g0130others(125): Show | 130 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.898+4860G>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73215298 | ||||||
| chr10:73215355
|
T | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0197 | 2 | HG01081.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.898+4917T>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73215355 | ||||||
| chr10:73215396
|
T | A | 83 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(80): Show | 83 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.898+4958T>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73215396 | ||||||
| chr10:73215414
|
G | A | 71 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(68): Show | 71 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.898+4976G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73215414 | ||||||
| chr10:73215623
|
C | G | 83 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(80): Show | 83 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.898+5185C>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73215623 | ||||||
| chr10:73215668
|
A | G | 1 | a0006c0006t0014g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.898+5230A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73215668 | ||||||
| chr10:73216115
|
A | ATCT | 83 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(80): Show | 83 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.898+5679_898+5681d others(5): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 73216115 | |||||
| chr10:73216178
|
T | G | 1 | a0002c0002t0002g0047 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.898+5740T>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73216178 | ||||||
| chr10:73216304
|
T | C | 83 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(80): Show | 83 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.898+5866T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73216304 | ||||||
| chr10:73216488
|
TG | T | 83 | a0001c0001t0001g0044a0001c0001t0002g0059a0002c0002t0002g0009others(80): Show | 83 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.898+6051delG | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73216488 | ||||||
| chr10:73216489
|
G | T | 9 | a0003c0003t0001g0112a0003c0003t0001g0121a0003c0003t0001g0122others(6): Show | 9 | HG02258.hp1 HG02559.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.898+6051G>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73216489 | ||||||
| chr10:73216561
|
G | A | 2 | a0003c0003t0012g0005a0003c0003t0012g0087 | 2 | HG01074.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.898+6123G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73216561 | ||||||
| chr10:73216645
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.898+6207A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73216645 | ||||||
| chr10:73217116
|
C | T | 1 | a0001c0001t0003g0224 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.898+6678C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73217116 | ||||||
| chr10:73217379
|
G | A | 4 | a0003c0003t0005g0025a0003c0003t0005g0083a0003c0003t0005g0084others(1): Show | 4 | HG02965.hp2 HG03453.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.898+6941G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73217379 | ||||||
| chr10:73217473
|
T | C | 2 | a0003c0003t0001g0101a0003c0003t0001g0193 | 2 | NA19054.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.898+7035T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73217473 | ||||||
| chr10:73217474
|
G | A | 15 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0223others(12): Show | 15 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.898+7036G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73217474 | ||||||
| chr10:73217581
|
A | C | 100 | a0001c0001t0002g0059a0001c0001t0003g0217a0001c0001t0003g0218others(97): Show | 100 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.898+7143A>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73217581 | ||||||
| chr10:73217624
|
T | C | 1 | a0006c0006t0014g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.898+7186T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73217624 | ||||||
| chr10:73217777
|
A | G | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.898+7339A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73217777 | ||||||
| chr10:73218023
|
C | T | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.898+7585C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73218023 | ||||||
| chr10:73218230
|
G | A | 1 | a0001c0001t0003g0222 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.898+7792G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73218230 | ||||||
| chr10:73218259
|
T | C | 21 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(18): Show | 21 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(18): Show |
intron_variant | MODIFIER | c.898+7821T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73218259 | ||||||
| chr10:73218427
|
T | A | 3 | a0002c0002t0002g0030a0002c0002t0002g0046a0002c0002t0002g0076 | 3 | HG02698.hp1 HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.898+7989T>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73218427 | ||||||
| chr10:73218643
|
A | G | 1 | a0001c0001t0003g0222 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.898+8205A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73218643 | ||||||
| chr10:73218657
|
T | C | 1 | a0002c0002t0002g0015 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.898+8219T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73218657 | ||||||
| chr10:73218795
|
G | A | 1 | a0007c0011t0020g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.898+8357G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73218795 | ||||||
| chr10:73218913
|
C | G | 2 | a0009c0007t0008g0008a0010c0005t0017g0007 | 2 | HG00642.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.898+8475C>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73218913 | ||||||
| chr10:73219405
|
G | A | 2 | a0002c0002t0002g0031a0002c0002t0002g0049 | 2 | HG00733.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.899-8655G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73219405 | ||||||
| chr10:73219517
|
G | T | 16 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0222others(13): Show | 16 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.899-8543G>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73219517 | ||||||
| chr10:73219831
|
A | C | 7 | a0003c0003t0005g0006a0003c0003t0005g0025a0003c0003t0005g0083others(4): Show | 7 | HG01074.hp2 HG01346.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.899-8229A>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73219831 | ||||||
| chr10:73219957
|
G | A | 1 | a0007c0011t0020g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.899-8103G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73219957 | ||||||
| chr10:73220131
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.899-7929A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73220131 | ||||||
| chr10:73220201
|
C | T | 1 | a0001c0001t0004g0162 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.899-7859C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73220201 | ||||||
| chr10:73220314
|
G | T | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.899-7746G>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73220314 | ||||||
| chr10:73220592
|
A | C | 4 | a0003c0003t0005g0025a0003c0003t0005g0083a0003c0003t0005g0084others(1): Show | 4 | HG02965.hp2 HG03453.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.899-7468A>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73220592 | ||||||
| chr10:73220637
|
G | T | 1 | a0001c0001t0001g0168 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.899-7423G>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73220637 | ||||||
| chr10:73220800
|
G | T | 1 | a0002c0002t0002g0013 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.899-7260G>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73220800 | ||||||
| chr10:73221182
|
T | C | 1 | a0001c0001t0001g0130 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.899-6878T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73221182 | ||||||
| chr10:73221299
|
A | T | 3 | a0001c0001t0001g0154a0001c0001t0001g0198a0001c0001t0003g0230 | 3 | HG00639.hp2 HG01243.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.899-6761A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73221299 | ||||||
| chr10:73221366
|
T | TAG | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.899-6694_899-6693i others(4): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73221366 | ||||||
| chr10:73221368
|
T | G | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.899-6692T>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73221368 | ||||||
| chr10:73221369
|
C | A | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.899-6691C>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73221369 | ||||||
| chr10:73221434
|
T | G | 1 | a0006c0006t0014g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.899-6626T>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73221434 | ||||||
| chr10:73221482
|
G | A | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.899-6578G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73221482 | ||||||
| chr10:73221501
|
A | G | 16 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0222others(13): Show | 16 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.899-6559A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73221501 | ||||||
| chr10:73221534
|
G | T | 100 | a0001c0001t0002g0059a0001c0001t0003g0217a0001c0001t0003g0218others(97): Show | 100 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.899-6526G>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73221534 | ||||||
| chr10:73221553
|
C | T | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.899-6507C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73221553 | ||||||
| chr10:73221600
|
C | T | 140 | a0001c0001t0001g0113a0001c0001t0001g0130a0001c0001t0001g0208others(137): Show | 142 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.899-6460C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73221600 | ||||||
| chr10:73222206
|
A | G | 4 | a0001c0001t0004g0118a0001c0001t0004g0119a0001c0001t0009g0220others(1): Show | 4 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.899-5854A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73222206 | ||||||
| chr10:73222246
|
C | G | 1 | a0002c0002t0002g0081 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.899-5814C>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73222246 | ||||||
| chr10:73222263
|
G | A | 2 | a0003c0003t0001g0124a0003c0003t0001g0126 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.899-5797G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73222263 | ||||||
| chr10:73222282
|
C | T | 1 | a0003c0003t0012g0087 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.899-5778C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73222282 | ||||||
| chr10:73222295
|
T | C | 1 | a0002c0002t0023g0086 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.899-5765T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73222295 | ||||||
| chr10:73222366
|
T | G | 1 | a0001c0001t0001g0210 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.899-5694T>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73222366 | ||||||
| chr10:73222661
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.899-5399C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73222661 | ||||||
| chr10:73222978
|
G | A | 1 | a0006c0006t0014g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.899-5082G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73222978 | ||||||
| chr10:73223202
|
C | G | 1 | a0002c0002t0002g0043 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.899-4858C>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73223202 | ||||||
| chr10:73223224
|
G | A | 15 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0223others(12): Show | 15 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.899-4836G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73223224 | ||||||
| chr10:73223233
|
C | T | 1 | a0003c0003t0008g0004 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.899-4827C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73223233 | ||||||
| chr10:73223237
|
A | AG | 233 | a0001c0001t0001g0002a0001c0001t0001g0044a0001c0001t0001g0092others(230): Show | 236 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.899-4823_899-4822i others(3): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73223237 | ||||||
| chr10:73223310
|
T | C | 1 | a0001c0001t0001g0184 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.899-4750T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73223310 | ||||||
| chr10:73223532
|
A | G | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.899-4528A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73223532 | ||||||
| chr10:73223633
|
G | A | 2 | a0002c0002t0011g0056a0002c0002t0011g0058 | 2 | NA18971.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.899-4427G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73223633 | ||||||
| chr10:73223636
|
T | C | 2 | a0002c0002t0002g0023a0002c0002t0002g0024 | 2 | HG01261.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.899-4424T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73223636 | ||||||
| chr10:73223734
|
G | GT | 14 | a0001c0001t0001g0100a0001c0001t0001g0139a0001c0001t0001g0146others(11): Show | 14 | HG00733.hp1 HG00735.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.899-4313dupT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 73223734 | |||||
| chr10:73223734
|
GT | G | 79 | a0001c0001t0002g0059a0001c0001t0003g0222a0002c0002t0002g0009others(76): Show | 79 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.899-4313delT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 73223734 | |||||
| chr10:73223737
|
T | A | 1 | a0008c0008t0005g0085 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.899-4323T>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73223737 | ||||||
| chr10:73223886
|
C | T | 21 | a0003c0003t0001g0001a0003c0003t0001g0089a0003c0003t0001g0090others(18): Show | 23 | HG00408.hp2 HG02257.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.899-4174C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73223886 | ||||||
| chr10:73224094
|
G | A | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.899-3966G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73224094 | ||||||
| chr10:73224380
|
A | G | 1 | a0002c0002t0002g0024 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.899-3680A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73224380 | ||||||
| chr10:73224471
|
C | CT | 24 | a0001c0001t0001g0113a0001c0001t0001g0116a0001c0001t0001g0160others(21): Show | 24 | HG00735.hp1 HG01243.hp1 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.899-3569dupT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 73224471 | |||||
| chr10:73224471
|
CT | C | 18 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0009g0220others(15): Show | 18 | HG00558.hp2 HG00621.hp2 HG02809.hp2 others(15): Show |
intron_variant | MODIFIER | c.899-3569delT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 73224471 | |||||
| chr10:73224630
|
C | G | 1 | a0001c0001t0001g0109 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.899-3430C>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73224630 | ||||||
| chr10:73224634
|
G | C | 1 | a0003c0003t0001g0123 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.899-3426G>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73224634 | ||||||
| chr10:73224724
|
G | A | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.899-3336G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73224724 | ||||||
| chr10:73224745
|
C | T | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.899-3315C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73224745 | ||||||
| chr10:73224763
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.899-3297C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73224763 | ||||||
| chr10:73224776
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.899-3284C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73224776 | ||||||
| chr10:73225126
|
C | T | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.899-2934C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73225126 | ||||||
| chr10:73225316
|
A | G | 1 | a0003c0003t0005g0006 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.899-2744A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73225316 | ||||||
| chr10:73225333
|
G | A | 7 | a0003c0003t0005g0006a0003c0003t0005g0025a0003c0003t0005g0083others(4): Show | 7 | HG01074.hp2 HG01346.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.899-2727G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73225333 | ||||||
| chr10:73225457
|
A | T | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.899-2603A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73225457 | ||||||
| chr10:73225757
|
A | G | 100 | a0001c0001t0002g0059a0001c0001t0003g0217a0001c0001t0003g0218others(97): Show | 100 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.899-2303A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73225757 | ||||||
| chr10:73226099
|
A | AT | 11 | a0001c0001t0001g0130a0001c0001t0001g0200a0001c0001t0004g0118others(8): Show | 11 | HG00438.hp1 HG02145.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.899-1943dupT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 73226099 | |||||
| chr10:73226099
|
ATT | A | 94 | a0001c0001t0002g0059a0001c0001t0003g0217a0001c0001t0003g0218others(91): Show | 94 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.899-1944_899-1943d others(4): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 73226099 | |||||
| chr10:73226178
|
T | C | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.899-1882T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73226178 | ||||||
| chr10:73226228
|
C | T | 1 | a0010c0005t0017g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.899-1832C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73226228 | ||||||
| chr10:73226416
|
A | G | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.899-1644A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73226416 | ||||||
| chr10:73226417
|
A | G | 4 | a0001c0001t0004g0118a0001c0001t0004g0119a0001c0001t0009g0220others(1): Show | 4 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.899-1643A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73226417 | ||||||
| chr10:73226485
|
A | G | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.899-1575A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73226485 | ||||||
| chr10:73226809
|
AC | A | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.899-1249delC | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 73226809 | |||||
| chr10:73227007
|
A | G | 2 | a0001c0001t0001g0113a0001c0001t0001g0130 | 2 | HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.899-1053A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73227007 | ||||||
| chr10:73227420
|
A | G | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.899-640A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73227420 | ||||||
| chr10:73227636
|
A | G | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.899-424A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73227636 | ||||||
| chr10:73227650
|
C | T | 16 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0222others(13): Show | 16 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.899-410C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73227650 | ||||||
| chr10:73227717
|
G | A | 100 | a0001c0001t0002g0059a0001c0001t0003g0217a0001c0001t0003g0218others(97): Show | 100 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.899-343G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73227717 | ||||||
| chr10:73227914
|
C | T | 1 | a0003c0003t0001g0175 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.899-146C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 7/13 | chr10 | 73227914 | ||||||
| chr10:73228461
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1023+277G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 8/13 | chr10 | 73228461 | ||||||
| chr10:73228609
|
A | AT | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1023+433dupT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr10 | 73228609 | |||||
| chr10:73228667
|
G | A | 1 | a0002c0002t0002g0075 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1023+483G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 8/13 | chr10 | 73228667 | ||||||
| chr10:73228681
|
T | A | 2 | a0009c0007t0008g0008a0010c0005t0017g0007 | 2 | HG00642.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1023+497T>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 8/13 | chr10 | 73228681 | ||||||
| chr10:73229135
|
A | G | 1 | a0003c0003t0008g0004 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1023+951A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 8/13 | chr10 | 73229135 | ||||||
| chr10:73229151
|
T | C | 4 | a0001c0001t0001g0103a0001c0001t0001g0114a0001c0001t0001g0115others(1): Show | 4 | NA18747.hp2 NA18999.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.1023+967T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 8/13 | chr10 | 73229151 | ||||||
| chr10:73229172
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1023+988G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 8/13 | chr10 | 73229172 | ||||||
| chr10:73229216
|
T | G | 1 | a0001c0001t0001g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1023+1032T>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 8/13 | chr10 | 73229216 | ||||||
| chr10:73229523
|
T | C | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1024-899T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 8/13 | chr10 | 73229523 | ||||||
| chr10:73229583
|
T | G | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1024-839T>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 8/13 | chr10 | 73229583 | ||||||
| chr10:73229692
|
G | A | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1024-730G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 8/13 | chr10 | 73229692 | ||||||
| chr10:73229725
|
C | T | 6 | a0001c0001t0001g0110a0001c0001t0001g0120a0001c0001t0001g0129others(3): Show | 6 | HG01346.hp1 HG01978.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.1024-697C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 8/13 | chr10 | 73229725 | ||||||
| chr10:73230249
|
C | A | 1 | a0001c0001t0001g0212 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1024-173C>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 8/13 | chr10 | 73230249 | ||||||
| chr10:73230369
|
A | T | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1024-53A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 8/13 | chr10 | 73230369 | ||||||
| chr10:73230552
|
T | C | 1 | a0003c0003t0001g0175 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1127+27T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/13 | chr10 | 73230552 | ||||||
| chr10:73230566
|
G | GAAACAGA others(57): Show |
1 | a0003c0003t0001g0102 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1127+45_1127+108du others(65): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 73230566 | |||||
| chr10:73230632
|
A | G | 1 | a0001c0001t0001g0142 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1127+107A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/13 | chr10 | 73230632 | ||||||
| chr10:73230715
|
C | T | 1 | a0001c0001t0004g0135 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1127+190C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/13 | chr10 | 73230715 | ||||||
| chr10:73230975
|
TAGA | T | 3 | a0001c0001t0001g0134a0001c0001t0001g0180a0001c0001t0001g0181 | 3 | HG02809.hp2 HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1127+455_1127+457d others(5): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 73230975 | |||||
| chr10:73231028
|
A | T | 1 | a0002c0002t0002g0041 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1127+503A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/13 | chr10 | 73231028 | ||||||
| chr10:73231031
|
A | G | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1127+506A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/13 | chr10 | 73231031 | ||||||
| chr10:73231053
|
C | T | 4 | a0003c0003t0008g0003a0003c0003t0008g0004a0009c0007t0008g0008others(1): Show | 4 | HG00642.hp1 HG02809.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1127+528C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/13 | chr10 | 73231053 | ||||||
| chr10:73231236
|
T | C | 1 | a0001c0001t0001g0148 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1127+711T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/13 | chr10 | 73231236 | ||||||
| chr10:73231286
|
CTAAA | C | 81 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(78): Show | 81 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1127+764_1127+767d others(6): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 73231286 | |||||
| chr10:73231627
|
A | T | 1 | a0003c0003t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1127+1102A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/13 | chr10 | 73231627 | ||||||
| chr10:73231640
|
G | GATAA | 100 | a0001c0001t0002g0059a0001c0001t0003g0217a0001c0001t0003g0218others(97): Show | 100 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1127+1115_1127+111 others(8): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/13 | chr10 | 73231640 | ||||||
| chr10:73231643
|
A | T | 100 | a0001c0001t0002g0059a0001c0001t0003g0217a0001c0001t0003g0218others(97): Show | 100 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1127+1118A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/13 | chr10 | 73231643 | ||||||
| chr10:73231644
|
A | C | 100 | a0001c0001t0002g0059a0001c0001t0003g0217a0001c0001t0003g0218others(97): Show | 100 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1127+1119A>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/13 | chr10 | 73231644 | ||||||
| chr10:73231646
|
T | A | 100 | a0001c0001t0002g0059a0001c0001t0003g0217a0001c0001t0003g0218others(97): Show | 100 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1127+1121T>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/13 | chr10 | 73231646 | ||||||
| chr10:73231647
|
T | G | 100 | a0001c0001t0002g0059a0001c0001t0003g0217a0001c0001t0003g0218others(97): Show | 100 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1127+1122T>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/13 | chr10 | 73231647 | ||||||
| chr10:73231733
|
T | A | 18 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0222others(15): Show | 18 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1128-1206T>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/13 | chr10 | 73231733 | ||||||
| chr10:73231797
|
G | C | 1 | a0002c0002t0023g0086 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1128-1142G>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/13 | chr10 | 73231797 | ||||||
| chr10:73231803
|
A | G | 100 | a0001c0001t0002g0059a0001c0001t0003g0217a0001c0001t0003g0218others(97): Show | 100 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1128-1136A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/13 | chr10 | 73231803 | ||||||
| chr10:73231925
|
T | TA | 33 | a0001c0001t0001g0099a0001c0001t0001g0104a0001c0001t0001g0105others(30): Show | 33 | HG00423.hp2 HG00735.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.1128-1000dupA | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 73231925 | |||||
| chr10:73231925
|
T | TAAA | 73 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(70): Show | 73 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1128-1002_1128-100 others(7): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 73231925 | |||||
| chr10:73231925
|
T | TAAAA | 5 | a0002c0002t0002g0018a0002c0002t0002g0021a0002c0002t0002g0022others(2): Show | 5 | HG01081.hp1 HG02080.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.1128-1003_1128-100 others(8): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 73231925 | |||||
| chr10:73232219
|
G | GA | 78 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(75): Show | 78 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1128-711dupA | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 73232219 | |||||
| chr10:73232399
|
A | C | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1128-540A>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/13 | chr10 | 73232399 | ||||||
| chr10:73232415
|
A | G | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1128-524A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/13 | chr10 | 73232415 | ||||||
| chr10:73232660
|
A | T | 1 | a0003c0003t0001g0125 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1128-279A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/13 | chr10 | 73232660 | ||||||
| chr10:73232856
|
T | C | 70 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(67): Show | 70 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.1128-83T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/13 | chr10 | 73232856 | ||||||
| chr10:73232870
|
C | A | 1 | a0001c0001t0001g0154 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1128-69C>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 9/13 | chr10 | 73232870 | ||||||
| chr10:73233225
|
A | G | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1352+62A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 10/13 | chr10 | 73233225 | ||||||
| chr10:73233438
|
A | T | 6 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0229others(3): Show | 6 | HG00735.hp1 HG01243.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1352+275A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 10/13 | chr10 | 73233438 | ||||||
| chr10:73233479
|
C | T | 1 | a0002c0002t0023g0086 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1352+316C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 10/13 | chr10 | 73233479 | ||||||
| chr10:73233605
|
A | C | 1 | a0001c0001t0003g0222 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1352+442A>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 10/13 | chr10 | 73233605 | ||||||
| chr10:73234040
|
G | C | 1 | a0001c0001t0001g0132 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1353-777G>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 10/13 | chr10 | 73234040 | ||||||
| chr10:73234126
|
A | T | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1353-691A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 10/13 | chr10 | 73234126 | ||||||
| chr10:73234263
|
C | G | 16 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0222others(13): Show | 16 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1353-554C>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 10/13 | chr10 | 73234263 | ||||||
| chr10:73234393
|
A | T | 1 | a0007c0011t0020g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1353-424A>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 10/13 | chr10 | 73234393 | ||||||
| chr10:73234473
|
G | C | 15 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0223others(12): Show | 15 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1353-344G>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 10/13 | chr10 | 73234473 | ||||||
| chr10:73234585
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1353-232C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 10/13 | chr10 | 73234585 | ||||||
| chr10:73234755
|
T | C | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1353-62T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 10/13 | chr10 | 73234755 | ||||||
| chr10:73234984
|
C | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0182a0001c0001t0001g0189 | 3 | NA18953.hp2 NA18970.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1476+44C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 11/13 | chr10 | 73234984 | ||||||
| chr10:73235121
|
C | T | 3 | a0002c0002t0002g0063a0002c0002t0002g0067a0002c0002t0002g0071 | 3 | NA18963.hp2 NA19003.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.1477-72C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 11/13 | chr10 | 73235121 | ||||||
| chr10:73235328
|
C | T | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1602+10C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 12/13 | chr10 | 73235328 | ||||||
| chr10:73235736
|
T | C | 2 | a0003c0003t0001g0124a0003c0003t0001g0126 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1602+418T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 12/13 | chr10 | 73235736 | ||||||
| chr10:73235753
|
C | T | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1602+435C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 12/13 | chr10 | 73235753 | ||||||
| chr10:73235953
|
C | T | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1602+635C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 12/13 | chr10 | 73235953 | ||||||
| chr10:73235978
|
G | A | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1602+660G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 12/13 | chr10 | 73235978 | ||||||
| chr10:73236069
|
G | A | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1602+751G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 12/13 | chr10 | 73236069 | ||||||
| chr10:73236212
|
CA | C | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1602+897delA | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 73236212 | |||||
| chr10:73236315
|
G | C | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1602+997G>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 12/13 | chr10 | 73236315 | ||||||
| chr10:73236413
|
C | CT | 16 | a0001c0001t0001g0044a0001c0001t0001g0099a0001c0001t0001g0104others(13): Show | 16 | HG01346.hp2 HG02071.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.1602+1113dupT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 73236413 | |||||
| chr10:73236413
|
CT | C | 24 | a0001c0001t0001g0114a0001c0001t0003g0217a0001c0001t0003g0218others(21): Show | 24 | HG00642.hp1 HG00735.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.1602+1113delT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 73236413 | |||||
| chr10:73236468
|
T | C | 2 | a0003c0003t0008g0003a0003c0003t0008g0004 | 2 | HG02809.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1602+1150T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 12/13 | chr10 | 73236468 | ||||||
| chr10:73236714
|
T | G | 1 | a0001c0001t0001g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1602+1396T>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 12/13 | chr10 | 73236714 | ||||||
| chr10:73236725
|
C | CT | 84 | a0001c0001t0001g0134a0001c0001t0001g0180a0001c0001t0002g0059others(81): Show | 84 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.1602+1422dupT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 73236725 | |||||
| chr10:73236864
|
T | G | 1 | a0006c0006t0014g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1602+1546T>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 12/13 | chr10 | 73236864 | ||||||
| chr10:73237067
|
C | A | 1 | a0001c0001t0001g0191 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1602+1749C>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 12/13 | chr10 | 73237067 | ||||||
| chr10:73237310
|
G | A | 2 | a0009c0007t0008g0008a0010c0005t0017g0007 | 2 | HG00642.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1602+1992G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 12/13 | chr10 | 73237310 | ||||||
| chr10:73237852
|
T | C | 1 | a0007c0011t0020g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1603-1460T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 12/13 | chr10 | 73237852 | ||||||
| chr10:73237996
|
C | A | 11 | a0003c0003t0005g0006a0003c0003t0005g0025a0003c0003t0005g0083others(8): Show | 11 | HG00642.hp1 HG01074.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.1603-1316C>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 12/13 | chr10 | 73237996 | ||||||
| chr10:73238001
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1603-1311C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 12/13 | chr10 | 73238001 | ||||||
| chr10:73238081
|
T | C | 100 | a0001c0001t0002g0059a0001c0001t0003g0217a0001c0001t0003g0218others(97): Show | 100 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1603-1231T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 12/13 | chr10 | 73238081 | ||||||
| chr10:73238157
|
T | C | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1603-1155T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 12/13 | chr10 | 73238157 | ||||||
| chr10:73238240
|
G | A | 1 | a0001c0001t0004g0194 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1603-1072G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 12/13 | chr10 | 73238240 | ||||||
| chr10:73238476
|
G | A | 3 | a0001c0001t0001g0138a0001c0001t0001g0151a0001c0001t0001g0159 | 3 | HG02055.hp2 HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1603-836G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 12/13 | chr10 | 73238476 | ||||||
| chr10:73238857
|
T | G | 1 | a0001c0001t0001g0157 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1603-455T>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 12/13 | chr10 | 73238857 | ||||||
| chr10:73238916
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1603-396T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 12/13 | chr10 | 73238916 | ||||||
| chr10:73238979
|
A | C | 1 | a0001c0001t0003g0233 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1603-333A>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 12/13 | chr10 | 73238979 | ||||||
| chr10:73239021
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1603-291G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 12/13 | chr10 | 73239021 | ||||||
| chr10:73239235
|
G | T | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1603-77G>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 12/13 | chr10 | 73239235 | ||||||
| chr10:73239249
|
G | C | 1 | a0007c0011t0020g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1603-63G>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 12/13 | chr10 | 73239249 | ||||||
| chr10:73239595
|
A | G | 4 | a0003c0003t0005g0025a0003c0003t0005g0083a0003c0003t0005g0084others(1): Show | 4 | HG02965.hp2 HG03453.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1675+211A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 13/13 | chr10 | 73239595 | ||||||
| chr10:73239603
|
A | G | 82 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(79): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1675+219A>G | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 13/13 | chr10 | 73239603 | ||||||
| chr10:73239652
|
CT | C | 21 | a0001c0001t0001g0178a0001c0001t0003g0217a0001c0001t0003g0218others(18): Show | 21 | HG00735.hp1 HG01074.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1675+282delT | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 73239652 | |||||
| chr10:73239779
|
CTGCTT | C | 2 | a0001c0001t0003g0227a0001c0001t0003g0228 | 2 | HG02280.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1675+398_1675+402d others(7): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 73239779 | |||||
| chr10:73239982
|
T | C | 15 | a0001c0001t0001g0154a0001c0001t0003g0217a0001c0001t0003g0218others(12): Show | 15 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1675+598T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 13/13 | chr10 | 73239982 | ||||||
| chr10:73240026
|
G | C | 1 | a0006c0006t0014g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1675+642G>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 13/13 | chr10 | 73240026 | ||||||
| chr10:73240440
|
T | C | 22 | a0001c0001t0001g0134a0001c0001t0001g0178a0001c0001t0001g0180others(19): Show | 22 | HG00639.hp2 HG00733.hp1 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.1676-506T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 13/13 | chr10 | 73240440 | ||||||
| chr10:73240450
|
T | C | 29 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0103others(26): Show | 29 | HG00735.hp2 HG01081.hp2 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.1676-496T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 13/13 | chr10 | 73240450 | ||||||
| chr10:73240467
|
C | T | 66 | a0001c0001t0001g0044a0001c0001t0001g0092a0001c0001t0001g0103others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1676-479C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 13/13 | chr10 | 73240467 | ||||||
| chr10:73240487
|
C | T | 17 | a0001c0001t0001g0099a0001c0001t0001g0137a0001c0001t0001g0141others(14): Show | 19 | HG00408.hp2 HG02257.hp2 HG02717.hp1 others(16): Show |
intron_variant | MODIFIER | c.1676-459C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 13/13 | chr10 | 73240487 | ||||||
| chr10:73240497
|
G | C | 1 | a0001c0001t0004g0135 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1676-449G>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 13/13 | chr10 | 73240497 | ||||||
| chr10:73240507
|
T | C | 1 | a0002c0002t0002g0063 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1676-439T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 13/13 | chr10 | 73240507 | ||||||
| chr10:73240523
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1676-423T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 13/13 | chr10 | 73240523 | ||||||
| chr10:73240528
|
T | C | 2 | a0001c0001t0001g0129a0007c0011t0020g0215 | 2 | HG01346.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1676-418T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 13/13 | chr10 | 73240528 | ||||||
| chr10:73240569
|
G | A | 2 | a0001c0001t0002g0059a0002c0002t0002g0082 | 2 | HG01978.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.1676-377G>A | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 13/13 | chr10 | 73240569 | ||||||
| chr10:73240599
|
C | T | 21 | a0001c0001t0001g0164a0003c0003t0001g0001a0003c0003t0001g0089others(18): Show | 23 | HG00408.hp2 HG02257.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.1676-347C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 13/13 | chr10 | 73240599 | ||||||
| chr10:73240714
|
C | CA | 14 | a0001c0001t0001g0172a0001c0001t0001g0201a0001c0001t0001g0226others(11): Show | 14 | HG01074.hp2 HG01346.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1676-217dupA | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 73240714 | |||||
| chr10:73240804
|
C | T | 3 | a0001c0001t0001g0136a0001c0001t0001g0148a0001c0001t0001g0173 | 3 | NA18940.hp1 NA18992.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1676-142C>T | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 13/13 | chr10 | 73240804 | ||||||
| chr10:73240839
|
T | TAAGAAAG others(309): Show |
1 | a0007c0011t0020g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1676-92_1676-91ins others(316): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 73240839 | |||||
| chr10:73240940
|
T | C | 83 | a0001c0001t0002g0059a0002c0002t0002g0009a0002c0002t0002g0010others(80): Show | 83 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(80): Show |
splice_region_variant&intron_variant | LOW | c.1676-6T>C | FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 13/13 | chr10 | 73240940 |