Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 27146 |
|---|---|
| ensemblid | ENSG00000047662.5 |
| hgncid | 29235 |
| symbol | FAM184B |
| name | family with sequence similarity 184 member B |
| refseq_nuc | NM_015688.2 |
| refseq_prot | NP_056503.1 |
| ensembl_nuc | ENST00000265018.4 |
| ensembl_prot | ENSP00000265018.3 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 17629306 |
| end | 17781621 |
| strand | - |
| ver | v1.2 |
| region | chr4:17629306-17781621 |
| region5000 | chr4:17624306-17786621 |
| regionname0 | FAM184B_chr4_17629306_17781621 |
| regionname5000 | FAM184B_chr4_17624306_17786621 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1060 | 89 | 44 | 11 | 20 | 4 | 10 | 12 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0002 | 0/1 | 1060 | 86 | 12 | 21 | 32 | 5 | 15 | 18 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0003 | 0/0 | 1060 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0004 | 0/0 | 1060 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0005 | 0/0 | 1060 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0006 | 0/0 | 1060 | 5 | 0 | 0 | 0 | 0 | 5 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0007 | 0/0 | 1060 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0008 | 0/0 | 1060 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0009 | 0/0 | 1060 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0010 | 0/0 | 1060 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0011 | 0/0 | 1060 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0012 | 1/0 | 1060 | 2 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0013 | 0/0 | 1060 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0014 | 0/0 | 1060 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0015 | 0/0 | 1060 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0016 | 0/0 | 1060 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0017 | 0/0 | 1060 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0018 | 0/0 | 1060 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0019 | 0/0 | 1060 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0020 | 0/0 | 1060 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0021 | 0/0 | 1060 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0022 | 0/0 | 1060 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0023 | 0/0 | 1060 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0024 | 0/0 | 1060 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0025 | 0/0 | 1060 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0026 | 0/0 | 1060 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0027 | 0/0 | 1060 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0028 | 0/0 | 1060 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0029 | 0/0 | 1060 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0030 | 0/0 | 1060 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0031 | 0/0 | 1060 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0032 | 0/0 | 1060 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0033 | 0/0 | 1060 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 3183 | 47 | 4 | 11 | 21 | 2 | 9 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0002 | 0/1 | 3183 | 32 | 4 | 10 | 8 | 3 | 6 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0003 | 0/0 | 3183 | 30 | 6 | 6 | 8 | 3 | 7 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0004 | 0/0 | 3183 | 11 | 8 | 3 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0005 | 0/0 | 3183 | 10 | 10 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0006 | 0/0 | 3183 | 10 | 0 | 0 | 8 | 0 | 2 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0007 | 0/0 | 3183 | 7 | 4 | 1 | 2 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0008 | 0/0 | 3183 | 6 | 3 | 1 | 1 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0009 | 0/0 | 3183 | 4 | 4 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0010 | 0/0 | 3183 | 4 | 4 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0011 | 0/0 | 3183 | 3 | 3 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0012 | 0/0 | 3183 | 3 | 3 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0013 | 0/0 | 3183 | 3 | 0 | 2 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0014 | 0/0 | 3183 | 3 | 0 | 0 | 0 | 0 | 3 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0015 | 0/0 | 3183 | 3 | 3 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0016 | 0/0 | 3183 | 3 | 3 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0017 | 0/0 | 3183 | 3 | 2 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0018 | 0/0 | 3183 | 2 | 2 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0019 | 0/0 | 3183 | 2 | 0 | 0 | 0 | 0 | 2 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0020 | 0/0 | 3183 | 2 | 1 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0021 | 0/0 | 3183 | 2 | 2 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0022 | 0/0 | 3183 | 2 | 0 | 0 | 2 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0023 | 0/0 | 3183 | 2 | 0 | 2 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0024 | 0/0 | 3183 | 2 | 0 | 0 | 2 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0025 | 0/0 | 3183 | 2 | 1 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0026 | 0/0 | 3183 | 2 | 0 | 2 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0027 | 0/0 | 3183 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0028 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0029 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0030 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0031 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0032 | 0/0 | 3183 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0033 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0034 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0035 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0036 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0037 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0038 | 1/0 | 3183 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0039 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0040 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0041 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0042 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0043 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0044 | 0/0 | 3183 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0045 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0046 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0047 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0048 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0049 | 0/0 | 3183 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0050 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0051 | 0/0 | 3183 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0052 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0053 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0054 | 0/0 | 3183 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0055 | 0/0 | 3183 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0056 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0057 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0058 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0059 | 0/0 | 3183 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0060 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0061 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0062 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0063 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| c0064 | 0/0 | 3183 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 3519 | 83 | 14 | 19 | 28 | 5 | 16 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0002 | 1/0 | 3549 | 11 | 3 | 2 | 3 | 1 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0003 | 0/0 | 3527 | 11 | 0 | 3 | 8 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0004 | 0/0 | 3545 | 7 | 2 | 5 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0005 | 0/0 | 3518 | 7 | 7 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0006 | 0/0 | 3518 | 7 | 7 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0007 | 0/0 | 3547 | 5 | 5 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0008 | 0/0 | 3546 | 5 | 0 | 3 | 1 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0009 | 0/0 | 3544 | 5 | 5 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0010 | 0/0 | 3529 | 5 | 3 | 0 | 0 | 2 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0011 | 0/0 | 3547 | 4 | 0 | 0 | 0 | 1 | 3 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0012 | 0/0 | 3519 | 4 | 4 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0013 | 0/0 | 3548 | 3 | 3 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0014 | 0/0 | 3546 | 3 | 3 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0015 | 0/0 | 3519 | 3 | 3 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0016 | 0/0 | 3520 | 3 | 0 | 0 | 2 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0017 | 0/0 | 3519 | 3 | 0 | 1 | 0 | 0 | 2 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0018 | 0/0 | 3530 | 3 | 3 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0019 | 0/0 | 3529 | 3 | 3 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0020 | 0/0 | 3549 | 2 | 0 | 0 | 2 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0021 | 0/0 | 3550 | 2 | 1 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0022 | 0/0 | 3549 | 2 | 2 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0023 | 0/0 | 3546 | 2 | 2 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0024 | 0/0 | 3546 | 2 | 0 | 1 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0025 | 0/0 | 3544 | 2 | 2 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0026 | 0/0 | 3543 | 2 | 2 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0027 | 0/0 | 3534 | 2 | 2 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0028 | 0/0 | 3528 | 2 | 0 | 0 | 0 | 0 | 2 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0029 | 0/0 | 3525 | 2 | 2 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0030 | 0/0 | 3522 | 2 | 1 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0031 | 0/0 | 3519 | 2 | 0 | 0 | 0 | 0 | 2 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0032 | 0/0 | 3519 | 2 | 0 | 0 | 2 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0033 | 0/0 | 3519 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0034 | 0/0 | 3519 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0035 | 0/0 | 3560 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0036 | 0/0 | 3559 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0037 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0038 | 0/0 | 3549 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0039 | 0/0 | 3549 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0040 | 0/0 | 3549 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0041 | 0/0 | 3546 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0042 | 0/0 | 3545 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0043 | 0/0 | 3545 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0044 | 0/0 | 3539 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0045 | 0/0 | 3545 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0046 | 0/0 | 3538 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0047 | 0/0 | 3534 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0048 | 0/0 | 3529 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0049 | 0/0 | 3528 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0050 | 0/0 | 3517 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0051 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0052 | 0/0 | 3518 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0053 | 0/0 | 3517 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0054 | 0/0 | 3522 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0055 | 0/0 | 3519 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0056 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0057 | 0/0 | 3519 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0058 | 0/0 | 3519 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0059 | 0/0 | 3519 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0060 | 0/0 | 3520 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0061 | 0/0 | 3521 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0062 | 0/0 | 3521 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0063 | 0/0 | 3518 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0064 | 0/0 | 3529 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0065 | 0/0 | 3529 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0066 | 0/0 | 3526 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0067 | 0/0 | 3546 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0068 | 0/0 | 3539 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| t0069 | 0/0 | 3520 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0025 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0034 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0003 | 0/0 | 3183 | 30 | 6 | 6 | 8 | 3 | 7 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0004 | 0/0 | 3183 | 11 | 8 | 3 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0005 | 0/0 | 3183 | 10 | 10 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0006 | 0/0 | 3183 | 10 | 0 | 0 | 8 | 0 | 2 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0007 | 0/0 | 3183 | 7 | 4 | 1 | 2 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0008 | 0/0 | 3183 | 6 | 3 | 1 | 1 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0012 | 0/0 | 3183 | 3 | 3 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0015 | 0/0 | 3183 | 3 | 3 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0017 | 0/0 | 3183 | 3 | 2 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0021 | 0/0 | 3183 | 2 | 2 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0029 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0033 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0047 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0060 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0002c0001 | 0/0 | 3183 | 47 | 4 | 11 | 21 | 2 | 9 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0002c0002 | 0/1 | 3183 | 32 | 4 | 10 | 8 | 3 | 6 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0002c0016 | 0/0 | 3183 | 3 | 3 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0002c0020 | 0/0 | 3183 | 2 | 1 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0002c0022 | 0/0 | 3183 | 2 | 0 | 0 | 2 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0003c0009 | 0/0 | 3183 | 4 | 4 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0003c0018 | 0/0 | 3183 | 2 | 2 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0004c0010 | 0/0 | 3183 | 4 | 4 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0004c0035 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0005c0028 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0005c0030 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0005c0031 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0005c0036 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0005c0042 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0006c0014 | 0/0 | 3183 | 3 | 0 | 0 | 0 | 0 | 3 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0006c0019 | 0/0 | 3183 | 2 | 0 | 0 | 0 | 0 | 2 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0007c0041 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0007c0043 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0007c0050 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0008c0034 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0008c0039 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0008c0049 | 0/0 | 3183 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0009c0011 | 0/0 | 3183 | 3 | 3 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0010c0013 | 0/0 | 3183 | 3 | 0 | 2 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0011c0023 | 0/0 | 3183 | 2 | 0 | 2 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0012c0038 | 1/0 | 3183 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0012c0046 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0013c0048 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0013c0058 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0014c0024 | 0/0 | 3183 | 2 | 0 | 0 | 2 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0015c0062 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0015c0063 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0016c0025 | 0/0 | 3183 | 2 | 1 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0017c0026 | 0/0 | 3183 | 2 | 0 | 2 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0018c0044 | 0/0 | 3183 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0019c0040 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0020c0054 | 0/0 | 3183 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0021c0052 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0022c0045 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0023c0053 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0024c0037 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0025c0056 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0026c0055 | 0/0 | 3183 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0027c0057 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0028c0032 | 0/0 | 3183 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0029c0059 | 0/0 | 3183 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0030c0051 | 0/0 | 3183 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0031c0027 | 0/0 | 3183 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0032c0061 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0033c0064 | 0/0 | 3183 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0003t0002 | 0/0 | 6731 | 6 | 1 | 1 | 3 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0003t0004 | 0/0 | 6727 | 4 | 1 | 3 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0003t0007 | 0/0 | 6729 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0003t0008 | 0/0 | 6728 | 4 | 0 | 2 | 1 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0003t0011 | 0/0 | 6729 | 3 | 0 | 0 | 0 | 1 | 2 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0003t0018 | 0/0 | 6712 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0003t0019 | 0/0 | 6711 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0003t0023 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0003t0037 | 0/0 | 6731 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0003t0040 | 0/0 | 6731 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0003t0044 | 0/0 | 6721 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0003t0046 | 0/0 | 6720 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0003t0047 | 0/0 | 6716 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0003t0049 | 0/0 | 6710 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0003t0060 | 0/0 | 6702 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0003t0066 | 0/0 | 6708 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0003t0067 | 0/0 | 6728 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0004t0003 | 0/0 | 6709 | 3 | 0 | 3 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0004t0009 | 0/0 | 6726 | 3 | 3 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0004t0025 | 0/0 | 6726 | 2 | 2 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0004t0026 | 0/0 | 6725 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0004t0042 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0004t0045 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0005t0007 | 0/0 | 6729 | 4 | 4 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0005t0013 | 0/0 | 6730 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0005t0014 | 0/0 | 6728 | 3 | 3 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0005t0027 | 0/0 | 6716 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0005t0029 | 0/0 | 6707 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0006t0003 | 0/0 | 6709 | 7 | 0 | 0 | 7 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0006t0028 | 0/0 | 6710 | 2 | 0 | 0 | 0 | 0 | 2 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0006t0048 | 0/0 | 6711 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0007t0004 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0007t0008 | 0/0 | 6728 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0007t0019 | 0/0 | 6711 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0007t0020 | 0/0 | 6731 | 2 | 0 | 0 | 2 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0007t0023 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0007t0039 | 0/0 | 6731 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0008t0002 | 0/0 | 6731 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0008t0004 | 0/0 | 6727 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0008t0011 | 0/0 | 6729 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0008t0018 | 0/0 | 6712 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0008t0019 | 0/0 | 6711 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0008t0068 | 0/0 | 6721 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0012t0009 | 0/0 | 6726 | 2 | 2 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0012t0026 | 0/0 | 6725 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0015t0013 | 0/0 | 6730 | 2 | 2 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0015t0029 | 0/0 | 6707 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0017t0010 | 0/0 | 6711 | 3 | 2 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0021t0018 | 0/0 | 6712 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0021t0064 | 0/0 | 6711 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0029t0005 | 0/0 | 6700 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0033t0003 | 0/0 | 6709 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0047t0010 | 0/0 | 6711 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0001c0060t0027 | 0/0 | 6716 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0002c0001t0001 | 0/0 | 6701 | 37 | 4 | 8 | 19 | 1 | 5 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0002c0001t0016 | 0/0 | 6702 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0002c0001t0017 | 0/0 | 6701 | 3 | 0 | 1 | 0 | 0 | 2 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0002c0001t0031 | 0/0 | 6701 | 2 | 0 | 0 | 0 | 0 | 2 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0002c0001t0033 | 0/0 | 6701 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0002c0001t0055 | 0/0 | 6701 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0002c0001t0058 | 0/0 | 6701 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0002c0001t0059 | 0/0 | 6701 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0002c0002t0001 | 0/1 | 6701 | 29 | 4 | 10 | 5 | 3 | 6 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0002c0002t0016 | 0/0 | 6702 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0002c0002t0032 | 0/0 | 6701 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0002c0002t0069 | 0/0 | 6702 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0002c0016t0001 | 0/0 | 6701 | 3 | 3 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0002c0020t0001 | 0/0 | 6701 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0002c0020t0016 | 0/0 | 6702 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0002c0022t0001 | 0/0 | 6701 | 2 | 0 | 0 | 2 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0003c0009t0005 | 0/0 | 6700 | 4 | 4 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0003c0018t0005 | 0/0 | 6700 | 2 | 2 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0004c0010t0006 | 0/0 | 6700 | 4 | 4 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0004c0035t0006 | 0/0 | 6700 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0005c0028t0006 | 0/0 | 6700 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0005c0030t0015 | 0/0 | 6701 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0005c0031t0015 | 0/0 | 6701 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0005c0036t0053 | 0/0 | 6699 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0005c0042t0006 | 0/0 | 6700 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0006c0014t0001 | 0/0 | 6701 | 2 | 0 | 0 | 0 | 0 | 2 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0006c0014t0063 | 0/0 | 6700 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0006c0019t0001 | 0/0 | 6701 | 2 | 0 | 0 | 0 | 0 | 2 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0007c0041t0012 | 0/0 | 6701 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0007c0043t0012 | 0/0 | 6701 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0007c0050t0012 | 0/0 | 6701 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0008c0034t0051 | 0/0 | 6701 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0008c0039t0015 | 0/0 | 6701 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0008c0049t0034 | 0/0 | 6701 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0009c0011t0001 | 0/0 | 6701 | 2 | 2 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0009c0011t0056 | 0/0 | 6701 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0010c0013t0002 | 0/0 | 6731 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0010c0013t0004 | 0/0 | 6727 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0010c0013t0024 | 0/0 | 6728 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0011c0023t0024 | 0/0 | 6728 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0011c0023t0043 | 0/0 | 6727 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0012c0038t0002 | 1/0 | 6731 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0012c0046t0002 | 0/0 | 6731 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0013c0048t0022 | 0/0 | 6731 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0013c0058t0022 | 0/0 | 6731 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0014c0024t0001 | 0/0 | 6701 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0014c0024t0032 | 0/0 | 6701 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0015c0062t0035 | 0/0 | 6742 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0015c0063t0054 | 0/0 | 6704 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0016c0025t0021 | 0/0 | 6732 | 2 | 1 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0017c0026t0038 | 0/0 | 6731 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0017c0026t0041 | 0/0 | 6728 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0018c0044t0001 | 0/0 | 6701 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0019c0040t0065 | 0/0 | 6711 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0020c0054t0001 | 0/0 | 6701 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0021c0052t0050 | 0/0 | 6699 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0022c0045t0001 | 0/0 | 6701 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0023c0053t0012 | 0/0 | 6701 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0024c0037t0052 | 0/0 | 6700 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0025c0056t0061 | 0/0 | 6703 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0026c0055t0002 | 0/0 | 6731 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0027c0057t0030 | 0/0 | 6704 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0028c0032t0062 | 0/0 | 6703 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0029c0059t0036 | 0/0 | 6741 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0030c0051t0010 | 0/0 | 6711 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0031c0027t0001 | 0/0 | 6701 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0032c0061t0030 | 0/0 | 6704 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| a0033c0064t0057 | 0/0 | 6701 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | copy fasta | chr4 | 17624306 | 17786621 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0003t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0003t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0003t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0003t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0003t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0003t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0003t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0003t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0003t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0003t0004g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0003t0007g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0003t0008g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0003t0008g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0003t0008g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0003t0008g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0003t0011g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0003t0011g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0003t0011g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0003t0018g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0003t0019g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0003t0023g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0003t0037g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0003t0040g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0003t0044g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0003t0046g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0003t0047g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0003t0049g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0003t0060g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0003t0066g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0003t0067g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0004t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0004t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0004t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0004t0009g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0004t0009g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0004t0009g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0004t0025g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0004t0025g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0004t0026g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0004t0042g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0004t0045g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0005t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0005t0007g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0005t0007g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0005t0007g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0005t0013g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0005t0014g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0005t0014g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0005t0014g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0005t0027g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0005t0029g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0006t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0006t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0006t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0006t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0006t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0006t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0006t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0006t0028g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0006t0028g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0006t0048g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0007t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0007t0008g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0007t0019g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0007t0020g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0007t0020g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0007t0023g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0007t0039g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0008t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0008t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0008t0011g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0008t0018g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0008t0019g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0008t0068g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0012t0009g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0012t0009g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0012t0026g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0015t0013g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0015t0013g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0015t0029g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0017t0010g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0017t0010g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0017t0010g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0021t0018g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0021t0064g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0029t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0033t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0047t0010g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0001c0060t0027g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0016g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0017g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0017g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0017g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0031g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0031g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0033g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0055g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0058g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0001t0059g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0001g0025 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0016g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0032g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0002t0069g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0016t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0016t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0016t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0020t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0020t0016g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0022t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0002c0022t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0003c0009t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0003c0009t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0003c0009t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0003c0009t0005g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0003c0018t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0003c0018t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0004c0010t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0004c0010t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0004c0010t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0004c0010t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0004c0035t0006g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0005c0028t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0005c0030t0015g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0005c0031t0015g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0005c0036t0053g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0005c0042t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0006c0014t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0006c0014t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0006c0014t0063g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0006c0019t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0006c0019t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0007c0041t0012g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0007c0043t0012g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0007c0050t0012g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0008c0034t0051g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0008c0039t0015g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0008c0049t0034g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0009c0011t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0009c0011t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0009c0011t0056g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0010c0013t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0010c0013t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0010c0013t0024g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0011c0023t0024g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0011c0023t0043g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0012c0038t0002g0034 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0012c0046t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0013c0048t0022g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0013c0058t0022g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0014c0024t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0014c0024t0032g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0015c0062t0035g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0015c0063t0054g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0016c0025t0021g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0016c0025t0021g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0017c0026t0038g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0017c0026t0041g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0018c0044t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0019c0040t0065g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0020c0054t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0021c0052t0050g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0022c0045t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0023c0053t0012g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0024c0037t0052g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0025c0056t0061g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0026c0055t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0027c0057t0030g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0028c0032t0062g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0029c0059t0036g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0030c0051t0010g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0031c0027t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0032c0061t0030g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| a0033c0064t0057g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0017 | t0010 | g0103 | EUR | GBR | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0043 | EUR | GBR | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG00140 | hp1 | a0001 | c0003 | t0008 | g0163 | EUR | GBR | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0119 | EUR | GBR | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG00280 | hp1 | a0026 | c0055 | t0002 | g0117 | EUR | FIN | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0056 | EUR | FIN | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG00323 | hp1 | a0020 | c0054 | t0001 | g0202 | EUR | FIN | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG00323 | hp2 | a0001 | c0003 | t0046 | g0059 | EUR | FIN | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG00423 | hp1 | a0001 | c0008 | t0068 | g0234 | EAS | CHS | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | CHS | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG00544 | hp1 | a0002 | c0001 | t0055 | g0144 | EAS | CHS | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG00544 | hp2 | a0001 | c0003 | t0067 | g0238 | EAS | CHS | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG00558 | hp1 | a0002 | c0022 | t0001 | g0085 | EAS | CHS | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG00558 | hp2 | a0022 | c0045 | t0001 | g0061 | EAS | CHS | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG00597 | hp1 | a0001 | c0003 | t0037 | g0219 | EAS | CHS | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG00597 | hp2 | a0002 | c0001 | t0001 | g0188 | EAS | CHS | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG00609 | hp1 | a0001 | c0007 | t0020 | g0060 | EAS | CHS | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG00609 | hp2 | a0002 | c0001 | t0001 | g0135 | EAS | CHS | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0050 | AMR | PUR | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG00639 | hp2 | a0002 | c0001 | t0001 | g0222 | AMR | PUR | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG00642 | hp1 | a0002 | c0001 | t0059 | g0127 | AMR | PUR | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0049 | AMR | PUR | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG00673 | hp1 | a0002 | c0001 | t0001 | g0190 | EAS | CHS | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG00673 | hp2 | a0001 | c0007 | t0020 | g0153 | EAS | CHS | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01069 | hp1 | a0002 | c0001 | t0001 | g0128 | AMR | PUR | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0066 | AMR | PUR | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0051 | AMR | PUR | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01071 | hp2 | a0002 | c0001 | t0001 | g0126 | AMR | PUR | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01074 | hp1 | a0001 | c0003 | t0004 | g0067 | AMR | PUR | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01074 | hp2 | a0002 | c0001 | t0001 | g0148 | AMR | PUR | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01081 | hp1 | a0017 | c0026 | t0041 | g0160 | AMR | PUR | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01081 | hp2 | a0001 | c0007 | t0008 | g0157 | AMR | PUR | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01099 | hp1 | a0001 | c0008 | t0004 | g0037 | AMR | PUR | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01099 | hp2 | a0001 | c0003 | t0004 | g0169 | AMR | PUR | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0063 | AMR | PUR | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01109 | hp2 | a0016 | c0025 | t0021 | g0224 | AMR | PUR | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01169 | hp1 | a0010 | c0013 | t0002 | g0231 | AMR | PUR | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0055 | AMR | PUR | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0036 | AMR | PUR | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01175 | hp2 | a0010 | c0013 | t0004 | g0232 | AMR | PUR | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0040 | AMR | PUR | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01192 | hp2 | a0001 | c0004 | t0003 | g0212 | AMR | PUR | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01243 | hp1 | a0033 | c0064 | t0057 | g0223 | AMR | PUR | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01243 | hp2 | a0008 | c0049 | t0034 | g0112 | AMR | PUR | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01257 | hp1 | a0001 | c0003 | t0008 | g0205 | AMR | CLM | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01257 | hp2 | a0002 | c0001 | t0001 | g0120 | AMR | CLM | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01258 | hp1 | a0002 | c0001 | t0001 | g0121 | AMR | CLM | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0210 | AMR | CLM | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01346 | hp1 | a0001 | c0003 | t0002 | g0227 | AMR | CLM | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01346 | hp2 | a0001 | c0003 | t0004 | g0057 | AMR | CLM | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01358 | hp1 | a0001 | c0003 | t0008 | g0216 | AMR | CLM | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01358 | hp2 | a0017 | c0026 | t0038 | g0098 | AMR | CLM | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01361 | hp1 | a0002 | c0001 | t0033 | g0001 | AMR | CLM | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01361 | hp2 | a0011 | c0023 | t0024 | g0209 | AMR | CLM | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01516 | hp1 | a0002 | c0001 | t0016 | g0130 | EUR | IBS | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01516 | hp2 | a0030 | c0051 | t0010 | g0041 | EUR | IBS | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01884 | hp1 | a0016 | c0025 | t0021 | g0225 | AFR | ACB | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01884 | hp2 | a0001 | c0003 | t0004 | g0018 | AFR | ACB | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01891 | hp1 | a0007 | c0041 | t0012 | g0011 | AFR | ACB | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01891 | hp2 | a0007 | c0043 | t0012 | g0105 | AFR | ACB | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01952 | hp1 | a0001 | c0004 | t0003 | g0213 | AMR | PEL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01952 | hp2 | a0002 | c0001 | t0001 | g0145 | AMR | PEL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02004 | hp1 | a0018 | c0044 | t0001 | g0062 | AMR | PEL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02004 | hp2 | a0002 | c0001 | t0001 | g0136 | AMR | PEL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02071 | hp1 | a0014 | c0024 | t0032 | g0237 | EAS | KHV | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02071 | hp2 | a0001 | c0003 | t0002 | g0149 | EAS | KHV | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02129 | hp1 | a0002 | c0001 | t0001 | g0082 | EAS | KHV | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | KHV | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02132 | hp1 | a0002 | c0001 | t0001 | g0186 | EAS | KHV | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02132 | hp2 | a0001 | c0003 | t0047 | g0199 | EAS | KHV | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02135 | hp1 | a0001 | c0003 | t0008 | g0208 | EAS | KHV | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02135 | hp2 | a0002 | c0001 | t0058 | g0173 | EAS | KHV | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02145 | hp1 | a0001 | c0005 | t0014 | g0170 | AFR | ACB | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02145 | hp2 | a0021 | c0052 | t0050 | g0076 | AFR | ACB | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02155 | hp1 | a0002 | c0001 | t0001 | g0181 | EAS | CDX | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | CDX | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02257 | hp1 | a0027 | c0057 | t0030 | g0096 | AFR | ACB | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0217 | AFR | ACB | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02258 | hp1 | a0001 | c0004 | t0025 | g0023 | AFR | ACB | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02258 | hp2 | a0001 | c0007 | t0004 | g0097 | AFR | ACB | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02280 | hp1 | a0013 | c0048 | t0022 | g0048 | AFR | ACB | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02280 | hp2 | a0005 | c0028 | t0006 | g0191 | AFR | ACB | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02293 | hp1 | a0011 | c0023 | t0043 | g0204 | AMR | PEL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0065 | AMR | PEL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02451 | hp1 | a0004 | c0010 | t0006 | g0107 | AFR | ACB | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02451 | hp2 | a0001 | c0008 | t0019 | g0102 | AFR | ACB | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02523 | hp1 | a0002 | c0001 | t0001 | g0101 | EAS | KHV | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02523 | hp2 | a0002 | c0020 | t0016 | g0089 | EAS | KHV | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02572 | hp1 | a0025 | c0056 | t0061 | g0078 | AFR | GWD | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02572 | hp2 | a0001 | c0005 | t0027 | g0111 | AFR | GWD | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0176 | SAS | PJL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02602 | hp2 | a0002 | c0001 | t0001 | g0197 | SAS | PJL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02615 | hp1 | a0023 | c0053 | t0012 | g0080 | AFR | GWD | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02615 | hp2 | a0005 | c0031 | t0015 | g0193 | AFR | GWD | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02622 | hp1 | a0001 | c0005 | t0007 | g0194 | AFR | GWD | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02622 | hp2 | a0001 | c0008 | t0002 | g0045 | AFR | GWD | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02630 | hp1 | a0001 | c0021 | t0064 | g0005 | AFR | GWD | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02630 | hp2 | a0013 | c0058 | t0022 | g0174 | AFR | GWD | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02647 | hp1 | a0001 | c0017 | t0010 | g0175 | AFR | GWD | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02647 | hp2 | a0001 | c0003 | t0002 | g0069 | AFR | GWD | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02683 | hp1 | a0001 | c0003 | t0002 | g0019 | SAS | PJL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02683 | hp2 | a0002 | c0001 | t0001 | g0226 | SAS | PJL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02698 | hp1 | a0001 | c0008 | t0011 | g0052 | SAS | PJL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02698 | hp2 | a0002 | c0001 | t0017 | g0137 | SAS | PJL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02717 | hp1 | a0001 | c0012 | t0026 | g0092 | AFR | GWD | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02717 | hp2 | a0009 | c0011 | t0056 | g0084 | AFR | GWD | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02723 | hp1 | a0001 | c0003 | t0023 | g0122 | AFR | GWD | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02723 | hp2 | a0001 | c0004 | t0009 | g0017 | AFR | GWD | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02735 | hp1 | a0006 | c0014 | t0063 | g0053 | SAS | PJL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02735 | hp2 | a0006 | c0014 | t0001 | g0008 | SAS | PJL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02738 | hp1 | a0031 | c0027 | t0001 | g0088 | SAS | PJL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02738 | hp2 | a0006 | c0014 | t0001 | g0042 | SAS | PJL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02809 | hp1 | a0001 | c0005 | t0014 | g0118 | AFR | GWD | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02809 | hp2 | a0001 | c0017 | t0010 | g0070 | AFR | GWD | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02818 | hp1 | a0001 | c0005 | t0029 | g0184 | AFR | GWD | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02818 | hp2 | a0002 | c0016 | t0001 | g0074 | AFR | GWD | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02886 | hp1 | a0001 | c0047 | t0010 | g0113 | AFR | GWD | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02886 | hp2 | a0009 | c0011 | t0001 | g0032 | AFR | GWD | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02895 | hp1 | a0007 | c0050 | t0012 | g0004 | AFR | GWD | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02895 | hp2 | a0001 | c0005 | t0007 | g0140 | AFR | GWD | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02897 | hp1 | a0004 | c0035 | t0006 | g0139 | AFR | GWD | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02897 | hp2 | a0001 | c0005 | t0007 | g0013 | AFR | GWD | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02922 | hp1 | a0001 | c0004 | t0045 | g0104 | AFR | ESN | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02922 | hp2 | a0008 | c0034 | t0051 | g0010 | AFR | ESN | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02965 | hp1 | a0015 | c0063 | t0054 | g0229 | AFR | ESN | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02965 | hp2 | a0009 | c0011 | t0001 | g0081 | AFR | ESN | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0114 | SAS | PJL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03017 | hp2 | a0028 | c0032 | t0062 | g0172 | SAS | PJL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03041 | hp1 | a0002 | c0001 | t0001 | g0141 | AFR | GWD | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03041 | hp2 | a0005 | c0036 | t0053 | g0233 | AFR | GWD | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03098 | hp1 | a0001 | c0015 | t0013 | g0003 | AFR | MSL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03098 | hp2 | a0004 | c0010 | t0006 | g0165 | AFR | MSL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03130 | hp1 | a0002 | c0001 | t0001 | g0142 | AFR | ESN | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03130 | hp2 | a0001 | c0007 | t0039 | g0124 | AFR | ESN | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03139 | hp1 | a0001 | c0003 | t0007 | g0220 | AFR | ESN | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03139 | hp2 | a0001 | c0015 | t0029 | g0164 | AFR | ESN | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03195 | hp1 | a0002 | c0020 | t0001 | g0079 | AFR | ESN | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03195 | hp2 | a0001 | c0004 | t0026 | g0073 | AFR | ESN | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03209 | hp1 | a0004 | c0010 | t0006 | g0109 | AFR | MSL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03209 | hp2 | a0001 | c0004 | t0009 | g0072 | AFR | MSL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03225 | hp1 | a0001 | c0007 | t0019 | g0143 | AFR | MSL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03225 | hp2 | a0001 | c0005 | t0014 | g0110 | AFR | MSL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0155 | SAS | PJL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03239 | hp2 | a0002 | c0001 | t0017 | g0091 | SAS | PJL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03453 | hp1 | a0002 | c0016 | t0001 | g0071 | AFR | MSL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03453 | hp2 | a0001 | c0012 | t0009 | g0161 | AFR | MSL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03486 | hp1 | a0001 | c0021 | t0018 | g0068 | AFR | MSL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03486 | hp2 | a0008 | c0039 | t0015 | g0016 | AFR | MSL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03490 | hp1 | a0001 | c0003 | t0060 | g0215 | SAS | PJL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03490 | hp2 | a0002 | c0001 | t0031 | g0178 | SAS | PJL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03491 | hp1 | a0001 | c0003 | t0049 | g0099 | SAS | PJL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03491 | hp2 | a0006 | c0019 | t0001 | g0064 | SAS | PJL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03492 | hp1 | a0002 | c0001 | t0031 | g0179 | SAS | PJL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03492 | hp2 | a0006 | c0019 | t0001 | g0100 | SAS | PJL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03516 | hp1 | a0001 | c0004 | t0009 | g0022 | AFR | ESN | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03516 | hp2 | a0001 | c0015 | t0013 | g0106 | AFR | ESN | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03540 | hp1 | a0001 | c0005 | t0007 | g0125 | AFR | GWD | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03540 | hp2 | a0004 | c0010 | t0006 | g0077 | AFR | GWD | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03579 | hp1 | a0019 | c0040 | t0065 | g0012 | AFR | MSL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03579 | hp2 | a0003 | c0009 | t0005 | g0133 | AFR | MSL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03654 | hp1 | a0029 | c0059 | t0036 | g0038 | SAS | PJL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03654 | hp2 | a0002 | c0001 | t0001 | g0198 | SAS | PJL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03704 | hp1 | a0002 | c0001 | t0001 | g0129 | SAS | PJL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03704 | hp2 | a0001 | c0003 | t0011 | g0168 | SAS | PJL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03710 | hp1 | a0010 | c0013 | t0024 | g0211 | SAS | PJL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03710 | hp2 | a0002 | c0001 | t0001 | g0087 | SAS | PJL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0180 | SAS | BEB | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03831 | hp2 | a0001 | c0006 | t0028 | g0014 | SAS | BEB | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03942 | hp1 | a0001 | c0003 | t0040 | g0201 | SAS | BEB | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0177 | SAS | BEB | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG04199 | hp1 | a0001 | c0003 | t0011 | g0167 | SAS | STU | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG04199 | hp2 | a0001 | c0006 | t0028 | g0015 | SAS | STU | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG04228 | hp1 | a0001 | c0003 | t0066 | g0150 | SAS | STU | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0054 | SAS | STU | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA18522 | hp1 | a0001 | c0003 | t0019 | g0095 | AFR | YRI | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA18522 | hp2 | a0001 | c0005 | t0013 | g0185 | AFR | YRI | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA18906 | hp1 | a0001 | c0007 | t0023 | g0123 | AFR | YRI | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA18906 | hp2 | a0003 | c0009 | t0005 | g0195 | AFR | YRI | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA18939 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA18939 | hp2 | a0032 | c0061 | t0030 | g0007 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA18950 | hp1 | a0002 | c0001 | t0001 | g0152 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA18950 | hp2 | a0001 | c0003 | t0002 | g0158 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA18956 | hp1 | a0002 | c0001 | t0001 | g0156 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA18956 | hp2 | a0001 | c0006 | t0003 | g0031 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA18972 | hp1 | a0002 | c0001 | t0001 | g0147 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA18972 | hp2 | a0014 | c0024 | t0001 | g0183 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA18995 | hp1 | a0002 | c0001 | t0001 | g0146 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA18995 | hp2 | a0001 | c0006 | t0003 | g0026 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA18998 | hp1 | a0001 | c0033 | t0003 | g0200 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA18998 | hp2 | a0002 | c0022 | t0001 | g0151 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA19000 | hp1 | a0002 | c0001 | t0001 | g0154 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA19000 | hp2 | a0001 | c0006 | t0048 | g0027 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA19001 | hp1 | a0001 | c0003 | t0044 | g0159 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA19001 | hp2 | a0002 | c0002 | t0016 | g0039 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA19004 | hp1 | a0001 | c0006 | t0003 | g0028 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA19004 | hp2 | a0002 | c0002 | t0032 | g0236 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA19012 | hp1 | a0001 | c0006 | t0003 | g0030 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA19030 | hp1 | a0001 | c0003 | t0018 | g0006 | AFR | LWK | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA19030 | hp2 | a0001 | c0004 | t0042 | g0108 | AFR | LWK | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA19043 | hp1 | a0024 | c0037 | t0052 | g0094 | AFR | LWK | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA19043 | hp2 | a0001 | c0029 | t0005 | g0115 | AFR | LWK | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA19056 | hp1 | a0002 | c0002 | t0069 | g0235 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA19056 | hp2 | a0001 | c0006 | t0003 | g0182 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA19064 | hp1 | a0001 | c0006 | t0003 | g0132 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA19064 | hp2 | a0002 | c0001 | t0001 | g0090 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA19081 | hp1 | a0001 | c0003 | t0002 | g0206 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA19081 | hp2 | a0002 | c0001 | t0001 | g0189 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA19084 | hp2 | a0002 | c0001 | t0001 | g0187 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA19086 | hp1 | a0002 | c0001 | t0001 | g0218 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA19086 | hp2 | a0002 | c0001 | t0001 | g0214 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA19240 | hp1 | a0001 | c0060 | t0027 | g0075 | AFR | YRI | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA19240 | hp2 | a0002 | c0016 | t0001 | g0221 | AFR | YRI | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA20129 | hp1 | a0005 | c0042 | t0006 | g0093 | AFR | ASW | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA20129 | hp2 | a0015 | c0062 | t0035 | g0230 | AFR | ASW | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA20752 | hp1 | a0001 | c0003 | t0011 | g0166 | EUR | TSI | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA20752 | hp2 | a0002 | c0001 | t0001 | g0083 | EUR | TSI | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01123 | hp1 | a0001 | c0004 | t0003 | g0207 | AMR | CLM | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG01123 | hp2 | a0002 | c0001 | t0017 | g0138 | AMR | CLM | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02109 | hp1 | a0003 | c0018 | t0005 | g0192 | AFR | ACB | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0044 | AFR | ACB | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02486 | hp1 | a0001 | c0012 | t0009 | g0035 | AFR | ACB | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0047 | AFR | ACB | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02559 | hp1 | a0003 | c0009 | t0005 | g0009 | AFR | ACB | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG02559 | hp2 | a0001 | c0004 | t0025 | g0024 | AFR | ACB | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03471 | hp1 | a0001 | c0008 | t0018 | g0020 | AFR | MSL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG03471 | hp2 | a0012 | c0046 | t0002 | g0021 | AFR | MSL | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG06807 | hp1 | a0003 | c0018 | t0005 | g0196 | AFR | USA | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| HG06807 | hp2 | a0002 | c0001 | t0001 | g0086 | AFR | USA | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA18955 | hp1 | a0001 | c0006 | t0003 | g0029 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA18955 | hp2 | a0002 | c0001 | t0001 | g0131 | EAS | JPT | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA20300 | hp1 | a0005 | c0030 | t0015 | g0033 | AFR | USA | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0228 | AFR | USA | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA21309 | hp1 | a0003 | c0009 | t0005 | g0162 | AFR | LWK | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| NA21309 | hp2 | a0002 | c0001 | t0001 | g0116 | AFR | LWK | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0025 | REF | REF | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| homoSapiens_grch38 | hp1 | a0012 | c0038 | t0002 | g0034 | REF | REF | FAM184B_chr4_17624306_17786621 | FAM184B | chr4 | 17624306 | 17786621 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:17632590
|
A | G | 32 | a0001a0002a0003others(29): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
missense_variant | MODERATE | c.3125T>C | p.Val1042Ala | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 3447/6731 | 3125/3183 | 1042/1060 | chr4 | 17632590 | ||
| chr4:17633713
|
G | A | 1 | a0011 | 2 | HG01361.hp2 HG02293.hp1 |
missense_variant | MODERATE | c.3065C>T | p.Ser1022Phe | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 17/18 | 3387/6731 | 3065/3183 | 1022/1060 | chr4 | 17633713 | ||
| chr4:17633765
|
G | T | 1 | a0021 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.3013C>A | p.Pro1005Thr | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 17/18 | 3335/6731 | 3013/3183 | 1005/1060 | chr4 | 17633765 | ||
| chr4:17633861
|
G | A | 1 | a0022 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.2917C>T | p.Arg973Cys | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 17/18 | 3239/6731 | 2917/3183 | 973/1060 | chr4 | 17633861 | ||
| chr4:17635043
|
T | C | 2 | a0013a0016 | 4 | HG01109.hp2 HG01884.hp1 HG02280.hp1 others(1): Show |
missense_variant | MODERATE | c.2855A>G | p.Asn952Ser | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 16/18 | 3177/6731 | 2855/3183 | 952/1060 | chr4 | 17635043 | ||
| chr4:17639257
|
C | G | 1 | a0026 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.2659G>C | p.Glu887Gln | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/18 | 2981/6731 | 2659/3183 | 887/1060 | chr4 | 17639257 | ||
| chr4:17639343
|
C | T | 1 | a0025 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.2573G>A | p.Arg858His | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/18 | 2895/6731 | 2573/3183 | 858/1060 | chr4 | 17639343 | ||
| chr4:17639358
|
T | C | 1 | a0027 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.2558A>G | p.Glu853Gly | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/18 | 2880/6731 | 2558/3183 | 853/1060 | chr4 | 17639358 | ||
| chr4:17642140
|
G | A | 1 | a0023 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.2435C>T | p.Ala812Val | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/18 | 2757/6731 | 2435/3183 | 812/1060 | chr4 | 17642140 | ||
| chr4:17642189
|
C | T | 1 | a0009 | 3 | HG02717.hp2 HG02886.hp2 HG02965.hp2 |
missense_variant | MODERATE | c.2386G>A | p.Ala796Thr | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/18 | 2708/6731 | 2386/3183 | 796/1060 | chr4 | 17642189 | ||
| chr4:17642225
|
G | A | 11 | a0002a0006a0007others(8): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
missense_variant | MODERATE | c.2350C>T | p.Arg784Trp | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/18 | 2672/6731 | 2350/3183 | 784/1060 | chr4 | 17642225 | ||
| chr4:17647672
|
G | A | 1 | a0028 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.2311C>T | p.Pro771Ser | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/18 | 2633/6731 | 2311/3183 | 771/1060 | chr4 | 17647672 | ||
| chr4:17652971
|
G | A | 1 | a0020 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.2050C>T | p.Arg684Cys | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/18 | 2372/6731 | 2050/3183 | 684/1060 | chr4 | 17652971 | ||
| chr4:17658398
|
G | C | 2 | a0003a0024 | 7 | HG02109.hp1 HG02559.hp1 HG03579.hp2 others(4): Show |
missense_variant | MODERATE | c.1989C>G | p.His663Gln | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/18 | 2311/6731 | 1989/3183 | 663/1060 | chr4 | 17658398 | ||
| chr4:17658459
|
C | T | 17 | a0002a0003a0004others(14): Show | 126 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(123): Show |
missense_variant | MODERATE | c.1928G>A | p.Arg643His | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/18 | 2250/6731 | 1928/3183 | 643/1060 | chr4 | 17658459 | ||
| chr4:17658534
|
T | C | 1 | a0029 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.1853A>G | p.Gln618Arg | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/18 | 2175/6731 | 1853/3183 | 618/1060 | chr4 | 17658534 | ||
| chr4:17660005
|
G | A | 2 | a0008a0019 | 4 | HG01243.hp2 HG02922.hp2 HG03486.hp2 others(1): Show |
missense_variant | MODERATE | c.1777C>T | p.Arg593Cys | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 9/18 | 2099/6731 | 1777/3183 | 593/1060 | chr4 | 17660005 | ||
| chr4:17664631
|
G | A | 4 | a0003a0004a0007others(1): Show | 15 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(12): Show |
missense_variant | MODERATE | c.1625C>T | p.Ser542Leu | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/18 | 1947/6731 | 1625/3183 | 542/1060 | chr4 | 17664631 | ||
| chr4:17688449
|
T | C | 2 | a0006a0030 | 6 | HG01516.hp2 HG02735.hp1 HG02735.hp2 others(3): Show |
missense_variant | MODERATE | c.1571A>G | p.Gln524Arg | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/18 | 1893/6731 | 1571/3183 | 524/1060 | chr4 | 17688449 | ||
| chr4:17705825
|
C | G | 1 | a0018 | 1 | HG02004.hp1 | missense_variant | MODERATE | c.1097G>C | p.Gly366Ala | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 4/18 | 1419/6731 | 1097/3183 | 366/1060 | chr4 | 17705825 | ||
| chr4:17705826
|
C | T | 1 | a0010 | 3 | HG01169.hp1 HG01175.hp2 HG03710.hp1 |
missense_variant | MODERATE | c.1096G>A | p.Gly366Ser | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 4/18 | 1418/6731 | 1096/3183 | 366/1060 | chr4 | 17705826 | ||
| chr4:17708963
|
C | G | 1 | a0031 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.823G>C | p.Asp275His | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/18 | 1145/6731 | 823/3183 | 275/1060 | chr4 | 17708963 | ||
| chr4:17709282
|
G | C | 2 | a0014a0032 | 3 | HG02071.hp1 NA18939.hp2 NA18972.hp2 |
missense_variant | MODERATE | c.504C>G | p.His168Gln | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/18 | 826/6731 | 504/3183 | 168/1060 | chr4 | 17709282 | ||
| chr4:17709541
|
T | C | 3 | a0015a0016a0033 | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
missense_variant | MODERATE | c.245A>G | p.Lys82Arg | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/18 | 567/6731 | 245/3183 | 82/1060 | chr4 | 17709541 | ||
| chr4:17709587
|
G | A | 1 | a0017 | 2 | HG01081.hp1 HG01358.hp2 |
missense_variant | MODERATE | c.199C>T | p.Arg67Trp | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/18 | 521/6731 | 199/3183 | 67/1060 | chr4 | 17709587 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:17633886
|
T | C | 1 | a0005c0031 | 1 | HG02615.hp2 | splice_region_variant&synonymous_variant | LOW | c.2892A>G | p.Lys964Lys | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 17/18 | 3214/6731 | 2892/3183 | 964/1060 | chr4 | 17633886 | ||
| chr4:17635015
|
G | C | 4 | a0001c0017a0001c0047a0015c0063others(1): Show | 6 | HG00099.hp1 HG01516.hp2 HG02647.hp1 others(3): Show |
synonymous_variant | LOW | c.2883C>G | p.Ser961Ser | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 16/18 | 3205/6731 | 2883/3183 | 961/1060 | chr4 | 17635015 | ||
| chr4:17636555
|
C | T | 3 | a0013c0048a0013c0058a0016c0025 | 4 | HG01109.hp2 HG01884.hp1 HG02280.hp1 others(1): Show |
synonymous_variant | LOW | c.2757G>A | p.Glu919Glu | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 15/18 | 3079/6731 | 2757/3183 | 919/1060 | chr4 | 17636555 | ||
| chr4:17639288
|
C | T | 15 | a0001c0029a0003c0009a0003c0018others(12): Show | 22 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(19): Show |
synonymous_variant | LOW | c.2628G>A | p.Gln876Gln | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/18 | 2950/6731 | 2628/3183 | 876/1060 | chr4 | 17639288 | ||
| chr4:17658389
|
G | A | 1 | a0019c0040 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.1998C>T | p.Ala666Ala | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/18 | 2320/6731 | 1998/3183 | 666/1060 | chr4 | 17658389 | ||
| chr4:17658410
|
G | A | 4 | a0025c0056a0027c0057a0028c0032others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG03017.hp2 others(1): Show |
synonymous_variant | LOW | c.1977C>T | p.Leu659Leu | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/18 | 2299/6731 | 1977/3183 | 659/1060 | chr4 | 17658410 | ||
| chr4:17658428
|
G | A | 7 | a0001c0004a0001c0006a0001c0012others(4): Show | 29 | HG01109.hp2 HG01123.hp1 HG01192.hp2 others(26): Show |
synonymous_variant | LOW | c.1959C>T | p.His653His | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/18 | 2281/6731 | 1959/3183 | 653/1060 | chr4 | 17658428 | ||
| chr4:17659976
|
C | T | 4 | a0001c0005a0001c0015a0001c0029others(1): Show | 15 | HG02145.hp1 HG02280.hp2 HG02572.hp2 others(12): Show |
synonymous_variant | LOW | c.1806G>A | p.Lys602Lys | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 9/18 | 2128/6731 | 1806/3183 | 602/1060 | chr4 | 17659976 | ||
| chr4:17664582
|
G | A | 1 | a0002c0022 | 2 | HG00558.hp1 NA18998.hp2 |
synonymous_variant | LOW | c.1674C>T | p.Thr558Thr | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/18 | 1996/6731 | 1674/3183 | 558/1060 | chr4 | 17664582 | ||
| chr4:17693320
|
A | G | 31 | a0001c0005a0001c0006a0001c0007others(28): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(145): Show |
synonymous_variant | LOW | c.1470T>C | p.Leu490Leu | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/18 | 1792/6731 | 1470/3183 | 490/1060 | chr4 | 17693320 | ||
| chr4:17705042
|
G | T | 2 | a0014c0024a0032c0061 | 3 | HG02071.hp1 NA18939.hp2 NA18972.hp2 |
synonymous_variant | LOW | c.1335C>A | p.Ser445Ser | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/18 | 1657/6731 | 1335/3183 | 445/1060 | chr4 | 17705042 | ||
| chr4:17705850
|
G | T | 2 | a0005c0042a0007c0043 | 2 | HG01891.hp2 NA20129.hp1 |
synonymous_variant | LOW | c.1072C>A | p.Arg358Arg | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 4/18 | 1394/6731 | 1072/3183 | 358/1060 | chr4 | 17705850 | ||
| chr4:17708930
|
G | A | 1 | a0001c0060 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.856C>T | p.Leu286Leu | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/18 | 1178/6731 | 856/3183 | 286/1060 | chr4 | 17708930 | ||
| chr4:17709453
|
T | C | 40 | a0001c0003a0001c0004a0001c0006others(37): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
synonymous_variant | LOW | c.333A>G | p.Gln111Gln | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/18 | 655/6731 | 333/3183 | 111/1060 | chr4 | 17709453 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:17629318
|
C | G | 1 | a0002c0001t0017 | 3 | HG01123.hp2 HG02698.hp2 HG03239.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3214G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 3214 | chr4 | 17629318 | |||||
| chr4:17629326
|
T | C | 2 | a0017c0026t0038a0017c0026t0041 | 2 | HG01081.hp1 HG01358.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3206A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 3206 | chr4 | 17629326 | |||||
| chr4:17629369
|
A | G | 1 | a0033c0064t0057 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3163T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 3163 | chr4 | 17629369 | |||||
| chr4:17629439
|
A | T | 1 | a0001c0004t0025 | 2 | HG02258.hp1 HG02559.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3093T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 3093 | chr4 | 17629439 | |||||
| chr4:17629537
|
C | T | 4 | a0001c0003t0007a0001c0005t0007a0001c0005t0013others(1): Show | 8 | HG02622.hp1 HG02895.hp2 HG02897.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2995G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 2995 | chr4 | 17629537 | |||||
| chr4:17629630
|
T | C | 85 | a0001c0003t0007a0001c0003t0018a0001c0003t0019others(82): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*2902A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 2902 | chr4 | 17629630 | |||||
| chr4:17629654
|
T | C | 1 | a0028c0032t0062 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2878A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 2878 | chr4 | 17629654 | |||||
| chr4:17629834
|
A | G | 1 | a0001c0003t0037 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2698T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 2698 | chr4 | 17629834 | |||||
| chr4:17629855
|
A | G | 9 | a0001c0029t0005a0003c0009t0005a0003c0018t0005others(6): Show | 13 | HG01243.hp2 HG02109.hp1 HG02559.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2677T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 2677 | chr4 | 17629855 | |||||
| chr4:17629907
|
T | C | 3 | a0001c0003t0023a0001c0007t0023a0001c0007t0039 | 3 | HG02723.hp1 HG03130.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2625A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 2625 | chr4 | 17629907 | |||||
| chr4:17630089
|
C | T | 1 | a0002c0001t0058 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2443G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 2443 | chr4 | 17630089 | |||||
| chr4:17630151
|
G | T | 5 | a0007c0041t0012a0007c0043t0012a0007c0050t0012others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2381C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 2381 | chr4 | 17630151 | |||||
| chr4:17630165
|
G | T | 7 | a0001c0003t0007a0001c0005t0007a0001c0005t0013others(4): Show | 13 | HG02145.hp1 HG02622.hp1 HG02809.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2367C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 2367 | chr4 | 17630165 | |||||
| chr4:17630476
|
C | T | 1 | a0009c0011t0056 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2056G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 2056 | chr4 | 17630476 | |||||
| chr4:17630601
|
C | T | 5 | a0001c0029t0005a0002c0001t0055a0003c0009t0005others(2): Show | 9 | HG00544.hp1 HG02109.hp1 HG02559.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1931G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 1931 | chr4 | 17630601 | |||||
| chr4:17630622
|
G | A | 1 | a0002c0001t0031 | 2 | HG03490.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1910C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 1910 | chr4 | 17630622 | |||||
| chr4:17630722
|
T | C | 1 | a0002c0001t0059 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1810A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 1810 | chr4 | 17630722 | |||||
| chr4:17630779
|
C | CT | 8 | a0001c0003t0007a0001c0005t0007a0001c0005t0013others(5): Show | 15 | HG01109.hp2 HG01884.hp1 HG02145.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1752dupA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 1752 | chr4 | 17630779 | |||||
| chr4:17630779
|
CT | C | 41 | a0001c0003t0018a0001c0003t0019a0001c0007t0019others(38): Show | 114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*1752delA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 1752 | chr4 | 17630779 | |||||
| chr4:17630877
|
A | G | 4 | a0025c0056t0061a0027c0057t0030a0028c0032t0062others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG03017.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1655T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 1655 | chr4 | 17630877 | |||||
| chr4:17630980
|
G | A | 1 | a0002c0001t0017 | 3 | HG01123.hp2 HG02698.hp2 HG03239.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1552C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 1552 | chr4 | 17630980 | |||||
| chr4:17631118
|
G | A | 1 | a0019c0040t0065 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1414C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 1414 | chr4 | 17631118 | |||||
| chr4:17631118
|
G | T | 4 | a0001c0029t0005a0003c0009t0005a0003c0018t0005others(1): Show | 8 | HG02109.hp1 HG02559.hp1 HG03579.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1414C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 1414 | chr4 | 17631118 | |||||
| chr4:17631143
|
A | G | 7 | a0001c0003t0018a0001c0003t0019a0001c0007t0019others(4): Show | 7 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1389T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 1389 | chr4 | 17631143 | |||||
| chr4:17631209
|
TA | T | 7 | a0001c0003t0018a0001c0003t0019a0001c0007t0019others(4): Show | 7 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1322delT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 1322 | chr4 | 17631209 | |||||
| chr4:17631211
|
T | C | 32 | a0002c0001t0001a0002c0001t0016a0002c0001t0017others(29): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*1321A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 1321 | chr4 | 17631211 | |||||
| chr4:17631212
|
A | T | 8 | a0001c0003t0018a0001c0003t0019a0001c0007t0019others(5): Show | 8 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1320T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 1320 | chr4 | 17631212 | |||||
| chr4:17631214
|
A | T | 8 | a0001c0003t0018a0001c0003t0019a0001c0007t0019others(5): Show | 8 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1318T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 1318 | chr4 | 17631214 | |||||
| chr4:17631216
|
A | T | 8 | a0001c0003t0018a0001c0003t0019a0001c0007t0019others(5): Show | 8 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1316T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 1316 | chr4 | 17631216 | |||||
| chr4:17631218
|
A | T | 8 | a0001c0003t0018a0001c0003t0019a0001c0007t0019others(5): Show | 8 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1314T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 1314 | chr4 | 17631218 | |||||
| chr4:17631220
|
A | T | 48 | a0001c0003t0018a0001c0003t0019a0001c0004t0003others(45): Show | 130 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*1312T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 1312 | chr4 | 17631220 | |||||
| chr4:17631222
|
T | A | 3 | a0010c0013t0024a0011c0023t0024a0011c0023t0043 | 3 | HG01361.hp2 HG02293.hp1 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1310A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 1310 | chr4 | 17631222 | |||||
| chr4:17631227
|
T | C | 8 | a0001c0003t0018a0001c0003t0019a0001c0007t0019others(5): Show | 8 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1305A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 1305 | chr4 | 17631227 | |||||
| chr4:17631331
|
CTAAT | C | 15 | a0001c0029t0005a0003c0009t0005a0003c0018t0005others(12): Show | 22 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1197_*1200delATTA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 1197 | chr4 | 17631331 | |||||
| chr4:17631365
|
G | C | 32 | a0002c0001t0001a0002c0001t0016a0002c0001t0017others(29): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*1167C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 1167 | chr4 | 17631365 | |||||
| chr4:17631426
|
A | G | 32 | a0002c0001t0001a0002c0001t0016a0002c0001t0017others(29): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*1106T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 1106 | chr4 | 17631426 | |||||
| chr4:17631454
|
G | A | 4 | a0001c0017t0010a0001c0047t0010a0015c0063t0054others(1): Show | 6 | HG00099.hp1 HG01516.hp2 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1078C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 1078 | chr4 | 17631454 | |||||
| chr4:17631585
|
C | A | 1 | a0001c0003t0040 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*947G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 947 | chr4 | 17631585 | |||||
| chr4:17631596
|
T | TAATTCC | 6 | a0001c0004t0009a0001c0004t0025a0001c0004t0026others(3): Show | 10 | HG02258.hp1 HG02486.hp1 HG02559.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*930_*935dupGGAATT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 935 | chr4 | 17631596 | |||||
| chr4:17631604
|
A | G | 15 | a0001c0029t0005a0003c0009t0005a0003c0018t0005others(12): Show | 22 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*928T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 928 | chr4 | 17631604 | |||||
| chr4:17631690
|
C | T | 1 | a0021c0052t0050 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*842G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 842 | chr4 | 17631690 | |||||
| chr4:17631810
|
A | G | 1 | a0001c0003t0047 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*722T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 722 | chr4 | 17631810 | |||||
| chr4:17631863
|
T | TG | 4 | a0025c0056t0061a0027c0057t0030a0028c0032t0062others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG03017.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*668dupC | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 668 | chr4 | 17631863 | |||||
| chr4:17631907
|
C | A | 1 | a0001c0021t0064 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*625G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 625 | chr4 | 17631907 | |||||
| chr4:17632042
|
AATTTTTT others(20): Show |
A | 1 | a0021c0052t0050 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*463_*489delAAAAAA others(21): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 463 | chr4 | 17632042 | |||||
| chr4:17632043
|
A | ATTTTTTT others(3): Show |
1 | a0029c0059t0036 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*479_*488dupAAAAAA others(4): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 488 | chr4 | 17632043 | |||||
| chr4:17632043
|
A | ATTTTTTT others(4): Show |
1 | a0015c0062t0035 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*478_*488dupAAAAAA others(5): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 488 | chr4 | 17632043 | |||||
| chr4:17632043
|
ATT | A | 4 | a0001c0003t0011a0001c0005t0013a0001c0008t0011others(1): Show | 7 | HG02698.hp1 HG03098.hp1 HG03516.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*487_*488delAA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 487 | chr4 | 17632043 | |||||
| chr4:17632043
|
ATTT | A | 10 | a0001c0003t0007a0001c0003t0008a0001c0003t0023others(7): Show | 16 | HG00140.hp1 HG00544.hp2 HG01081.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*486_*488delAAA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 486 | chr4 | 17632043 | |||||
| chr4:17632043
|
ATTTT | A | 7 | a0001c0003t0004a0001c0004t0042a0001c0005t0014others(4): Show | 12 | HG01074.hp1 HG01099.hp1 HG01099.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*485_*488delAAAA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 485 | chr4 | 17632043 | |||||
| chr4:17632043
|
ATTTTTTT others(3): Show |
A | 3 | a0001c0003t0044a0001c0004t0045a0001c0008t0068 | 3 | HG00423.hp1 HG02922.hp1 NA19001.hp1 |
3_prime_UTR_variant | MODIFIER | c.*479_*488delAAAAAA others(4): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 479 | chr4 | 17632043 | |||||
| chr4:17632043
|
ATTTTTTT others(4): Show |
A | 4 | a0001c0003t0046a0001c0004t0009a0001c0004t0025others(1): Show | 8 | HG00323.hp2 HG02258.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*478_*488delAAAAAA others(5): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 478 | chr4 | 17632043 | |||||
| chr4:17632043
|
ATTTTTTT others(5): Show |
A | 2 | a0001c0004t0026a0001c0012t0026 | 2 | HG02717.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*477_*488delAAAAAA others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 477 | chr4 | 17632043 | |||||
| chr4:17632043
|
ATTTTTTT others(8): Show |
A | 3 | a0001c0003t0047a0001c0005t0027a0001c0060t0027 | 3 | HG02132.hp2 HG02572.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*474_*488delAAAAAA others(9): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 474 | chr4 | 17632043 | |||||
| chr4:17632043
|
ATTTTTTT others(10): Show |
A | 3 | a0001c0003t0018a0001c0008t0018a0001c0021t0018 | 3 | HG03471.hp1 HG03486.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*472_*488delAAAAAA others(11): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 472 | chr4 | 17632043 | |||||
| chr4:17632043
|
ATTTTTTT others(11): Show |
A | 4 | a0001c0003t0019a0001c0007t0019a0001c0008t0019others(1): Show | 4 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*471_*488delAAAAAA others(12): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 471 | chr4 | 17632043 | |||||
| chr4:17632043
|
ATTTTTTT others(12): Show |
A | 1 | a0019c0040t0065 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*470_*488delAAAAAA others(13): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 470 | chr4 | 17632043 | |||||
| chr4:17632043
|
ATTTTTTT others(13): Show |
A | 4 | a0001c0006t0048a0001c0017t0010a0001c0047t0010others(1): Show | 6 | HG00099.hp1 HG01516.hp2 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*469_*488delAAAAAA others(14): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 469 | chr4 | 17632043 | |||||
| chr4:17632043
|
ATTTTTTT others(14): Show |
A | 2 | a0001c0003t0049a0001c0006t0028 | 3 | HG03491.hp1 HG03831.hp2 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*468_*488delAAAAAA others(15): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 468 | chr4 | 17632043 | |||||
| chr4:17632043
|
ATTTTTTT others(15): Show |
A | 3 | a0001c0004t0003a0001c0006t0003a0001c0033t0003 | 11 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*467_*488delAAAAAA others(16): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 467 | chr4 | 17632043 | |||||
| chr4:17632043
|
ATTTTTTT others(16): Show |
A | 1 | a0001c0003t0066 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*466_*488delAAAAAA others(17): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 466 | chr4 | 17632043 | |||||
| chr4:17632043
|
ATTTTTTT others(18): Show |
A | 2 | a0001c0005t0029a0001c0015t0029 | 2 | HG02818.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*464_*488delAAAAAA others(19): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 464 | chr4 | 17632043 | |||||
| chr4:17632043
|
ATTTTTTT others(19): Show |
A | 5 | a0005c0030t0015a0005c0031t0015a0008c0034t0051others(2): Show | 5 | HG01243.hp2 HG02615.hp2 HG02922.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*463_*488delAAAAAA others(20): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 463 | chr4 | 17632043 | |||||
| chr4:17632043
|
ATTTTTTT others(20): Show |
A | 10 | a0001c0029t0005a0003c0009t0005a0003c0018t0005others(7): Show | 17 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*462_*488delAAAAAA others(21): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 462 | chr4 | 17632043 | |||||
| chr4:17632043
|
ATTTTTTT others(21): Show |
A | 5 | a0002c0001t0016a0002c0002t0016a0002c0020t0016others(2): Show | 5 | HG01516.hp1 HG02257.hp1 HG02523.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*461_*488delAAAAAA others(22): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 461 | chr4 | 17632043 | |||||
| chr4:17632043
|
ATTTTTTT others(22): Show |
A | 31 | a0001c0003t0060a0002c0001t0001a0002c0001t0017others(28): Show | 104 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*460_*488delAAAAAA others(23): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 460 | chr4 | 17632043 | |||||
| chr4:17632043
|
ATTTTTTT others(23): Show |
A | 1 | a0006c0014t0063 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*459_*488delAAAAAA others(24): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 459 | chr4 | 17632043 | |||||
| chr4:17632103
|
C | T | 1 | a0008c0049t0034 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*429G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 429 | chr4 | 17632103 | |||||
| chr4:17632187
|
G | A | 9 | a0001c0003t0018a0001c0003t0019a0001c0003t0066others(6): Show | 9 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*345C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 345 | chr4 | 17632187 | |||||
| chr4:17632284
|
A | G | 1 | a0001c0007t0020 | 2 | HG00609.hp1 HG00673.hp2 |
3_prime_UTR_variant | MODIFIER | c.*248T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 18/18 | 248 | chr4 | 17632284 | |||||
| chr4:17781380
|
G | C | 5 | a0001c0003t0067a0001c0008t0068a0002c0002t0032others(2): Show | 5 | HG00423.hp1 HG00544.hp2 HG02071.hp1 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-81C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/18 | chr4 | 17781380 | ||||||
| chr4:17781465
|
C | T | 1 | a0002c0001t0033 | 1 | HG01361.hp1 | 5_prime_UTR_variant | MODIFIER | c.-166G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/18 | 166 | chr4 | 17781465 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:17632632
|
G | A | 139 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(136): Show |
splice_region_variant&intron_variant | LOW | c.3090-7C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 17/17 | chr4 | 17632632 | ||||||
| chr4:17632633
|
C | CAA | 109 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(106): Show | 109 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.3090-10_3090-9dupT others(1): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 17/17 | chr4 | 17632633 | ||||||
| chr4:17632690
|
A | ACC | 6 | a0001c0017t0010g0070a0001c0017t0010g0103a0001c0017t0010g0175others(3): Show | 6 | HG00099.hp1 HG01516.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.3090-67_3090-66dup others(2): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 17/17 | chr4 | 17632690 | ||||||
| chr4:17632737
|
C | T | 22 | a0001c0029t0005g0115a0003c0009t0005g0009a0003c0009t0005g0133others(19): Show | 22 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.3090-112G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 17/17 | chr4 | 17632737 | ||||||
| chr4:17632819
|
G | T | 139 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.3090-194C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 17/17 | chr4 | 17632819 | ||||||
| chr4:17632847
|
T | C | 1 | a0003c0009t0005g0195 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3090-222A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 17/17 | chr4 | 17632847 | ||||||
| chr4:17633016
|
G | T | 2 | a0004c0010t0006g0165a0019c0040t0065g0012 | 2 | HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3090-391C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 17/17 | chr4 | 17633016 | ||||||
| chr4:17633048
|
G | A | 22 | a0001c0029t0005g0115a0003c0009t0005g0009a0003c0009t0005g0133others(19): Show | 22 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.3090-423C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 17/17 | chr4 | 17633048 | ||||||
| chr4:17633218
|
G | A | 8 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(5): Show | 8 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.3089+471C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 17/17 | chr4 | 17633218 | ||||||
| chr4:17633245
|
A | G | 1 | a0028c0032t0062g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3089+444T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 17/17 | chr4 | 17633245 | ||||||
| chr4:17633321
|
C | T | 1 | a0025c0056t0061g0078 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3089+368G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 17/17 | chr4 | 17633321 | ||||||
| chr4:17633363
|
G | A | 1 | a0032c0061t0030g0007 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.3089+326C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 17/17 | chr4 | 17633363 | ||||||
| chr4:17633933
|
CAAAAT | C | 100 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.2890-50_2890-46del others(5): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 16/17 | chr4 | 17633933 | ||||||
| chr4:17633987
|
C | T | 8 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(5): Show | 8 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.2890-99G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 16/17 | chr4 | 17633987 | ||||||
| chr4:17633988
|
G | A | 1 | a0002c0002t0001g0180 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2890-100C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 16/17 | chr4 | 17633988 | ||||||
| chr4:17634028
|
T | C | 8 | a0001c0029t0005g0115a0003c0009t0005g0009a0003c0009t0005g0133others(5): Show | 8 | HG02109.hp1 HG02559.hp1 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.2890-140A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 16/17 | chr4 | 17634028 | ||||||
| chr4:17634080
|
G | A | 3 | a0002c0001t0017g0091a0002c0001t0017g0137a0002c0001t0017g0138 | 3 | HG01123.hp2 HG02698.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.2890-192C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 16/17 | chr4 | 17634080 | ||||||
| chr4:17634264
|
A | T | 105 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2890-376T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 16/17 | chr4 | 17634264 | ||||||
| chr4:17634387
|
G | A | 1 | a0001c0003t0040g0201 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2890-499C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 16/17 | chr4 | 17634387 | ||||||
| chr4:17634409
|
C | T | 105 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2890-521G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 16/17 | chr4 | 17634409 | ||||||
| chr4:17634427
|
G | A | 1 | a0021c0052t0050g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2890-539C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 16/17 | chr4 | 17634427 | ||||||
| chr4:17634441
|
G | A | 3 | a0006c0014t0063g0053a0018c0044t0001g0062a0020c0054t0001g0202 | 3 | HG00323.hp1 HG02004.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.2890-553C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 16/17 | chr4 | 17634441 | ||||||
| chr4:17634448
|
T | A | 8 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(5): Show | 8 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.2890-560A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 16/17 | chr4 | 17634448 | ||||||
| chr4:17634525
|
C | T | 1 | a0002c0001t0001g0198 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2889+484G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 16/17 | chr4 | 17634525 | ||||||
| chr4:17634526
|
G | A | 2 | a0025c0056t0061g0078a0027c0057t0030g0096 | 2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2889+483C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 16/17 | chr4 | 17634526 | ||||||
| chr4:17634575
|
C | T | 1 | a0007c0041t0012g0011 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2889+434G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 16/17 | chr4 | 17634575 | ||||||
| chr4:17634618
|
C | T | 9 | a0004c0010t0006g0077a0004c0010t0006g0107a0004c0010t0006g0109others(6): Show | 9 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2889+391G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 16/17 | chr4 | 17634618 | ||||||
| chr4:17634696
|
A | C | 131 | a0001c0029t0005g0115a0002c0001t0001g0002a0002c0001t0001g0082others(128): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.2889+313T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 16/17 | chr4 | 17634696 | ||||||
| chr4:17634857
|
C | T | 1 | a0028c0032t0062g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2889+152G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 16/17 | chr4 | 17634857 | ||||||
| chr4:17634884
|
G | GT | 115 | a0001c0003t0007g0220a0002c0001t0001g0002a0002c0001t0001g0082others(112): Show | 115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.2889+124dupA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 16/17 | chr4 | 17634884 | ||||||
| chr4:17634896
|
CAATG | C | 4 | a0013c0048t0022g0048a0013c0058t0022g0174a0016c0025t0021g0224others(1): Show | 4 | HG01109.hp2 HG01884.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.2889+109_2889+112d others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 16/17 | chr4 | 17634896 | ||||||
| chr4:17634915
|
C | T | 22 | a0001c0029t0005g0115a0003c0009t0005g0009a0003c0009t0005g0133others(19): Show | 22 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.2889+94G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 16/17 | chr4 | 17634915 | ||||||
| chr4:17635215
|
C | G | 1 | a0028c0032t0062g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2785-102G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 15/17 | chr4 | 17635215 | ||||||
| chr4:17635258
|
C | T | 1 | a0028c0032t0062g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2785-145G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 15/17 | chr4 | 17635258 | ||||||
| chr4:17635354
|
A | G | 6 | a0001c0017t0010g0070a0001c0017t0010g0103a0001c0017t0010g0175others(3): Show | 6 | HG00099.hp1 HG01516.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2785-241T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 15/17 | chr4 | 17635354 | ||||||
| chr4:17635405
|
CAAAG | C | 4 | a0002c0001t0001g0131a0002c0002t0001g0051a0002c0022t0001g0085others(1): Show | 4 | HG00558.hp1 HG01071.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.2785-296_2785-293d others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 15/17 | chr4 | 17635405 | ||||||
| chr4:17635443
|
C | T | 4 | a0004c0035t0006g0139a0005c0028t0006g0191a0005c0036t0053g0233others(1): Show | 4 | HG02280.hp2 HG02897.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2785-330G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 15/17 | chr4 | 17635443 | ||||||
| chr4:17635486
|
A | G | 1 | a0002c0002t0016g0039 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2785-373T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 15/17 | chr4 | 17635486 | ||||||
| chr4:17635489
|
T | C | 1 | a0002c0002t0001g0066 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2785-376A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 15/17 | chr4 | 17635489 | ||||||
| chr4:17635557
|
TTGTG | T | 14 | a0001c0003t0007g0220a0001c0005t0007g0013a0001c0005t0007g0125others(11): Show | 14 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2785-448_2785-445d others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 15/17 | chr4 | 17635557 | ||||||
| chr4:17635587
|
C | G | 11 | a0002c0001t0001g0126a0002c0001t0001g0128a0002c0001t0033g0001others(8): Show | 11 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.2785-474G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 15/17 | chr4 | 17635587 | ||||||
| chr4:17635675
|
T | A | 1 | a0015c0062t0035g0230 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2785-562A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 15/17 | chr4 | 17635675 | ||||||
| chr4:17635675
|
T | TA | 113 | a0001c0029t0005g0115a0002c0001t0001g0002a0002c0001t0001g0082others(110): Show | 113 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.2785-563dupT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 15/17 | chr4 | 17635675 | ||||||
| chr4:17635675
|
T | TAA | 9 | a0002c0001t0001g0131a0002c0002t0001g0177a0002c0020t0001g0079others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.2785-564_2785-563d others(4): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 15/17 | chr4 | 17635675 | ||||||
| chr4:17635675
|
TA | T | 51 | a0001c0003t0007g0220a0001c0003t0018g0006a0001c0003t0019g0095others(48): Show | 51 | HG01109.hp2 HG01123.hp1 HG01192.hp2 others(48): Show |
intron_variant | MODIFIER | c.2785-563delT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 15/17 | chr4 | 17635675 | ||||||
| chr4:17635677
|
A | AAG | 5 | a0005c0030t0015g0033a0005c0031t0015g0193a0008c0034t0051g0010others(2): Show | 5 | HG01243.hp2 HG02615.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2785-565_2785-564i others(4): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 15/17 | chr4 | 17635677 | ||||||
| chr4:17635711
|
G | A | 1 | a0015c0062t0035g0230 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2785-598C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 15/17 | chr4 | 17635711 | ||||||
| chr4:17635785
|
G | A | 2 | a0002c0001t0001g0218a0002c0002t0001g0176 | 2 | HG02602.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.2785-672C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 15/17 | chr4 | 17635785 | ||||||
| chr4:17635936
|
TCTA | T | 2 | a0001c0004t0025g0023a0001c0004t0025g0024 | 2 | HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2784+589_2784+591d others(5): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 15/17 | chr4 | 17635936 | ||||||
| chr4:17636041
|
AT | A | 145 | a0001c0004t0003g0207a0001c0004t0003g0212a0001c0004t0003g0213others(142): Show | 145 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.2784+486delA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 15/17 | chr4 | 17636041 | ||||||
| chr4:17636140
|
C | T | 6 | a0001c0017t0010g0070a0001c0017t0010g0103a0001c0017t0010g0175others(3): Show | 6 | HG00099.hp1 HG01516.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2784+388G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 15/17 | chr4 | 17636140 | ||||||
| chr4:17636369
|
C | G | 7 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(4): Show | 7 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.2784+159G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 15/17 | chr4 | 17636369 | ||||||
| chr4:17636379
|
A | T | 4 | a0001c0003t0019g0095a0001c0007t0019g0143a0001c0008t0019g0102others(1): Show | 4 | HG02451.hp2 HG03225.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2784+149T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 15/17 | chr4 | 17636379 | ||||||
| chr4:17636397
|
A | C | 139 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.2784+131T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 15/17 | chr4 | 17636397 | ||||||
| chr4:17636433
|
C | T | 1 | a0001c0015t0013g0003 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2784+95G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 15/17 | chr4 | 17636433 | ||||||
| chr4:17636456
|
T | G | 4 | a0001c0003t0019g0095a0001c0007t0019g0143a0001c0008t0019g0102others(1): Show | 4 | HG02451.hp2 HG03225.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2784+72A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 15/17 | chr4 | 17636456 | ||||||
| chr4:17636519
|
C | CA | 6 | a0001c0017t0010g0070a0001c0017t0010g0103a0001c0017t0010g0175others(3): Show | 6 | HG00099.hp1 HG01516.hp2 HG02647.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.2784+8dupT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 15/17 | chr4 | 17636519 | ||||||
| chr4:17636707
|
A | AC | 14 | a0001c0004t0003g0207a0001c0004t0003g0212a0001c0004t0003g0213others(11): Show | 14 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.2667-63dupG | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17636707 | ||||||
| chr4:17636824
|
GCT | G | 2 | a0017c0026t0038g0098a0017c0026t0041g0160 | 2 | HG01081.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.2667-181_2667-180d others(4): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17636824 | ||||||
| chr4:17636867
|
C | G | 1 | a0002c0002t0001g0114 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2667-222G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17636867 | ||||||
| chr4:17636880
|
A | G | 6 | a0001c0017t0010g0070a0001c0017t0010g0103a0001c0017t0010g0175others(3): Show | 6 | HG00099.hp1 HG01516.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2667-235T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17636880 | ||||||
| chr4:17636897
|
C | T | 9 | a0004c0010t0006g0077a0004c0010t0006g0107a0004c0010t0006g0109others(6): Show | 9 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2667-252G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17636897 | ||||||
| chr4:17637078
|
G | GTGCAATG others(17): Show |
4 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(1): Show | 4 | HG02622.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2667-457_2667-434d others(26): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17637078 | ||||||
| chr4:17637098
|
C | G | 4 | a0025c0056t0061g0078a0027c0057t0030g0096a0028c0032t0062g0172others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.2667-453G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17637098 | ||||||
| chr4:17637099
|
T | G | 2 | a0001c0005t0014g0170a0008c0034t0051g0010 | 2 | HG02145.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2667-454A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17637099 | ||||||
| chr4:17637107
|
A | G | 4 | a0002c0001t0001g0147a0002c0002t0001g0171a0002c0002t0001g0203others(1): Show | 4 | HG02129.hp2 HG02257.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.2667-462T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17637107 | ||||||
| chr4:17637125
|
C | T | 8 | a0001c0004t0009g0017a0001c0004t0009g0022a0001c0004t0009g0072others(5): Show | 8 | HG02486.hp1 HG02717.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2667-480G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17637125 | ||||||
| chr4:17637226
|
A | T | 29 | a0001c0004t0003g0207a0001c0004t0003g0212a0001c0004t0003g0213others(26): Show | 29 | HG01109.hp2 HG01123.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.2667-581T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17637226 | ||||||
| chr4:17637276
|
C | G | 5 | a0001c0003t0004g0057a0001c0003t0008g0163a0001c0003t0008g0216others(2): Show | 5 | HG00140.hp1 HG01346.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.2667-631G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17637276 | ||||||
| chr4:17637277
|
T | C | 105 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2667-632A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17637277 | ||||||
| chr4:17637323
|
G | C | 1 | a0002c0002t0001g0058 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2667-678C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17637323 | ||||||
| chr4:17637605
|
G | A | 8 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(5): Show | 8 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.2667-960C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17637605 | ||||||
| chr4:17637657
|
G | C | 1 | a0001c0047t0010g0113 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2667-1012C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17637657 | ||||||
| chr4:17637672
|
C | CAG | 137 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(134): Show | 137 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.2667-1028_2667-102 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17637672 | ||||||
| chr4:17637684
|
T | C | 1 | a0002c0001t0055g0144 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2667-1039A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17637684 | ||||||
| chr4:17637993
|
C | T | 2 | a0002c0001t0031g0178a0002c0001t0031g0179 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2666+1257G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17637993 | ||||||
| chr4:17637994
|
T | A | 2 | a0001c0017t0010g0070a0001c0017t0010g0175 | 2 | HG02647.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2666+1256A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17637994 | ||||||
| chr4:17637996
|
TCA | T | 2 | a0001c0017t0010g0070a0001c0017t0010g0175 | 2 | HG02647.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2666+1252_2666+125 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17637996 | ||||||
| chr4:17637998
|
A | ACT | 225 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.2666+1250_2666+125 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17637998 | ||||||
| chr4:17638110
|
G | A | 6 | a0001c0006t0003g0182a0001c0033t0003g0200a0007c0043t0012g0105others(3): Show | 6 | HG01243.hp1 HG01891.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2666+1140C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638110 | ||||||
| chr4:17638134
|
C | CT | 29 | a0001c0003t0002g0149a0001c0003t0002g0158a0001c0003t0004g0018others(26): Show | 29 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.2666+1115dupA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638134 | ||||||
| chr4:17638134
|
C | CTT | 11 | a0001c0003t0002g0019a0001c0003t0002g0227a0001c0003t0004g0067others(8): Show | 11 | HG00423.hp1 HG00609.hp1 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.2666+1114_2666+111 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638134 | ||||||
| chr4:17638134
|
C | CTTTTTTT others(1): Show |
7 | a0001c0006t0003g0026a0001c0006t0003g0028a0001c0006t0003g0029others(4): Show | 7 | NA18955.hp1 NA18956.hp2 NA18995.hp2 others(4): Show |
intron_variant | MODIFIER | c.2666+1108_2666+111 others(12): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638134 | ||||||
| chr4:17638134
|
C | CTTTTTTT others(3): Show |
4 | a0001c0004t0003g0207a0001c0004t0003g0212a0001c0004t0003g0213others(1): Show | 4 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.2666+1106_2666+111 others(14): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638134 | ||||||
| chr4:17638134
|
CTTTTTTT others(1): Show |
C | 8 | a0001c0029t0005g0115a0003c0009t0005g0009a0003c0009t0005g0162others(5): Show | 8 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.2666+1108_2666+111 others(12): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638134 | ||||||
| chr4:17638134
|
CTTTTTTT others(2): Show |
C | 19 | a0001c0003t0004g0169a0001c0017t0010g0070a0001c0017t0010g0103others(16): Show | 19 | HG00099.hp1 HG00323.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.2666+1107_2666+111 others(13): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638134 | ||||||
| chr4:17638134
|
CTTTTTTT others(3): Show |
C | 105 | a0001c0003t0007g0220a0001c0005t0007g0013a0001c0005t0007g0125others(102): Show | 105 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.2666+1106_2666+111 others(14): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638134 | ||||||
| chr4:17638134
|
CTTTTTTT others(4): Show |
C | 11 | a0002c0001t0001g0002a0002c0001t0016g0130a0002c0002t0001g0047others(8): Show | 11 | HG00140.hp2 HG01243.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.2666+1105_2666+111 others(15): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638134 | ||||||
| chr4:17638134
|
CTTTTTTT others(5): Show |
C | 6 | a0004c0010t0006g0077a0004c0010t0006g0165a0013c0048t0022g0048others(3): Show | 6 | HG01109.hp2 HG01884.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2666+1104_2666+111 others(16): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638134 | ||||||
| chr4:17638134
|
CTTTTTTT others(6): Show |
C | 12 | a0001c0004t0009g0017a0001c0004t0009g0022a0001c0004t0009g0072others(9): Show | 12 | HG02258.hp1 HG02486.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.2666+1103_2666+111 others(17): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638134 | ||||||
| chr4:17638135
|
T | C | 5 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0008t0018g0020others(2): Show | 5 | HG02451.hp2 HG03471.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2666+1115A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638135 | ||||||
| chr4:17638136
|
T | C | 1 | a0001c0007t0019g0143 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2666+1114A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638136 | ||||||
| chr4:17638176
|
AT | A | 7 | a0001c0003t0004g0169a0001c0017t0010g0070a0001c0017t0010g0103others(4): Show | 7 | HG00099.hp1 HG01099.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.2666+1073delA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638176 | ||||||
| chr4:17638180
|
TTTTTG | T | 5 | a0001c0003t0019g0095a0001c0003t0023g0122a0001c0007t0019g0143others(2): Show | 5 | HG02451.hp2 HG02723.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2666+1065_2666+106 others(9): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638180 | ||||||
| chr4:17638192
|
T | C | 146 | a0001c0003t0007g0220a0001c0005t0007g0013a0001c0005t0007g0125others(143): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.2666+1058A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638192 | ||||||
| chr4:17638196
|
T | C | 4 | a0004c0010t0006g0077a0004c0010t0006g0107a0004c0010t0006g0109others(1): Show | 4 | HG02451.hp1 HG03098.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2666+1054A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638196 | ||||||
| chr4:17638301
|
G | A | 9 | a0001c0029t0005g0115a0003c0009t0005g0009a0003c0009t0005g0133others(6): Show | 9 | HG01243.hp2 HG02109.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.2666+949C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638301 | ||||||
| chr4:17638354
|
A | AT | 21 | a0001c0006t0003g0182a0001c0017t0010g0070a0001c0017t0010g0103others(18): Show | 21 | HG00099.hp1 HG01243.hp2 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.2666+895dupA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638354 | ||||||
| chr4:17638354
|
A | ATT | 42 | a0001c0003t0007g0220a0001c0004t0003g0207a0001c0004t0003g0212others(39): Show | 42 | HG01123.hp1 HG01192.hp2 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.2666+894_2666+895d others(4): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638354 | ||||||
| chr4:17638522
|
G | A | 8 | a0004c0010t0006g0077a0004c0010t0006g0107a0004c0010t0006g0109others(5): Show | 8 | HG02280.hp2 HG02451.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.2666+728C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638522 | ||||||
| chr4:17638608
|
G | A | 1 | a0002c0002t0001g0114 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2666+642C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638608 | ||||||
| chr4:17638660
|
T | A | 139 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.2666+590A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638660 | ||||||
| chr4:17638696
|
G | A | 6 | a0001c0017t0010g0070a0001c0017t0010g0103a0001c0017t0010g0175others(3): Show | 6 | HG00099.hp1 HG01516.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2666+554C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638696 | ||||||
| chr4:17638758
|
A | G | 1 | a0028c0032t0062g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2666+492T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638758 | ||||||
| chr4:17638784
|
G | GGAACATA | 22 | a0001c0029t0005g0115a0003c0009t0005g0009a0003c0009t0005g0133others(19): Show | 22 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.2666+459_2666+465d others(9): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638784 | ||||||
| chr4:17638798
|
T | G | 5 | a0005c0030t0015g0033a0005c0031t0015g0193a0008c0034t0051g0010others(2): Show | 5 | HG01243.hp2 HG02615.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2666+452A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638798 | ||||||
| chr4:17638814
|
T | G | 1 | a0008c0034t0051g0010 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2666+436A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638814 | ||||||
| chr4:17638840
|
A | G | 109 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(106): Show | 109 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.2666+410T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638840 | ||||||
| chr4:17638903
|
C | T | 105 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2666+347G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638903 | ||||||
| chr4:17638906
|
C | T | 22 | a0001c0029t0005g0115a0003c0009t0005g0009a0003c0009t0005g0133others(19): Show | 22 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.2666+344G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638906 | ||||||
| chr4:17638981
|
C | T | 2 | a0001c0029t0005g0115a0003c0009t0005g0009 | 2 | HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2666+269G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17638981 | ||||||
| chr4:17639031
|
G | A | 100 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.2666+219C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17639031 | ||||||
| chr4:17639049
|
G | A | 1 | a0008c0049t0034g0112 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2666+201C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17639049 | ||||||
| chr4:17639081
|
G | A | 2 | a0010c0013t0024g0211a0026c0055t0002g0117 | 2 | HG00280.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2666+169C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17639081 | ||||||
| chr4:17639122
|
C | T | 29 | a0001c0004t0003g0207a0001c0004t0003g0212a0001c0004t0003g0213others(26): Show | 29 | HG01109.hp2 HG01123.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.2666+128G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17639122 | ||||||
| chr4:17639150
|
A | G | 8 | a0002c0001t0001g0082a0002c0001t0001g0101a0002c0001t0001g0152others(5): Show | 8 | HG00597.hp2 HG02129.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.2666+100T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17639150 | ||||||
| chr4:17639235
|
C | T | 109 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(106): Show | 109 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.2666+15G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 14/17 | chr4 | 17639235 | ||||||
| chr4:17639565
|
A | G | 188 | a0001c0003t0007g0220a0001c0003t0018g0006a0001c0003t0019g0095others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.2520-169T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17639565 | ||||||
| chr4:17639831
|
C | CT | 24 | a0001c0003t0007g0220a0001c0003t0018g0006a0001c0005t0007g0013others(21): Show | 24 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.2520-436dupA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17639831 | ||||||
| chr4:17639831
|
C | CTT | 8 | a0004c0010t0006g0077a0004c0010t0006g0107a0004c0010t0006g0109others(5): Show | 8 | HG02280.hp2 HG02451.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.2520-437_2520-436d others(4): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17639831 | ||||||
| chr4:17639871
|
C | G | 22 | a0001c0029t0005g0115a0003c0009t0005g0009a0003c0009t0005g0133others(19): Show | 22 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.2520-475G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17639871 | ||||||
| chr4:17639897
|
C | T | 22 | a0001c0029t0005g0115a0003c0009t0005g0009a0003c0009t0005g0133others(19): Show | 22 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.2520-501G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17639897 | ||||||
| chr4:17639973
|
C | T | 1 | a0019c0040t0065g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2520-577G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17639973 | ||||||
| chr4:17640009
|
T | C | 13 | a0001c0029t0005g0115a0003c0009t0005g0009a0003c0009t0005g0133others(10): Show | 13 | HG01243.hp2 HG02109.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.2520-613A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17640009 | ||||||
| chr4:17640060
|
G | C | 7 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(4): Show | 7 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.2520-664C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17640060 | ||||||
| chr4:17640111
|
CG | C | 109 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(106): Show | 109 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.2520-716delC | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17640111 | ||||||
| chr4:17640112
|
G | A | 3 | a0005c0030t0015g0033a0005c0031t0015g0193a0008c0039t0015g0016 | 3 | HG02615.hp2 HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2520-716C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17640112 | ||||||
| chr4:17640211
|
A | G | 139 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.2520-815T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17640211 | ||||||
| chr4:17640232
|
G | A | 105 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2520-836C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17640232 | ||||||
| chr4:17640298
|
T | C | 139 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.2520-902A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17640298 | ||||||
| chr4:17640302
|
C | T | 29 | a0001c0004t0003g0207a0001c0004t0003g0212a0001c0004t0003g0213others(26): Show | 29 | HG01109.hp2 HG01123.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.2520-906G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17640302 | ||||||
| chr4:17640307
|
C | G | 105 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2520-911G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17640307 | ||||||
| chr4:17640316
|
C | CA | 16 | a0001c0003t0002g0019a0001c0003t0002g0158a0001c0003t0004g0057others(13): Show | 16 | HG01123.hp1 HG01175.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.2520-921dupT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17640316 | ||||||
| chr4:17640316
|
CA | C | 15 | a0001c0004t0009g0017a0001c0004t0009g0022a0001c0004t0009g0072others(12): Show | 15 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.2520-921delT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17640316 | ||||||
| chr4:17640316
|
CAAA | C | 11 | a0001c0008t0019g0102a0001c0021t0018g0068a0001c0029t0005g0115others(8): Show | 11 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2520-923_2520-921d others(5): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17640316 | ||||||
| chr4:17640316
|
CAAAA | C | 133 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.2520-924_2520-921d others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17640316 | ||||||
| chr4:17640343
|
G | A | 131 | a0001c0029t0005g0115a0002c0001t0001g0002a0002c0001t0001g0082others(128): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.2520-947C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17640343 | ||||||
| chr4:17640421
|
T | C | 1 | a0027c0057t0030g0096 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2520-1025A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17640421 | ||||||
| chr4:17640424
|
C | G | 5 | a0005c0030t0015g0033a0005c0031t0015g0193a0008c0034t0051g0010others(2): Show | 5 | HG01243.hp2 HG02615.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2520-1028G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17640424 | ||||||
| chr4:17640433
|
G | A | 1 | a0005c0031t0015g0193 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2520-1037C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17640433 | ||||||
| chr4:17640481
|
C | CA | 35 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0004t0003g0207others(32): Show | 35 | HG01123.hp1 HG01192.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.2520-1086dupT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17640481 | ||||||
| chr4:17640481
|
C | CAA | 104 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(101): Show | 104 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.2520-1087_2520-108 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17640481 | ||||||
| chr4:17640501
|
T | G | 1 | a0027c0057t0030g0096 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2520-1105A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17640501 | ||||||
| chr4:17640507
|
A | G | 1 | a0010c0013t0004g0232 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2520-1111T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17640507 | ||||||
| chr4:17640532
|
A | C | 1 | a0032c0061t0030g0007 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2520-1136T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17640532 | ||||||
| chr4:17640553
|
G | A | 4 | a0013c0048t0022g0048a0013c0058t0022g0174a0016c0025t0021g0224others(1): Show | 4 | HG01109.hp2 HG01884.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.2520-1157C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17640553 | ||||||
| chr4:17640582
|
A | AG | 145 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.2520-1187_2520-118 others(5): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17640582 | ||||||
| chr4:17640638
|
G | C | 8 | a0001c0029t0005g0115a0003c0009t0005g0009a0003c0009t0005g0133others(5): Show | 8 | HG02109.hp1 HG02559.hp1 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.2520-1242C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17640638 | ||||||
| chr4:17640675
|
G | C | 9 | a0004c0010t0006g0077a0004c0010t0006g0107a0004c0010t0006g0109others(6): Show | 9 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2520-1279C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17640675 | ||||||
| chr4:17640701
|
G | T | 4 | a0025c0056t0061g0078a0027c0057t0030g0096a0028c0032t0062g0172others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.2520-1305C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17640701 | ||||||
| chr4:17640980
|
C | CTGAA | 8 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(5): Show | 8 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.2519+1072_2519+107 others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17640980 | ||||||
| chr4:17641007
|
C | T | 131 | a0001c0029t0005g0115a0002c0001t0001g0002a0002c0001t0001g0082others(128): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.2519+1049G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641007 | ||||||
| chr4:17641040
|
C | A | 6 | a0001c0017t0010g0070a0001c0017t0010g0103a0001c0017t0010g0175others(3): Show | 6 | HG00099.hp1 HG01516.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2519+1016G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641040 | ||||||
| chr4:17641058
|
C | A | 6 | a0001c0017t0010g0070a0001c0017t0010g0103a0001c0017t0010g0175others(3): Show | 6 | HG00099.hp1 HG01516.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2519+998G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641058 | ||||||
| chr4:17641095
|
G | C | 1 | a0003c0009t0005g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2519+961C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641095 | ||||||
| chr4:17641170
|
G | C | 1 | a0028c0032t0062g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2519+886C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641170 | ||||||
| chr4:17641186
|
A | G | 1 | a0032c0061t0030g0007 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2519+870T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641186 | ||||||
| chr4:17641305
|
A | G | 6 | a0001c0017t0010g0070a0001c0017t0010g0103a0001c0017t0010g0175others(3): Show | 6 | HG00099.hp1 HG01516.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2519+751T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641305 | ||||||
| chr4:17641314
|
T | A | 105 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2519+742A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641314 | ||||||
| chr4:17641427
|
G | A | 100 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.2519+629C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641427 | ||||||
| chr4:17641429
|
C | A | 13 | a0001c0029t0005g0115a0003c0009t0005g0009a0003c0009t0005g0133others(10): Show | 13 | HG01243.hp2 HG02109.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.2519+627G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641429 | ||||||
| chr4:17641461
|
C | CT | 14 | a0001c0003t0002g0149a0001c0003t0002g0206a0001c0003t0008g0163others(11): Show | 14 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.2519+594dupA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641461 | ||||||
| chr4:17641461
|
C | CTT | 15 | a0001c0003t0002g0158a0001c0003t0002g0227a0001c0003t0004g0018others(12): Show | 15 | HG00423.hp1 HG01099.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.2519+593_2519+594d others(4): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641461 | ||||||
| chr4:17641461
|
C | CTTT | 9 | a0001c0003t0002g0019a0001c0003t0011g0167a0001c0003t0023g0122others(6): Show | 9 | HG00597.hp1 HG01175.hp2 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.2519+592_2519+594d others(5): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641461 | ||||||
| chr4:17641461
|
C | CTTTTTTT others(3): Show |
2 | a0001c0005t0007g0125a0001c0015t0013g0106 | 2 | HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2519+585_2519+594d others(12): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641461 | ||||||
| chr4:17641461
|
C | CTTTTTTT others(7): Show |
1 | a0001c0015t0013g0003 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2519+581_2519+594d others(16): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641461 | ||||||
| chr4:17641461
|
C | CTTTTTTT others(8): Show |
1 | a0001c0015t0029g0164 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2519+580_2519+594d others(17): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641461 | ||||||
| chr4:17641461
|
C | CTTTTTTT others(10): Show |
1 | a0001c0003t0007g0220 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2519+578_2519+594d others(19): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641461 | ||||||
| chr4:17641461
|
C | CTTTTTTT others(12): Show |
1 | a0001c0005t0014g0170 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2519+576_2519+594d others(21): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641461 | ||||||
| chr4:17641461
|
C | CTTTTTTT others(14): Show |
1 | a0001c0005t0027g0111 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2519+574_2519+594d others(23): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641461 | ||||||
| chr4:17641461
|
C | CTTTTTTT others(16): Show |
1 | a0001c0005t0014g0118 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2519+572_2519+594d others(25): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641461 | ||||||
| chr4:17641461
|
C | CTTTTTTT others(20): Show |
1 | a0001c0005t0014g0110 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2519+568_2519+594d others(29): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641461 | ||||||
| chr4:17641461
|
CTTTTT | C | 5 | a0001c0004t0003g0207a0001c0004t0003g0212a0001c0004t0003g0213others(2): Show | 5 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.2519+590_2519+594d others(7): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641461 | ||||||
| chr4:17641461
|
CTTTTTT | C | 15 | a0001c0004t0009g0022a0001c0004t0025g0023a0001c0004t0025g0024others(12): Show | 15 | HG02258.hp1 HG02559.hp2 HG03098.hp2 others(12): Show |
intron_variant | MODIFIER | c.2519+589_2519+594d others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641461 | ||||||
| chr4:17641461
|
CTTTTTTT | C | 13 | a0001c0003t0019g0095a0001c0004t0009g0017a0001c0004t0009g0072others(10): Show | 13 | HG01109.hp2 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.2519+588_2519+594d others(9): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641461 | ||||||
| chr4:17641461
|
CTTTTTTT others(1): Show |
C | 8 | a0001c0003t0018g0006a0001c0007t0020g0060a0001c0008t0018g0020others(5): Show | 8 | HG00597.hp2 HG00609.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.2519+587_2519+594d others(10): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641461 | ||||||
| chr4:17641461
|
CTTTTTTT others(3): Show |
C | 6 | a0001c0017t0010g0175a0002c0001t0001g0154a0002c0001t0059g0127others(3): Show | 6 | HG00642.hp1 HG01071.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.2519+585_2519+594d others(12): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641461 | ||||||
| chr4:17641461
|
CTTTTTTT others(4): Show |
C | 96 | a0001c0017t0010g0070a0001c0060t0027g0075a0002c0001t0001g0002others(93): Show | 96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.2519+584_2519+594d others(13): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641461 | ||||||
| chr4:17641461
|
CTTTTTTT others(5): Show |
C | 9 | a0001c0017t0010g0103a0001c0047t0010g0113a0002c0001t0001g0181others(6): Show | 9 | HG00099.hp1 HG01516.hp1 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.2519+583_2519+594d others(14): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641461 | ||||||
| chr4:17641461
|
CTTTTTTT others(7): Show |
C | 3 | a0003c0009t0005g0133a0005c0030t0015g0033a0024c0037t0052g0094 | 3 | HG03579.hp2 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2519+581_2519+594d others(16): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641461 | ||||||
| chr4:17641461
|
CTTTTTTT others(8): Show |
C | 12 | a0001c0007t0008g0157a0001c0029t0005g0115a0003c0009t0005g0009others(9): Show | 12 | HG01081.hp1 HG01081.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.2519+580_2519+594d others(17): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641461 | ||||||
| chr4:17641461
|
CTTTTTTT others(9): Show |
C | 1 | a0028c0032t0062g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2519+579_2519+594d others(18): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641461 | ||||||
| chr4:17641461
|
CTTTTTTT others(10): Show |
C | 1 | a0032c0061t0030g0007 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2519+578_2519+594d others(19): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641461 | ||||||
| chr4:17641547
|
T | C | 131 | a0001c0029t0005g0115a0002c0001t0001g0002a0002c0001t0001g0082others(128): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.2519+509A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641547 | ||||||
| chr4:17641643
|
C | CT | 38 | a0001c0003t0002g0019a0001c0003t0007g0220a0001c0003t0008g0163others(35): Show | 38 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.2519+412dupA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641643 | ||||||
| chr4:17641643
|
C | CTT | 22 | a0001c0003t0023g0122a0001c0004t0003g0207a0001c0004t0003g0212others(19): Show | 22 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(19): Show |
intron_variant | MODIFIER | c.2519+411_2519+412d others(4): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641643 | ||||||
| chr4:17641643
|
C | CTTT | 5 | a0001c0006t0003g0026a0001c0006t0003g0030a0001c0006t0048g0027others(2): Show | 5 | HG03225.hp1 HG03579.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.2519+410_2519+412d others(5): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641643 | ||||||
| chr4:17641643
|
C | CTTTTT | 7 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0008t0018g0020others(4): Show | 7 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2519+408_2519+412d others(7): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641643 | ||||||
| chr4:17641643
|
C | CTTTTTTT others(2): Show |
9 | a0002c0001t0001g0116a0002c0001t0031g0178a0002c0001t0031g0179others(6): Show | 9 | HG01169.hp2 HG02615.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.2519+404_2519+412d others(11): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641643 | ||||||
| chr4:17641643
|
C | CTTTTTTT others(3): Show |
38 | a0002c0001t0001g0086a0002c0001t0001g0087a0002c0001t0001g0121others(35): Show | 38 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.2519+403_2519+412d others(12): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641643 | ||||||
| chr4:17641643
|
C | CTTTTTTT others(4): Show |
32 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(29): Show | 32 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.2519+402_2519+412d others(13): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641643 | ||||||
| chr4:17641643
|
C | CTTTTTTT others(5): Show |
8 | a0002c0001t0001g0090a0002c0001t0001g0101a0002c0001t0001g0152others(5): Show | 8 | HG00423.hp2 HG02523.hp1 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.2519+401_2519+412d others(14): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641643 | ||||||
| chr4:17641643
|
C | CTTTTTTT others(6): Show |
2 | a0002c0001t0001g0147a0002c0022t0001g0085 | 2 | HG00558.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.2519+400_2519+412d others(15): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641643 | ||||||
| chr4:17641643
|
C | CTTTTTTT others(7): Show |
3 | a0002c0001t0001g0214a0002c0022t0001g0151a0014c0024t0001g0183 | 3 | NA18972.hp2 NA18998.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.2519+399_2519+412d others(16): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641643 | ||||||
| chr4:17641643
|
C | CTTTTTTT others(9): Show |
1 | a0002c0001t0001g0136 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2519+397_2519+412d others(18): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641643 | ||||||
| chr4:17641643
|
C | CTTTTTTT others(10): Show |
3 | a0002c0001t0001g0142a0002c0001t0001g0146a0002c0001t0001g0222 | 3 | HG00639.hp2 HG03130.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.2519+396_2519+412d others(19): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641643 | ||||||
| chr4:17641643
|
C | CTTTTTTT others(12): Show |
1 | a0002c0002t0001g0051 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2519+394_2519+412d others(21): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641643 | ||||||
| chr4:17641643
|
C | CTTTTTTT others(13): Show |
1 | a0002c0001t0001g0148 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2519+393_2519+412d others(22): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641643 | ||||||
| chr4:17641643
|
C | CTTTTTTT others(16): Show |
1 | a0002c0001t0001g0154 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2519+390_2519+412d others(25): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641643 | ||||||
| chr4:17641643
|
C | T | 1 | a0001c0006t0003g0182 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2519+413G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641643 | ||||||
| chr4:17641643
|
CT | C | 13 | a0001c0003t0002g0206a0001c0003t0060g0215a0001c0004t0009g0022others(10): Show | 13 | HG01123.hp2 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.2519+412delA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641643 | ||||||
| chr4:17641643
|
CTT | C | 5 | a0002c0001t0017g0091a0002c0001t0017g0137a0005c0030t0015g0033others(2): Show | 5 | HG02615.hp2 HG02698.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.2519+411_2519+412d others(4): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641643 | ||||||
| chr4:17641643
|
CTTTTTTT others(7): Show |
C | 4 | a0004c0010t0006g0077a0004c0010t0006g0107a0004c0010t0006g0109others(1): Show | 4 | HG02451.hp1 HG03098.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2519+399_2519+412d others(16): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641643 | ||||||
| chr4:17641714
|
G | A | 5 | a0005c0030t0015g0033a0005c0031t0015g0193a0008c0034t0051g0010others(2): Show | 5 | HG01243.hp2 HG02615.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2519+342C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641714 | ||||||
| chr4:17641832
|
C | T | 1 | a0021c0052t0050g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2519+224G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641832 | ||||||
| chr4:17641845
|
C | T | 234 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.2519+211G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641845 | ||||||
| chr4:17641988
|
A | AG | 6 | a0001c0003t0007g0220a0001c0005t0007g0013a0001c0005t0007g0125others(3): Show | 6 | HG02622.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2519+67dupC | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641988 | ||||||
| chr4:17641994
|
A | AG | 23 | a0001c0003t0008g0208a0001c0003t0011g0167a0001c0003t0037g0219others(20): Show | 23 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.2519+61dupC | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641994 | ||||||
| chr4:17641994
|
A | G | 7 | a0001c0003t0007g0220a0001c0005t0007g0013a0001c0005t0007g0125others(4): Show | 7 | HG02622.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2519+62T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641994 | ||||||
| chr4:17641997
|
G | A | 109 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(106): Show | 109 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.2519+59C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641997 | ||||||
| chr4:17641999
|
G | A | 1 | a0001c0017t0010g0103 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2519+57C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17641999 | ||||||
| chr4:17642041
|
C | T | 1 | a0027c0057t0030g0096 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2519+15G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 13/17 | chr4 | 17642041 | ||||||
| chr4:17642248
|
G | A | 8 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(5): Show | 8 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.2347-20C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17642248 | ||||||
| chr4:17642477
|
C | G | 9 | a0004c0010t0006g0077a0004c0010t0006g0107a0004c0010t0006g0109others(6): Show | 9 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2347-249G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17642477 | ||||||
| chr4:17642525
|
C | T | 6 | a0001c0017t0010g0070a0001c0017t0010g0103a0001c0017t0010g0175others(3): Show | 6 | HG00099.hp1 HG01516.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2347-297G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17642525 | ||||||
| chr4:17642735
|
CTCTTCA | C | 10 | a0001c0004t0009g0017a0001c0004t0009g0022a0001c0004t0009g0072others(7): Show | 10 | HG02258.hp1 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.2347-513_2347-508d others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17642735 | ||||||
| chr4:17642790
|
G | A | 2 | a0002c0022t0001g0085a0002c0022t0001g0151 | 2 | HG00558.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.2347-562C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17642790 | ||||||
| chr4:17642849
|
A | G | 145 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.2347-621T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17642849 | ||||||
| chr4:17642929
|
CCCGA | C | 5 | a0007c0041t0012g0011a0007c0043t0012g0105a0007c0050t0012g0004others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.2347-705_2347-702d others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17642929 | ||||||
| chr4:17642985
|
C | T | 15 | a0001c0004t0009g0017a0001c0004t0009g0022a0001c0004t0009g0072others(12): Show | 15 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.2347-757G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17642985 | ||||||
| chr4:17643105
|
G | T | 2 | a0028c0032t0062g0172a0032c0061t0030g0007 | 2 | HG03017.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.2347-877C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17643105 | ||||||
| chr4:17643204
|
T | G | 8 | a0001c0004t0009g0017a0001c0004t0009g0022a0001c0004t0009g0072others(5): Show | 8 | HG02486.hp1 HG02717.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2347-976A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17643204 | ||||||
| chr4:17643214
|
A | G | 3 | a0005c0030t0015g0033a0005c0031t0015g0193a0008c0039t0015g0016 | 3 | HG02615.hp2 HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2347-986T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17643214 | ||||||
| chr4:17643277
|
T | C | 9 | a0004c0010t0006g0077a0004c0010t0006g0107a0004c0010t0006g0109others(6): Show | 9 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2347-1049A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17643277 | ||||||
| chr4:17643406
|
T | TA | 2 | a0001c0003t0002g0069a0001c0008t0002g0045 | 2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2347-1179_2347-117 others(5): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17643406 | ||||||
| chr4:17643435
|
G | C | 8 | a0001c0029t0005g0115a0003c0009t0005g0009a0003c0009t0005g0133others(5): Show | 8 | HG02109.hp1 HG02559.hp1 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.2347-1207C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17643435 | ||||||
| chr4:17643508
|
C | G | 1 | a0001c0006t0003g0132 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2347-1280G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17643508 | ||||||
| chr4:17643539
|
T | C | 1 | a0032c0061t0030g0007 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2347-1311A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17643539 | ||||||
| chr4:17643610
|
C | T | 100 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.2347-1382G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17643610 | ||||||
| chr4:17643613
|
G | A | 9 | a0002c0001t0001g0126a0002c0001t0001g0128a0002c0002t0001g0025others(6): Show | 9 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.2347-1385C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17643613 | ||||||
| chr4:17643642
|
A | G | 7 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(4): Show | 7 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.2347-1414T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17643642 | ||||||
| chr4:17643646
|
G | A | 8 | a0001c0029t0005g0115a0003c0009t0005g0009a0003c0009t0005g0133others(5): Show | 8 | HG02109.hp1 HG02559.hp1 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.2347-1418C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17643646 | ||||||
| chr4:17643727
|
C | T | 15 | a0001c0004t0009g0017a0001c0004t0009g0022a0001c0004t0009g0072others(12): Show | 15 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.2347-1499G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17643727 | ||||||
| chr4:17643753
|
C | T | 105 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2347-1525G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17643753 | ||||||
| chr4:17643846
|
C | T | 29 | a0001c0004t0003g0207a0001c0004t0003g0212a0001c0004t0003g0213others(26): Show | 29 | HG01109.hp2 HG01123.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.2347-1618G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17643846 | ||||||
| chr4:17643931
|
A | C | 1 | a0021c0052t0050g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2347-1703T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17643931 | ||||||
| chr4:17643944
|
G | T | 1 | a0001c0003t0040g0201 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2347-1716C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17643944 | ||||||
| chr4:17644087
|
G | A | 105 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2347-1859C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17644087 | ||||||
| chr4:17644110
|
C | T | 8 | a0001c0029t0005g0115a0003c0009t0005g0009a0003c0009t0005g0133others(5): Show | 8 | HG02109.hp1 HG02559.hp1 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.2347-1882G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17644110 | ||||||
| chr4:17644245
|
G | A | 6 | a0001c0017t0010g0070a0001c0017t0010g0103a0001c0017t0010g0175others(3): Show | 6 | HG00099.hp1 HG01516.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2347-2017C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17644245 | ||||||
| chr4:17644292
|
C | T | 145 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.2347-2064G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17644292 | ||||||
| chr4:17644319
|
T | C | 175 | a0001c0003t0002g0069a0001c0003t0018g0006a0001c0003t0019g0095others(172): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.2347-2091A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17644319 | ||||||
| chr4:17644393
|
A | T | 2 | a0001c0004t0025g0023a0001c0004t0025g0024 | 2 | HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2347-2165T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17644393 | ||||||
| chr4:17644475
|
C | T | 24 | a0001c0003t0004g0067a0001c0003t0004g0169a0001c0029t0005g0115others(21): Show | 24 | HG01074.hp1 HG01099.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.2347-2247G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17644475 | ||||||
| chr4:17644501
|
T | C | 5 | a0005c0030t0015g0033a0005c0031t0015g0193a0008c0034t0051g0010others(2): Show | 5 | HG01243.hp2 HG02615.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2347-2273A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17644501 | ||||||
| chr4:17644510
|
A | G | 1 | a0024c0037t0052g0094 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2347-2282T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17644510 | ||||||
| chr4:17644537
|
C | G | 1 | a0001c0006t0028g0014 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2347-2309G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17644537 | ||||||
| chr4:17644564
|
T | C | 4 | a0025c0056t0061g0078a0027c0057t0030g0096a0028c0032t0062g0172others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.2347-2336A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17644564 | ||||||
| chr4:17644673
|
G | A | 1 | a0027c0057t0030g0096 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2347-2445C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17644673 | ||||||
| chr4:17644779
|
A | T | 1 | a0021c0052t0050g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2347-2551T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17644779 | ||||||
| chr4:17644810
|
G | A | 8 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(5): Show | 8 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.2347-2582C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17644810 | ||||||
| chr4:17645058
|
A | G | 6 | a0001c0017t0010g0070a0001c0017t0010g0103a0001c0017t0010g0175others(3): Show | 6 | HG00099.hp1 HG01516.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2346+2579T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17645058 | ||||||
| chr4:17645144
|
T | C | 1 | a0032c0061t0030g0007 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2346+2493A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17645144 | ||||||
| chr4:17645258
|
T | C | 140 | a0001c0003t0002g0069a0001c0003t0018g0006a0001c0003t0019g0095others(137): Show | 140 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.2346+2379A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17645258 | ||||||
| chr4:17645260
|
C | T | 1 | a0015c0062t0035g0230 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2346+2377G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17645260 | ||||||
| chr4:17645261
|
G | A | 15 | a0001c0004t0009g0017a0001c0004t0009g0022a0001c0004t0009g0072others(12): Show | 15 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.2346+2376C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17645261 | ||||||
| chr4:17645264
|
G | A | 1 | a0002c0001t0001g0145 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2346+2373C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17645264 | ||||||
| chr4:17645382
|
T | C | 1 | a0007c0041t0012g0011 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2346+2255A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17645382 | ||||||
| chr4:17645430
|
G | A | 34 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(31): Show | 34 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(31): Show |
intron_variant | MODIFIER | c.2346+2207C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17645430 | ||||||
| chr4:17645441
|
A | G | 105 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2346+2196T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17645441 | ||||||
| chr4:17645447
|
G | A | 6 | a0002c0001t0001g0083a0002c0001t0001g0087a0002c0001t0001g0226others(3): Show | 6 | HG00323.hp1 HG02004.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.2346+2190C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17645447 | ||||||
| chr4:17645502
|
G | A | 2 | a0028c0032t0062g0172a0032c0061t0030g0007 | 2 | HG03017.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.2346+2135C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17645502 | ||||||
| chr4:17645527
|
T | G | 2 | a0025c0056t0061g0078a0027c0057t0030g0096 | 2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2346+2110A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17645527 | ||||||
| chr4:17645597
|
A | C | 3 | a0002c0001t0001g0218a0002c0002t0001g0047a0002c0002t0001g0176 | 3 | HG02486.hp2 HG02602.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.2346+2040T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17645597 | ||||||
| chr4:17645625
|
T | C | 12 | a0001c0029t0005g0115a0003c0009t0005g0009a0003c0009t0005g0162others(9): Show | 12 | HG01243.hp2 HG02109.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.2346+2012A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17645625 | ||||||
| chr4:17645653
|
G | T | 4 | a0002c0002t0001g0228a0002c0016t0001g0071a0002c0016t0001g0074others(1): Show | 4 | HG02818.hp2 HG03453.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.2346+1984C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17645653 | ||||||
| chr4:17645660
|
G | A | 1 | a0001c0003t0049g0099 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2346+1977C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17645660 | ||||||
| chr4:17645708
|
A | G | 1 | a0015c0063t0054g0229 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2346+1929T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17645708 | ||||||
| chr4:17645736
|
TTAAAC | T | 9 | a0004c0010t0006g0077a0004c0010t0006g0107a0004c0010t0006g0109others(6): Show | 9 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2346+1896_2346+190 others(9): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17645736 | ||||||
| chr4:17645777
|
A | G | 39 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(36): Show | 39 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.2346+1860T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17645777 | ||||||
| chr4:17645817
|
C | T | 1 | a0001c0006t0003g0026 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2346+1820G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17645817 | ||||||
| chr4:17645885
|
AAAAC | A | 8 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(5): Show | 8 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.2346+1748_2346+175 others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17645885 | ||||||
| chr4:17646049
|
G | C | 6 | a0001c0017t0010g0070a0001c0017t0010g0103a0001c0017t0010g0175others(3): Show | 6 | HG00099.hp1 HG01516.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2346+1588C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17646049 | ||||||
| chr4:17646055
|
T | C | 4 | a0004c0035t0006g0139a0005c0028t0006g0191a0005c0036t0053g0233others(1): Show | 4 | HG02280.hp2 HG02897.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2346+1582A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17646055 | ||||||
| chr4:17646113
|
A | G | 5 | a0005c0030t0015g0033a0005c0031t0015g0193a0008c0034t0051g0010others(2): Show | 5 | HG01243.hp2 HG02615.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2346+1524T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17646113 | ||||||
| chr4:17646118
|
G | T | 6 | a0001c0017t0010g0070a0001c0017t0010g0103a0001c0017t0010g0175others(3): Show | 6 | HG00099.hp1 HG01516.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2346+1519C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17646118 | ||||||
| chr4:17646181
|
A | G | 1 | a0032c0061t0030g0007 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2346+1456T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17646181 | ||||||
| chr4:17646202
|
C | T | 8 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(5): Show | 8 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.2346+1435G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17646202 | ||||||
| chr4:17646280
|
G | A | 8 | a0004c0010t0006g0077a0004c0010t0006g0107a0004c0010t0006g0109others(5): Show | 8 | HG02280.hp2 HG02451.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.2346+1357C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17646280 | ||||||
| chr4:17646283
|
T | A | 1 | a0002c0002t0001g0180 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2346+1354A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17646283 | ||||||
| chr4:17646289
|
C | T | 100 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.2346+1348G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17646289 | ||||||
| chr4:17646293
|
A | G | 100 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.2346+1344T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17646293 | ||||||
| chr4:17646294
|
A | G | 100 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.2346+1343T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17646294 | ||||||
| chr4:17646430
|
G | T | 14 | a0001c0003t0007g0220a0001c0005t0007g0013a0001c0005t0007g0125others(11): Show | 14 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2346+1207C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17646430 | ||||||
| chr4:17646496
|
C | T | 1 | a0002c0001t0001g0156 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2346+1141G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17646496 | ||||||
| chr4:17646497
|
A | G | 174 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0004t0003g0207others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.2346+1140T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17646497 | ||||||
| chr4:17646568
|
C | G | 1 | a0003c0009t0005g0162 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2346+1069G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17646568 | ||||||
| chr4:17646653
|
A | G | 1 | a0008c0034t0051g0010 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2346+984T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17646653 | ||||||
| chr4:17646718
|
TTAAAA | T | 4 | a0025c0056t0061g0078a0027c0057t0030g0096a0028c0032t0062g0172others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.2346+914_2346+918d others(7): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17646718 | ||||||
| chr4:17646721
|
A | C | 2 | a0001c0003t0004g0067a0001c0003t0004g0169 | 2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.2346+916T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17646721 | ||||||
| chr4:17646724
|
T | C | 1 | a0001c0003t0002g0227 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2346+913A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17646724 | ||||||
| chr4:17646825
|
G | A | 1 | a0002c0002t0001g0177 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2346+812C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17646825 | ||||||
| chr4:17646962
|
G | A | 1 | a0002c0002t0001g0025 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2346+675C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17646962 | ||||||
| chr4:17646963
|
C | A | 1 | a0002c0002t0001g0025 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2346+674G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17646963 | ||||||
| chr4:17647126
|
C | CT | 120 | a0001c0004t0042g0108a0001c0047t0010g0113a0002c0001t0001g0002others(117): Show | 120 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.2346+510dupA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17647126 | ||||||
| chr4:17647144
|
G | A | 8 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(5): Show | 8 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.2346+493C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17647144 | ||||||
| chr4:17647186
|
G | A | 22 | a0001c0029t0005g0115a0003c0009t0005g0009a0003c0009t0005g0133others(19): Show | 22 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.2346+451C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17647186 | ||||||
| chr4:17647216
|
G | C | 1 | a0019c0040t0065g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2346+421C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17647216 | ||||||
| chr4:17647252
|
CT | C | 66 | a0001c0003t0007g0220a0001c0003t0008g0208a0001c0003t0018g0006others(63): Show | 66 | HG00099.hp1 HG00323.hp2 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.2346+384delA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17647252 | ||||||
| chr4:17647252
|
CTT | C | 115 | a0001c0003t0019g0095a0001c0006t0028g0014a0001c0007t0019g0143others(112): Show | 115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.2346+383_2346+384d others(4): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17647252 | ||||||
| chr4:17647272
|
A | C | 1 | a0002c0001t0001g0198 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2346+365T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17647272 | ||||||
| chr4:17647410
|
G | A | 1 | a0025c0056t0061g0078 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2346+227C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17647410 | ||||||
| chr4:17647610
|
T | G | 145 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.2346+27A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 12/17 | chr4 | 17647610 | ||||||
| chr4:17647871
|
T | C | 138 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(135): Show | 138 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.2192-80A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17647871 | ||||||
| chr4:17647876
|
T | G | 139 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.2192-85A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17647876 | ||||||
| chr4:17647906
|
G | T | 6 | a0001c0017t0010g0070a0001c0017t0010g0103a0001c0017t0010g0175others(3): Show | 6 | HG00099.hp1 HG01516.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2192-115C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17647906 | ||||||
| chr4:17648060
|
A | G | 3 | a0005c0030t0015g0033a0005c0031t0015g0193a0008c0039t0015g0016 | 3 | HG02615.hp2 HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2192-269T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17648060 | ||||||
| chr4:17648265
|
GA | G | 2 | a0025c0056t0061g0078a0027c0057t0030g0096 | 2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2192-475delT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17648265 | ||||||
| chr4:17648278
|
T | C | 8 | a0004c0010t0006g0077a0004c0010t0006g0107a0004c0010t0006g0109others(5): Show | 8 | HG02280.hp2 HG02451.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.2192-487A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17648278 | ||||||
| chr4:17648288
|
G | A | 10 | a0001c0004t0009g0017a0001c0004t0009g0022a0001c0004t0009g0072others(7): Show | 10 | HG02258.hp1 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.2192-497C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17648288 | ||||||
| chr4:17648295
|
C | T | 1 | a0026c0055t0002g0117 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2192-504G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17648295 | ||||||
| chr4:17648355
|
A | AT | 10 | a0001c0006t0048g0027a0004c0010t0006g0077a0004c0010t0006g0107others(7): Show | 10 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.2192-565dupA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17648355 | ||||||
| chr4:17648519
|
A | AT | 24 | a0001c0003t0007g0220a0001c0003t0018g0006a0001c0003t0019g0095others(21): Show | 24 | HG00099.hp1 HG01358.hp2 HG01516.hp2 others(21): Show |
intron_variant | MODIFIER | c.2192-729dupA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17648519 | ||||||
| chr4:17648519
|
AT | A | 118 | a0001c0003t0060g0215a0001c0029t0005g0115a0002c0001t0001g0002others(115): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.2192-729delA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17648519 | ||||||
| chr4:17648582
|
G | A | 1 | a0001c0003t0002g0227 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2192-791C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17648582 | ||||||
| chr4:17648604
|
T | C | 7 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(4): Show | 7 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.2192-813A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17648604 | ||||||
| chr4:17648635
|
G | A | 1 | a0011c0023t0043g0204 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2192-844C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17648635 | ||||||
| chr4:17648642
|
A | G | 9 | a0004c0010t0006g0077a0004c0010t0006g0107a0004c0010t0006g0109others(6): Show | 9 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2192-851T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17648642 | ||||||
| chr4:17648658
|
A | G | 131 | a0001c0029t0005g0115a0002c0001t0001g0002a0002c0001t0001g0082others(128): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.2192-867T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17648658 | ||||||
| chr4:17648727
|
G | T | 6 | a0001c0017t0010g0070a0001c0017t0010g0103a0001c0017t0010g0175others(3): Show | 6 | HG00099.hp1 HG01516.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2192-936C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17648727 | ||||||
| chr4:17648728
|
T | C | 139 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.2192-937A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17648728 | ||||||
| chr4:17648745
|
T | A | 1 | a0028c0032t0062g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2192-954A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17648745 | ||||||
| chr4:17648794
|
G | A | 2 | a0002c0001t0001g0189a0002c0001t0001g0190 | 2 | HG00673.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.2192-1003C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17648794 | ||||||
| chr4:17648856
|
C | A | 1 | a0021c0052t0050g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2192-1065G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17648856 | ||||||
| chr4:17649020
|
G | A | 1 | a0023c0053t0012g0080 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2192-1229C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17649020 | ||||||
| chr4:17649119
|
A | C | 7 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(4): Show | 7 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.2192-1328T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17649119 | ||||||
| chr4:17649135
|
A | G | 139 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.2192-1344T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17649135 | ||||||
| chr4:17649310
|
C | T | 1 | a0028c0032t0062g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2192-1519G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17649310 | ||||||
| chr4:17649369
|
G | C | 1 | a0001c0003t0008g0216 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2192-1578C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17649369 | ||||||
| chr4:17649392
|
G | A | 1 | a0023c0053t0012g0080 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2192-1601C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17649392 | ||||||
| chr4:17649417
|
T | C | 1 | a0001c0008t0068g0234 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2192-1626A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17649417 | ||||||
| chr4:17649510
|
G | A | 1 | a0023c0053t0012g0080 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2192-1719C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17649510 | ||||||
| chr4:17649541
|
A | G | 139 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.2192-1750T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17649541 | ||||||
| chr4:17649578
|
C | T | 109 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(106): Show | 109 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.2192-1787G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17649578 | ||||||
| chr4:17649583
|
C | CA | 7 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0003t0040g0201others(4): Show | 7 | HG02630.hp1 HG03225.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.2192-1793dupT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17649583 | ||||||
| chr4:17649583
|
CA | C | 27 | a0001c0006t0003g0031a0001c0029t0005g0115a0002c0001t0001g0152others(24): Show | 27 | HG00639.hp2 HG01243.hp2 HG01516.hp2 others(24): Show |
intron_variant | MODIFIER | c.2192-1793delT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17649583 | ||||||
| chr4:17649583
|
CAA | C | 106 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(103): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.2192-1794_2192-179 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17649583 | ||||||
| chr4:17649660
|
T | TA | 8 | a0001c0029t0005g0115a0003c0009t0005g0009a0003c0009t0005g0133others(5): Show | 8 | HG02109.hp1 HG02559.hp1 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.2192-1870dupT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17649660 | ||||||
| chr4:17649660
|
T | TAA | 11 | a0004c0010t0006g0077a0004c0010t0006g0107a0004c0010t0006g0109others(8): Show | 11 | HG01243.hp2 HG02451.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2192-1871_2192-187 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17649660 | ||||||
| chr4:17649681
|
C | G | 131 | a0001c0029t0005g0115a0002c0001t0001g0002a0002c0001t0001g0082others(128): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.2192-1890G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17649681 | ||||||
| chr4:17649751
|
G | A | 2 | a0004c0010t0006g0077a0004c0010t0006g0165 | 2 | HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2192-1960C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17649751 | ||||||
| chr4:17649868
|
T | TCATCCAT others(1): Show |
105 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2192-2085_2192-207 others(12): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17649868 | ||||||
| chr4:17649885
|
C | CATCCATC others(13): Show |
39 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(36): Show | 39 | HG00099.hp1 HG01243.hp2 HG01516.hp2 others(36): Show |
intron_variant | MODIFIER | c.2192-2095_2192-209 others(24): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17649885 | ||||||
| chr4:17649885
|
C | T | 105 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2192-2094G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17649885 | ||||||
| chr4:17649887
|
T | TCCATCCA others(9): Show |
1 | a0032c0061t0030g0007 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2192-2097_2192-209 others(20): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17649887 | ||||||
| chr4:17649969
|
G | A | 2 | a0006c0014t0001g0008a0006c0014t0001g0042 | 2 | HG02735.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.2192-2178C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17649969 | ||||||
| chr4:17649988
|
G | T | 2 | a0002c0002t0001g0036a0002c0002t0001g0055 | 2 | HG01169.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.2192-2197C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17649988 | ||||||
| chr4:17650078
|
G | GTCCA | 141 | a0001c0004t0003g0207a0001c0004t0003g0212a0001c0004t0003g0213others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.2192-2291_2192-228 others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17650078 | ||||||
| chr4:17650134
|
C | A | 139 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.2192-2343G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17650134 | ||||||
| chr4:17650182
|
GTCCATCC others(5): Show |
G | 1 | a0008c0049t0034g0112 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2192-2403_2192-239 others(16): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17650182 | ||||||
| chr4:17650316
|
G | T | 1 | a0001c0003t0011g0166 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2191+2514C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17650316 | ||||||
| chr4:17650362
|
A | T | 1 | a0028c0032t0062g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2191+2468T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17650362 | ||||||
| chr4:17650364
|
G | A | 22 | a0001c0029t0005g0115a0003c0009t0005g0009a0003c0009t0005g0133others(19): Show | 22 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.2191+2466C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17650364 | ||||||
| chr4:17650408
|
G | C | 105 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2191+2422C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17650408 | ||||||
| chr4:17650441
|
G | A | 2 | a0001c0017t0010g0070a0001c0017t0010g0175 | 2 | HG02647.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2191+2389C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17650441 | ||||||
| chr4:17650487
|
T | C | 1 | a0002c0002t0001g0050 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2191+2343A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17650487 | ||||||
| chr4:17650510
|
T | C | 188 | a0001c0003t0007g0220a0001c0003t0018g0006a0001c0003t0019g0095others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.2191+2320A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17650510 | ||||||
| chr4:17650537
|
A | G | 1 | a0006c0014t0001g0008 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2191+2293T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17650537 | ||||||
| chr4:17650602
|
C | T | 2 | a0025c0056t0061g0078a0027c0057t0030g0096 | 2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2191+2228G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17650602 | ||||||
| chr4:17650716
|
G | A | 22 | a0001c0029t0005g0115a0003c0009t0005g0009a0003c0009t0005g0133others(19): Show | 22 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.2191+2114C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17650716 | ||||||
| chr4:17650729
|
G | A | 105 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2191+2101C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17650729 | ||||||
| chr4:17650827
|
A | C | 105 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2191+2003T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17650827 | ||||||
| chr4:17650888
|
T | C | 1 | a0001c0008t0011g0052 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2191+1942A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17650888 | ||||||
| chr4:17650902
|
A | AT | 16 | a0001c0004t0003g0207a0001c0004t0003g0212a0001c0004t0003g0213others(13): Show | 16 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.2191+1927dupA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17650902 | ||||||
| chr4:17650903
|
T | A | 139 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.2191+1927A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17650903 | ||||||
| chr4:17651021
|
C | T | 1 | a0022c0045t0001g0061 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2191+1809G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17651021 | ||||||
| chr4:17651058
|
C | T | 2 | a0017c0026t0038g0098a0017c0026t0041g0160 | 2 | HG01081.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.2191+1772G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17651058 | ||||||
| chr4:17651131
|
G | A | 1 | a0032c0061t0030g0007 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2191+1699C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17651131 | ||||||
| chr4:17651333
|
C | T | 103 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(100): Show | 103 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.2191+1497G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17651333 | ||||||
| chr4:17651353
|
C | T | 7 | a0001c0004t0009g0072a0001c0017t0010g0070a0001c0017t0010g0103others(4): Show | 7 | HG00099.hp1 HG01516.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2191+1477G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17651353 | ||||||
| chr4:17651394
|
C | T | 9 | a0004c0010t0006g0077a0004c0010t0006g0107a0004c0010t0006g0109others(6): Show | 9 | HG01891.hp1 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2191+1436G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17651394 | ||||||
| chr4:17651430
|
C | T | 6 | a0001c0017t0010g0070a0001c0017t0010g0103a0001c0017t0010g0175others(3): Show | 6 | HG00099.hp1 HG01516.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2191+1400G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17651430 | ||||||
| chr4:17651463
|
A | G | 135 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(132): Show | 135 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.2191+1367T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17651463 | ||||||
| chr4:17651537
|
C | CA | 21 | a0001c0003t0008g0163a0001c0003t0060g0215a0001c0003t0066g0150others(18): Show | 21 | HG00140.hp1 HG01109.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.2191+1292dupT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17651537 | ||||||
| chr4:17651537
|
C | CAA | 87 | a0001c0003t0007g0220a0001c0004t0009g0017a0001c0004t0042g0108others(84): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.2191+1291_2191+129 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17651537 | ||||||
| chr4:17651537
|
C | CAAA | 53 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0004t0003g0212others(50): Show | 53 | HG00597.hp2 HG00609.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.2191+1290_2191+129 others(7): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17651537 | ||||||
| chr4:17651537
|
C | CAAAA | 16 | a0001c0004t0003g0207a0001c0006t0003g0026a0001c0006t0003g0030others(13): Show | 16 | HG01123.hp1 HG02559.hp1 HG02698.hp2 others(13): Show |
intron_variant | MODIFIER | c.2191+1289_2191+129 others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17651537 | ||||||
| chr4:17651537
|
C | CAAAAAAA others(8): Show |
1 | a0028c0032t0062g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2191+1278_2191+129 others(19): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17651537 | ||||||
| chr4:17651537
|
C | CAAAAAAA others(10): Show |
1 | a0027c0057t0030g0096 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2191+1276_2191+129 others(21): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17651537 | ||||||
| chr4:17651537
|
CA | C | 10 | a0001c0003t0002g0206a0001c0017t0010g0070a0001c0017t0010g0103others(7): Show | 10 | HG00099.hp1 HG00280.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2191+1292delT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17651537 | ||||||
| chr4:17651537
|
CAAAAAAA others(5): Show |
C | 3 | a0009c0011t0001g0032a0009c0011t0001g0081a0009c0011t0056g0084 | 3 | HG02717.hp2 HG02886.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2191+1281_2191+129 others(16): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17651537 | ||||||
| chr4:17651537
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0004t0009g0022 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2191+1279_2191+129 others(18): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17651537 | ||||||
| chr4:17651589
|
T | C | 1 | a0032c0061t0030g0007 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2191+1241A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17651589 | ||||||
| chr4:17651600
|
A | C | 9 | a0004c0010t0006g0077a0004c0010t0006g0107a0004c0010t0006g0109others(6): Show | 9 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2191+1230T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17651600 | ||||||
| chr4:17651613
|
C | G | 1 | a0010c0013t0024g0211 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2191+1217G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17651613 | ||||||
| chr4:17651662
|
A | T | 174 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0004t0003g0207others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.2191+1168T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17651662 | ||||||
| chr4:17651984
|
G | A | 14 | a0001c0003t0007g0220a0001c0005t0007g0013a0001c0005t0007g0125others(11): Show | 14 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2191+846C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17651984 | ||||||
| chr4:17652050
|
T | C | 1 | a0019c0040t0065g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2191+780A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17652050 | ||||||
| chr4:17652129
|
C | CT | 8 | a0001c0008t0002g0045a0001c0017t0010g0070a0001c0017t0010g0103others(5): Show | 8 | HG00099.hp1 HG01516.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2191+700dupA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17652129 | ||||||
| chr4:17652129
|
C | CTTTT | 5 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0008t0018g0020others(2): Show | 5 | HG02451.hp2 HG02630.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.2191+697_2191+700d others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17652129 | ||||||
| chr4:17652129
|
CT | C | 16 | a0001c0004t0009g0017a0001c0004t0009g0022a0001c0004t0009g0072others(13): Show | 16 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2191+700delA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17652129 | ||||||
| chr4:17652129
|
CTT | C | 13 | a0001c0004t0003g0207a0001c0004t0003g0212a0001c0004t0003g0213others(10): Show | 13 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.2191+699_2191+700d others(4): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17652129 | ||||||
| chr4:17652146
|
T | TTTTG | 122 | a0001c0029t0005g0115a0002c0001t0001g0002a0002c0001t0001g0082others(119): Show | 122 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.2191+683_2191+684i others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17652146 | ||||||
| chr4:17652146
|
T | TTTTTG | 8 | a0002c0002t0001g0040a0002c0002t0001g0054a0002c0002t0001g0056others(5): Show | 8 | HG00280.hp2 HG00423.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.2191+683_2191+684i others(7): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17652146 | ||||||
| chr4:17652155
|
T | C | 188 | a0001c0003t0007g0220a0001c0003t0018g0006a0001c0003t0019g0095others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.2191+675A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17652155 | ||||||
| chr4:17652163
|
C | T | 1 | a0002c0001t0001g0198 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2191+667G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17652163 | ||||||
| chr4:17652250
|
G | A | 1 | a0021c0052t0050g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2191+580C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17652250 | ||||||
| chr4:17652268
|
A | G | 174 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0004t0003g0207others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.2191+562T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17652268 | ||||||
| chr4:17652281
|
C | T | 1 | a0001c0003t0008g0216 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2191+549G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17652281 | ||||||
| chr4:17652286
|
G | A | 1 | a0025c0056t0061g0078 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2191+544C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17652286 | ||||||
| chr4:17652515
|
A | C | 29 | a0001c0004t0003g0207a0001c0004t0003g0212a0001c0004t0003g0213others(26): Show | 29 | HG01109.hp2 HG01123.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.2191+315T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17652515 | ||||||
| chr4:17652598
|
C | A | 8 | a0001c0029t0005g0115a0003c0009t0005g0009a0003c0009t0005g0133others(5): Show | 8 | HG02109.hp1 HG02559.hp1 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.2191+232G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17652598 | ||||||
| chr4:17652718
|
G | A | 109 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(106): Show | 109 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.2191+112C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17652718 | ||||||
| chr4:17652740
|
C | T | 1 | a0001c0005t0007g0194 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2191+90G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 11/17 | chr4 | 17652740 | ||||||
| chr4:17653025
|
T | C | 139 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.2038-42A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653025 | ||||||
| chr4:17653081
|
C | T | 2 | a0004c0010t0006g0077a0004c0010t0006g0165 | 2 | HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2038-98G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653081 | ||||||
| chr4:17653125
|
C | G | 8 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(5): Show | 8 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.2038-142G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653125 | ||||||
| chr4:17653150
|
GC | G | 22 | a0001c0029t0005g0115a0003c0009t0005g0009a0003c0009t0005g0133others(19): Show | 22 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.2038-168delG | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653150 | ||||||
| chr4:17653223
|
CCAAT | C | 22 | a0001c0029t0005g0115a0003c0009t0005g0009a0003c0009t0005g0133others(19): Show | 22 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.2038-244_2038-241d others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653223 | ||||||
| chr4:17653355
|
T | C | 22 | a0001c0029t0005g0115a0003c0009t0005g0009a0003c0009t0005g0133others(19): Show | 22 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.2038-372A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653355 | ||||||
| chr4:17653405
|
G | A | 5 | a0005c0030t0015g0033a0005c0031t0015g0193a0008c0034t0051g0010others(2): Show | 5 | HG01243.hp2 HG02615.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2038-422C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653405 | ||||||
| chr4:17653436
|
T | C | 14 | a0001c0003t0007g0220a0001c0005t0007g0013a0001c0005t0007g0125others(11): Show | 14 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2038-453A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653436 | ||||||
| chr4:17653473
|
A | G | 145 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.2038-490T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653473 | ||||||
| chr4:17653493
|
G | C | 7 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(4): Show | 7 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.2038-510C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653493 | ||||||
| chr4:17653523
|
TATTC | T | 29 | a0001c0004t0003g0207a0001c0004t0003g0212a0001c0004t0003g0213others(26): Show | 29 | HG01109.hp2 HG01123.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.2038-544_2038-541d others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653523 | ||||||
| chr4:17653788
|
G | C | 1 | a0005c0036t0053g0233 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2038-805C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653788 | ||||||
| chr4:17653796
|
T | C | 1 | a0001c0015t0013g0106 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2038-813A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653796 | ||||||
| chr4:17653824
|
A | C | 21 | a0003c0009t0005g0009a0003c0009t0005g0133a0003c0009t0005g0162others(18): Show | 21 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.2038-841T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653824 | ||||||
| chr4:17653870
|
G | A | 4 | a0004c0035t0006g0139a0005c0028t0006g0191a0005c0036t0053g0233others(1): Show | 4 | HG02280.hp2 HG02897.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2038-887C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653870 | ||||||
| chr4:17653919
|
A | AGGGAGGG others(51): Show |
5 | a0005c0030t0015g0033a0005c0031t0015g0193a0008c0034t0051g0010others(2): Show | 5 | HG01243.hp2 HG02615.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2038-937_2038-936i others(60): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653919 | ||||||
| chr4:17653919
|
A | AGGGAGGG others(53): Show |
1 | a0027c0057t0030g0096 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2038-937_2038-936i others(62): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653919 | ||||||
| chr4:17653919
|
A | AGGGAGGG others(45): Show |
15 | a0003c0009t0005g0009a0003c0009t0005g0133a0003c0009t0005g0162others(12): Show | 15 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.2038-937_2038-936i others(54): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653919 | ||||||
| chr4:17653919
|
A | AGGGAGGG others(51): Show |
16 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(13): Show | 16 | HG00099.hp1 HG01516.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.2038-937_2038-936i others(60): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653919 | ||||||
| chr4:17653919
|
A | AGGGAGGG others(52): Show |
4 | a0007c0041t0012g0011a0007c0043t0012g0105a0007c0050t0012g0004others(1): Show | 4 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.2038-937_2038-936i others(61): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653919 | ||||||
| chr4:17653919
|
A | AGGGAGGG others(43): Show |
13 | a0001c0004t0009g0017a0001c0004t0009g0022a0001c0004t0009g0072others(10): Show | 13 | HG01884.hp1 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.2038-937_2038-936i others(52): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653919 | ||||||
| chr4:17653919
|
A | AGGGAGGG others(49): Show |
10 | a0001c0004t0003g0207a0001c0004t0003g0213a0001c0006t0003g0026others(7): Show | 10 | HG01123.hp1 HG01952.hp1 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.2038-937_2038-936i others(58): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653919 | ||||||
| chr4:17653919
|
A | AGGGAGGG others(52): Show |
1 | a0032c0061t0030g0007 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2038-937_2038-936i others(61): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653919 | ||||||
| chr4:17653919
|
A | AGGGAGGG others(44): Show |
2 | a0013c0048t0022g0048a0016c0025t0021g0224 | 2 | HG01109.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.2038-937_2038-936i others(53): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653919 | ||||||
| chr4:17653919
|
A | AGGGAGGG others(50): Show |
2 | a0001c0006t0003g0028a0001c0006t0028g0015 | 2 | HG04199.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.2038-937_2038-936i others(59): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653919 | ||||||
| chr4:17653919
|
A | AGGGAGGG others(52): Show |
2 | a0001c0004t0003g0212a0001c0006t0048g0027 | 2 | HG01192.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.2038-937_2038-936i others(61): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653919 | ||||||
| chr4:17653919
|
A | AGGGAGGG others(84): Show |
1 | a0002c0002t0001g0114 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2038-937_2038-936i others(93): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653919 | ||||||
| chr4:17653919
|
A | AGGGAGGG others(68): Show |
1 | a0023c0053t0012g0080 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2038-937_2038-936i others(77): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653919 | ||||||
| chr4:17653919
|
A | AGGGAGGG others(52): Show |
1 | a0002c0002t0016g0039 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2038-937_2038-936i others(61): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653919 | ||||||
| chr4:17653919
|
A | AGGGAGGG others(52): Show |
87 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(84): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.2038-937_2038-936i others(61): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653919 | ||||||
| chr4:17653919
|
A | AGGGAGGG others(53): Show |
1 | a0002c0001t0001g0131 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2038-937_2038-936i others(62): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653919 | ||||||
| chr4:17653919
|
A | AGGGAGGG others(53): Show |
7 | a0002c0001t0001g0154a0002c0001t0001g0188a0002c0001t0016g0130others(4): Show | 7 | HG00597.hp2 HG01109.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.2038-937_2038-936i others(62): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653919 | ||||||
| chr4:17653919
|
A | AGGGAGGG others(53): Show |
2 | a0006c0014t0001g0042a0031c0027t0001g0088 | 2 | HG02738.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2038-937_2038-936i others(62): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653919 | ||||||
| chr4:17653919
|
A | AGGGAGGG others(46): Show |
1 | a0021c0052t0050g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2038-937_2038-936i others(55): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653919 | ||||||
| chr4:17653919
|
A | AGGGAGGG others(45): Show |
1 | a0001c0003t0008g0205 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2038-937_2038-936i others(54): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653919 | ||||||
| chr4:17653919
|
A | AGGGAGGG others(46): Show |
41 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0206others(38): Show | 41 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.2038-937_2038-936i others(55): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653919 | ||||||
| chr4:17653919
|
A | AGGGAGGG others(47): Show |
21 | a0001c0003t0002g0149a0001c0003t0002g0158a0001c0003t0007g0220others(18): Show | 21 | HG00140.hp1 HG00544.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.2038-937_2038-936i others(56): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653919 | ||||||
| chr4:17653919
|
A | AGGGAGGG others(48): Show |
1 | a0001c0003t0004g0018 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2038-937_2038-936i others(57): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653919 | ||||||
| chr4:17653923
|
A | AGGGAGAG others(54): Show |
1 | a0002c0001t0001g0087 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2038-941_2038-940i others(63): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653923 | ||||||
| chr4:17653937
|
T | A | 1 | a0019c0040t0065g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2038-954A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17653937 | ||||||
| chr4:17654056
|
A | G | 1 | a0001c0007t0019g0143 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2038-1073T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17654056 | ||||||
| chr4:17654144
|
G | A | 21 | a0003c0009t0005g0009a0003c0009t0005g0133a0003c0009t0005g0162others(18): Show | 21 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.2038-1161C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17654144 | ||||||
| chr4:17654174
|
G | A | 1 | a0021c0052t0050g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2038-1191C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17654174 | ||||||
| chr4:17654193
|
C | CT | 13 | a0001c0004t0003g0212a0001c0017t0010g0103a0002c0001t0001g0101others(10): Show | 13 | HG00099.hp1 HG00597.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.2038-1211dupA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17654193 | ||||||
| chr4:17654193
|
C | CTT | 12 | a0004c0010t0006g0077a0004c0010t0006g0107a0004c0010t0006g0109others(9): Show | 12 | HG01243.hp2 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.2038-1212_2038-121 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17654193 | ||||||
| chr4:17654193
|
CT | C | 5 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(2): Show | 5 | HG02622.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2038-1211delA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17654193 | ||||||
| chr4:17654310
|
A | G | 8 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(5): Show | 8 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.2038-1327T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17654310 | ||||||
| chr4:17654355
|
T | A | 2 | a0002c0001t0001g0086a0002c0001t0001g0129 | 2 | HG03704.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2038-1372A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17654355 | ||||||
| chr4:17654451
|
G | T | 8 | a0004c0010t0006g0077a0004c0010t0006g0107a0004c0010t0006g0109others(5): Show | 8 | HG02280.hp2 HG02451.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.2038-1468C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17654451 | ||||||
| chr4:17654480
|
A | G | 130 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(127): Show | 130 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.2038-1497T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17654480 | ||||||
| chr4:17654484
|
C | T | 105 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2038-1501G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17654484 | ||||||
| chr4:17654581
|
G | A | 4 | a0025c0056t0061g0078a0027c0057t0030g0096a0028c0032t0062g0172others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.2038-1598C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17654581 | ||||||
| chr4:17654604
|
G | A | 6 | a0001c0017t0010g0070a0001c0017t0010g0103a0001c0017t0010g0175others(3): Show | 6 | HG00099.hp1 HG01516.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2038-1621C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17654604 | ||||||
| chr4:17654785
|
G | A | 29 | a0001c0004t0003g0207a0001c0004t0003g0212a0001c0004t0003g0213others(26): Show | 29 | HG01109.hp2 HG01123.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.2038-1802C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17654785 | ||||||
| chr4:17654849
|
GTCTTTT | G | 6 | a0001c0017t0010g0070a0001c0017t0010g0103a0001c0017t0010g0175others(3): Show | 6 | HG00099.hp1 HG01516.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2038-1872_2038-186 others(10): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17654849 | ||||||
| chr4:17654887
|
C | G | 9 | a0004c0010t0006g0077a0004c0010t0006g0107a0004c0010t0006g0109others(6): Show | 9 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2038-1904G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17654887 | ||||||
| chr4:17654912
|
C | T | 8 | a0004c0010t0006g0077a0004c0010t0006g0107a0004c0010t0006g0109others(5): Show | 8 | HG02280.hp2 HG02451.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.2038-1929G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17654912 | ||||||
| chr4:17654913
|
G | A | 105 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2038-1930C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17654913 | ||||||
| chr4:17654952
|
A | G | 12 | a0003c0009t0005g0009a0003c0009t0005g0133a0003c0009t0005g0162others(9): Show | 12 | HG01243.hp2 HG02109.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.2038-1969T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17654952 | ||||||
| chr4:17655115
|
G | C | 105 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2038-2132C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17655115 | ||||||
| chr4:17655229
|
C | T | 2 | a0025c0056t0061g0078a0027c0057t0030g0096 | 2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2038-2246G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17655229 | ||||||
| chr4:17655428
|
G | A | 100 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.2038-2445C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17655428 | ||||||
| chr4:17655689
|
C | T | 1 | a0001c0008t0011g0052 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2037+2661G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17655689 | ||||||
| chr4:17655737
|
G | A | 125 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(122): Show | 125 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.2037+2613C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17655737 | ||||||
| chr4:17655955
|
A | G | 12 | a0003c0009t0005g0009a0003c0009t0005g0133a0003c0009t0005g0162others(9): Show | 12 | HG01243.hp2 HG02109.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.2037+2395T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17655955 | ||||||
| chr4:17656025
|
G | A | 1 | a0019c0040t0065g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2037+2325C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17656025 | ||||||
| chr4:17656027
|
C | T | 105 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2037+2323G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17656027 | ||||||
| chr4:17656230
|
C | A | 188 | a0001c0003t0007g0220a0001c0003t0018g0006a0001c0003t0019g0095others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.2037+2120G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17656230 | ||||||
| chr4:17656241
|
G | C | 5 | a0005c0030t0015g0033a0005c0031t0015g0193a0008c0034t0051g0010others(2): Show | 5 | HG01243.hp2 HG02615.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2037+2109C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17656241 | ||||||
| chr4:17656262
|
C | A | 2 | a0005c0036t0053g0233a0005c0042t0006g0093 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2037+2088G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17656262 | ||||||
| chr4:17656298
|
G | A | 1 | a0005c0036t0053g0233 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2037+2052C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17656298 | ||||||
| chr4:17656329
|
A | T | 21 | a0003c0009t0005g0009a0003c0009t0005g0133a0003c0009t0005g0162others(18): Show | 21 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.2037+2021T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17656329 | ||||||
| chr4:17656363
|
G | A | 105 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2037+1987C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17656363 | ||||||
| chr4:17656398
|
CTTTCTTT | C | 15 | a0001c0003t0007g0220a0001c0005t0007g0013a0001c0005t0007g0125others(12): Show | 15 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.2037+1945_2037+195 others(11): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17656398 | ||||||
| chr4:17656471
|
A | G | 1 | a0025c0056t0061g0078 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2037+1879T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17656471 | ||||||
| chr4:17656494
|
C | T | 1 | a0021c0052t0050g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2037+1856G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17656494 | ||||||
| chr4:17656495
|
A | G | 144 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.2037+1855T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17656495 | ||||||
| chr4:17656581
|
T | C | 5 | a0007c0041t0012g0011a0007c0043t0012g0105a0007c0050t0012g0004others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.2037+1769A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17656581 | ||||||
| chr4:17656704
|
C | CT | 7 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(4): Show | 7 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.2037+1645dupA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17656704 | ||||||
| chr4:17656918
|
T | A | 12 | a0003c0009t0005g0009a0003c0009t0005g0133a0003c0009t0005g0162others(9): Show | 12 | HG01243.hp2 HG02109.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.2037+1432A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17656918 | ||||||
| chr4:17657022
|
T | A | 105 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2037+1328A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17657022 | ||||||
| chr4:17657215
|
T | C | 105 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2037+1135A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17657215 | ||||||
| chr4:17657411
|
C | T | 173 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0004t0003g0207others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.2037+939G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17657411 | ||||||
| chr4:17657416
|
T | C | 173 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0004t0003g0207others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.2037+934A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17657416 | ||||||
| chr4:17657431
|
C | T | 5 | a0005c0030t0015g0033a0005c0031t0015g0193a0008c0034t0051g0010others(2): Show | 5 | HG01243.hp2 HG02615.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2037+919G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17657431 | ||||||
| chr4:17657555
|
T | C | 7 | a0003c0009t0005g0009a0003c0009t0005g0133a0003c0009t0005g0162others(4): Show | 7 | HG02109.hp1 HG02559.hp1 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.2037+795A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17657555 | ||||||
| chr4:17657642
|
T | C | 1 | a0002c0016t0001g0071 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2037+708A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17657642 | ||||||
| chr4:17657655
|
C | CT | 22 | a0001c0003t0004g0169a0001c0004t0003g0207a0001c0004t0003g0212others(19): Show | 22 | HG00099.hp1 HG01099.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.2037+694dupA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17657655 | ||||||
| chr4:17657655
|
C | CTT | 33 | a0001c0004t0009g0017a0001c0004t0009g0022a0001c0004t0009g0072others(30): Show | 33 | HG00323.hp1 HG01109.hp2 HG01516.hp2 others(30): Show |
intron_variant | MODIFIER | c.2037+693_2037+694d others(4): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17657655 | ||||||
| chr4:17657655
|
C | CTTT | 97 | a0001c0006t0048g0027a0002c0001t0001g0002a0002c0001t0001g0082others(94): Show | 97 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.2037+692_2037+694d others(5): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17657655 | ||||||
| chr4:17657655
|
C | CTTTT | 15 | a0002c0001t0001g0120a0002c0001t0001g0145a0002c0002t0001g0036others(12): Show | 15 | HG01175.hp1 HG01192.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2037+691_2037+694d others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17657655 | ||||||
| chr4:17657696
|
A | G | 9 | a0004c0010t0006g0077a0004c0010t0006g0107a0004c0010t0006g0109others(6): Show | 9 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2037+654T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17657696 | ||||||
| chr4:17657775
|
G | C | 1 | a0028c0032t0062g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2037+575C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17657775 | ||||||
| chr4:17657903
|
C | G | 134 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(131): Show | 134 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.2037+447G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17657903 | ||||||
| chr4:17657975
|
T | C | 144 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.2037+375A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17657975 | ||||||
| chr4:17657992
|
C | T | 1 | a0008c0039t0015g0016 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2037+358G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17657992 | ||||||
| chr4:17658118
|
G | C | 5 | a0005c0030t0015g0033a0005c0031t0015g0193a0008c0034t0051g0010others(2): Show | 5 | HG01243.hp2 HG02615.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2037+232C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17658118 | ||||||
| chr4:17658275
|
G | C | 21 | a0003c0009t0005g0009a0003c0009t0005g0133a0003c0009t0005g0162others(18): Show | 21 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.2037+75C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17658275 | ||||||
| chr4:17658276
|
G | A | 5 | a0005c0030t0015g0033a0005c0031t0015g0193a0008c0034t0051g0010others(2): Show | 5 | HG01243.hp2 HG02615.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2037+74C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17658276 | ||||||
| chr4:17658313
|
G | T | 105 | a0002c0001t0001g0002a0002c0001t0001g0082a0002c0001t0001g0083others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2037+37C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 10/17 | chr4 | 17658313 | ||||||
| chr4:17658614
|
T | C | 149 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0003t0023g0122others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.1825-52A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 9/17 | chr4 | 17658614 | ||||||
| chr4:17658619
|
T | C | 29 | a0001c0004t0003g0207a0001c0004t0003g0212a0001c0004t0003g0213others(26): Show | 29 | HG01109.hp2 HG01123.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.1825-57A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 9/17 | chr4 | 17658619 | ||||||
| chr4:17658784
|
T | C | 178 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0003t0023g0122others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.1825-222A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 9/17 | chr4 | 17658784 | ||||||
| chr4:17658811
|
G | T | 1 | a0024c0037t0052g0094 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1825-249C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 9/17 | chr4 | 17658811 | ||||||
| chr4:17659108
|
CT | C | 47 | a0001c0003t0008g0216a0001c0003t0018g0006a0001c0003t0019g0095others(44): Show | 47 | HG00099.hp1 HG00323.hp1 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.1825-547delA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 9/17 | chr4 | 17659108 | ||||||
| chr4:17659108
|
CTT | C | 7 | a0001c0006t0003g0182a0004c0010t0006g0077a0004c0010t0006g0107others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1825-548_1825-547d others(4): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 9/17 | chr4 | 17659108 | ||||||
| chr4:17659172
|
C | G | 7 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(4): Show | 7 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1825-610G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 9/17 | chr4 | 17659172 | ||||||
| chr4:17659218
|
G | A | 6 | a0001c0017t0010g0070a0001c0017t0010g0103a0001c0017t0010g0175others(3): Show | 6 | HG00099.hp1 HG01516.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1825-656C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 9/17 | chr4 | 17659218 | ||||||
| chr4:17659476
|
T | A | 3 | a0002c0001t0017g0091a0002c0001t0017g0137a0002c0001t0017g0138 | 3 | HG01123.hp2 HG02698.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1824+482A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 9/17 | chr4 | 17659476 | ||||||
| chr4:17659502
|
T | C | 1 | a0002c0001t0001g0090 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1824+456A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 9/17 | chr4 | 17659502 | ||||||
| chr4:17659511
|
G | C | 7 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(4): Show | 7 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1824+447C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 9/17 | chr4 | 17659511 | ||||||
| chr4:17659545
|
G | A | 1 | a0002c0002t0001g0025 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1824+413C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 9/17 | chr4 | 17659545 | ||||||
| chr4:17659558
|
C | T | 1 | a0001c0003t0008g0216 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1824+400G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 9/17 | chr4 | 17659558 | ||||||
| chr4:17659609
|
C | A | 1 | a0002c0002t0001g0025 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1824+349G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 9/17 | chr4 | 17659609 | ||||||
| chr4:17659631
|
C | T | 1 | a0019c0040t0065g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1824+327G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 9/17 | chr4 | 17659631 | ||||||
| chr4:17659686
|
A | G | 2 | a0001c0017t0010g0070a0001c0017t0010g0175 | 2 | HG02647.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1824+272T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 9/17 | chr4 | 17659686 | ||||||
| chr4:17659722
|
G | T | 1 | a0009c0011t0001g0032 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1824+236C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 9/17 | chr4 | 17659722 | ||||||
| chr4:17659737
|
C | T | 1 | a0028c0032t0062g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1824+221G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 9/17 | chr4 | 17659737 | ||||||
| chr4:17659770
|
G | A | 1 | a0019c0040t0065g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1824+188C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 9/17 | chr4 | 17659770 | ||||||
| chr4:17659775
|
C | T | 112 | a0001c0003t0023g0122a0001c0007t0004g0097a0001c0007t0008g0157others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1824+183G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 9/17 | chr4 | 17659775 | ||||||
| chr4:17659804
|
A | G | 1 | a0001c0003t0004g0169 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1824+154T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 9/17 | chr4 | 17659804 | ||||||
| chr4:17659911
|
G | A | 2 | a0002c0002t0001g0036a0002c0002t0001g0055 | 2 | HG01169.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1824+47C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 9/17 | chr4 | 17659911 | ||||||
| chr4:17660157
|
G | A | 1 | a0028c0032t0062g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1695-70C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17660157 | ||||||
| chr4:17660266
|
T | C | 104 | a0001c0004t0042g0108a0001c0007t0004g0097a0001c0007t0008g0157others(101): Show | 104 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.1695-179A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17660266 | ||||||
| chr4:17660454
|
G | T | 1 | a0025c0056t0061g0078 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1695-367C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17660454 | ||||||
| chr4:17660462
|
T | G | 3 | a0025c0056t0061g0078a0028c0032t0062g0172a0032c0061t0030g0007 | 3 | HG02572.hp1 HG03017.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.1695-375A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17660462 | ||||||
| chr4:17660528
|
C | T | 2 | a0023c0053t0012g0080a0024c0037t0052g0094 | 2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1695-441G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17660528 | ||||||
| chr4:17660613
|
C | A | 2 | a0002c0001t0001g0082a0002c0001t0001g0181 | 2 | HG02129.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.1695-526G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17660613 | ||||||
| chr4:17660737
|
A | C | 109 | a0001c0003t0023g0122a0001c0007t0004g0097a0001c0007t0008g0157others(106): Show | 109 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1695-650T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17660737 | ||||||
| chr4:17660761
|
TG | T | 13 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(10): Show | 13 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1695-675delC | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17660761 | ||||||
| chr4:17660784
|
C | T | 2 | a0009c0011t0001g0032a0009c0011t0056g0084 | 2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1695-697G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17660784 | ||||||
| chr4:17660785
|
A | G | 109 | a0001c0003t0023g0122a0001c0007t0004g0097a0001c0007t0008g0157others(106): Show | 109 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1695-698T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17660785 | ||||||
| chr4:17660848
|
T | C | 179 | a0001c0003t0007g0220a0001c0003t0018g0006a0001c0003t0019g0095others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.1695-761A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17660848 | ||||||
| chr4:17660864
|
A | T | 3 | a0025c0056t0061g0078a0028c0032t0062g0172a0032c0061t0030g0007 | 3 | HG02572.hp1 HG03017.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.1695-777T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17660864 | ||||||
| chr4:17660865
|
C | T | 9 | a0005c0036t0053g0233a0005c0042t0006g0093a0008c0034t0051g0010others(6): Show | 9 | HG01243.hp2 HG02145.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1695-778G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17660865 | ||||||
| chr4:17661000
|
C | T | 2 | a0002c0002t0001g0047a0002c0002t0001g0119 | 2 | HG00140.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1695-913G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17661000 | ||||||
| chr4:17661108
|
G | A | 100 | a0001c0003t0023g0122a0001c0007t0004g0097a0001c0007t0008g0157others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.1695-1021C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17661108 | ||||||
| chr4:17661189
|
C | G | 3 | a0005c0036t0053g0233a0005c0042t0006g0093a0021c0052t0050g0076 | 3 | HG02145.hp2 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1695-1102G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17661189 | ||||||
| chr4:17661209
|
A | G | 3 | a0025c0056t0061g0078a0028c0032t0062g0172a0032c0061t0030g0007 | 3 | HG02572.hp1 HG03017.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.1695-1122T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17661209 | ||||||
| chr4:17661322
|
G | C | 3 | a0001c0004t0009g0022a0001c0004t0025g0023a0001c0004t0025g0024 | 3 | HG02258.hp1 HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1695-1235C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17661322 | ||||||
| chr4:17661325
|
T | C | 1 | a0002c0002t0001g0040 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1695-1238A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17661325 | ||||||
| chr4:17661348
|
C | T | 1 | a0003c0009t0005g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1695-1261G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17661348 | ||||||
| chr4:17661445
|
T | G | 118 | a0001c0003t0023g0122a0001c0007t0004g0097a0001c0007t0008g0157others(115): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1695-1358A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17661445 | ||||||
| chr4:17661576
|
G | A | 153 | a0001c0003t0007g0220a0001c0003t0023g0122a0001c0004t0003g0207others(150): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1695-1489C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17661576 | ||||||
| chr4:17661605
|
C | A | 1 | a0001c0004t0026g0073 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1695-1518G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17661605 | ||||||
| chr4:17661656
|
G | C | 1 | a0002c0001t0001g0197 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1695-1569C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17661656 | ||||||
| chr4:17661719
|
G | A | 1 | a0025c0056t0061g0078 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1695-1632C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17661719 | ||||||
| chr4:17661791
|
A | G | 180 | a0001c0003t0007g0220a0001c0003t0018g0006a0001c0003t0019g0095others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.1695-1704T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17661791 | ||||||
| chr4:17661815
|
C | T | 1 | a0001c0003t0008g0216 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1695-1728G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17661815 | ||||||
| chr4:17662092
|
C | T | 61 | a0001c0003t0007g0220a0001c0003t0018g0006a0001c0003t0019g0095others(58): Show | 61 | HG00099.hp1 HG00423.hp1 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.1695-2005G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17662092 | ||||||
| chr4:17662133
|
A | T | 9 | a0004c0010t0006g0077a0004c0010t0006g0107a0004c0010t0006g0109others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1695-2046T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17662133 | ||||||
| chr4:17662278
|
G | A | 1 | a0020c0054t0001g0202 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1695-2191C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17662278 | ||||||
| chr4:17662317
|
A | G | 1 | a0001c0004t0042g0108 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1695-2230T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17662317 | ||||||
| chr4:17662344
|
CT | C | 151 | a0001c0003t0004g0169a0001c0003t0007g0220a0001c0003t0018g0006others(148): Show | 151 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1694+2217delA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17662344 | ||||||
| chr4:17662375
|
TCACA | T | 7 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(4): Show | 7 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1694+2183_1694+218 others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17662375 | ||||||
| chr4:17662438
|
A | G | 18 | a0001c0004t0003g0207a0001c0004t0003g0212a0001c0004t0003g0213others(15): Show | 18 | HG00423.hp1 HG01123.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1694+2124T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17662438 | ||||||
| chr4:17662523
|
C | T | 2 | a0028c0032t0062g0172a0032c0061t0030g0007 | 2 | HG03017.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.1694+2039G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17662523 | ||||||
| chr4:17662584
|
G | A | 1 | a0025c0056t0061g0078 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1694+1978C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17662584 | ||||||
| chr4:17662736
|
T | C | 1 | a0002c0002t0001g0040 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1694+1826A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17662736 | ||||||
| chr4:17662850
|
G | T | 99 | a0001c0003t0023g0122a0001c0007t0004g0097a0001c0007t0008g0157others(96): Show | 99 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.1694+1712C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17662850 | ||||||
| chr4:17663154
|
C | T | 1 | a0005c0036t0053g0233 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1694+1408G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17663154 | ||||||
| chr4:17663183
|
A | T | 170 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(167): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.1694+1379T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17663183 | ||||||
| chr4:17663216
|
C | T | 2 | a0028c0032t0062g0172a0032c0061t0030g0007 | 2 | HG03017.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.1694+1346G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17663216 | ||||||
| chr4:17663318
|
G | A | 2 | a0003c0009t0005g0195a0003c0018t0005g0192 | 2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1694+1244C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17663318 | ||||||
| chr4:17663409
|
A | G | 99 | a0001c0003t0023g0122a0001c0007t0004g0097a0001c0007t0008g0157others(96): Show | 99 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.1694+1153T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17663409 | ||||||
| chr4:17663479
|
C | G | 1 | a0009c0011t0001g0081 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1694+1083G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17663479 | ||||||
| chr4:17663486
|
T | G | 170 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(167): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.1694+1076A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17663486 | ||||||
| chr4:17663564
|
C | T | 1 | a0025c0056t0061g0078 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1694+998G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17663564 | ||||||
| chr4:17663615
|
A | AACACACA others(7): Show |
5 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0008t0018g0020others(2): Show | 5 | HG02630.hp1 HG03471.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1694+933_1694+946d others(16): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17663615 | ||||||
| chr4:17663615
|
A | AACACACA others(9): Show |
1 | a0001c0008t0019g0102 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1694+931_1694+946d others(18): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17663615 | ||||||
| chr4:17663615
|
A | AACACACA others(6): Show |
1 | a0032c0061t0030g0007 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1694+946_1694+947i others(15): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17663615 | ||||||
| chr4:17663615
|
A | AACACACA others(8): Show |
1 | a0028c0032t0062g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1694+946_1694+947i others(17): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17663615 | ||||||
| chr4:17663615
|
A | T | 50 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(47): Show | 50 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1694+947T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17663615 | ||||||
| chr4:17663615
|
AAC | A | 58 | a0001c0004t0003g0207a0001c0004t0003g0212a0001c0004t0003g0213others(55): Show | 58 | HG00099.hp1 HG00423.hp1 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.1694+945_1694+946d others(4): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17663615 | ||||||
| chr4:17663615
|
AACAC | A | 3 | a0001c0004t0042g0108a0002c0001t0017g0091a0002c0001t0017g0137 | 3 | HG02698.hp2 HG03239.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1694+943_1694+946d others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17663615 | ||||||
| chr4:17663615
|
AACACAC | A | 94 | a0001c0003t0023g0122a0001c0007t0004g0097a0001c0007t0008g0157others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.1694+941_1694+946d others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17663615 | ||||||
| chr4:17663622
|
A | ACAC | 50 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(47): Show | 50 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1694+937_1694+939d others(5): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17663622 | ||||||
| chr4:17663634
|
A | C | 50 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(47): Show | 50 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1694+928T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17663634 | ||||||
| chr4:17663689
|
G | A | 1 | a0002c0002t0001g0217 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1694+873C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17663689 | ||||||
| chr4:17663778
|
C | T | 11 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(8): Show | 11 | HG01243.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1694+784G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17663778 | ||||||
| chr4:17663809
|
T | C | 9 | a0001c0004t0042g0108a0001c0017t0010g0070a0001c0017t0010g0103others(6): Show | 9 | HG00099.hp1 HG01516.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1694+753A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17663809 | ||||||
| chr4:17663833
|
C | T | 100 | a0001c0003t0023g0122a0001c0007t0004g0097a0001c0007t0008g0157others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.1694+729G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17663833 | ||||||
| chr4:17663875
|
A | T | 50 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(47): Show | 50 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1694+687T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17663875 | ||||||
| chr4:17664041
|
G | A | 7 | a0002c0001t0001g0082a0002c0001t0001g0101a0002c0001t0001g0152others(4): Show | 7 | HG00597.hp2 HG02129.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.1694+521C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17664041 | ||||||
| chr4:17664051
|
A | G | 1 | a0032c0061t0030g0007 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1694+511T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17664051 | ||||||
| chr4:17664218
|
C | A | 2 | a0023c0053t0012g0080a0024c0037t0052g0094 | 2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1694+344G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17664218 | ||||||
| chr4:17664481
|
A | C | 2 | a0005c0036t0053g0233a0005c0042t0006g0093 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1694+81T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 8/17 | chr4 | 17664481 | ||||||
| chr4:17664665
|
G | T | 1 | a0008c0034t0051g0010 | 1 | HG02922.hp2 | splice_region_variant&intron_variant | LOW | c.1597-6C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17664665 | ||||||
| chr4:17664680
|
G | GA | 12 | a0001c0004t0042g0108a0001c0017t0010g0070a0001c0017t0010g0103others(9): Show | 12 | HG00099.hp1 HG01516.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1597-22dupT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17664680 | ||||||
| chr4:17664680
|
GA | G | 12 | a0001c0003t0007g0220a0001c0004t0009g0017a0001c0004t0009g0022others(9): Show | 12 | HG00280.hp1 HG02258.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1597-22delT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17664680 | ||||||
| chr4:17664680
|
GAA | G | 7 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(4): Show | 7 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1597-23_1597-22del others(2): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17664680 | ||||||
| chr4:17664793
|
C | T | 50 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(47): Show | 50 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1597-134G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17664793 | ||||||
| chr4:17664838
|
A | T | 7 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(4): Show | 7 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1597-179T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17664838 | ||||||
| chr4:17664878
|
C | T | 3 | a0005c0036t0053g0233a0005c0042t0006g0093a0021c0052t0050g0076 | 3 | HG02145.hp2 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1597-219G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17664878 | ||||||
| chr4:17665018
|
G | C | 7 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0007t0019g0143others(4): Show | 7 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1597-359C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17665018 | ||||||
| chr4:17665026
|
C | G | 4 | a0007c0041t0012g0011a0007c0043t0012g0105a0007c0050t0012g0004others(1): Show | 4 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.1597-367G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17665026 | ||||||
| chr4:17665205
|
C | T | 1 | a0023c0053t0012g0080 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1597-546G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17665205 | ||||||
| chr4:17665212
|
G | A | 1 | a0028c0032t0062g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1597-553C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17665212 | ||||||
| chr4:17665468
|
C | T | 1 | a0005c0030t0015g0033 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1597-809G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17665468 | ||||||
| chr4:17665482
|
T | C | 4 | a0008c0034t0051g0010a0008c0039t0015g0016a0008c0049t0034g0112others(1): Show | 4 | HG01243.hp2 HG02922.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1597-823A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17665482 | ||||||
| chr4:17665641
|
G | A | 1 | a0021c0052t0050g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1597-982C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17665641 | ||||||
| chr4:17665678
|
C | T | 1 | a0020c0054t0001g0202 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1597-1019G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17665678 | ||||||
| chr4:17665798
|
G | A | 26 | a0001c0004t0003g0207a0001c0004t0003g0212a0001c0004t0003g0213others(23): Show | 26 | HG00423.hp1 HG01123.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.1597-1139C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17665798 | ||||||
| chr4:17665898
|
G | GC | 52 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(49): Show | 52 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1597-1240dupG | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17665898 | ||||||
| chr4:17665931
|
T | C | 2 | a0005c0036t0053g0233a0005c0042t0006g0093 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1597-1272A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17665931 | ||||||
| chr4:17665966
|
C | T | 1 | a0002c0016t0001g0074 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1597-1307G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17665966 | ||||||
| chr4:17666124
|
T | G | 26 | a0001c0004t0003g0207a0001c0004t0003g0212a0001c0004t0003g0213others(23): Show | 26 | HG00423.hp1 HG01123.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.1597-1465A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17666124 | ||||||
| chr4:17666143
|
G | A | 51 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(48): Show | 51 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.1597-1484C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17666143 | ||||||
| chr4:17666188
|
C | G | 1 | a0028c0032t0062g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1597-1529G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17666188 | ||||||
| chr4:17666305
|
C | CT | 22 | a0001c0003t0046g0059a0001c0005t0007g0013a0001c0005t0007g0125others(19): Show | 22 | HG00323.hp2 HG02145.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.1597-1647dupA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17666305 | ||||||
| chr4:17666305
|
C | CTT | 49 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0206others(46): Show | 49 | HG00140.hp1 HG00280.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1597-1648_1597-164 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17666305 | ||||||
| chr4:17666305
|
CT | C | 32 | a0001c0003t0002g0069a0001c0004t0003g0207a0001c0004t0003g0212others(29): Show | 32 | HG00423.hp1 HG01109.hp2 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.1597-1647delA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17666305 | ||||||
| chr4:17666364
|
C | T | 117 | a0001c0003t0023g0122a0001c0007t0004g0097a0001c0007t0008g0157others(114): Show | 117 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1597-1705G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17666364 | ||||||
| chr4:17666365
|
G | A | 1 | a0015c0063t0054g0229 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1597-1706C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17666365 | ||||||
| chr4:17666469
|
C | CT | 56 | a0001c0003t0002g0069a0001c0003t0018g0006a0001c0003t0019g0095others(53): Show | 56 | HG00423.hp1 HG01109.hp2 HG01123.hp1 others(53): Show |
intron_variant | MODIFIER | c.1597-1811dupA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17666469 | ||||||
| chr4:17666469
|
C | CTT | 18 | a0001c0004t0042g0108a0001c0006t0003g0029a0001c0006t0048g0027others(15): Show | 18 | HG00558.hp2 HG00609.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.1597-1812_1597-181 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17666469 | ||||||
| chr4:17666469
|
C | CTTT | 73 | a0001c0003t0023g0122a0001c0007t0004g0097a0001c0007t0008g0157others(70): Show | 73 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.1597-1813_1597-181 others(7): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17666469 | ||||||
| chr4:17666469
|
C | CTTTT | 65 | a0001c0003t0002g0019a0001c0003t0002g0158a0001c0003t0002g0206others(62): Show | 65 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.1597-1814_1597-181 others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17666469 | ||||||
| chr4:17666469
|
C | CTTTTT | 15 | a0001c0003t0002g0149a0001c0003t0008g0208a0001c0003t0008g0216others(12): Show | 15 | HG00597.hp2 HG01175.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.1597-1815_1597-181 others(9): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17666469 | ||||||
| chr4:17666516
|
G | A | 1 | a0002c0001t0001g0190 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1597-1857C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17666516 | ||||||
| chr4:17666577
|
G | A | 52 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(49): Show | 52 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1597-1918C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17666577 | ||||||
| chr4:17666584
|
A | T | 1 | a0031c0027t0001g0088 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1597-1925T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17666584 | ||||||
| chr4:17666731
|
C | T | 1 | a0002c0002t0001g0114 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1597-2072G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17666731 | ||||||
| chr4:17666845
|
C | A | 1 | a0028c0032t0062g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1597-2186G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17666845 | ||||||
| chr4:17666881
|
C | A | 113 | a0001c0003t0023g0122a0001c0007t0004g0097a0001c0007t0008g0157others(110): Show | 113 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1597-2222G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17666881 | ||||||
| chr4:17666939
|
TTTTTTTT others(1): Show |
T | 9 | a0001c0004t0042g0108a0001c0017t0010g0070a0001c0017t0010g0103others(6): Show | 9 | HG00099.hp1 HG01516.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1597-2288_1597-228 others(12): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17666939 | ||||||
| chr4:17666994
|
C | T | 7 | a0001c0003t0002g0069a0002c0016t0001g0071a0002c0016t0001g0074others(4): Show | 7 | HG01109.hp2 HG01884.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1597-2335G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17666994 | ||||||
| chr4:17667015
|
G | C | 5 | a0004c0010t0006g0077a0004c0010t0006g0107a0004c0010t0006g0109others(2): Show | 5 | HG02451.hp1 HG02897.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1597-2356C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17667015 | ||||||
| chr4:17667264
|
C | T | 1 | a0001c0003t0004g0018 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1597-2605G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17667264 | ||||||
| chr4:17667494
|
C | T | 6 | a0001c0003t0018g0006a0001c0007t0019g0143a0001c0008t0018g0020others(3): Show | 6 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-2835G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17667494 | ||||||
| chr4:17667528
|
C | T | 1 | a0021c0052t0050g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1597-2869G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17667528 | ||||||
| chr4:17667562
|
G | A | 100 | a0001c0003t0023g0122a0001c0007t0004g0097a0001c0007t0008g0157others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.1597-2903C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17667562 | ||||||
| chr4:17667590
|
G | C | 1 | a0004c0010t0006g0077 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1597-2931C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17667590 | ||||||
| chr4:17667695
|
C | T | 2 | a0028c0032t0062g0172a0032c0061t0030g0007 | 2 | HG03017.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.1597-3036G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17667695 | ||||||
| chr4:17667849
|
A | G | 193 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1597-3190T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17667849 | ||||||
| chr4:17668101
|
G | A | 6 | a0001c0003t0018g0006a0001c0007t0019g0143a0001c0008t0018g0020others(3): Show | 6 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-3442C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17668101 | ||||||
| chr4:17668159
|
A | T | 1 | a0002c0001t0001g0226 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1597-3500T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17668159 | ||||||
| chr4:17668169
|
T | C | 5 | a0004c0010t0006g0077a0004c0010t0006g0107a0004c0010t0006g0109others(2): Show | 5 | HG02451.hp1 HG02897.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1597-3510A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17668169 | ||||||
| chr4:17668215
|
G | A | 1 | a0002c0001t0017g0091 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1597-3556C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17668215 | ||||||
| chr4:17668280
|
T | C | 1 | a0028c0032t0062g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1597-3621A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17668280 | ||||||
| chr4:17668329
|
T | C | 1 | a0002c0002t0001g0046 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1597-3670A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17668329 | ||||||
| chr4:17668484
|
G | T | 52 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(49): Show | 52 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1597-3825C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17668484 | ||||||
| chr4:17668555
|
C | T | 3 | a0007c0041t0012g0011a0023c0053t0012g0080a0024c0037t0052g0094 | 3 | HG01891.hp1 HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1597-3896G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17668555 | ||||||
| chr4:17668811
|
C | T | 1 | a0002c0001t0001g0002 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1597-4152G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17668811 | ||||||
| chr4:17669041
|
G | C | 54 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(51): Show | 54 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.1597-4382C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17669041 | ||||||
| chr4:17669054
|
C | T | 191 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.1597-4395G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17669054 | ||||||
| chr4:17669199
|
A | G | 1 | a0003c0009t0005g0195 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1597-4540T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17669199 | ||||||
| chr4:17669238
|
T | C | 100 | a0001c0003t0023g0122a0001c0007t0004g0097a0001c0007t0008g0157others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.1597-4579A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17669238 | ||||||
| chr4:17669369
|
T | C | 7 | a0001c0003t0002g0069a0002c0016t0001g0071a0002c0016t0001g0074others(4): Show | 7 | HG01109.hp2 HG01884.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1597-4710A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17669369 | ||||||
| chr4:17669572
|
A | G | 216 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1597-4913T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17669572 | ||||||
| chr4:17669677
|
C | T | 2 | a0023c0053t0012g0080a0024c0037t0052g0094 | 2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1597-5018G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17669677 | ||||||
| chr4:17669683
|
C | T | 6 | a0001c0003t0018g0006a0001c0007t0019g0143a0001c0008t0018g0020others(3): Show | 6 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-5024G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17669683 | ||||||
| chr4:17669859
|
AT | A | 2 | a0023c0053t0012g0080a0024c0037t0052g0094 | 2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1597-5201delA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17669859 | ||||||
| chr4:17669951
|
A | G | 6 | a0001c0003t0018g0006a0001c0007t0019g0143a0001c0008t0018g0020others(3): Show | 6 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-5292T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17669951 | ||||||
| chr4:17670615
|
A | G | 9 | a0001c0004t0042g0108a0001c0017t0010g0070a0001c0017t0010g0103others(6): Show | 9 | HG00099.hp1 HG01516.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1597-5956T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17670615 | ||||||
| chr4:17670739
|
A | G | 1 | a0001c0047t0010g0113 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1597-6080T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17670739 | ||||||
| chr4:17670842
|
A | G | 9 | a0001c0004t0042g0108a0001c0017t0010g0070a0001c0017t0010g0103others(6): Show | 9 | HG00099.hp1 HG01516.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1597-6183T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17670842 | ||||||
| chr4:17670866
|
G | T | 6 | a0001c0003t0018g0006a0001c0007t0019g0143a0001c0008t0018g0020others(3): Show | 6 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-6207C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17670866 | ||||||
| chr4:17671036
|
A | C | 1 | a0002c0001t0001g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1597-6377T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17671036 | ||||||
| chr4:17671040
|
A | C | 3 | a0001c0003t0018g0006a0001c0008t0018g0020a0001c0021t0064g0005 | 3 | HG02630.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1597-6381T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17671040 | ||||||
| chr4:17671141
|
T | C | 7 | a0001c0003t0002g0069a0002c0016t0001g0071a0002c0016t0001g0074others(4): Show | 7 | HG01109.hp2 HG01884.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1597-6482A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17671141 | ||||||
| chr4:17671261
|
T | C | 193 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1597-6602A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17671261 | ||||||
| chr4:17671313
|
C | A | 1 | a0004c0035t0006g0139 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1597-6654G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17671313 | ||||||
| chr4:17671473
|
G | A | 6 | a0001c0003t0018g0006a0001c0007t0019g0143a0001c0008t0018g0020others(3): Show | 6 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-6814C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17671473 | ||||||
| chr4:17671703
|
G | A | 6 | a0001c0003t0018g0006a0001c0007t0019g0143a0001c0008t0018g0020others(3): Show | 6 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-7044C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17671703 | ||||||
| chr4:17671783
|
G | C | 1 | a0002c0001t0001g0197 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1597-7124C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17671783 | ||||||
| chr4:17671865
|
G | T | 6 | a0001c0003t0018g0006a0001c0007t0019g0143a0001c0008t0018g0020others(3): Show | 6 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-7206C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17671865 | ||||||
| chr4:17671950
|
C | CA | 107 | a0001c0003t0002g0069a0001c0003t0023g0122a0001c0007t0004g0097others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1597-7292dupT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17671950 | ||||||
| chr4:17672054
|
C | A | 6 | a0001c0003t0018g0006a0001c0007t0019g0143a0001c0008t0018g0020others(3): Show | 6 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-7395G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17672054 | ||||||
| chr4:17672117
|
A | G | 1 | a0001c0003t0011g0166 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1597-7458T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17672117 | ||||||
| chr4:17672180
|
C | T | 6 | a0001c0003t0018g0006a0001c0007t0019g0143a0001c0008t0018g0020others(3): Show | 6 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-7521G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17672180 | ||||||
| chr4:17672258
|
T | TA | 180 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(177): Show | 180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.1597-7600dupT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17672258 | ||||||
| chr4:17672276
|
A | C | 1 | a0032c0061t0030g0007 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1597-7617T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17672276 | ||||||
| chr4:17672290
|
G | A | 2 | a0028c0032t0062g0172a0032c0061t0030g0007 | 2 | HG03017.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.1597-7631C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17672290 | ||||||
| chr4:17672298
|
C | G | 1 | a0021c0052t0050g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1597-7639G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17672298 | ||||||
| chr4:17672411
|
G | C | 1 | a0011c0023t0043g0204 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1597-7752C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17672411 | ||||||
| chr4:17672534
|
C | T | 194 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1597-7875G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17672534 | ||||||
| chr4:17672589
|
G | C | 1 | a0004c0010t0006g0109 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1597-7930C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17672589 | ||||||
| chr4:17672658
|
C | G | 3 | a0002c0001t0017g0091a0002c0001t0017g0137a0002c0001t0017g0138 | 3 | HG01123.hp2 HG02698.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1597-7999G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17672658 | ||||||
| chr4:17672707
|
C | T | 1 | a0015c0063t0054g0229 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1597-8048G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17672707 | ||||||
| chr4:17672926
|
A | G | 1 | a0002c0001t0001g0218 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1597-8267T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17672926 | ||||||
| chr4:17672935
|
C | A | 128 | a0001c0003t0002g0069a0001c0003t0018g0006a0001c0003t0023g0122others(125): Show | 128 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1597-8276G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17672935 | ||||||
| chr4:17673032
|
C | T | 122 | a0001c0003t0002g0069a0001c0003t0023g0122a0001c0007t0004g0097others(119): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1597-8373G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17673032 | ||||||
| chr4:17673065
|
C | T | 4 | a0002c0001t0001g0147a0002c0002t0001g0171a0002c0002t0001g0203others(1): Show | 4 | HG02129.hp2 HG02257.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.1597-8406G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17673065 | ||||||
| chr4:17673265
|
T | C | 2 | a0001c0003t0004g0067a0001c0003t0004g0169 | 2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1597-8606A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17673265 | ||||||
| chr4:17673338
|
T | C | 6 | a0003c0009t0005g0009a0003c0009t0005g0133a0003c0009t0005g0162others(3): Show | 6 | HG02109.hp1 HG02559.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1597-8679A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17673338 | ||||||
| chr4:17673396
|
C | A | 39 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.1597-8737G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17673396 | ||||||
| chr4:17673533
|
C | T | 1 | a0003c0009t0005g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1597-8874G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17673533 | ||||||
| chr4:17673771
|
T | G | 128 | a0001c0003t0002g0069a0001c0003t0018g0006a0001c0003t0023g0122others(125): Show | 128 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1597-9112A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17673771 | ||||||
| chr4:17673814
|
T | A | 1 | a0028c0032t0062g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1597-9155A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17673814 | ||||||
| chr4:17673841
|
C | CA | 192 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.1597-9183dupT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17673841 | ||||||
| chr4:17673926
|
T | A | 7 | a0001c0003t0018g0006a0001c0007t0019g0143a0001c0008t0018g0020others(4): Show | 7 | HG02451.hp2 HG02523.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1597-9267A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17673926 | ||||||
| chr4:17673969
|
C | G | 107 | a0001c0003t0002g0069a0001c0003t0023g0122a0001c0007t0004g0097others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1597-9310G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17673969 | ||||||
| chr4:17674036
|
T | A | 1 | a0002c0001t0001g0086 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1597-9377A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17674036 | ||||||
| chr4:17674309
|
A | G | 67 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(64): Show | 67 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.1597-9650T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17674309 | ||||||
| chr4:17674315
|
A | T | 2 | a0002c0001t0001g0135a0022c0045t0001g0061 | 2 | HG00558.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.1597-9656T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17674315 | ||||||
| chr4:17674434
|
T | A | 1 | a0002c0001t0001g0131 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1597-9775A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17674434 | ||||||
| chr4:17674574
|
G | T | 5 | a0004c0010t0006g0077a0004c0010t0006g0107a0004c0010t0006g0109others(2): Show | 5 | HG02451.hp1 HG02897.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1597-9915C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17674574 | ||||||
| chr4:17674581
|
T | C | 19 | a0001c0004t0003g0207a0001c0004t0003g0212a0001c0004t0003g0213others(16): Show | 19 | HG00423.hp1 HG01123.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.1597-9922A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17674581 | ||||||
| chr4:17674648
|
A | G | 1 | a0001c0003t0066g0150 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1597-9989T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17674648 | ||||||
| chr4:17674683
|
G | T | 5 | a0001c0003t0002g0227a0001c0003t0004g0057a0001c0003t0046g0059others(2): Show | 5 | HG00323.hp2 HG01346.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.1597-10024C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17674683 | ||||||
| chr4:17674763
|
A | C | 107 | a0001c0003t0002g0069a0001c0003t0023g0122a0001c0007t0004g0097others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1597-10104T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17674763 | ||||||
| chr4:17674814
|
C | G | 107 | a0001c0003t0002g0069a0001c0003t0023g0122a0001c0007t0004g0097others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1597-10155G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17674814 | ||||||
| chr4:17674853
|
C | A | 107 | a0001c0003t0002g0069a0001c0003t0023g0122a0001c0007t0004g0097others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1597-10194G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17674853 | ||||||
| chr4:17674906
|
A | G | 6 | a0001c0003t0018g0006a0001c0007t0019g0143a0001c0008t0018g0020others(3): Show | 6 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-10247T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17674906 | ||||||
| chr4:17674990
|
GT | G | 6 | a0001c0003t0018g0006a0001c0007t0019g0143a0001c0008t0018g0020others(3): Show | 6 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-10332delA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17674990 | ||||||
| chr4:17675167
|
G | A | 6 | a0001c0003t0018g0006a0001c0007t0019g0143a0001c0008t0018g0020others(3): Show | 6 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-10508C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17675167 | ||||||
| chr4:17675248
|
G | T | 79 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1597-10589C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17675248 | ||||||
| chr4:17675373
|
A | C | 7 | a0001c0003t0002g0069a0002c0016t0001g0071a0002c0016t0001g0074others(4): Show | 7 | HG01109.hp2 HG01884.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1597-10714T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17675373 | ||||||
| chr4:17675450
|
T | G | 2 | a0028c0032t0062g0172a0032c0061t0030g0007 | 2 | HG03017.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.1597-10791A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17675450 | ||||||
| chr4:17675540
|
G | A | 77 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.1597-10881C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17675540 | ||||||
| chr4:17675567
|
T | C | 1 | a0008c0049t0034g0112 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1597-10908A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17675567 | ||||||
| chr4:17675614
|
T | A | 6 | a0001c0003t0018g0006a0001c0007t0019g0143a0001c0008t0018g0020others(3): Show | 6 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-10955A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17675614 | ||||||
| chr4:17675667
|
G | A | 1 | a0010c0013t0024g0211 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1597-11008C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17675667 | ||||||
| chr4:17675673
|
C | T | 2 | a0028c0032t0062g0172a0032c0061t0030g0007 | 2 | HG03017.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.1597-11014G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17675673 | ||||||
| chr4:17675682
|
C | G | 107 | a0001c0003t0002g0069a0001c0003t0023g0122a0001c0007t0004g0097others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1597-11023G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17675682 | ||||||
| chr4:17675849
|
A | G | 1 | a0002c0001t0001g0131 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1597-11190T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17675849 | ||||||
| chr4:17675894
|
GGGAATGT others(3): Show |
G | 1 | a0032c0061t0030g0007 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1597-11245_1597-11 others(16): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17675894 | ||||||
| chr4:17675942
|
C | G | 67 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(64): Show | 67 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.1597-11283G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17675942 | ||||||
| chr4:17676606
|
T | G | 1 | a0001c0006t0003g0031 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1596+11818A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17676606 | ||||||
| chr4:17676651
|
T | C | 2 | a0023c0053t0012g0080a0024c0037t0052g0094 | 2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1596+11773A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17676651 | ||||||
| chr4:17676809
|
TGTACA | T | 216 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1596+11610_1596+11 others(11): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17676809 | ||||||
| chr4:17676833
|
C | T | 100 | a0001c0003t0023g0122a0001c0007t0004g0097a0001c0007t0008g0157others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.1596+11591G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17676833 | ||||||
| chr4:17676977
|
C | T | 106 | a0001c0003t0018g0006a0001c0003t0023g0122a0001c0007t0004g0097others(103): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1596+11447G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17676977 | ||||||
| chr4:17677026
|
G | A | 113 | a0001c0003t0002g0069a0001c0003t0018g0006a0001c0003t0023g0122others(110): Show | 113 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1596+11398C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17677026 | ||||||
| chr4:17677080
|
C | T | 1 | a0028c0032t0062g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1596+11344G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17677080 | ||||||
| chr4:17677104
|
G | A | 2 | a0001c0017t0010g0103a0030c0051t0010g0041 | 2 | HG00099.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1596+11320C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17677104 | ||||||
| chr4:17677182
|
G | A | 1 | a0001c0004t0003g0213 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1596+11242C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17677182 | ||||||
| chr4:17677204
|
C | T | 4 | a0007c0041t0012g0011a0007c0043t0012g0105a0007c0050t0012g0004others(1): Show | 4 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+11220G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17677204 | ||||||
| chr4:17677551
|
A | T | 107 | a0001c0003t0002g0069a0001c0003t0023g0122a0001c0007t0004g0097others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1596+10873T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17677551 | ||||||
| chr4:17677654
|
C | G | 2 | a0023c0053t0012g0080a0024c0037t0052g0094 | 2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1596+10770G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17677654 | ||||||
| chr4:17677970
|
TC | T | 100 | a0001c0003t0023g0122a0001c0007t0004g0097a0001c0007t0008g0157others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.1596+10453delG | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17677970 | ||||||
| chr4:17678045
|
C | A | 1 | a0001c0006t0003g0132 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1596+10379G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17678045 | ||||||
| chr4:17678072
|
C | T | 113 | a0001c0003t0002g0069a0001c0003t0018g0006a0001c0003t0023g0122others(110): Show | 113 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1596+10352G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17678072 | ||||||
| chr4:17678128
|
T | C | 77 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.1596+10296A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17678128 | ||||||
| chr4:17678135
|
A | G | 1 | a0024c0037t0052g0094 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1596+10289T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17678135 | ||||||
| chr4:17678329
|
G | A | 2 | a0002c0002t0001g0050a0002c0002t0001g0210 | 2 | HG00639.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1596+10095C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17678329 | ||||||
| chr4:17678381
|
C | T | 5 | a0004c0010t0006g0077a0004c0010t0006g0107a0004c0010t0006g0109others(2): Show | 5 | HG02451.hp1 HG02897.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+10043G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17678381 | ||||||
| chr4:17678525
|
T | C | 113 | a0001c0003t0002g0069a0001c0003t0018g0006a0001c0003t0023g0122others(110): Show | 113 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1596+9899A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17678525 | ||||||
| chr4:17678633
|
C | T | 106 | a0001c0003t0018g0006a0001c0003t0023g0122a0001c0007t0004g0097others(103): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1596+9791G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17678633 | ||||||
| chr4:17678669
|
G | A | 100 | a0001c0003t0023g0122a0001c0007t0004g0097a0001c0007t0008g0157others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.1596+9755C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17678669 | ||||||
| chr4:17678692
|
A | G | 1 | a0024c0037t0052g0094 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1596+9732T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17678692 | ||||||
| chr4:17678693
|
T | C | 1 | a0002c0001t0001g0214 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1596+9731A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17678693 | ||||||
| chr4:17678768
|
A | G | 10 | a0003c0009t0005g0009a0003c0009t0005g0133a0003c0009t0005g0162others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1596+9656T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17678768 | ||||||
| chr4:17678791
|
A | G | 5 | a0001c0003t0002g0227a0001c0003t0004g0057a0001c0003t0046g0059others(2): Show | 5 | HG00323.hp2 HG01346.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+9633T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17678791 | ||||||
| chr4:17678800
|
A | G | 2 | a0023c0053t0012g0080a0024c0037t0052g0094 | 2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1596+9624T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17678800 | ||||||
| chr4:17678925
|
G | C | 13 | a0001c0003t0002g0069a0001c0003t0018g0006a0001c0007t0019g0143others(10): Show | 13 | HG01109.hp2 HG01884.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1596+9499C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17678925 | ||||||
| chr4:17679275
|
T | C | 113 | a0001c0003t0002g0069a0001c0003t0018g0006a0001c0003t0023g0122others(110): Show | 113 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1596+9149A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17679275 | ||||||
| chr4:17679374
|
A | G | 19 | a0001c0004t0003g0207a0001c0004t0003g0212a0001c0004t0003g0213others(16): Show | 19 | HG00423.hp1 HG01123.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.1596+9050T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17679374 | ||||||
| chr4:17679397
|
T | C | 2 | a0001c0017t0010g0103a0030c0051t0010g0041 | 2 | HG00099.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1596+9027A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17679397 | ||||||
| chr4:17679643
|
A | G | 1 | a0001c0015t0029g0164 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1596+8781T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17679643 | ||||||
| chr4:17679724
|
G | T | 1 | a0001c0006t0028g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1596+8700C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17679724 | ||||||
| chr4:17679794
|
G | A | 2 | a0023c0053t0012g0080a0024c0037t0052g0094 | 2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1596+8630C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17679794 | ||||||
| chr4:17679799
|
TA | T | 117 | a0001c0003t0002g0069a0001c0003t0023g0122a0001c0007t0004g0097others(114): Show | 117 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1596+8624delT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17679799 | ||||||
| chr4:17679849
|
A | G | 1 | a0002c0002t0001g0040 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1596+8575T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17679849 | ||||||
| chr4:17680272
|
G | A | 2 | a0002c0001t0001g0218a0002c0002t0001g0176 | 2 | HG02602.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1596+8152C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17680272 | ||||||
| chr4:17680303
|
G | A | 6 | a0001c0003t0018g0006a0001c0007t0019g0143a0001c0008t0018g0020others(3): Show | 6 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+8121C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17680303 | ||||||
| chr4:17680407
|
G | A | 115 | a0001c0003t0002g0069a0001c0003t0018g0006a0001c0003t0023g0122others(112): Show | 115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1596+8017C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17680407 | ||||||
| chr4:17680455
|
T | C | 3 | a0001c0007t0019g0143a0001c0008t0019g0102a0001c0021t0018g0068 | 3 | HG02451.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1596+7969A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17680455 | ||||||
| chr4:17680481
|
A | G | 15 | a0003c0009t0005g0009a0003c0009t0005g0133a0003c0009t0005g0162others(12): Show | 15 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1596+7943T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17680481 | ||||||
| chr4:17680507
|
T | C | 194 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1596+7917A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17680507 | ||||||
| chr4:17680572
|
T | A | 1 | a0002c0002t0001g0176 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1596+7852A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17680572 | ||||||
| chr4:17680595
|
C | T | 77 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.1596+7829G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17680595 | ||||||
| chr4:17680639
|
A | G | 194 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1596+7785T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17680639 | ||||||
| chr4:17680671
|
G | A | 3 | a0002c0002t0001g0049a0002c0002t0001g0050a0002c0002t0001g0210 | 3 | HG00639.hp1 HG00642.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1596+7753C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17680671 | ||||||
| chr4:17680686
|
G | A | 1 | a0001c0003t0046g0059 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1596+7738C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17680686 | ||||||
| chr4:17680736
|
T | C | 3 | a0001c0007t0019g0143a0001c0008t0019g0102a0001c0021t0018g0068 | 3 | HG02451.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1596+7688A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17680736 | ||||||
| chr4:17680971
|
G | T | 2 | a0023c0053t0012g0080a0024c0037t0052g0094 | 2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1596+7453C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17680971 | ||||||
| chr4:17680974
|
C | T | 97 | a0001c0003t0023g0122a0001c0007t0004g0097a0001c0007t0008g0157others(94): Show | 97 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1596+7450G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17680974 | ||||||
| chr4:17681055
|
A | T | 2 | a0001c0006t0003g0182a0001c0033t0003g0200 | 2 | NA18998.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1596+7369T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17681055 | ||||||
| chr4:17681114
|
A | G | 1 | a0001c0005t0014g0170 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1596+7310T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17681114 | ||||||
| chr4:17681126
|
G | T | 1 | a0021c0052t0050g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1596+7298C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17681126 | ||||||
| chr4:17681211
|
T | C | 112 | a0001c0003t0023g0122a0001c0007t0004g0097a0001c0007t0008g0157others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1596+7213A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17681211 | ||||||
| chr4:17681252
|
G | A | 1 | a0002c0001t0001g0186 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1596+7172C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17681252 | ||||||
| chr4:17681523
|
G | T | 1 | a0001c0003t0002g0206 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1596+6901C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17681523 | ||||||
| chr4:17681595
|
C | T | 1 | a0001c0060t0027g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1596+6829G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17681595 | ||||||
| chr4:17681596
|
G | A | 100 | a0001c0003t0023g0122a0001c0007t0004g0097a0001c0007t0008g0157others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.1596+6828C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17681596 | ||||||
| chr4:17681724
|
T | C | 6 | a0001c0003t0018g0006a0001c0007t0019g0143a0001c0008t0018g0020others(3): Show | 6 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+6700A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17681724 | ||||||
| chr4:17681765
|
G | C | 6 | a0001c0003t0018g0006a0001c0007t0019g0143a0001c0008t0018g0020others(3): Show | 6 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+6659C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17681765 | ||||||
| chr4:17681999
|
C | G | 1 | a0002c0001t0001g0135 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1596+6425G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17681999 | ||||||
| chr4:17682012
|
G | C | 6 | a0001c0003t0018g0006a0001c0007t0019g0143a0001c0008t0018g0020others(3): Show | 6 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+6412C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17682012 | ||||||
| chr4:17682142
|
C | T | 19 | a0001c0004t0003g0207a0001c0004t0003g0212a0001c0004t0003g0213others(16): Show | 19 | HG00423.hp1 HG01123.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.1596+6282G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17682142 | ||||||
| chr4:17682157
|
A | G | 216 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1596+6267T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17682157 | ||||||
| chr4:17682188
|
G | A | 108 | a0001c0003t0002g0069a0001c0003t0023g0122a0001c0007t0004g0097others(105): Show | 108 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1596+6236C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17682188 | ||||||
| chr4:17682293
|
T | A | 76 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(73): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.1596+6131A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17682293 | ||||||
| chr4:17682431
|
C | T | 1 | a0001c0003t0023g0122 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1596+5993G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17682431 | ||||||
| chr4:17682563
|
G | A | 103 | a0001c0003t0018g0006a0001c0007t0004g0097a0001c0007t0008g0157others(100): Show | 103 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1596+5861C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17682563 | ||||||
| chr4:17682641
|
G | C | 1 | a0032c0061t0030g0007 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1596+5783C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17682641 | ||||||
| chr4:17682711
|
C | G | 108 | a0001c0003t0002g0069a0001c0003t0023g0122a0001c0007t0004g0097others(105): Show | 108 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1596+5713G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17682711 | ||||||
| chr4:17682722
|
C | T | 1 | a0002c0002t0001g0119 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1596+5702G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17682722 | ||||||
| chr4:17682769
|
G | T | 108 | a0001c0003t0002g0069a0001c0003t0023g0122a0001c0007t0004g0097others(105): Show | 108 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1596+5655C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17682769 | ||||||
| chr4:17683086
|
A | T | 1 | a0002c0001t0001g0141 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1596+5338T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17683086 | ||||||
| chr4:17683207
|
G | T | 2 | a0028c0032t0062g0172a0032c0061t0030g0007 | 2 | HG03017.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.1596+5217C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17683207 | ||||||
| chr4:17683263
|
A | G | 108 | a0001c0003t0002g0069a0001c0003t0023g0122a0001c0007t0004g0097others(105): Show | 108 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1596+5161T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17683263 | ||||||
| chr4:17683279
|
A | T | 6 | a0001c0003t0018g0006a0001c0007t0019g0143a0001c0008t0018g0020others(3): Show | 6 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+5145T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17683279 | ||||||
| chr4:17683328
|
G | A | 114 | a0001c0003t0002g0069a0001c0003t0018g0006a0001c0003t0023g0122others(111): Show | 114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.1596+5096C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17683328 | ||||||
| chr4:17683685
|
G | T | 108 | a0001c0003t0002g0069a0001c0003t0023g0122a0001c0007t0004g0097others(105): Show | 108 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1596+4739C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17683685 | ||||||
| chr4:17683713
|
A | T | 108 | a0001c0003t0002g0069a0001c0003t0023g0122a0001c0007t0004g0097others(105): Show | 108 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1596+4711T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17683713 | ||||||
| chr4:17683723
|
C | A | 108 | a0001c0003t0002g0069a0001c0003t0023g0122a0001c0007t0004g0097others(105): Show | 108 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1596+4701G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17683723 | ||||||
| chr4:17683801
|
C | T | 6 | a0001c0003t0018g0006a0001c0007t0019g0143a0001c0008t0018g0020others(3): Show | 6 | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+4623G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17683801 | ||||||
| chr4:17683808
|
G | A | 1 | a0002c0002t0001g0025 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1596+4616C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17683808 | ||||||
| chr4:17683880
|
A | G | 108 | a0001c0003t0002g0069a0001c0003t0023g0122a0001c0007t0004g0097others(105): Show | 108 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1596+4544T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17683880 | ||||||
| chr4:17683904
|
C | T | 1 | a0001c0003t0067g0238 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1596+4520G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17683904 | ||||||
| chr4:17683905
|
G | A | 2 | a0028c0032t0062g0172a0032c0061t0030g0007 | 2 | HG03017.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.1596+4519C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17683905 | ||||||
| chr4:17683943
|
G | A | 2 | a0002c0002t0001g0228a0007c0041t0012g0011 | 2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1596+4481C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17683943 | ||||||
| chr4:17683984
|
A | G | 1 | a0028c0032t0062g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1596+4440T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17683984 | ||||||
| chr4:17684084
|
A | C | 108 | a0001c0003t0002g0069a0001c0003t0023g0122a0001c0007t0004g0097others(105): Show | 108 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1596+4340T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17684084 | ||||||
| chr4:17684087
|
G | A | 1 | a0001c0003t0011g0167 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1596+4337C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17684087 | ||||||
| chr4:17684094
|
C | CTAT | 106 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(103): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.1596+4327_1596+432 others(7): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17684094 | ||||||
| chr4:17684097
|
TTA | T | 128 | a0001c0003t0002g0069a0001c0003t0023g0122a0001c0004t0003g0207others(125): Show | 128 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1596+4325_1596+432 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17684097 | ||||||
| chr4:17684101
|
A | G | 1 | a0001c0003t0008g0205 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1596+4323T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17684101 | ||||||
| chr4:17684107
|
G | T | 128 | a0001c0003t0002g0069a0001c0003t0023g0122a0001c0004t0003g0207others(125): Show | 128 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1596+4317C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17684107 | ||||||
| chr4:17684111
|
AAAATAAT others(3): Show |
A | 128 | a0001c0003t0002g0069a0001c0003t0023g0122a0001c0004t0003g0207others(125): Show | 128 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1596+4303_1596+431 others(14): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17684111 | ||||||
| chr4:17684122
|
A | G | 128 | a0001c0003t0002g0069a0001c0003t0023g0122a0001c0004t0003g0207others(125): Show | 128 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1596+4302T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17684122 | ||||||
| chr4:17684150
|
A | C | 108 | a0001c0003t0002g0069a0001c0003t0023g0122a0001c0007t0004g0097others(105): Show | 108 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1596+4274T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17684150 | ||||||
| chr4:17684175
|
AAATAATT others(13): Show |
A | 2 | a0002c0001t0001g0141a0002c0001t0001g0142 | 2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1596+4229_1596+424 others(24): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17684175 | ||||||
| chr4:17684181
|
T | C | 3 | a0009c0011t0001g0032a0009c0011t0001g0081a0009c0011t0056g0084 | 3 | HG02717.hp2 HG02886.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1596+4243A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17684181 | ||||||
| chr4:17684195
|
G | A | 211 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1596+4229C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17684195 | ||||||
| chr4:17684203
|
A | T | 108 | a0001c0003t0002g0069a0001c0003t0023g0122a0001c0007t0004g0097others(105): Show | 108 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1596+4221T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17684203 | ||||||
| chr4:17684222
|
CTAT | C | 104 | a0001c0003t0018g0006a0001c0007t0004g0097a0001c0007t0008g0157others(101): Show | 104 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1596+4199_1596+420 others(7): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17684222 | ||||||
| chr4:17684334
|
T | C | 1 | a0028c0032t0062g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1596+4090A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17684334 | ||||||
| chr4:17684467
|
G | A | 61 | a0001c0007t0004g0097a0001c0007t0008g0157a0001c0007t0023g0123others(58): Show | 61 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.1596+3957C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17684467 | ||||||
| chr4:17684605
|
C | T | 61 | a0001c0007t0004g0097a0001c0007t0008g0157a0001c0007t0023g0123others(58): Show | 61 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.1596+3819G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17684605 | ||||||
| chr4:17684714
|
T | C | 72 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(69): Show | 72 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.1596+3710A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17684714 | ||||||
| chr4:17684734
|
C | G | 63 | a0001c0007t0004g0097a0001c0007t0008g0157a0001c0007t0023g0123others(60): Show | 63 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.1596+3690G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17684734 | ||||||
| chr4:17684747
|
G | A | 3 | a0001c0007t0019g0143a0001c0008t0019g0102a0001c0021t0018g0068 | 3 | HG02451.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1596+3677C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17684747 | ||||||
| chr4:17684860
|
G | T | 10 | a0001c0003t0002g0069a0001c0003t0023g0122a0001c0017t0010g0070others(7): Show | 10 | HG01109.hp2 HG01884.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1596+3564C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17684860 | ||||||
| chr4:17684881
|
T | C | 3 | a0002c0022t0001g0085a0002c0022t0001g0151a0014c0024t0032g0237 | 3 | HG00558.hp1 HG02071.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1596+3543A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17684881 | ||||||
| chr4:17684927
|
C | A | 3 | a0005c0036t0053g0233a0005c0042t0006g0093a0023c0053t0012g0080 | 3 | HG02615.hp1 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1596+3497G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17684927 | ||||||
| chr4:17684988
|
G | A | 2 | a0002c0002t0001g0036a0002c0002t0001g0055 | 2 | HG01169.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1596+3436C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17684988 | ||||||
| chr4:17684991
|
A | C | 2 | a0002c0002t0001g0036a0002c0002t0001g0055 | 2 | HG01169.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1596+3433T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17684991 | ||||||
| chr4:17685017
|
G | A | 3 | a0002c0022t0001g0085a0002c0022t0001g0151a0028c0032t0062g0172 | 3 | HG00558.hp1 HG03017.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1596+3407C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17685017 | ||||||
| chr4:17685198
|
TA | T | 14 | a0001c0003t0046g0059a0001c0003t0066g0150a0001c0005t0007g0140others(11): Show | 14 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(11): Show |
intron_variant | MODIFIER | c.1596+3225delT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17685198 | ||||||
| chr4:17685213
|
A | G | 2 | a0001c0003t0018g0006a0001c0008t0018g0020 | 2 | HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1596+3211T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17685213 | ||||||
| chr4:17685242
|
A | G | 2 | a0002c0016t0001g0221a0005c0036t0053g0233 | 2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1596+3182T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17685242 | ||||||
| chr4:17685405
|
C | T | 78 | a0001c0006t0003g0026a0001c0006t0003g0028a0001c0006t0003g0029others(75): Show | 78 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1596+3019G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17685405 | ||||||
| chr4:17685430
|
T | G | 2 | a0005c0042t0006g0093a0007c0043t0012g0105 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1596+2994A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17685430 | ||||||
| chr4:17685558
|
C | CA | 11 | a0001c0003t0018g0006a0001c0003t0046g0059a0001c0005t0007g0140others(8): Show | 11 | HG00323.hp2 HG00558.hp1 HG00609.hp1 others(8): Show |
intron_variant | MODIFIER | c.1596+2865dupT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17685558 | ||||||
| chr4:17685558
|
C | CAA | 81 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(78): Show | 81 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.1596+2864_1596+286 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17685558 | ||||||
| chr4:17685558
|
CA | C | 83 | a0001c0003t0019g0095a0001c0004t0009g0022a0001c0004t0025g0023others(80): Show | 83 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.1596+2865delT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17685558 | ||||||
| chr4:17685634
|
C | T | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+2790G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17685634 | ||||||
| chr4:17686170
|
T | C | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+2254A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17686170 | ||||||
| chr4:17686435
|
T | A | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+1989A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17686435 | ||||||
| chr4:17686458
|
A | G | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+1966T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17686458 | ||||||
| chr4:17686580
|
G | T | 1 | a0002c0002t0001g0228 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1596+1844C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17686580 | ||||||
| chr4:17686613
|
C | T | 1 | a0001c0012t0026g0092 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1596+1811G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17686613 | ||||||
| chr4:17686667
|
C | T | 1 | a0005c0036t0053g0233 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1596+1757G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17686667 | ||||||
| chr4:17686668
|
A | C | 1 | a0003c0009t0005g0195 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1596+1756T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17686668 | ||||||
| chr4:17686715
|
G | A | 59 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(56): Show | 59 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.1596+1709C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17686715 | ||||||
| chr4:17686726
|
G | A | 1 | a0002c0002t0001g0228 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1596+1698C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17686726 | ||||||
| chr4:17686819
|
G | A | 1 | a0002c0001t0001g0156 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1596+1605C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17686819 | ||||||
| chr4:17686946
|
CA | C | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+1477delT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17686946 | ||||||
| chr4:17686959
|
G | A | 64 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.1596+1465C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17686959 | ||||||
| chr4:17686988
|
T | C | 43 | a0001c0008t0002g0045a0001c0008t0011g0052a0001c0008t0018g0020others(40): Show | 43 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.1596+1436A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17686988 | ||||||
| chr4:17687136
|
G | A | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+1288C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17687136 | ||||||
| chr4:17687215
|
A | G | 2 | a0002c0001t0031g0178a0002c0001t0031g0179 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1596+1209T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17687215 | ||||||
| chr4:17687265
|
T | C | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+1159A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17687265 | ||||||
| chr4:17687343
|
T | C | 1 | a0002c0001t0001g0135 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1596+1081A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17687343 | ||||||
| chr4:17687517
|
T | G | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+907A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17687517 | ||||||
| chr4:17687534
|
T | C | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+890A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17687534 | ||||||
| chr4:17687555
|
C | T | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+869G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17687555 | ||||||
| chr4:17687654
|
G | A | 1 | a0002c0002t0016g0039 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1596+770C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17687654 | ||||||
| chr4:17687673
|
A | G | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+751T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17687673 | ||||||
| chr4:17687827
|
T | C | 10 | a0001c0003t0023g0122a0002c0002t0001g0228a0002c0016t0001g0221others(7): Show | 10 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1596+597A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17687827 | ||||||
| chr4:17687844
|
C | T | 51 | a0001c0003t0019g0095a0001c0004t0009g0022a0001c0004t0025g0023others(48): Show | 51 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1596+580G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17687844 | ||||||
| chr4:17687855
|
G | A | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+569C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17687855 | ||||||
| chr4:17687861
|
G | C | 3 | a0001c0007t0020g0060a0001c0007t0020g0153a0032c0061t0030g0007 | 3 | HG00609.hp1 HG00673.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.1596+563C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17687861 | ||||||
| chr4:17687861
|
G | T | 3 | a0002c0022t0001g0085a0002c0022t0001g0151a0014c0024t0032g0237 | 3 | HG00558.hp1 HG02071.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1596+563C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17687861 | ||||||
| chr4:17687930
|
A | C | 1 | a0002c0001t0058g0173 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1596+494T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17687930 | ||||||
| chr4:17688092
|
C | T | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+332G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17688092 | ||||||
| chr4:17688128
|
C | T | 1 | a0001c0060t0027g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1596+296G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17688128 | ||||||
| chr4:17688129
|
G | T | 64 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.1596+295C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17688129 | ||||||
| chr4:17688139
|
C | T | 3 | a0002c0022t0001g0085a0002c0022t0001g0151a0014c0024t0032g0237 | 3 | HG00558.hp1 HG02071.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1596+285G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17688139 | ||||||
| chr4:17688148
|
T | A | 1 | a0001c0004t0009g0017 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1596+276A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17688148 | ||||||
| chr4:17688248
|
T | G | 3 | a0001c0003t0023g0122a0002c0002t0001g0228a0002c0016t0001g0221 | 3 | HG02723.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1596+176A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17688248 | ||||||
| chr4:17688278
|
AT | A | 231 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(228): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1596+145delA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17688278 | ||||||
| chr4:17688311
|
G | A | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+113C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17688311 | ||||||
| chr4:17688351
|
T | C | 234 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.1596+73A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 7/17 | chr4 | 17688351 | ||||||
| chr4:17688599
|
C | T | 1 | a0002c0002t0001g0114 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1489-68G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17688599 | ||||||
| chr4:17688644
|
C | T | 2 | a0001c0003t0002g0149a0001c0003t0047g0199 | 2 | HG02071.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.1489-113G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17688644 | ||||||
| chr4:17688680
|
C | CT | 37 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0003t0023g0122others(34): Show | 37 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.1489-150dupA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17688680 | ||||||
| chr4:17688680
|
C | CTT | 54 | a0001c0003t0002g0149a0001c0003t0002g0158a0001c0003t0002g0206others(51): Show | 54 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.1489-151_1489-150d others(4): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17688680 | ||||||
| chr4:17688680
|
C | CTTT | 12 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0227others(9): Show | 12 | HG01123.hp1 HG01175.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.1489-152_1489-150d others(5): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17688680 | ||||||
| chr4:17688680
|
CT | C | 12 | a0001c0006t0028g0014a0001c0007t0004g0097a0001c0007t0008g0157others(9): Show | 12 | HG01069.hp2 HG01081.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.1489-150delA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17688680 | ||||||
| chr4:17688680
|
CTTTTTTT others(5): Show |
C | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1489-161_1489-150d others(14): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17688680 | ||||||
| chr4:17688707
|
T | C | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1489-176A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17688707 | ||||||
| chr4:17688782
|
C | T | 1 | a0023c0053t0012g0080 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1489-251G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17688782 | ||||||
| chr4:17688973
|
G | A | 2 | a0002c0001t0001g0126a0002c0001t0001g0131 | 2 | HG01071.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.1489-442C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17688973 | ||||||
| chr4:17688987
|
C | G | 1 | a0001c0021t0064g0005 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1489-456G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17688987 | ||||||
| chr4:17688989
|
G | A | 2 | a0001c0003t0023g0122a0002c0016t0001g0221 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1489-458C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17688989 | ||||||
| chr4:17689089
|
A | G | 1 | a0001c0005t0014g0170 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1489-558T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17689089 | ||||||
| chr4:17689424
|
T | C | 60 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.1489-893A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17689424 | ||||||
| chr4:17689543
|
C | A | 148 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(145): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.1489-1012G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17689543 | ||||||
| chr4:17689578
|
T | G | 1 | a0001c0004t0042g0108 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1489-1047A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17689578 | ||||||
| chr4:17689582
|
A | T | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1489-1051T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17689582 | ||||||
| chr4:17689607
|
T | C | 148 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(145): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.1489-1076A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17689607 | ||||||
| chr4:17689871
|
G | A | 1 | a0012c0046t0002g0021 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1489-1340C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17689871 | ||||||
| chr4:17689901
|
A | C | 230 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(227): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1489-1370T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17689901 | ||||||
| chr4:17689944
|
T | A | 1 | a0023c0053t0012g0080 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1489-1413A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17689944 | ||||||
| chr4:17689953
|
T | A | 143 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(140): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1489-1422A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17689953 | ||||||
| chr4:17689964
|
C | T | 3 | a0001c0021t0064g0005a0023c0053t0012g0080a0025c0056t0061g0078 | 3 | HG02572.hp1 HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1489-1433G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17689964 | ||||||
| chr4:17689980
|
C | A | 3 | a0002c0001t0001g0083a0002c0001t0001g0087a0002c0001t0001g0226 | 3 | HG02683.hp2 HG03710.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1489-1449G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17689980 | ||||||
| chr4:17689996
|
C | T | 1 | a0002c0002t0069g0235 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1489-1465G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17689996 | ||||||
| chr4:17690017
|
G | A | 83 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(80): Show | 83 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.1489-1486C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17690017 | ||||||
| chr4:17690026
|
T | C | 61 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.1489-1495A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17690026 | ||||||
| chr4:17690095
|
C | T | 1 | a0008c0039t0015g0016 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1489-1564G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17690095 | ||||||
| chr4:17690155
|
A | T | 143 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(140): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1489-1624T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17690155 | ||||||
| chr4:17690157
|
A | T | 3 | a0001c0021t0064g0005a0023c0053t0012g0080a0025c0056t0061g0078 | 3 | HG02572.hp1 HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1489-1626T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17690157 | ||||||
| chr4:17690173
|
A | G | 143 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(140): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1489-1642T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17690173 | ||||||
| chr4:17690284
|
G | T | 2 | a0009c0011t0001g0081a0009c0011t0056g0084 | 2 | HG02717.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1489-1753C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17690284 | ||||||
| chr4:17690303
|
G | T | 1 | a0001c0003t0018g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1489-1772C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17690303 | ||||||
| chr4:17690423
|
G | A | 1 | a0002c0001t0001g0190 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1489-1892C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17690423 | ||||||
| chr4:17690696
|
A | C | 143 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(140): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1489-2165T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17690696 | ||||||
| chr4:17690799
|
C | G | 148 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(145): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.1489-2268G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17690799 | ||||||
| chr4:17690836
|
A | T | 1 | a0018c0044t0001g0062 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1489-2305T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17690836 | ||||||
| chr4:17690856
|
G | C | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1489-2325C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17690856 | ||||||
| chr4:17691062
|
T | G | 78 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(75): Show | 78 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.1488+2240A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17691062 | ||||||
| chr4:17691092
|
C | G | 143 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(140): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1488+2210G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17691092 | ||||||
| chr4:17691142
|
C | T | 3 | a0005c0036t0053g0233a0008c0039t0015g0016a0019c0040t0065g0012 | 3 | HG03041.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1488+2160G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17691142 | ||||||
| chr4:17691151
|
G | T | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1488+2151C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17691151 | ||||||
| chr4:17691158
|
C | T | 1 | a0001c0047t0010g0113 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1488+2144G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17691158 | ||||||
| chr4:17691159
|
A | G | 143 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(140): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1488+2143T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17691159 | ||||||
| chr4:17691240
|
C | T | 60 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.1488+2062G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17691240 | ||||||
| chr4:17691255
|
G | C | 144 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(141): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1488+2047C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17691255 | ||||||
| chr4:17691381
|
T | C | 1 | a0001c0003t0004g0018 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1488+1921A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17691381 | ||||||
| chr4:17691403
|
G | T | 1 | a0017c0026t0041g0160 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1488+1899C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17691403 | ||||||
| chr4:17691404
|
G | T | 1 | a0017c0026t0041g0160 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1488+1898C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17691404 | ||||||
| chr4:17691423
|
C | T | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1488+1879G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17691423 | ||||||
| chr4:17691455
|
A | G | 144 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(141): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1488+1847T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17691455 | ||||||
| chr4:17691456
|
T | C | 144 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(141): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1488+1846A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17691456 | ||||||
| chr4:17691486
|
G | A | 8 | a0001c0003t0019g0095a0001c0004t0009g0022a0001c0004t0025g0023others(5): Show | 8 | HG02258.hp1 HG02559.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.1488+1816C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17691486 | ||||||
| chr4:17691599
|
T | C | 1 | a0008c0049t0034g0112 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1488+1703A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17691599 | ||||||
| chr4:17691642
|
C | T | 144 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(141): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1488+1660G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17691642 | ||||||
| chr4:17691685
|
CA | C | 5 | a0001c0012t0026g0092a0002c0002t0001g0055a0002c0020t0001g0079others(2): Show | 5 | HG01169.hp2 HG02717.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1488+1616delT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17691685 | ||||||
| chr4:17691685
|
CAA | C | 7 | a0001c0003t0002g0158a0001c0003t0002g0206a0001c0003t0004g0169others(4): Show | 7 | HG01099.hp2 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.1488+1615_1488+161 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17691685 | ||||||
| chr4:17691685
|
CAAA | C | 67 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(64): Show | 67 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.1488+1614_1488+161 others(7): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17691685 | ||||||
| chr4:17691851
|
G | A | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1488+1451C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17691851 | ||||||
| chr4:17691869
|
A | G | 1 | a0002c0020t0001g0079 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1488+1433T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17691869 | ||||||
| chr4:17691950
|
G | A | 144 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(141): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1488+1352C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17691950 | ||||||
| chr4:17691984
|
C | T | 1 | a0002c0001t0001g0189 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1488+1318G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17691984 | ||||||
| chr4:17692038
|
C | A | 144 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(141): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1488+1264G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17692038 | ||||||
| chr4:17692051
|
CA | C | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1488+1250delT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17692051 | ||||||
| chr4:17692051
|
CAA | C | 11 | a0001c0006t0048g0027a0001c0007t0004g0097a0001c0007t0008g0157others(8): Show | 11 | HG01081.hp2 HG01516.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1488+1249_1488+125 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17692051 | ||||||
| chr4:17692051
|
CAAA | C | 133 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(130): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.1488+1248_1488+125 others(7): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17692051 | ||||||
| chr4:17692082
|
G | T | 1 | a0005c0036t0053g0233 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1488+1220C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17692082 | ||||||
| chr4:17692132
|
T | C | 149 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(146): Show | 149 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1488+1170A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17692132 | ||||||
| chr4:17692135
|
A | G | 1 | a0017c0026t0041g0160 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1488+1167T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17692135 | ||||||
| chr4:17692171
|
G | A | 145 | a0001c0003t0018g0006a0001c0005t0007g0013a0001c0005t0007g0125others(142): Show | 145 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1488+1131C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17692171 | ||||||
| chr4:17692213
|
G | A | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1488+1089C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17692213 | ||||||
| chr4:17692244
|
C | T | 144 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(141): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1488+1058G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17692244 | ||||||
| chr4:17692288
|
C | A | 1 | a0001c0021t0064g0005 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1488+1014G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17692288 | ||||||
| chr4:17692411
|
G | A | 144 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(141): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1488+891C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17692411 | ||||||
| chr4:17692502
|
T | C | 144 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(141): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1488+800A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17692502 | ||||||
| chr4:17692584
|
C | T | 1 | a0001c0060t0027g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1488+718G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17692584 | ||||||
| chr4:17692600
|
A | G | 144 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(141): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1488+702T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17692600 | ||||||
| chr4:17692616
|
T | G | 1 | a0002c0001t0001g0082 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1488+686A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17692616 | ||||||
| chr4:17692770
|
G | A | 3 | a0001c0003t0023g0122a0001c0021t0064g0005a0002c0016t0001g0221 | 3 | HG02630.hp1 HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1488+532C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17692770 | ||||||
| chr4:17693029
|
GCAGGC | G | 144 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(141): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1488+268_1488+272d others(7): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17693029 | ||||||
| chr4:17693257
|
G | C | 145 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(142): Show | 145 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1488+45C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17693257 | ||||||
| chr4:17693293
|
A | G | 149 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.1488+9T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 6/17 | chr4 | 17693293 | ||||||
| chr4:17693450
|
G | A | 3 | a0014c0024t0001g0183a0014c0024t0032g0237a0032c0061t0030g0007 | 3 | HG02071.hp1 NA18939.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.1378-38C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17693450 | ||||||
| chr4:17693583
|
C | G | 60 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(57): Show | 60 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.1378-171G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17693583 | ||||||
| chr4:17693605
|
T | C | 3 | a0014c0024t0001g0183a0014c0024t0032g0237a0032c0061t0030g0007 | 3 | HG02071.hp1 NA18939.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.1378-193A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17693605 | ||||||
| chr4:17693830
|
A | G | 155 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1378-418T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17693830 | ||||||
| chr4:17693864
|
C | A | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1378-452G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17693864 | ||||||
| chr4:17693876
|
C | A | 4 | a0002c0001t0001g0120a0002c0001t0001g0121a0002c0001t0001g0222others(1): Show | 4 | HG00639.hp2 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1378-464G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17693876 | ||||||
| chr4:17693901
|
C | T | 1 | a0025c0056t0061g0078 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1378-489G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17693901 | ||||||
| chr4:17693910
|
G | C | 1 | a0001c0012t0026g0092 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1378-498C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17693910 | ||||||
| chr4:17694032
|
T | C | 153 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.1378-620A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17694032 | ||||||
| chr4:17694036
|
C | T | 1 | a0002c0002t0001g0180 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1378-624G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17694036 | ||||||
| chr4:17694087
|
C | T | 1 | a0002c0002t0001g0228 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1378-675G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17694087 | ||||||
| chr4:17694099
|
G | A | 153 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.1378-687C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17694099 | ||||||
| chr4:17694437
|
G | A | 9 | a0001c0003t0019g0095a0001c0004t0009g0022a0001c0004t0025g0023others(6): Show | 9 | HG02258.hp1 HG02559.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1378-1025C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17694437 | ||||||
| chr4:17694522
|
C | CA | 145 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.1378-1111dupT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17694522 | ||||||
| chr4:17694522
|
C | CAA | 9 | a0002c0001t0001g0146a0014c0024t0001g0183a0014c0024t0032g0237others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1378-1112_1378-111 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17694522 | ||||||
| chr4:17694583
|
A | T | 2 | a0001c0003t0002g0158a0001c0003t0044g0159 | 2 | NA18950.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1378-1171T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17694583 | ||||||
| chr4:17694620
|
C | T | 8 | a0001c0006t0003g0026a0001c0006t0003g0028a0001c0006t0003g0029others(5): Show | 8 | NA18955.hp1 NA18956.hp2 NA18995.hp2 others(5): Show |
intron_variant | MODIFIER | c.1378-1208G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17694620 | ||||||
| chr4:17694657
|
T | C | 154 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1378-1245A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17694657 | ||||||
| chr4:17694755
|
G | T | 154 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1378-1343C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17694755 | ||||||
| chr4:17694786
|
A | G | 154 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1378-1374T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17694786 | ||||||
| chr4:17694799
|
A | G | 151 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.1378-1387T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17694799 | ||||||
| chr4:17694811
|
G | A | 42 | a0001c0008t0002g0045a0001c0008t0004g0037a0001c0008t0011g0052others(39): Show | 42 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(39): Show |
intron_variant | MODIFIER | c.1378-1399C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17694811 | ||||||
| chr4:17694854
|
G | T | 154 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1378-1442C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17694854 | ||||||
| chr4:17694999
|
AG | A | 5 | a0001c0003t0008g0216a0011c0023t0024g0209a0011c0023t0043g0204others(2): Show | 5 | HG00323.hp1 HG01358.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1378-1588delC | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17694999 | ||||||
| chr4:17695003
|
C | CCTGG | 153 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.1378-1595_1378-159 others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17695003 | ||||||
| chr4:17695155
|
C | CTGGGGTT others(1): Show |
153 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.1378-1744_1378-174 others(12): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17695155 | ||||||
| chr4:17695159
|
G | T | 154 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1378-1747C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17695159 | ||||||
| chr4:17695162
|
GT | G | 76 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(73): Show | 76 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.1378-1751delA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17695162 | ||||||
| chr4:17695164
|
T | TG | 154 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1378-1753_1378-175 others(5): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17695164 | ||||||
| chr4:17695166
|
T | G | 9 | a0001c0003t0019g0095a0001c0004t0009g0022a0001c0004t0025g0023others(6): Show | 9 | HG02258.hp1 HG02559.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1378-1754A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17695166 | ||||||
| chr4:17695181
|
C | G | 4 | a0001c0007t0019g0143a0002c0001t0017g0091a0002c0001t0017g0137others(1): Show | 4 | HG01123.hp2 HG02698.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1378-1769G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17695181 | ||||||
| chr4:17695233
|
G | A | 1 | a0002c0002t0069g0235 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1378-1821C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17695233 | ||||||
| chr4:17695243
|
C | G | 154 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1378-1831G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17695243 | ||||||
| chr4:17695320
|
GC | G | 3 | a0001c0033t0003g0200a0002c0001t0001g0135a0002c0001t0001g0214 | 3 | HG00609.hp2 NA18998.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1378-1909delG | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17695320 | ||||||
| chr4:17695341
|
A | T | 154 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1378-1929T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17695341 | ||||||
| chr4:17695385
|
T | C | 235 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.1378-1973A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17695385 | ||||||
| chr4:17695386
|
G | A | 160 | a0001c0003t0019g0095a0001c0004t0009g0022a0001c0004t0025g0023others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.1378-1974C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17695386 | ||||||
| chr4:17695564
|
A | G | 66 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(63): Show | 66 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.1378-2152T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17695564 | ||||||
| chr4:17695594
|
T | C | 154 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1378-2182A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17695594 | ||||||
| chr4:17695677
|
G | A | 1 | a0025c0056t0061g0078 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1378-2265C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17695677 | ||||||
| chr4:17695685
|
T | C | 231 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(228): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1378-2273A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17695685 | ||||||
| chr4:17695687
|
GGA | G | 66 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(63): Show | 66 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.1378-2277_1378-227 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17695687 | ||||||
| chr4:17695691
|
A | T | 2 | a0001c0003t0023g0122a0002c0016t0001g0221 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1378-2279T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17695691 | ||||||
| chr4:17695738
|
A | C | 1 | a0008c0049t0034g0112 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1378-2326T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17695738 | ||||||
| chr4:17695755
|
C | A | 1 | a0001c0003t0018g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1378-2343G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17695755 | ||||||
| chr4:17695798
|
A | C | 154 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1378-2386T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17695798 | ||||||
| chr4:17695923
|
G | T | 154 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1378-2511C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17695923 | ||||||
| chr4:17696064
|
G | A | 59 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.1378-2652C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17696064 | ||||||
| chr4:17696212
|
G | C | 154 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1378-2800C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17696212 | ||||||
| chr4:17696234
|
A | G | 1 | a0001c0029t0005g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1378-2822T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17696234 | ||||||
| chr4:17696283
|
C | G | 42 | a0001c0008t0002g0045a0001c0008t0004g0037a0001c0008t0011g0052others(39): Show | 42 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(39): Show |
intron_variant | MODIFIER | c.1378-2871G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17696283 | ||||||
| chr4:17696442
|
C | A | 1 | a0002c0001t0001g0218 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1378-3030G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17696442 | ||||||
| chr4:17696465
|
A | G | 154 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1378-3053T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17696465 | ||||||
| chr4:17696604
|
G | A | 2 | a0006c0019t0001g0064a0006c0019t0001g0100 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1378-3192C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17696604 | ||||||
| chr4:17696632
|
C | T | 154 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1378-3220G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17696632 | ||||||
| chr4:17696713
|
C | T | 4 | a0006c0014t0001g0008a0006c0014t0001g0042a0006c0014t0063g0053others(1): Show | 4 | HG01516.hp2 HG02735.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1378-3301G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17696713 | ||||||
| chr4:17696738
|
A | G | 1 | a0005c0036t0053g0233 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1378-3326T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17696738 | ||||||
| chr4:17696745
|
C | T | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1378-3333G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17696745 | ||||||
| chr4:17696814
|
A | AAATG | 147 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1378-3406_1378-340 others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17696814 | ||||||
| chr4:17696814
|
A | AAATGAAT others(1): Show |
6 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(3): Show | 6 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.1378-3410_1378-340 others(12): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17696814 | ||||||
| chr4:17696814
|
A | AAATGAAT others(9): Show |
1 | a0002c0002t0001g0228 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1378-3418_1378-340 others(20): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17696814 | ||||||
| chr4:17696830
|
G | GAATA | 8 | a0001c0003t0002g0227a0001c0003t0004g0057a0001c0003t0019g0095others(5): Show | 8 | HG01346.hp1 HG01346.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1378-3422_1378-341 others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17696830 | ||||||
| chr4:17696830
|
GAATA | G | 5 | a0001c0003t0023g0122a0001c0003t0046g0059a0001c0004t0042g0108others(2): Show | 5 | HG00323.hp2 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1378-3422_1378-341 others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17696830 | ||||||
| chr4:17696834
|
A | G | 154 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1378-3422T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17696834 | ||||||
| chr4:17696838
|
A | G | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1378-3426T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17696838 | ||||||
| chr4:17697087
|
G | A | 1 | a0001c0021t0064g0005 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1378-3675C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17697087 | ||||||
| chr4:17697102
|
G | A | 155 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1378-3690C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17697102 | ||||||
| chr4:17697158
|
G | C | 154 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1378-3746C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17697158 | ||||||
| chr4:17697225
|
G | A | 1 | a0002c0001t0001g0189 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1378-3813C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17697225 | ||||||
| chr4:17697350
|
C | T | 2 | a0023c0053t0012g0080a0025c0056t0061g0078 | 2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1378-3938G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17697350 | ||||||
| chr4:17697416
|
AC | A | 83 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(80): Show | 83 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.1378-4005delG | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17697416 | ||||||
| chr4:17697417
|
C | A | 71 | a0001c0006t0003g0026a0001c0006t0003g0028a0001c0006t0003g0029others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.1378-4005G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17697417 | ||||||
| chr4:17697667
|
T | A | 1 | a0001c0003t0037g0219 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1378-4255A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17697667 | ||||||
| chr4:17697886
|
A | G | 154 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1378-4474T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17697886 | ||||||
| chr4:17698040
|
G | A | 1 | a0002c0001t0001g0082 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1378-4628C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17698040 | ||||||
| chr4:17698093
|
C | CA | 8 | a0001c0003t0019g0095a0001c0004t0009g0022a0001c0004t0025g0023others(5): Show | 8 | HG02258.hp1 HG02559.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.1378-4682dupT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17698093 | ||||||
| chr4:17698167
|
G | T | 154 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1378-4755C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17698167 | ||||||
| chr4:17698319
|
C | T | 7 | a0001c0003t0002g0069a0001c0017t0010g0070a0001c0017t0010g0175others(4): Show | 7 | HG02630.hp2 HG02647.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1378-4907G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17698319 | ||||||
| chr4:17698418
|
G | GAAC | 154 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1378-5009_1378-500 others(7): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17698418 | ||||||
| chr4:17698436
|
C | A | 234 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.1378-5024G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17698436 | ||||||
| chr4:17698539
|
A | T | 2 | a0023c0053t0012g0080a0025c0056t0061g0078 | 2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1378-5127T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17698539 | ||||||
| chr4:17698553
|
G | A | 155 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1378-5141C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17698553 | ||||||
| chr4:17698695
|
G | A | 231 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(228): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1378-5283C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17698695 | ||||||
| chr4:17698851
|
C | T | 154 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1378-5439G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17698851 | ||||||
| chr4:17699195
|
AGAAATTA others(8): Show |
A | 154 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1377+5790_1378-578 others(19): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17699195 | ||||||
| chr4:17699301
|
G | T | 1 | a0001c0012t0009g0035 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1377+5699C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17699301 | ||||||
| chr4:17699306
|
A | AAAT | 154 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1377+5691_1377+569 others(7): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17699306 | ||||||
| chr4:17699328
|
T | C | 2 | a0001c0006t0028g0014a0001c0006t0028g0015 | 2 | HG03831.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1377+5672A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17699328 | ||||||
| chr4:17699329
|
T | A | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1377+5671A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17699329 | ||||||
| chr4:17699401
|
A | T | 42 | a0001c0008t0002g0045a0001c0008t0004g0037a0001c0008t0011g0052others(39): Show | 42 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(39): Show |
intron_variant | MODIFIER | c.1377+5599T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17699401 | ||||||
| chr4:17699408
|
C | T | 220 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.1377+5592G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17699408 | ||||||
| chr4:17699497
|
G | A | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1377+5503C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17699497 | ||||||
| chr4:17699630
|
A | C | 154 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1377+5370T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17699630 | ||||||
| chr4:17699674
|
G | A | 45 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(42): Show | 45 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1377+5326C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17699674 | ||||||
| chr4:17699843
|
A | G | 217 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1377+5157T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17699843 | ||||||
| chr4:17699844
|
A | G | 217 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1377+5156T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17699844 | ||||||
| chr4:17699876
|
A | G | 217 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1377+5124T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17699876 | ||||||
| chr4:17700140
|
G | T | 1 | a0013c0058t0022g0174 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1377+4860C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17700140 | ||||||
| chr4:17700262
|
G | A | 3 | a0001c0015t0013g0106a0004c0010t0006g0107a0004c0010t0006g0109 | 3 | HG02451.hp1 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1377+4738C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17700262 | ||||||
| chr4:17700288
|
T | G | 1 | a0001c0008t0011g0052 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1377+4712A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17700288 | ||||||
| chr4:17700350
|
G | A | 1 | a0001c0003t0018g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1377+4650C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17700350 | ||||||
| chr4:17700361
|
G | A | 1 | a0001c0021t0064g0005 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1377+4639C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17700361 | ||||||
| chr4:17700404
|
A | T | 3 | a0014c0024t0001g0183a0014c0024t0032g0237a0032c0061t0030g0007 | 3 | HG02071.hp1 NA18939.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.1377+4596T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17700404 | ||||||
| chr4:17700645
|
C | T | 1 | a0001c0008t0011g0052 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1377+4355G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17700645 | ||||||
| chr4:17700893
|
T | G | 220 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.1377+4107A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17700893 | ||||||
| chr4:17700902
|
A | G | 154 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1377+4098T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17700902 | ||||||
| chr4:17700903
|
A | C | 1 | a0025c0056t0061g0078 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1377+4097T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17700903 | ||||||
| chr4:17701142
|
T | C | 220 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.1377+3858A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17701142 | ||||||
| chr4:17701367
|
C | A | 3 | a0014c0024t0001g0183a0014c0024t0032g0237a0032c0061t0030g0007 | 3 | HG02071.hp1 NA18939.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.1377+3633G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17701367 | ||||||
| chr4:17701636
|
G | A | 3 | a0014c0024t0001g0183a0014c0024t0032g0237a0032c0061t0030g0007 | 3 | HG02071.hp1 NA18939.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.1377+3364C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17701636 | ||||||
| chr4:17701797
|
G | A | 1 | a0002c0020t0001g0079 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1377+3203C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17701797 | ||||||
| chr4:17701938
|
A | C | 1 | a0009c0011t0001g0081 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1377+3062T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17701938 | ||||||
| chr4:17701991
|
G | T | 65 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(62): Show | 65 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.1377+3009C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17701991 | ||||||
| chr4:17702011
|
A | G | 217 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1377+2989T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17702011 | ||||||
| chr4:17702054
|
T | C | 155 | a0001c0003t0002g0069a0001c0005t0007g0013a0001c0005t0007g0125others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1377+2946A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17702054 | ||||||
| chr4:17702094
|
C | T | 1 | a0002c0002t0001g0228 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1377+2906G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17702094 | ||||||
| chr4:17702118
|
A | T | 1 | a0002c0001t0017g0138 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1377+2882T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17702118 | ||||||
| chr4:17702318
|
C | T | 3 | a0014c0024t0001g0183a0014c0024t0032g0237a0032c0061t0030g0007 | 3 | HG02071.hp1 NA18939.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.1377+2682G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17702318 | ||||||
| chr4:17702326
|
T | C | 155 | a0001c0003t0002g0069a0001c0005t0007g0013a0001c0005t0007g0125others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1377+2674A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17702326 | ||||||
| chr4:17702360
|
T | G | 9 | a0001c0003t0019g0095a0001c0004t0009g0022a0001c0004t0025g0023others(6): Show | 9 | HG02258.hp1 HG02559.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1377+2640A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17702360 | ||||||
| chr4:17702449
|
C | G | 1 | a0002c0002t0001g0228 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1377+2551G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17702449 | ||||||
| chr4:17702844
|
T | C | 1 | a0020c0054t0001g0202 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1377+2156A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17702844 | ||||||
| chr4:17703044
|
C | T | 65 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(62): Show | 65 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.1377+1956G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17703044 | ||||||
| chr4:17703328
|
C | G | 1 | a0012c0046t0002g0021 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1377+1672G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17703328 | ||||||
| chr4:17703477
|
A | AAG | 5 | a0001c0006t0003g0026a0001c0006t0003g0029a0001c0006t0003g0030others(2): Show | 5 | NA18955.hp1 NA18956.hp2 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.1377+1521_1377+152 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17703477 | ||||||
| chr4:17703497
|
C | CA | 155 | a0001c0003t0023g0122a0001c0004t0009g0017a0001c0005t0007g0013others(152): Show | 155 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.1377+1502dupT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17703497 | ||||||
| chr4:17703803
|
T | C | 3 | a0002c0001t0001g0083a0002c0001t0001g0087a0002c0001t0001g0226 | 3 | HG02683.hp2 HG03710.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1377+1197A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17703803 | ||||||
| chr4:17703804
|
G | T | 3 | a0002c0001t0001g0083a0002c0001t0001g0087a0002c0001t0001g0226 | 3 | HG02683.hp2 HG03710.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1377+1196C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17703804 | ||||||
| chr4:17703810
|
G | A | 3 | a0002c0001t0001g0083a0002c0001t0001g0087a0002c0001t0001g0226 | 3 | HG02683.hp2 HG03710.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1377+1190C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17703810 | ||||||
| chr4:17703811
|
G | A | 3 | a0002c0001t0001g0083a0002c0001t0001g0087a0002c0001t0001g0226 | 3 | HG02683.hp2 HG03710.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1377+1189C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17703811 | ||||||
| chr4:17703812
|
T | C | 1 | a0002c0002t0069g0235 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1377+1188A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17703812 | ||||||
| chr4:17703823
|
T | C | 3 | a0002c0001t0001g0083a0002c0001t0001g0087a0002c0001t0001g0226 | 3 | HG02683.hp2 HG03710.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1377+1177A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17703823 | ||||||
| chr4:17703824
|
G | A | 3 | a0002c0001t0001g0083a0002c0001t0001g0087a0002c0001t0001g0226 | 3 | HG02683.hp2 HG03710.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1377+1176C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17703824 | ||||||
| chr4:17703849
|
T | G | 3 | a0002c0001t0001g0083a0002c0001t0001g0087a0002c0001t0001g0226 | 3 | HG02683.hp2 HG03710.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1377+1151A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17703849 | ||||||
| chr4:17703856
|
G | A | 3 | a0002c0001t0001g0083a0002c0001t0001g0087a0002c0001t0001g0226 | 3 | HG02683.hp2 HG03710.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1377+1144C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17703856 | ||||||
| chr4:17703858
|
C | G | 3 | a0002c0001t0001g0083a0002c0001t0001g0087a0002c0001t0001g0226 | 3 | HG02683.hp2 HG03710.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1377+1142G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17703858 | ||||||
| chr4:17703866
|
G | C | 3 | a0002c0001t0001g0083a0002c0001t0001g0087a0002c0001t0001g0226 | 3 | HG02683.hp2 HG03710.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1377+1134C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17703866 | ||||||
| chr4:17703870
|
G | A | 3 | a0002c0001t0001g0083a0002c0001t0001g0087a0002c0001t0001g0226 | 3 | HG02683.hp2 HG03710.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1377+1130C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17703870 | ||||||
| chr4:17703879
|
C | T | 3 | a0002c0001t0001g0083a0002c0001t0001g0087a0002c0001t0001g0226 | 3 | HG02683.hp2 HG03710.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1377+1121G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17703879 | ||||||
| chr4:17703885
|
T | C | 3 | a0002c0001t0001g0083a0002c0001t0001g0087a0002c0001t0001g0226 | 3 | HG02683.hp2 HG03710.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1377+1115A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17703885 | ||||||
| chr4:17703886
|
G | A | 3 | a0002c0001t0001g0083a0002c0001t0001g0087a0002c0001t0001g0226 | 3 | HG02683.hp2 HG03710.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1377+1114C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17703886 | ||||||
| chr4:17703887
|
C | A | 3 | a0002c0001t0001g0083a0002c0001t0001g0087a0002c0001t0001g0226 | 3 | HG02683.hp2 HG03710.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1377+1113G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17703887 | ||||||
| chr4:17703925
|
G | A | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1377+1075C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17703925 | ||||||
| chr4:17703929
|
C | CA | 115 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.1377+1070dupT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17703929 | ||||||
| chr4:17703929
|
C | CAA | 5 | a0001c0003t0023g0122a0002c0016t0001g0221a0003c0009t0005g0162others(2): Show | 5 | HG01891.hp2 HG02723.hp1 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.1377+1069_1377+107 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17703929 | ||||||
| chr4:17703971
|
C | T | 1 | a0001c0005t0014g0118 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1377+1029G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17703971 | ||||||
| chr4:17704519
|
G | A | 145 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.1377+481C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17704519 | ||||||
| chr4:17704564
|
G | T | 143 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.1377+436C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17704564 | ||||||
| chr4:17704629
|
G | A | 1 | a0001c0004t0042g0108 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1377+371C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17704629 | ||||||
| chr4:17704631
|
A | T | 3 | a0002c0001t0017g0091a0002c0001t0017g0137a0002c0001t0017g0138 | 3 | HG01123.hp2 HG02698.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1377+369T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17704631 | ||||||
| chr4:17704816
|
A | G | 143 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.1377+184T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17704816 | ||||||
| chr4:17704844
|
T | A | 1 | a0001c0015t0013g0003 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1377+156A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17704844 | ||||||
| chr4:17704911
|
G | A | 8 | a0001c0003t0019g0095a0001c0004t0009g0022a0001c0004t0025g0023others(5): Show | 8 | HG02258.hp1 HG02559.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.1377+89C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 5/17 | chr4 | 17704911 | ||||||
| chr4:17705305
|
T | G | 66 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(63): Show | 66 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.1171-99A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 4/17 | chr4 | 17705305 | ||||||
| chr4:17705409
|
G | A | 230 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(227): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1171-203C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 4/17 | chr4 | 17705409 | ||||||
| chr4:17705464
|
T | C | 1 | a0016c0025t0021g0225 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1171-258A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 4/17 | chr4 | 17705464 | ||||||
| chr4:17705541
|
C | T | 1 | a0001c0021t0064g0005 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1170+211G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 4/17 | chr4 | 17705541 | ||||||
| chr4:17705596
|
G | A | 3 | a0014c0024t0001g0183a0014c0024t0032g0237a0032c0061t0030g0007 | 3 | HG02071.hp1 NA18939.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.1170+156C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 4/17 | chr4 | 17705596 | ||||||
| chr4:17705678
|
C | T | 81 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(78): Show | 81 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.1170+74G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 4/17 | chr4 | 17705678 | ||||||
| chr4:17705738
|
G | A | 68 | a0001c0006t0003g0026a0001c0006t0003g0028a0001c0006t0003g0029others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.1170+14C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 4/17 | chr4 | 17705738 | ||||||
| chr4:17705972
|
G | A | 2 | a0023c0053t0012g0080a0025c0056t0061g0078 | 2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1031-81C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 3/17 | chr4 | 17705972 | ||||||
| chr4:17706004
|
C | A | 41 | a0001c0008t0002g0045a0001c0008t0004g0037a0001c0008t0011g0052others(38): Show | 41 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.1031-113G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 3/17 | chr4 | 17706004 | ||||||
| chr4:17706045
|
T | C | 147 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.1031-154A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 3/17 | chr4 | 17706045 | ||||||
| chr4:17706106
|
G | A | 1 | a0001c0007t0004g0097 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1031-215C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 3/17 | chr4 | 17706106 | ||||||
| chr4:17706147
|
G | A | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1031-256C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 3/17 | chr4 | 17706147 | ||||||
| chr4:17706396
|
G | A | 1 | a0001c0003t0018g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1031-505C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 3/17 | chr4 | 17706396 | ||||||
| chr4:17706553
|
C | G | 1 | a0008c0049t0034g0112 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1031-662G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 3/17 | chr4 | 17706553 | ||||||
| chr4:17706695
|
G | A | 147 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.1031-804C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 3/17 | chr4 | 17706695 | ||||||
| chr4:17706735
|
A | G | 147 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.1031-844T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 3/17 | chr4 | 17706735 | ||||||
| chr4:17706792
|
AT | A | 24 | a0001c0006t0003g0026a0001c0006t0003g0028a0001c0006t0003g0029others(21): Show | 24 | HG00423.hp1 HG02559.hp1 HG02615.hp1 others(21): Show |
intron_variant | MODIFIER | c.1030+856delA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 3/17 | chr4 | 17706792 | ||||||
| chr4:17706796
|
T | C | 1 | a0002c0001t0001g0083 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1030+853A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 3/17 | chr4 | 17706796 | ||||||
| chr4:17706834
|
G | T | 1 | a0001c0012t0026g0092 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1030+815C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 3/17 | chr4 | 17706834 | ||||||
| chr4:17706960
|
G | A | 1 | a0004c0010t0006g0165 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1030+689C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 3/17 | chr4 | 17706960 | ||||||
| chr4:17707192
|
C | A | 65 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(62): Show | 65 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.1030+457G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 3/17 | chr4 | 17707192 | ||||||
| chr4:17707405
|
G | A | 2 | a0014c0024t0001g0183a0014c0024t0032g0237 | 2 | HG02071.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1030+244C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 3/17 | chr4 | 17707405 | ||||||
| chr4:17707610
|
C | A | 2 | a0001c0006t0028g0014a0001c0006t0028g0015 | 2 | HG03831.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1030+39G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 3/17 | chr4 | 17707610 | ||||||
| chr4:17707829
|
A | G | 1 | a0002c0002t0001g0203 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.895-45T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17707829 | ||||||
| chr4:17707944
|
A | G | 1 | a0008c0034t0051g0010 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.895-160T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17707944 | ||||||
| chr4:17708009
|
G | A | 1 | a0012c0046t0002g0021 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.895-225C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708009 | ||||||
| chr4:17708034
|
C | T | 1 | a0001c0021t0064g0005 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.895-250G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708034 | ||||||
| chr4:17708052
|
T | G | 9 | a0001c0003t0002g0069a0001c0017t0010g0070a0001c0017t0010g0175others(6): Show | 9 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.895-268A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708052 | ||||||
| chr4:17708092
|
C | G | 1 | a0002c0020t0001g0079 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.895-308G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708092 | ||||||
| chr4:17708338
|
A | T | 3 | a0014c0024t0001g0183a0014c0024t0032g0237a0032c0061t0030g0007 | 3 | HG02071.hp1 NA18939.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.894+554T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708338 | ||||||
| chr4:17708367
|
G | C | 3 | a0014c0024t0001g0183a0014c0024t0032g0237a0032c0061t0030g0007 | 3 | HG02071.hp1 NA18939.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.894+525C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708367 | ||||||
| chr4:17708519
|
C | T | 3 | a0001c0012t0026g0092a0002c0020t0001g0079a0024c0037t0052g0094 | 3 | HG02717.hp1 HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.894+373G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708519 | ||||||
| chr4:17708568
|
C | G | 1 | a0023c0053t0012g0080 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.894+324G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708568 | ||||||
| chr4:17708663
|
C | CTA | 16 | a0001c0003t0002g0069a0001c0003t0004g0067a0001c0003t0046g0059others(13): Show | 16 | HG00323.hp2 HG00609.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.894+227_894+228dup others(2): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708663 | ||||||
| chr4:17708663
|
C | CTATA | 25 | a0001c0003t0002g0019a0001c0003t0011g0168a0001c0003t0044g0159others(22): Show | 25 | HG00544.hp2 HG01192.hp1 HG02129.hp1 others(22): Show |
intron_variant | MODIFIER | c.894+225_894+228dup others(4): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708663 | ||||||
| chr4:17708663
|
C | CTATACAT others(7): Show |
2 | a0002c0001t0001g0128a0002c0001t0059g0127 | 2 | HG00642.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.894+228_894+229ins others(14): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708663 | ||||||
| chr4:17708663
|
C | CTATATA | 54 | a0001c0003t0002g0227a0001c0003t0004g0018a0001c0003t0004g0057others(51): Show | 54 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.894+223_894+228dup others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708663 | ||||||
| chr4:17708663
|
C | CTATATAT others(1): Show |
49 | a0001c0003t0002g0158a0001c0003t0002g0206a0001c0003t0007g0220others(46): Show | 49 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.894+221_894+228dup others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708663 | ||||||
| chr4:17708663
|
C | CTATATAT others(3): Show |
18 | a0001c0003t0037g0219a0001c0005t0007g0013a0001c0005t0007g0194others(15): Show | 18 | HG00099.hp2 HG00597.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.894+219_894+228dup others(10): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708663 | ||||||
| chr4:17708663
|
C | CTATATAT others(5): Show |
10 | a0001c0015t0013g0003a0001c0021t0018g0068a0002c0001t0001g0136others(7): Show | 10 | HG00423.hp2 HG00642.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.894+217_894+228dup others(12): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708663 | ||||||
| chr4:17708663
|
C | CTATATAT others(7): Show |
1 | a0001c0004t0045g0104 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.894+215_894+228dup others(14): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708663 | ||||||
| chr4:17708663
|
C | CTATATAT others(9): Show |
2 | a0001c0003t0008g0163a0001c0004t0025g0024 | 2 | HG00140.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.894+213_894+228dup others(16): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708663 | ||||||
| chr4:17708663
|
C | CTATATAT others(11): Show |
1 | a0001c0003t0004g0169 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.894+211_894+228dup others(18): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708663 | ||||||
| chr4:17708663
|
CTA | C | 2 | a0001c0003t0011g0167a0001c0008t0068g0234 | 2 | HG00423.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.894+227_894+228del others(2): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708663 | ||||||
| chr4:17708663
|
CTATA | C | 10 | a0001c0003t0011g0166a0001c0006t0003g0182a0001c0006t0028g0014others(7): Show | 10 | HG01123.hp2 HG02602.hp1 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.894+225_894+228del others(4): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708663 | ||||||
| chr4:17708663
|
CTATATA | C | 2 | a0001c0006t0003g0028a0003c0018t0005g0196 | 2 | HG06807.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.894+223_894+228del others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708663 | ||||||
| chr4:17708663
|
CTATATAT others(1): Show |
C | 4 | a0001c0005t0029g0184a0001c0012t0009g0035a0002c0002t0001g0177others(1): Show | 4 | HG02486.hp1 HG02818.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.894+221_894+228del others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708663 | ||||||
| chr4:17708663
|
CTATATAT others(3): Show |
C | 1 | a0018c0044t0001g0062 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.894+219_894+228del others(10): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708663 | ||||||
| chr4:17708663
|
CTATATAT others(5): Show |
C | 4 | a0001c0007t0020g0153a0011c0023t0024g0209a0011c0023t0043g0204others(1): Show | 4 | HG00673.hp2 HG01361.hp2 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.894+217_894+228del others(12): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708663 | ||||||
| chr4:17708663
|
CTATATAT others(7): Show |
C | 2 | a0001c0003t0002g0149a0001c0003t0047g0199 | 2 | HG02071.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.894+215_894+228del others(14): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708663 | ||||||
| chr4:17708663
|
CTATATAT others(9): Show |
C | 4 | a0001c0015t0029g0164a0004c0010t0006g0165a0008c0034t0051g0010others(1): Show | 4 | HG02922.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.894+213_894+228del others(16): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708663 | ||||||
| chr4:17708663
|
CTATATAT others(11): Show |
C | 5 | a0001c0003t0018g0006a0001c0006t0003g0132a0006c0014t0001g0008others(2): Show | 5 | HG02257.hp1 HG02735.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.894+211_894+228del others(18): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708663 | ||||||
| chr4:17708663
|
CTATATAT others(13): Show |
C | 8 | a0001c0006t0003g0026a0001c0006t0003g0029a0001c0006t0003g0030others(5): Show | 8 | HG01516.hp2 HG02280.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.894+209_894+228del others(20): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708663 | ||||||
| chr4:17708663
|
CTATATAT others(15): Show |
C | 2 | a0001c0012t0026g0092a0024c0037t0052g0094 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.894+207_894+228del others(22): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708663 | ||||||
| chr4:17708663
|
CTATATAT others(25): Show |
C | 1 | a0002c0001t0001g0189 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.894+197_894+228del others(32): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708663 | ||||||
| chr4:17708688
|
TATATATA others(8): Show |
T | 1 | a0002c0020t0001g0079 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.894+189_894+203del others(15): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708688 | ||||||
| chr4:17708704
|
T | G | 1 | a0002c0020t0001g0079 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.894+188A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708704 | ||||||
| chr4:17708705
|
A | G | 1 | a0002c0020t0001g0079 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.894+187T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708705 | ||||||
| chr4:17708707
|
A | G | 1 | a0002c0020t0001g0079 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.894+185T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708707 | ||||||
| chr4:17708709
|
A | ATATATGG others(5): Show |
1 | a0013c0058t0022g0174 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.894+182_894+183ins others(12): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708709 | ||||||
| chr4:17708709
|
A | G | 2 | a0001c0012t0026g0092a0024c0037t0052g0094 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.894+183T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708709 | ||||||
| chr4:17708710
|
G | C | 1 | a0002c0020t0001g0079 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.894+182C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708710 | ||||||
| chr4:17708714
|
C | CTG | 124 | a0001c0003t0002g0149a0001c0003t0002g0158a0001c0003t0002g0206others(121): Show | 124 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.894+176_894+177dup others(2): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708714 | ||||||
| chr4:17708714
|
C | CTGTG | 7 | a0001c0012t0026g0092a0002c0001t0001g0086a0002c0001t0001g0147others(4): Show | 7 | HG01243.hp2 HG02071.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.894+174_894+177dup others(4): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708714 | ||||||
| chr4:17708714
|
C | CTGTGTG | 19 | a0001c0017t0010g0070a0001c0017t0010g0175a0001c0033t0003g0200others(16): Show | 19 | HG00609.hp2 HG00642.hp1 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.894+172_894+177dup others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708714 | ||||||
| chr4:17708714
|
C | CTGTGTGT others(1): Show |
4 | a0001c0003t0002g0069a0002c0002t0001g0040a0002c0016t0001g0071others(1): Show | 4 | HG01192.hp1 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.894+170_894+177dup others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708714 | ||||||
| chr4:17708714
|
C | G | 2 | a0002c0020t0001g0079a0013c0058t0022g0174 | 2 | HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.894+178G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708714 | ||||||
| chr4:17708714
|
CTG | C | 26 | a0001c0003t0019g0095a0001c0004t0009g0022a0001c0004t0025g0023others(23): Show | 26 | HG00423.hp1 HG02258.hp1 HG02559.hp1 others(23): Show |
intron_variant | MODIFIER | c.894+176_894+177del others(2): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708714 | ||||||
| chr4:17708738
|
G | T | 2 | a0002c0002t0001g0176a0002c0002t0001g0177 | 2 | HG02602.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.894+154C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 2/17 | chr4 | 17708738 | ||||||
| chr4:17709707
|
G | A | 1 | a0007c0041t0012g0011 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.142-63C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17709707 | ||||||
| chr4:17709803
|
A | G | 142 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.142-159T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17709803 | ||||||
| chr4:17709851
|
T | G | 1 | a0002c0002t0001g0228 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.142-207A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17709851 | ||||||
| chr4:17709931
|
A | G | 145 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.142-287T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17709931 | ||||||
| chr4:17709980
|
T | C | 1 | a0001c0003t0018g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-336A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17709980 | ||||||
| chr4:17710011
|
T | C | 149 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.142-367A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17710011 | ||||||
| chr4:17710195
|
G | A | 2 | a0002c0001t0001g0141a0002c0001t0001g0142 | 2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.142-551C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17710195 | ||||||
| chr4:17710259
|
G | A | 2 | a0009c0011t0001g0081a0009c0011t0056g0084 | 2 | HG02717.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.142-615C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17710259 | ||||||
| chr4:17710302
|
C | T | 3 | a0001c0004t0003g0207a0001c0004t0003g0212a0001c0004t0003g0213 | 3 | HG01123.hp1 HG01192.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.142-658G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17710302 | ||||||
| chr4:17710327
|
A | AAAAC | 88 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(85): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.142-687_142-684dup others(4): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17710327 | ||||||
| chr4:17710327
|
A | AAAACAAA others(1): Show |
54 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0003t0066g0150others(51): Show | 54 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.142-691_142-684dup others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17710327 | ||||||
| chr4:17710347
|
G | C | 144 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.142-703C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17710347 | ||||||
| chr4:17710882
|
C | T | 1 | a0002c0020t0001g0079 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.142-1238G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17710882 | ||||||
| chr4:17710969
|
G | T | 1 | a0011c0023t0043g0204 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.142-1325C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17710969 | ||||||
| chr4:17710976
|
A | G | 1 | a0008c0049t0034g0112 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.142-1332T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17710976 | ||||||
| chr4:17711084
|
G | A | 1 | a0001c0003t0018g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-1440C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17711084 | ||||||
| chr4:17711161
|
T | C | 92 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(89): Show | 92 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.142-1517A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17711161 | ||||||
| chr4:17711256
|
G | A | 41 | a0001c0008t0002g0045a0001c0008t0004g0037a0001c0008t0011g0052others(38): Show | 41 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.142-1612C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17711256 | ||||||
| chr4:17711335
|
C | T | 1 | a0002c0001t0001g0082 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.142-1691G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17711335 | ||||||
| chr4:17711538
|
C | T | 1 | a0002c0001t0001g0198 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.142-1894G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17711538 | ||||||
| chr4:17711742
|
C | T | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-2098G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17711742 | ||||||
| chr4:17711919
|
T | C | 49 | a0001c0003t0019g0095a0001c0004t0009g0022a0001c0004t0025g0023others(46): Show | 49 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.142-2275A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17711919 | ||||||
| chr4:17712082
|
G | A | 3 | a0014c0024t0001g0183a0014c0024t0032g0237a0032c0061t0030g0007 | 3 | HG02071.hp1 NA18939.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.142-2438C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17712082 | ||||||
| chr4:17712094
|
T | G | 142 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.142-2450A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17712094 | ||||||
| chr4:17712191
|
G | C | 142 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.142-2547C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17712191 | ||||||
| chr4:17712258
|
C | A | 1 | a0002c0002t0001g0155 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.142-2614G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17712258 | ||||||
| chr4:17712285
|
T | A | 142 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.142-2641A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17712285 | ||||||
| chr4:17712302
|
G | C | 10 | a0001c0003t0002g0069a0001c0017t0010g0070a0001c0017t0010g0175others(7): Show | 10 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-2658C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17712302 | ||||||
| chr4:17712336
|
A | C | 1 | a0023c0053t0012g0080 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.142-2692T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17712336 | ||||||
| chr4:17712417
|
C | G | 1 | a0004c0010t0006g0077 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.142-2773G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17712417 | ||||||
| chr4:17712480
|
C | T | 1 | a0004c0010t0006g0165 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.142-2836G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17712480 | ||||||
| chr4:17712726
|
C | G | 2 | a0001c0015t0029g0164a0004c0010t0006g0165 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.142-3082G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17712726 | ||||||
| chr4:17712746
|
C | CA | 22 | a0001c0004t0009g0072a0001c0004t0045g0104a0001c0006t0003g0026others(19): Show | 22 | HG00423.hp1 HG02559.hp1 HG02886.hp1 others(19): Show |
intron_variant | MODIFIER | c.142-3103dupT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17712746 | ||||||
| chr4:17712755
|
AG | A | 2 | a0001c0015t0029g0164a0004c0010t0006g0165 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.142-3112delC | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17712755 | ||||||
| chr4:17712789
|
A | G | 3 | a0001c0015t0013g0106a0004c0010t0006g0107a0004c0010t0006g0109 | 3 | HG02451.hp1 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.142-3145T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17712789 | ||||||
| chr4:17712962
|
C | T | 8 | a0001c0003t0019g0095a0001c0004t0009g0022a0001c0004t0025g0023others(5): Show | 8 | HG02258.hp1 HG02559.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.142-3318G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17712962 | ||||||
| chr4:17713251
|
G | A | 2 | a0001c0003t0023g0122a0002c0016t0001g0221 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.142-3607C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17713251 | ||||||
| chr4:17713259
|
G | T | 1 | a0001c0004t0025g0024 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.142-3615C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17713259 | ||||||
| chr4:17713306
|
C | G | 2 | a0001c0003t0023g0122a0002c0016t0001g0221 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.142-3662G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17713306 | ||||||
| chr4:17713471
|
T | C | 1 | a0008c0049t0034g0112 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.142-3827A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17713471 | ||||||
| chr4:17713574
|
T | C | 2 | a0002c0002t0001g0046a0002c0002t0016g0039 | 2 | HG02155.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.142-3930A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17713574 | ||||||
| chr4:17713617
|
A | C | 2 | a0001c0003t0002g0158a0001c0003t0044g0159 | 2 | NA18950.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.142-3973T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17713617 | ||||||
| chr4:17713770
|
G | A | 6 | a0001c0006t0003g0026a0001c0006t0003g0028a0001c0006t0003g0029others(3): Show | 6 | NA18955.hp1 NA18956.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-4126C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17713770 | ||||||
| chr4:17713791
|
T | C | 3 | a0001c0015t0013g0106a0004c0010t0006g0107a0004c0010t0006g0109 | 3 | HG02451.hp1 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.142-4147A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17713791 | ||||||
| chr4:17713873
|
C | A | 6 | a0001c0006t0003g0026a0001c0006t0003g0028a0001c0006t0003g0029others(3): Show | 6 | NA18955.hp1 NA18956.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-4229G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17713873 | ||||||
| chr4:17713935
|
G | A | 1 | a0001c0007t0008g0157 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.142-4291C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17713935 | ||||||
| chr4:17713940
|
T | C | 142 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.142-4296A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17713940 | ||||||
| chr4:17714077
|
A | G | 142 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.142-4433T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17714077 | ||||||
| chr4:17714165
|
C | T | 142 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.142-4521G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17714165 | ||||||
| chr4:17714168
|
T | G | 149 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.142-4524A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17714168 | ||||||
| chr4:17714529
|
C | T | 3 | a0014c0024t0001g0183a0014c0024t0032g0237a0032c0061t0030g0007 | 3 | HG02071.hp1 NA18939.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.142-4885G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17714529 | ||||||
| chr4:17714532
|
G | A | 6 | a0001c0007t0004g0097a0001c0007t0008g0157a0001c0007t0023g0123others(3): Show | 6 | HG01081.hp2 HG02258.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-4888C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17714532 | ||||||
| chr4:17714581
|
C | T | 1 | a0032c0061t0030g0007 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.142-4937G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17714581 | ||||||
| chr4:17714986
|
C | G | 1 | a0001c0003t0046g0059 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.142-5342G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17714986 | ||||||
| chr4:17715042
|
C | T | 1 | a0007c0041t0012g0011 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.142-5398G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17715042 | ||||||
| chr4:17715087
|
A | G | 128 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.142-5443T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17715087 | ||||||
| chr4:17715317
|
A | C | 1 | a0001c0003t0018g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-5673T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17715317 | ||||||
| chr4:17715373
|
G | T | 1 | a0001c0006t0003g0132 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.142-5729C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17715373 | ||||||
| chr4:17715399
|
C | T | 1 | a0001c0003t0018g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-5755G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17715399 | ||||||
| chr4:17715572
|
A | G | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-5928T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17715572 | ||||||
| chr4:17715738
|
A | G | 5 | a0001c0003t0019g0095a0001c0004t0009g0022a0001c0004t0025g0023others(2): Show | 5 | HG02258.hp1 HG02559.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-6094T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17715738 | ||||||
| chr4:17715781
|
A | T | 4 | a0001c0007t0019g0143a0002c0001t0017g0091a0002c0001t0017g0137others(1): Show | 4 | HG01123.hp2 HG02698.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-6137T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17715781 | ||||||
| chr4:17715788
|
AAG | A | 21 | a0001c0004t0009g0072a0001c0004t0045g0104a0001c0006t0003g0026others(18): Show | 21 | HG00423.hp1 HG02559.hp1 HG02886.hp1 others(18): Show |
intron_variant | MODIFIER | c.142-6146_142-6145d others(4): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17715788 | ||||||
| chr4:17716707
|
T | G | 1 | a0001c0008t0004g0037 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.142-7063A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17716707 | ||||||
| chr4:17716938
|
T | A | 3 | a0010c0013t0002g0231a0010c0013t0004g0232a0010c0013t0024g0211 | 3 | HG01169.hp1 HG01175.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.142-7294A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17716938 | ||||||
| chr4:17717047
|
G | T | 1 | a0002c0001t0001g0186 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.142-7403C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17717047 | ||||||
| chr4:17717083
|
T | A | 1 | a0008c0049t0034g0112 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.142-7439A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17717083 | ||||||
| chr4:17717278
|
C | G | 1 | a0002c0001t0001g0126 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.142-7634G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17717278 | ||||||
| chr4:17717350
|
T | C | 6 | a0001c0003t0019g0095a0001c0004t0009g0022a0001c0004t0025g0023others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-7706A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17717350 | ||||||
| chr4:17717458
|
C | T | 1 | a0001c0015t0029g0164 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.142-7814G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17717458 | ||||||
| chr4:17717513
|
C | T | 1 | a0008c0049t0034g0112 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.142-7869G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17717513 | ||||||
| chr4:17717523
|
T | C | 230 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(227): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.142-7879A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17717523 | ||||||
| chr4:17717635
|
G | A | 1 | a0007c0041t0012g0011 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.142-7991C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17717635 | ||||||
| chr4:17717845
|
G | A | 1 | a0001c0004t0009g0022 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.142-8201C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17717845 | ||||||
| chr4:17717919
|
C | A | 202 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.142-8275G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17717919 | ||||||
| chr4:17718337
|
C | T | 1 | a0032c0061t0030g0007 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.142-8693G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17718337 | ||||||
| chr4:17718390
|
C | T | 1 | a0024c0037t0052g0094 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.142-8746G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17718390 | ||||||
| chr4:17718437
|
A | G | 1 | a0001c0003t0019g0095 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.142-8793T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17718437 | ||||||
| chr4:17718507
|
A | G | 7 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0032g0236others(4): Show | 7 | HG00423.hp1 HG02071.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-8863T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17718507 | ||||||
| chr4:17718587
|
T | G | 9 | a0001c0003t0018g0006a0001c0008t0068g0234a0001c0015t0029g0164others(6): Show | 9 | HG00423.hp1 HG02071.hp1 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.142-8943A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17718587 | ||||||
| chr4:17718750
|
G | A | 2 | a0002c0002t0001g0228a0023c0053t0012g0080 | 2 | HG02615.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.142-9106C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17718750 | ||||||
| chr4:17718799
|
C | T | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-9155G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17718799 | ||||||
| chr4:17718910
|
C | T | 1 | a0013c0058t0022g0174 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.142-9266G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17718910 | ||||||
| chr4:17719013
|
G | T | 1 | a0004c0010t0006g0077 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.142-9369C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17719013 | ||||||
| chr4:17719034
|
T | C | 1 | a0002c0001t0001g0226 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.142-9390A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17719034 | ||||||
| chr4:17719038
|
C | T | 1 | a0001c0004t0042g0108 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.142-9394G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17719038 | ||||||
| chr4:17719157
|
C | T | 2 | a0007c0050t0012g0004a0008c0049t0034g0112 | 2 | HG01243.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.142-9513G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17719157 | ||||||
| chr4:17719185
|
C | T | 1 | a0001c0021t0064g0005 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.142-9541G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17719185 | ||||||
| chr4:17719190
|
A | G | 1 | a0031c0027t0001g0088 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.142-9546T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17719190 | ||||||
| chr4:17719195
|
G | A | 11 | a0002c0001t0001g0082a0002c0001t0001g0086a0002c0001t0001g0090others(8): Show | 11 | HG00642.hp1 HG01069.hp1 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.142-9551C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17719195 | ||||||
| chr4:17719211
|
T | C | 7 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0032g0236others(4): Show | 7 | HG00423.hp1 HG02071.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-9567A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17719211 | ||||||
| chr4:17719238
|
T | C | 6 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0032g0236others(3): Show | 6 | HG00423.hp1 HG02071.hp1 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-9594A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17719238 | ||||||
| chr4:17720029
|
T | A | 2 | a0001c0003t0011g0167a0001c0003t0011g0168 | 2 | HG03704.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.142-10385A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17720029 | ||||||
| chr4:17720065
|
C | T | 1 | a0001c0015t0029g0164 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.142-10421G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17720065 | ||||||
| chr4:17720130
|
C | T | 1 | a0032c0061t0030g0007 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.142-10486G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17720130 | ||||||
| chr4:17720190
|
C | T | 15 | a0001c0004t0009g0072a0001c0004t0045g0104a0001c0006t0003g0026others(12): Show | 15 | HG02886.hp1 HG02922.hp1 HG03209.hp2 others(12): Show |
intron_variant | MODIFIER | c.142-10546G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17720190 | ||||||
| chr4:17720203
|
G | A | 2 | a0001c0005t0029g0184a0003c0018t0005g0196 | 2 | HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.142-10559C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17720203 | ||||||
| chr4:17720254
|
C | A | 1 | a0008c0039t0015g0016 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.142-10610G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17720254 | ||||||
| chr4:17720348
|
A | G | 15 | a0001c0004t0009g0072a0001c0004t0045g0104a0001c0006t0003g0026others(12): Show | 15 | HG02886.hp1 HG02922.hp1 HG03209.hp2 others(12): Show |
intron_variant | MODIFIER | c.142-10704T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17720348 | ||||||
| chr4:17720564
|
T | A | 7 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0032g0236others(4): Show | 7 | HG00423.hp1 HG02071.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-10920A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17720564 | ||||||
| chr4:17720612
|
G | T | 1 | a0001c0060t0027g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.142-10968C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17720612 | ||||||
| chr4:17720658
|
G | C | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-11014C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17720658 | ||||||
| chr4:17720701
|
C | T | 1 | a0002c0001t0055g0144 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.142-11057G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17720701 | ||||||
| chr4:17720791
|
C | T | 1 | a0001c0012t0026g0092 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.142-11147G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17720791 | ||||||
| chr4:17720800
|
C | T | 2 | a0001c0003t0002g0158a0001c0003t0044g0159 | 2 | NA18950.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.142-11156G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17720800 | ||||||
| chr4:17720883
|
TA | T | 207 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.142-11240delT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17720883 | ||||||
| chr4:17720883
|
TAA | T | 19 | a0001c0003t0023g0122a0001c0003t0044g0159a0001c0005t0013g0185others(16): Show | 19 | HG00423.hp2 HG01109.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.142-11241_142-1124 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17720883 | ||||||
| chr4:17721110
|
C | T | 6 | a0001c0012t0026g0092a0001c0021t0064g0005a0002c0020t0001g0079others(3): Show | 6 | HG01243.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-11466G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17721110 | ||||||
| chr4:17721253
|
G | A | 1 | a0007c0041t0012g0011 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.142-11609C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17721253 | ||||||
| chr4:17721257
|
G | A | 4 | a0001c0012t0026g0092a0001c0021t0064g0005a0002c0020t0001g0079others(1): Show | 4 | HG02630.hp1 HG02717.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-11613C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17721257 | ||||||
| chr4:17721362
|
C | T | 1 | a0001c0015t0029g0164 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.142-11718G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17721362 | ||||||
| chr4:17721383
|
C | CAAAAAAA others(3): Show |
2 | a0001c0003t0018g0006a0001c0004t0025g0023 | 2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.142-11749_142-1174 others(14): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17721383 | ||||||
| chr4:17721383
|
C | CAAAAAAA others(4): Show |
12 | a0001c0004t0009g0022a0001c0004t0009g0072a0001c0004t0025g0024others(9): Show | 12 | HG02280.hp1 HG02559.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.142-11750_142-1174 others(15): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17721383 | ||||||
| chr4:17721383
|
C | CAAAAAAA others(5): Show |
10 | a0001c0003t0019g0095a0001c0006t0003g0026a0001c0006t0003g0030others(7): Show | 10 | HG02155.hp2 HG02451.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-11751_142-1174 others(16): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17721383 | ||||||
| chr4:17721383
|
C | CAAAAAAA others(6): Show |
21 | a0001c0003t0002g0227a0001c0003t0008g0163a0001c0003t0044g0159others(18): Show | 21 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(18): Show |
intron_variant | MODIFIER | c.142-11752_142-1174 others(17): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17721383 | ||||||
| chr4:17721383
|
C | CAAAAAAA others(7): Show |
38 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(35): Show | 38 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.142-11753_142-1174 others(18): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17721383 | ||||||
| chr4:17721383
|
C | CAAAAAAA others(8): Show |
24 | a0001c0003t0002g0158a0001c0003t0011g0166a0001c0003t0011g0167others(21): Show | 24 | HG00140.hp2 HG00639.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.142-11754_142-1174 others(19): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17721383 | ||||||
| chr4:17721383
|
C | CAAAAAAA others(9): Show |
6 | a0001c0003t0060g0215a0001c0003t0066g0150a0001c0008t0002g0045others(3): Show | 6 | HG00423.hp2 HG01361.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-11755_142-1174 others(20): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17721383 | ||||||
| chr4:17721383
|
C | CAAAAAAA others(10): Show |
4 | a0001c0003t0008g0216a0001c0003t0067g0238a0001c0021t0018g0068others(1): Show | 4 | HG00544.hp2 HG01081.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-11756_142-1174 others(21): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17721383 | ||||||
| chr4:17721383
|
C | CAAAAAAA others(11): Show |
3 | a0001c0003t0008g0208a0001c0003t0037g0219a0023c0053t0012g0080 | 3 | HG00597.hp1 HG02135.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.142-11757_142-1174 others(22): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17721383 | ||||||
| chr4:17721383
|
C | CAAAAAAA others(14): Show |
3 | a0001c0003t0008g0205a0015c0063t0054g0229a0017c0026t0038g0098 | 3 | HG01257.hp1 HG01358.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.142-11760_142-1174 others(25): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17721383 | ||||||
| chr4:17721383
|
C | CAAAAAAA others(16): Show |
1 | a0015c0062t0035g0230 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.142-11762_142-1174 others(27): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17721383 | ||||||
| chr4:17721383
|
C | CAAAAAAA others(18): Show |
1 | a0016c0025t0021g0225 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.142-11740_142-1173 others(29): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17721383 | ||||||
| chr4:17721383
|
C | CAAAAAAA others(21): Show |
1 | a0016c0025t0021g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.142-11740_142-1173 others(32): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17721383 | ||||||
| chr4:17721383
|
C | CAAAAAAA others(23): Show |
1 | a0033c0064t0057g0223 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.142-11740_142-1173 others(34): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17721383 | ||||||
| chr4:17721383
|
CA | C | 70 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(67): Show | 70 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.142-11740delT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17721383 | ||||||
| chr4:17721383
|
CAA | C | 7 | a0001c0004t0042g0108a0001c0008t0068g0234a0002c0001t0001g0120others(4): Show | 7 | HG00423.hp1 HG00639.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-11741_142-1174 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17721383 | ||||||
| chr4:17721383
|
CAAA | C | 10 | a0001c0012t0026g0092a0001c0021t0064g0005a0002c0002t0001g0134others(7): Show | 10 | HG02071.hp1 HG02630.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-11742_142-1174 others(7): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17721383 | ||||||
| chr4:17721459
|
G | A | 1 | a0002c0002t0001g0180 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.142-11815C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17721459 | ||||||
| chr4:17721545
|
G | A | 16 | a0001c0004t0009g0072a0001c0004t0045g0104a0001c0006t0003g0026others(13): Show | 16 | HG02886.hp1 HG02922.hp1 HG03017.hp2 others(13): Show |
intron_variant | MODIFIER | c.142-11901C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17721545 | ||||||
| chr4:17721691
|
A | G | 2 | a0002c0001t0001g0086a0002c0001t0001g0129 | 2 | HG03704.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.142-12047T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17721691 | ||||||
| chr4:17721699
|
G | A | 5 | a0001c0003t0002g0227a0001c0003t0008g0163a0011c0023t0024g0209others(2): Show | 5 | HG00140.hp1 HG00323.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-12055C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17721699 | ||||||
| chr4:17721769
|
C | T | 1 | a0002c0001t0017g0091 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.142-12125G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17721769 | ||||||
| chr4:17721874
|
T | C | 1 | a0002c0001t0001g0146 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.142-12230A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17721874 | ||||||
| chr4:17721917
|
C | G | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-12273G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17721917 | ||||||
| chr4:17721992
|
G | A | 6 | a0001c0003t0019g0095a0001c0004t0009g0022a0001c0004t0025g0023others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-12348C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17721992 | ||||||
| chr4:17722296
|
T | C | 1 | a0004c0010t0006g0077 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.142-12652A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17722296 | ||||||
| chr4:17722301
|
C | T | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-12657G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17722301 | ||||||
| chr4:17722377
|
T | C | 2 | a0001c0003t0023g0122a0002c0016t0001g0221 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.142-12733A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17722377 | ||||||
| chr4:17722454
|
T | C | 1 | a0002c0001t0001g0082 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.142-12810A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17722454 | ||||||
| chr4:17722567
|
C | T | 1 | a0031c0027t0001g0088 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.142-12923G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17722567 | ||||||
| chr4:17722653
|
C | T | 1 | a0001c0021t0064g0005 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.142-13009G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17722653 | ||||||
| chr4:17722840
|
C | G | 3 | a0003c0009t0005g0162a0005c0042t0006g0093a0007c0043t0012g0105 | 3 | HG01891.hp2 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.142-13196G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17722840 | ||||||
| chr4:17722896
|
T | C | 1 | a0001c0015t0029g0164 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.142-13252A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17722896 | ||||||
| chr4:17722951
|
A | T | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-13307T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17722951 | ||||||
| chr4:17722979
|
A | C | 6 | a0001c0003t0019g0095a0001c0004t0009g0022a0001c0004t0025g0023others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-13335T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17722979 | ||||||
| chr4:17723066
|
T | C | 2 | a0002c0002t0001g0228a0023c0053t0012g0080 | 2 | HG02615.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.142-13422A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17723066 | ||||||
| chr4:17723212
|
G | A | 3 | a0001c0015t0013g0106a0004c0010t0006g0107a0004c0010t0006g0109 | 3 | HG02451.hp1 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.142-13568C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17723212 | ||||||
| chr4:17723318
|
G | A | 1 | a0007c0041t0012g0011 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.142-13674C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17723318 | ||||||
| chr4:17723366
|
C | A | 1 | a0001c0003t0008g0208 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.142-13722G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17723366 | ||||||
| chr4:17723398
|
T | C | 1 | a0002c0002t0001g0155 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.142-13754A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17723398 | ||||||
| chr4:17723448
|
G | A | 1 | a0001c0003t0004g0057 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.142-13804C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17723448 | ||||||
| chr4:17723468
|
A | G | 231 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(228): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.142-13824T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17723468 | ||||||
| chr4:17723938
|
C | T | 1 | a0007c0041t0012g0011 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.142-14294G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17723938 | ||||||
| chr4:17724111
|
T | TCA | 13 | a0001c0003t0037g0219a0001c0005t0014g0118a0001c0012t0026g0092others(10): Show | 13 | HG00558.hp1 HG00597.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.142-14469_142-1446 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17724111 | ||||||
| chr4:17724111
|
T | TCACA | 55 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(52): Show | 55 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.142-14471_142-1446 others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17724111 | ||||||
| chr4:17724111
|
T | TCACACA | 3 | a0003c0009t0005g0162a0007c0050t0012g0004a0017c0026t0038g0098 | 3 | HG01358.hp2 HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.142-14473_142-1446 others(10): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17724111 | ||||||
| chr4:17724111
|
TCACA | T | 50 | a0001c0003t0004g0057a0001c0003t0008g0216a0001c0003t0011g0166others(47): Show | 50 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.142-14471_142-1446 others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17724111 | ||||||
| chr4:17724210
|
G | A | 3 | a0001c0012t0026g0092a0002c0020t0001g0079a0024c0037t0052g0094 | 3 | HG02717.hp1 HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.142-14566C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17724210 | ||||||
| chr4:17724236
|
T | C | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-14592A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17724236 | ||||||
| chr4:17724349
|
C | G | 1 | a0002c0002t0001g0063 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.142-14705G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17724349 | ||||||
| chr4:17724485
|
T | A | 1 | a0013c0058t0022g0174 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.142-14841A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17724485 | ||||||
| chr4:17724555
|
G | A | 1 | a0007c0041t0012g0011 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.142-14911C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17724555 | ||||||
| chr4:17724583
|
T | C | 15 | a0001c0004t0009g0072a0001c0004t0045g0104a0001c0006t0003g0026others(12): Show | 15 | HG02886.hp1 HG02922.hp1 HG03209.hp2 others(12): Show |
intron_variant | MODIFIER | c.142-14939A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17724583 | ||||||
| chr4:17724616
|
G | A | 4 | a0001c0004t0009g0022a0001c0004t0025g0023a0001c0004t0025g0024others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-14972C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17724616 | ||||||
| chr4:17724872
|
A | G | 2 | a0002c0002t0001g0228a0023c0053t0012g0080 | 2 | HG02615.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.142-15228T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17724872 | ||||||
| chr4:17724927
|
G | A | 7 | a0002c0001t0001g0136a0002c0001t0001g0145a0002c0001t0001g0146others(4): Show | 7 | HG00544.hp1 HG01074.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-15283C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17724927 | ||||||
| chr4:17725012
|
C | T | 1 | a0001c0003t0002g0149 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.142-15368G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17725012 | ||||||
| chr4:17725147
|
C | T | 51 | a0001c0003t0004g0057a0001c0003t0008g0216a0001c0003t0011g0166others(48): Show | 51 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.142-15503G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17725147 | ||||||
| chr4:17725327
|
T | C | 1 | a0001c0006t0003g0132 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.142-15683A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17725327 | ||||||
| chr4:17725445
|
T | G | 1 | a0012c0046t0002g0021 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.142-15801A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17725445 | ||||||
| chr4:17725504
|
C | T | 1 | a0001c0060t0027g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.142-15860G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17725504 | ||||||
| chr4:17725609
|
T | C | 1 | a0001c0003t0066g0150 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.142-15965A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17725609 | ||||||
| chr4:17725837
|
T | C | 1 | a0001c0003t0018g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-16193A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17725837 | ||||||
| chr4:17725907
|
G | A | 1 | a0001c0033t0003g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.142-16263C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17725907 | ||||||
| chr4:17726037
|
T | C | 231 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(228): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.142-16393A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17726037 | ||||||
| chr4:17726136
|
G | A | 3 | a0005c0036t0053g0233a0008c0039t0015g0016a0019c0040t0065g0012 | 3 | HG03041.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.142-16492C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17726136 | ||||||
| chr4:17726143
|
C | T | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-16499G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17726143 | ||||||
| chr4:17726154
|
G | A | 1 | a0008c0049t0034g0112 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.142-16510C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17726154 | ||||||
| chr4:17726179
|
G | A | 1 | a0001c0007t0019g0143 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.142-16535C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17726179 | ||||||
| chr4:17726318
|
G | A | 68 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(65): Show | 68 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.142-16674C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17726318 | ||||||
| chr4:17726401
|
T | C | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-16757A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17726401 | ||||||
| chr4:17726480
|
T | C | 1 | a0031c0027t0001g0088 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.142-16836A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17726480 | ||||||
| chr4:17726664
|
G | A | 6 | a0001c0003t0019g0095a0001c0004t0009g0022a0001c0004t0025g0023others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-17020C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17726664 | ||||||
| chr4:17726695
|
T | C | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-17051A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17726695 | ||||||
| chr4:17726701
|
C | T | 1 | a0001c0003t0018g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-17057G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17726701 | ||||||
| chr4:17726733
|
C | T | 51 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(48): Show | 51 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.142-17089G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17726733 | ||||||
| chr4:17726983
|
C | A | 1 | a0002c0001t0001g0101 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.142-17339G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17726983 | ||||||
| chr4:17727134
|
A | C | 1 | a0002c0002t0016g0039 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.142-17490T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17727134 | ||||||
| chr4:17727174
|
C | T | 149 | a0001c0003t0004g0057a0001c0003t0008g0216a0001c0003t0011g0166others(146): Show | 149 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.142-17530G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17727174 | ||||||
| chr4:17727177
|
A | G | 1 | a0001c0021t0064g0005 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.142-17533T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17727177 | ||||||
| chr4:17727195
|
T | G | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-17551A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17727195 | ||||||
| chr4:17727228
|
G | A | 1 | a0002c0002t0001g0114 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142-17584C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17727228 | ||||||
| chr4:17727509
|
T | C | 1 | a0002c0001t0001g0214 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.142-17865A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17727509 | ||||||
| chr4:17727637
|
C | G | 5 | a0001c0017t0010g0103a0002c0002t0001g0025a0002c0002t0001g0049others(2): Show | 5 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-17993G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17727637 | ||||||
| chr4:17727691
|
C | T | 1 | a0001c0015t0013g0003 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.142-18047G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17727691 | ||||||
| chr4:17727947
|
C | T | 7 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0032g0236others(4): Show | 7 | HG00423.hp1 HG02071.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-18303G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17727947 | ||||||
| chr4:17728169
|
G | A | 1 | a0001c0015t0029g0164 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.142-18525C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17728169 | ||||||
| chr4:17728234
|
A | G | 3 | a0001c0004t0009g0072a0001c0004t0045g0104a0013c0058t0022g0174 | 3 | HG02630.hp2 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.142-18590T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17728234 | ||||||
| chr4:17728274
|
C | T | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-18630G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17728274 | ||||||
| chr4:17728336
|
A | C | 1 | a0002c0001t0001g0190 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.142-18692T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17728336 | ||||||
| chr4:17728397
|
A | G | 5 | a0001c0005t0014g0170a0001c0012t0026g0092a0005c0042t0006g0093others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-18753T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17728397 | ||||||
| chr4:17728545
|
G | A | 1 | a0001c0029t0005g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.142-18901C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17728545 | ||||||
| chr4:17728644
|
G | A | 161 | a0001c0003t0004g0057a0001c0003t0008g0216a0001c0003t0011g0166others(158): Show | 161 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.142-19000C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17728644 | ||||||
| chr4:17728720
|
C | T | 2 | a0002c0002t0001g0228a0023c0053t0012g0080 | 2 | HG02615.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.142-19076G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17728720 | ||||||
| chr4:17728754
|
A | T | 2 | a0001c0005t0014g0110a0001c0005t0027g0111 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.142-19110T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17728754 | ||||||
| chr4:17728815
|
C | T | 7 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0032g0236others(4): Show | 7 | HG00423.hp1 HG02071.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-19171G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17728815 | ||||||
| chr4:17728816
|
G | A | 53 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(50): Show | 53 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.142-19172C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17728816 | ||||||
| chr4:17728821
|
C | T | 7 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0032g0236others(4): Show | 7 | HG00423.hp1 HG02071.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-19177G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17728821 | ||||||
| chr4:17728827
|
A | G | 1 | a0002c0002t0001g0049 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.142-19183T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17728827 | ||||||
| chr4:17728864
|
C | T | 2 | a0001c0003t0023g0122a0002c0016t0001g0221 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.142-19220G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17728864 | ||||||
| chr4:17728927
|
C | T | 2 | a0001c0004t0009g0072a0001c0004t0045g0104 | 2 | HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.142-19283G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17728927 | ||||||
| chr4:17728962
|
G | A | 1 | a0001c0004t0042g0108 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.142-19318C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17728962 | ||||||
| chr4:17729018
|
C | T | 3 | a0001c0004t0009g0072a0001c0004t0045g0104a0013c0058t0022g0174 | 3 | HG02630.hp2 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.142-19374G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17729018 | ||||||
| chr4:17729101
|
TC | T | 6 | a0007c0041t0012g0011a0015c0062t0035g0230a0015c0063t0054g0229others(3): Show | 6 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-19458delG | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17729101 | ||||||
| chr4:17729104
|
C | T | 2 | a0001c0004t0009g0072a0001c0004t0045g0104 | 2 | HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.142-19460G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17729104 | ||||||
| chr4:17729127
|
C | T | 50 | a0001c0003t0004g0057a0001c0003t0008g0216a0001c0003t0011g0166others(47): Show | 50 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.142-19483G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17729127 | ||||||
| chr4:17729189
|
A | G | 228 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(225): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.142-19545T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17729189 | ||||||
| chr4:17729302
|
G | A | 2 | a0002c0002t0001g0228a0023c0053t0012g0080 | 2 | HG02615.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.142-19658C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17729302 | ||||||
| chr4:17729377
|
G | A | 81 | a0001c0004t0042g0108a0001c0005t0007g0013a0001c0005t0007g0125others(78): Show | 81 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.142-19733C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17729377 | ||||||
| chr4:17729515
|
C | G | 10 | a0001c0003t0004g0057a0001c0003t0011g0166a0001c0003t0011g0167others(7): Show | 10 | HG00323.hp2 HG01099.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-19871G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17729515 | ||||||
| chr4:17729615
|
G | A | 13 | a0001c0006t0003g0026a0001c0006t0003g0028a0001c0006t0003g0029others(10): Show | 13 | HG02886.hp1 HG03579.hp2 HG03831.hp2 others(10): Show |
intron_variant | MODIFIER | c.142-19971C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17729615 | ||||||
| chr4:17729824
|
G | A | 1 | a0001c0007t0019g0143 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.142-20180C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17729824 | ||||||
| chr4:17729842
|
G | C | 1 | a0023c0053t0012g0080 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.142-20198C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17729842 | ||||||
| chr4:17729855
|
T | C | 1 | a0023c0053t0012g0080 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.142-20211A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17729855 | ||||||
| chr4:17729883
|
T | C | 1 | a0001c0005t0014g0170 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.142-20239A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17729883 | ||||||
| chr4:17729933
|
G | A | 1 | a0013c0058t0022g0174 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.142-20289C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17729933 | ||||||
| chr4:17729966
|
C | T | 2 | a0006c0019t0001g0064a0006c0019t0001g0100 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.142-20322G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17729966 | ||||||
| chr4:17730075
|
C | T | 81 | a0001c0004t0042g0108a0001c0005t0007g0013a0001c0005t0007g0125others(78): Show | 81 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.142-20431G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17730075 | ||||||
| chr4:17730126
|
C | T | 7 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0032g0236others(4): Show | 7 | HG00423.hp1 HG02071.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-20482G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17730126 | ||||||
| chr4:17730133
|
G | A | 1 | a0025c0056t0061g0078 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.142-20489C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17730133 | ||||||
| chr4:17730156
|
A | G | 6 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0032g0236others(3): Show | 6 | HG00423.hp1 HG02071.hp1 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-20512T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17730156 | ||||||
| chr4:17730195
|
C | T | 1 | a0030c0051t0010g0041 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.142-20551G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17730195 | ||||||
| chr4:17730276
|
A | G | 2 | a0002c0020t0001g0079a0008c0049t0034g0112 | 2 | HG01243.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.142-20632T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17730276 | ||||||
| chr4:17730383
|
G | A | 6 | a0001c0003t0019g0095a0001c0004t0009g0022a0001c0004t0025g0023others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-20739C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17730383 | ||||||
| chr4:17730445
|
C | T | 2 | a0002c0001t0001g0086a0002c0001t0001g0129 | 2 | HG03704.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.142-20801G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17730445 | ||||||
| chr4:17730457
|
T | C | 6 | a0007c0041t0012g0011a0015c0062t0035g0230a0015c0063t0054g0229others(3): Show | 6 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-20813A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17730457 | ||||||
| chr4:17730579
|
C | T | 13 | a0001c0006t0003g0026a0001c0006t0003g0028a0001c0006t0003g0029others(10): Show | 13 | HG02886.hp1 HG03579.hp2 HG03831.hp2 others(10): Show |
intron_variant | MODIFIER | c.142-20935G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17730579 | ||||||
| chr4:17730676
|
G | A | 1 | a0001c0015t0029g0164 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.142-21032C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17730676 | ||||||
| chr4:17730775
|
G | A | 46 | a0001c0003t0004g0057a0001c0003t0008g0216a0001c0003t0011g0166others(43): Show | 46 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.142-21131C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17730775 | ||||||
| chr4:17730876
|
G | A | 40 | a0001c0005t0007g0013a0001c0005t0007g0125a0001c0005t0007g0140others(37): Show | 40 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.142-21232C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17730876 | ||||||
| chr4:17730931
|
G | T | 7 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0032g0236others(4): Show | 7 | HG00423.hp1 HG02071.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-21287C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17730931 | ||||||
| chr4:17731019
|
C | A | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-21375G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17731019 | ||||||
| chr4:17731118
|
C | G | 2 | a0002c0002t0001g0043a0002c0002t0001g0044 | 2 | HG00099.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.142-21474G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17731118 | ||||||
| chr4:17731216
|
A | G | 1 | a0001c0015t0029g0164 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.142-21572T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17731216 | ||||||
| chr4:17731221
|
C | T | 50 | a0001c0003t0004g0057a0001c0003t0008g0216a0001c0003t0011g0166others(47): Show | 50 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.142-21577G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17731221 | ||||||
| chr4:17731259
|
A | C | 2 | a0002c0002t0001g0228a0023c0053t0012g0080 | 2 | HG02615.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.142-21615T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17731259 | ||||||
| chr4:17731471
|
G | C | 7 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0032g0236others(4): Show | 7 | HG00423.hp1 HG02071.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-21827C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17731471 | ||||||
| chr4:17731571
|
G | C | 6 | a0001c0003t0019g0095a0001c0004t0009g0022a0001c0004t0025g0023others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-21927C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17731571 | ||||||
| chr4:17731604
|
G | T | 1 | a0002c0020t0016g0089 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.142-21960C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17731604 | ||||||
| chr4:17731917
|
C | T | 231 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(228): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.142-22273G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17731917 | ||||||
| chr4:17731941
|
C | A | 1 | a0002c0001t0001g0002 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.142-22297G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17731941 | ||||||
| chr4:17731950
|
G | A | 2 | a0001c0021t0064g0005a0025c0056t0061g0078 | 2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.142-22306C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17731950 | ||||||
| chr4:17732004
|
T | A | 53 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(50): Show | 53 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.142-22360A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17732004 | ||||||
| chr4:17732022
|
C | T | 1 | a0014c0024t0032g0237 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-22378G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17732022 | ||||||
| chr4:17732127
|
T | C | 1 | a0007c0050t0012g0004 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.142-22483A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17732127 | ||||||
| chr4:17732179
|
T | C | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-22535A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17732179 | ||||||
| chr4:17732314
|
A | G | 1 | a0002c0001t0001g0142 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.142-22670T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17732314 | ||||||
| chr4:17732316
|
G | A | 6 | a0001c0003t0019g0095a0001c0004t0009g0022a0001c0004t0025g0023others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-22672C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17732316 | ||||||
| chr4:17732460
|
A | G | 13 | a0001c0006t0003g0026a0001c0006t0003g0028a0001c0006t0003g0029others(10): Show | 13 | HG02886.hp1 HG03579.hp2 HG03831.hp2 others(10): Show |
intron_variant | MODIFIER | c.142-22816T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17732460 | ||||||
| chr4:17732461
|
G | C | 164 | a0001c0003t0004g0057a0001c0003t0008g0216a0001c0003t0011g0166others(161): Show | 164 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.142-22817C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17732461 | ||||||
| chr4:17732540
|
T | C | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-22896A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17732540 | ||||||
| chr4:17732586
|
G | A | 1 | a0002c0001t0001g0002 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.142-22942C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17732586 | ||||||
| chr4:17732748
|
A | C | 2 | a0002c0002t0001g0228a0023c0053t0012g0080 | 2 | HG02615.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.142-23104T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17732748 | ||||||
| chr4:17732834
|
T | C | 1 | a0001c0005t0014g0170 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.142-23190A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17732834 | ||||||
| chr4:17732877
|
C | T | 2 | a0002c0002t0001g0176a0002c0002t0001g0177 | 2 | HG02602.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.142-23233G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17732877 | ||||||
| chr4:17732917
|
C | T | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-23273G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17732917 | ||||||
| chr4:17732932
|
C | T | 1 | a0005c0031t0015g0193 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.142-23288G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17732932 | ||||||
| chr4:17732962
|
G | C | 3 | a0002c0020t0001g0079a0007c0050t0012g0004a0008c0049t0034g0112 | 3 | HG01243.hp2 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.142-23318C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17732962 | ||||||
| chr4:17733096
|
T | C | 1 | a0002c0001t0001g0218 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.142-23452A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17733096 | ||||||
| chr4:17733205
|
C | T | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-23561G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17733205 | ||||||
| chr4:17733241
|
G | A | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-23597C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17733241 | ||||||
| chr4:17733242
|
T | C | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-23598A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17733242 | ||||||
| chr4:17733265
|
G | A | 4 | a0001c0007t0019g0143a0002c0001t0017g0091a0002c0001t0017g0137others(1): Show | 4 | HG01123.hp2 HG02698.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-23621C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17733265 | ||||||
| chr4:17733287
|
T | C | 6 | a0007c0041t0012g0011a0015c0062t0035g0230a0015c0063t0054g0229others(3): Show | 6 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-23643A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17733287 | ||||||
| chr4:17733412
|
A | G | 1 | a0001c0003t0018g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-23768T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17733412 | ||||||
| chr4:17733717
|
G | A | 1 | a0032c0061t0030g0007 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.142-24073C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17733717 | ||||||
| chr4:17733751
|
T | TG | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-24108_142-2410 others(5): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17733751 | ||||||
| chr4:17733768
|
T | G | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-24124A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17733768 | ||||||
| chr4:17733909
|
C | T | 1 | a0002c0001t0001g0214 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.142-24265G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17733909 | ||||||
| chr4:17733910
|
G | A | 1 | a0002c0001t0001g0214 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.142-24266C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17733910 | ||||||
| chr4:17733928
|
C | A | 1 | a0001c0021t0064g0005 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.142-24284G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17733928 | ||||||
| chr4:17733986
|
T | C | 1 | a0001c0060t0027g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.142-24342A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17733986 | ||||||
| chr4:17734006
|
G | A | 7 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0032g0236others(4): Show | 7 | HG00423.hp1 HG02071.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-24362C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17734006 | ||||||
| chr4:17734028
|
A | G | 2 | a0001c0021t0064g0005a0025c0056t0061g0078 | 2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.142-24384T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17734028 | ||||||
| chr4:17734070
|
A | G | 37 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(34): Show | 37 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.142-24426T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17734070 | ||||||
| chr4:17734104
|
G | T | 7 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0032g0236others(4): Show | 7 | HG00423.hp1 HG02071.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-24460C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17734104 | ||||||
| chr4:17734163
|
C | T | 3 | a0001c0004t0009g0072a0001c0004t0045g0104a0013c0058t0022g0174 | 3 | HG02630.hp2 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.142-24519G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17734163 | ||||||
| chr4:17734239
|
C | G | 13 | a0001c0006t0003g0026a0001c0006t0003g0028a0001c0006t0003g0029others(10): Show | 13 | HG02886.hp1 HG03579.hp2 HG03831.hp2 others(10): Show |
intron_variant | MODIFIER | c.142-24595G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17734239 | ||||||
| chr4:17734310
|
C | G | 3 | a0005c0036t0053g0233a0008c0039t0015g0016a0019c0040t0065g0012 | 3 | HG03041.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.142-24666G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17734310 | ||||||
| chr4:17734372
|
A | G | 6 | a0001c0003t0019g0095a0001c0004t0009g0022a0001c0004t0025g0023others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-24728T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17734372 | ||||||
| chr4:17734424
|
C | T | 1 | a0002c0001t0001g0187 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.142-24780G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17734424 | ||||||
| chr4:17734626
|
A | G | 13 | a0001c0006t0003g0026a0001c0006t0003g0028a0001c0006t0003g0029others(10): Show | 13 | HG02886.hp1 HG03579.hp2 HG03831.hp2 others(10): Show |
intron_variant | MODIFIER | c.142-24982T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17734626 | ||||||
| chr4:17734651
|
G | C | 4 | a0001c0003t0018g0006a0001c0015t0029g0164a0002c0001t0001g0116others(1): Show | 4 | HG03139.hp2 HG03471.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-25007C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17734651 | ||||||
| chr4:17734721
|
A | C | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-25077T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17734721 | ||||||
| chr4:17734770
|
C | T | 231 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(228): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.142-25126G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17734770 | ||||||
| chr4:17734773
|
C | T | 81 | a0001c0004t0042g0108a0001c0005t0007g0013a0001c0005t0007g0125others(78): Show | 81 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.142-25129G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17734773 | ||||||
| chr4:17734829
|
A | G | 1 | a0021c0052t0050g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.142-25185T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17734829 | ||||||
| chr4:17734967
|
A | G | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-25323T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17734967 | ||||||
| chr4:17734984
|
T | C | 1 | a0002c0002t0069g0235 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.142-25340A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17734984 | ||||||
| chr4:17735126
|
A | G | 3 | a0001c0003t0011g0166a0001c0003t0011g0167a0001c0003t0011g0168 | 3 | HG03704.hp2 HG04199.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.142-25482T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17735126 | ||||||
| chr4:17735172
|
G | A | 1 | a0001c0004t0042g0108 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.142-25528C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17735172 | ||||||
| chr4:17735219
|
A | G | 1 | a0002c0002t0001g0040 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.142-25575T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17735219 | ||||||
| chr4:17735278
|
A | G | 1 | a0001c0015t0029g0164 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.142-25634T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17735278 | ||||||
| chr4:17735368
|
C | T | 1 | a0002c0020t0016g0089 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.142-25724G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17735368 | ||||||
| chr4:17735382
|
A | T | 7 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0032g0236others(4): Show | 7 | HG00423.hp1 HG02071.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-25738T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17735382 | ||||||
| chr4:17735571
|
G | T | 1 | a0013c0058t0022g0174 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.142-25927C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17735571 | ||||||
| chr4:17735609
|
A | G | 6 | a0001c0003t0019g0095a0001c0004t0009g0022a0001c0004t0025g0023others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-25965T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17735609 | ||||||
| chr4:17735633
|
T | C | 61 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.142-25989A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17735633 | ||||||
| chr4:17735643
|
G | GAAAAAGA others(246): Show |
2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-26000_142-2599 others(257): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17735643 | ||||||
| chr4:17735923
|
G | C | 1 | a0001c0003t0018g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-26279C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17735923 | ||||||
| chr4:17735985
|
T | C | 1 | a0002c0020t0001g0079 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.142-26341A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17735985 | ||||||
| chr4:17736019
|
T | C | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-26375A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17736019 | ||||||
| chr4:17736284
|
C | G | 4 | a0001c0008t0018g0020a0001c0008t0019g0102a0001c0021t0018g0068others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-26640G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17736284 | ||||||
| chr4:17736479
|
G | A | 7 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0032g0236others(4): Show | 7 | HG00423.hp1 HG02071.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-26835C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17736479 | ||||||
| chr4:17736488
|
T | C | 1 | a0002c0002t0001g0058 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.142-26844A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17736488 | ||||||
| chr4:17736669
|
G | A | 14 | a0001c0033t0003g0200a0002c0001t0001g0082a0002c0001t0001g0086others(11): Show | 14 | HG00609.hp2 HG00642.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-27025C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17736669 | ||||||
| chr4:17736750
|
T | C | 1 | a0002c0020t0001g0079 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.142-27106A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17736750 | ||||||
| chr4:17736777
|
G | A | 6 | a0007c0041t0012g0011a0015c0062t0035g0230a0015c0063t0054g0229others(3): Show | 6 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-27133C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17736777 | ||||||
| chr4:17736860
|
G | A | 3 | a0001c0004t0009g0072a0001c0004t0045g0104a0013c0058t0022g0174 | 3 | HG02630.hp2 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.142-27216C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17736860 | ||||||
| chr4:17736971
|
G | C | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-27327C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17736971 | ||||||
| chr4:17737067
|
C | T | 1 | a0002c0001t0001g0135 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.142-27423G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17737067 | ||||||
| chr4:17737200
|
C | A | 5 | a0001c0005t0014g0170a0001c0012t0026g0092a0005c0042t0006g0093others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-27556G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17737200 | ||||||
| chr4:17737638
|
G | A | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-27994C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17737638 | ||||||
| chr4:17737727
|
T | C | 3 | a0001c0003t0018g0006a0001c0015t0029g0164a0020c0054t0001g0202 | 3 | HG00323.hp1 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-28083A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17737727 | ||||||
| chr4:17737880
|
G | A | 1 | a0006c0014t0001g0008 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.142-28236C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17737880 | ||||||
| chr4:17737962
|
C | T | 3 | a0001c0004t0009g0072a0001c0004t0045g0104a0013c0058t0022g0174 | 3 | HG02630.hp2 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.142-28318G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17737962 | ||||||
| chr4:17738057
|
C | T | 5 | a0001c0005t0014g0170a0001c0012t0026g0092a0005c0042t0006g0093others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-28413G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17738057 | ||||||
| chr4:17738080
|
G | A | 1 | a0002c0002t0001g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.142-28436C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17738080 | ||||||
| chr4:17738183
|
A | G | 3 | a0002c0020t0001g0079a0007c0050t0012g0004a0008c0049t0034g0112 | 3 | HG01243.hp2 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.142-28539T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17738183 | ||||||
| chr4:17738262
|
C | T | 7 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0032g0236others(4): Show | 7 | HG00423.hp1 HG02071.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-28618G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17738262 | ||||||
| chr4:17738631
|
TA | T | 6 | a0007c0041t0012g0011a0015c0062t0035g0230a0015c0063t0054g0229others(3): Show | 6 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-28988delT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17738631 | ||||||
| chr4:17738806
|
C | T | 2 | a0002c0001t0031g0178a0002c0001t0031g0179 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.142-29162G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17738806 | ||||||
| chr4:17738990
|
T | A | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-29346A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17738990 | ||||||
| chr4:17739085
|
C | T | 3 | a0002c0002t0001g0054a0002c0002t0001g0056a0002c0002t0001g0065 | 3 | HG00280.hp2 HG02293.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.142-29441G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17739085 | ||||||
| chr4:17739168
|
C | T | 13 | a0001c0006t0003g0026a0001c0006t0003g0028a0001c0006t0003g0029others(10): Show | 13 | HG02886.hp1 HG03579.hp2 HG03831.hp2 others(10): Show |
intron_variant | MODIFIER | c.142-29524G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17739168 | ||||||
| chr4:17739487
|
G | A | 85 | a0001c0004t0042g0108a0001c0005t0007g0013a0001c0005t0007g0125others(82): Show | 85 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.142-29843C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17739487 | ||||||
| chr4:17739540
|
T | C | 4 | a0002c0001t0001g0120a0002c0001t0001g0121a0002c0001t0001g0222others(1): Show | 4 | HG00639.hp2 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-29896A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17739540 | ||||||
| chr4:17739553
|
C | CTGTTTTT others(7): Show |
1 | a0002c0001t0001g0186 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.142-29923_142-2991 others(18): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17739553 | ||||||
| chr4:17739555
|
G | GTTTTTGT others(7): Show |
3 | a0001c0007t0004g0097a0001c0007t0008g0157a0001c0007t0023g0123 | 3 | HG01081.hp2 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.142-29912_142-2991 others(18): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17739555 | ||||||
| chr4:17739555
|
G | GTTTTTGT others(8): Show |
1 | a0001c0007t0039g0124 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.142-29912_142-2991 others(19): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17739555 | ||||||
| chr4:17739555
|
G | GTTTTTTT others(10): Show |
1 | a0001c0015t0029g0164 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.142-29912_142-2991 others(21): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17739555 | ||||||
| chr4:17739555
|
G | GTTTTTTT others(5): Show |
1 | a0024c0037t0052g0094 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.142-29923_142-2991 others(16): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17739555 | ||||||
| chr4:17739555
|
G | GTTTTTTT others(7): Show |
1 | a0009c0011t0001g0032 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.142-29912_142-2991 others(18): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17739555 | ||||||
| chr4:17739555
|
G | GTTTTTTT others(6): Show |
43 | a0001c0003t0002g0227a0001c0003t0004g0057a0001c0003t0008g0216others(40): Show | 43 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.142-29924_142-2991 others(17): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17739555 | ||||||
| chr4:17739555
|
G | GTTTTTTT others(7): Show |
98 | a0001c0003t0004g0018a0001c0003t0004g0067a0001c0003t0007g0220others(95): Show | 98 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.142-29925_142-2991 others(18): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17739555 | ||||||
| chr4:17739555
|
G | GTTTTTTT others(8): Show |
63 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(60): Show | 63 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.142-29926_142-2991 others(19): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17739555 | ||||||
| chr4:17739555
|
G | GTTTTTTT others(9): Show |
16 | a0001c0003t0002g0069a0001c0003t0008g0208a0001c0003t0044g0159others(13): Show | 16 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.142-29927_142-2991 others(20): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17739555 | ||||||
| chr4:17739555
|
G | GTTTTTTT others(10): Show |
1 | a0001c0003t0018g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-29912_142-2991 others(21): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17739555 | ||||||
| chr4:17739557
|
T | TTTTTTTT others(7): Show |
1 | a0010c0013t0002g0231 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.142-29914_142-2991 others(18): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17739557 | ||||||
| chr4:17739602
|
G | A | 1 | a0002c0002t0001g0180 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.142-29958C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17739602 | ||||||
| chr4:17739614
|
C | T | 1 | a0001c0003t0037g0219 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.142-29970G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17739614 | ||||||
| chr4:17739975
|
T | C | 103 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.142-30331A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17739975 | ||||||
| chr4:17740112
|
G | T | 1 | a0001c0021t0064g0005 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.142-30468C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17740112 | ||||||
| chr4:17740250
|
A | G | 232 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(229): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.142-30606T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17740250 | ||||||
| chr4:17740308
|
C | T | 2 | a0001c0003t0023g0122a0002c0016t0001g0221 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.142-30664G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17740308 | ||||||
| chr4:17740313
|
C | A | 1 | a0001c0005t0013g0185 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.142-30669G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17740313 | ||||||
| chr4:17740351
|
C | CA | 192 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.142-30708dupT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17740351 | ||||||
| chr4:17740351
|
C | CAA | 18 | a0001c0003t0002g0158a0001c0003t0011g0167a0001c0004t0003g0207others(15): Show | 18 | HG00323.hp1 HG00642.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.142-30709_142-3070 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17740351 | ||||||
| chr4:17740351
|
C | CAAA | 7 | a0001c0005t0014g0170a0001c0008t0068g0234a0002c0002t0001g0134others(4): Show | 7 | HG00423.hp1 HG01361.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.142-30710_142-3070 others(7): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17740351 | ||||||
| chr4:17740351
|
C | CAAAA | 5 | a0001c0012t0026g0092a0002c0002t0032g0236a0005c0042t0006g0093others(2): Show | 5 | HG01891.hp2 HG02717.hp1 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-30711_142-3070 others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17740351 | ||||||
| chr4:17740403
|
T | C | 2 | a0001c0003t0023g0122a0002c0016t0001g0221 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.142-30759A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17740403 | ||||||
| chr4:17740526
|
CT | C | 13 | a0001c0006t0003g0026a0001c0006t0003g0028a0001c0006t0003g0029others(10): Show | 13 | HG02886.hp1 HG03579.hp2 HG03831.hp2 others(10): Show |
intron_variant | MODIFIER | c.142-30883delA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17740526 | ||||||
| chr4:17740609
|
T | C | 1 | a0001c0003t0044g0159 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.142-30965A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17740609 | ||||||
| chr4:17740717
|
C | G | 2 | a0002c0001t0031g0178a0002c0001t0031g0179 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.142-31073G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17740717 | ||||||
| chr4:17740751
|
G | A | 1 | a0018c0044t0001g0062 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.142-31107C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17740751 | ||||||
| chr4:17740773
|
A | G | 235 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.142-31129T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17740773 | ||||||
| chr4:17741119
|
T | C | 232 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(229): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.142-31475A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17741119 | ||||||
| chr4:17741302
|
G | T | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-31658C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17741302 | ||||||
| chr4:17741555
|
G | A | 2 | a0002c0002t0001g0051a0002c0002t0001g0066 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.142-31911C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17741555 | ||||||
| chr4:17741642
|
G | A | 2 | a0002c0002t0001g0228a0023c0053t0012g0080 | 2 | HG02615.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.142-31998C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17741642 | ||||||
| chr4:17741716
|
C | T | 1 | a0017c0026t0038g0098 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.142-32072G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17741716 | ||||||
| chr4:17741728
|
G | A | 3 | a0005c0036t0053g0233a0008c0039t0015g0016a0019c0040t0065g0012 | 3 | HG03041.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.142-32084C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17741728 | ||||||
| chr4:17741758
|
G | A | 6 | a0001c0005t0007g0125a0001c0005t0007g0140a0002c0001t0001g0141others(3): Show | 6 | HG02895.hp2 HG02897.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-32114C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17741758 | ||||||
| chr4:17741814
|
T | C | 4 | a0002c0001t0001g0120a0002c0001t0001g0121a0002c0001t0001g0222others(1): Show | 4 | HG00639.hp2 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-32170A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17741814 | ||||||
| chr4:17741847
|
T | C | 5 | a0001c0005t0014g0170a0001c0012t0026g0092a0005c0042t0006g0093others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-32203A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17741847 | ||||||
| chr4:17741932
|
A | C | 1 | a0032c0061t0030g0007 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.142-32288T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17741932 | ||||||
| chr4:17741979
|
T | C | 1 | a0001c0005t0007g0194 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.142-32335A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17741979 | ||||||
| chr4:17742055
|
G | C | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-32411C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742055 | ||||||
| chr4:17742077
|
G | A | 5 | a0001c0005t0014g0170a0001c0012t0026g0092a0005c0042t0006g0093others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-32433C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742077 | ||||||
| chr4:17742137
|
AATAT | A | 2 | a0008c0039t0015g0016a0019c0040t0065g0012 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.142-32497_142-3249 others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742137 | ||||||
| chr4:17742137
|
AATATATA others(1): Show |
A | 44 | a0001c0003t0004g0057a0001c0003t0008g0216a0001c0003t0011g0166others(41): Show | 44 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.142-32501_142-3249 others(12): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742137 | ||||||
| chr4:17742137
|
AATATATA others(3): Show |
A | 26 | a0001c0003t0002g0206a0001c0003t0007g0220a0001c0003t0008g0163others(23): Show | 26 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.142-32503_142-3249 others(14): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742137 | ||||||
| chr4:17742137
|
AATATATA others(9): Show |
A | 2 | a0001c0003t0023g0122a0002c0016t0001g0221 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.142-32509_142-3249 others(20): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742137 | ||||||
| chr4:17742155
|
TATATATA others(2): Show |
T | 21 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(18): Show | 21 | HG01074.hp1 HG01081.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.142-32520_142-3251 others(13): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742155 | ||||||
| chr4:17742155
|
TATATATA others(4): Show |
T | 1 | a0001c0005t0014g0170 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.142-32522_142-3251 others(15): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742155 | ||||||
| chr4:17742157
|
TATATATA others(2): Show |
T | 27 | a0001c0003t0002g0069a0001c0003t0008g0208a0001c0003t0046g0059others(24): Show | 27 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.142-32522_142-3251 others(13): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742157 | ||||||
| chr4:17742157
|
TATATATA others(4): Show |
T | 3 | a0001c0005t0007g0194a0015c0062t0035g0230a0015c0063t0054g0229 | 3 | HG02622.hp1 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.142-32524_142-3251 others(15): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742157 | ||||||
| chr4:17742158
|
ATATATAT others(4): Show |
A | 9 | a0001c0012t0026g0092a0001c0047t0010g0113a0004c0010t0006g0077others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.142-32525_142-3251 others(15): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742158 | ||||||
| chr4:17742159
|
TATATATA | T | 7 | a0001c0015t0013g0106a0002c0002t0001g0114a0002c0002t0001g0119others(4): Show | 7 | HG00140.hp2 HG02280.hp1 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.142-32522_142-3251 others(11): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742159 | ||||||
| chr4:17742159
|
TATATATA others(2): Show |
T | 55 | a0001c0005t0007g0125a0001c0005t0007g0140a0001c0005t0013g0185others(52): Show | 55 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.142-32524_142-3251 others(13): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742159 | ||||||
| chr4:17742160
|
ATATATAT others(2): Show |
A | 9 | a0001c0004t0042g0108a0001c0007t0020g0060a0001c0033t0003g0200others(6): Show | 9 | HG00609.hp1 HG01071.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.142-32525_142-3251 others(13): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742160 | ||||||
| chr4:17742160
|
ATATATAT others(4): Show |
A | 12 | a0001c0006t0003g0026a0001c0006t0003g0028a0001c0006t0003g0029others(9): Show | 12 | HG03579.hp2 HG03831.hp2 HG04199.hp2 others(9): Show |
intron_variant | MODIFIER | c.142-32527_142-3251 others(15): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742160 | ||||||
| chr4:17742161
|
TATATATA | T | 6 | a0001c0003t0018g0006a0002c0002t0001g0047a0002c0002t0001g0051others(3): Show | 6 | HG00423.hp2 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-32524_142-3251 others(11): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742161 | ||||||
| chr4:17742163
|
TATATA | T | 2 | a0002c0001t0017g0091a0002c0001t0017g0137 | 2 | HG02698.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.142-32524_142-3252 others(9): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742163 | ||||||
| chr4:17742164
|
A | T | 3 | a0001c0004t0003g0212a0002c0002t0001g0040a0026c0055t0002g0117 | 3 | HG00280.hp1 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.142-32520T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742164 | ||||||
| chr4:17742166
|
A | T | 58 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(55): Show | 58 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.142-32522T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742166 | ||||||
| chr4:17742168
|
A | ATATATAT others(8): Show |
1 | a0023c0053t0012g0080 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.142-32525_142-3252 others(19): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742168 | ||||||
| chr4:17742168
|
A | T | 116 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.142-32524T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742168 | ||||||
| chr4:17742195
|
A | G | 5 | a0001c0005t0014g0170a0001c0012t0026g0092a0005c0042t0006g0093others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-32551T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742195 | ||||||
| chr4:17742236
|
G | A | 8 | a0001c0003t0007g0220a0001c0004t0009g0017a0001c0004t0009g0072others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.142-32592C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742236 | ||||||
| chr4:17742248
|
G | A | 5 | a0001c0005t0014g0170a0001c0012t0026g0092a0005c0042t0006g0093others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-32604C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742248 | ||||||
| chr4:17742434
|
G | A | 3 | a0016c0025t0021g0224a0016c0025t0021g0225a0033c0064t0057g0223 | 3 | HG01109.hp2 HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.142-32790C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742434 | ||||||
| chr4:17742513
|
C | T | 200 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.142-32869G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742513 | ||||||
| chr4:17742605
|
T | C | 1 | a0002c0001t0001g0141 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.142-32961A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742605 | ||||||
| chr4:17742629
|
C | T | 5 | a0001c0005t0014g0170a0001c0012t0026g0092a0005c0042t0006g0093others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-32985G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742629 | ||||||
| chr4:17742664
|
A | T | 3 | a0001c0015t0013g0106a0004c0010t0006g0107a0004c0010t0006g0109 | 3 | HG02451.hp1 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.142-33020T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742664 | ||||||
| chr4:17742747
|
G | T | 1 | a0001c0015t0029g0164 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.142-33103C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742747 | ||||||
| chr4:17742842
|
C | T | 5 | a0015c0062t0035g0230a0015c0063t0054g0229a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-33198G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742842 | ||||||
| chr4:17742898
|
A | C | 6 | a0001c0003t0019g0095a0001c0004t0009g0022a0001c0004t0025g0023others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-33254T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742898 | ||||||
| chr4:17742946
|
G | A | 1 | a0013c0058t0022g0174 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.142-33302C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17742946 | ||||||
| chr4:17743105
|
A | T | 2 | a0002c0002t0001g0228a0023c0053t0012g0080 | 2 | HG02615.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.142-33461T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17743105 | ||||||
| chr4:17743109
|
G | T | 1 | a0013c0058t0022g0174 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.142-33465C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17743109 | ||||||
| chr4:17743311
|
A | G | 5 | a0001c0005t0014g0170a0001c0012t0026g0092a0005c0042t0006g0093others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-33667T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17743311 | ||||||
| chr4:17743426
|
C | T | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-33782G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17743426 | ||||||
| chr4:17743600
|
T | C | 1 | a0002c0001t0017g0138 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.142-33956A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17743600 | ||||||
| chr4:17743668
|
G | A | 1 | a0001c0015t0029g0164 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.142-34024C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17743668 | ||||||
| chr4:17743718
|
C | T | 2 | a0002c0002t0001g0228a0023c0053t0012g0080 | 2 | HG02615.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.142-34074G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17743718 | ||||||
| chr4:17743829
|
C | A | 2 | a0002c0002t0001g0228a0023c0053t0012g0080 | 2 | HG02615.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.142-34185G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17743829 | ||||||
| chr4:17743873
|
G | A | 1 | a0023c0053t0012g0080 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.142-34229C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17743873 | ||||||
| chr4:17743877
|
G | A | 1 | a0013c0058t0022g0174 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.142-34233C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17743877 | ||||||
| chr4:17744150
|
A | G | 6 | a0001c0003t0018g0006a0001c0015t0029g0164a0003c0009t0005g0009others(3): Show | 6 | HG02559.hp1 HG03041.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-34506T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17744150 | ||||||
| chr4:17744312
|
C | T | 1 | a0001c0015t0029g0164 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.142-34668G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17744312 | ||||||
| chr4:17744461
|
T | TCA | 63 | a0001c0003t0004g0067a0001c0004t0042g0108a0001c0007t0004g0097others(60): Show | 63 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.142-34819_142-3481 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17744461 | ||||||
| chr4:17744461
|
T | TCACA | 3 | a0002c0001t0001g0188a0002c0001t0001g0197a0002c0001t0017g0138 | 3 | HG00597.hp2 HG01123.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.142-34821_142-3481 others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17744461 | ||||||
| chr4:17744461
|
TCA | T | 5 | a0001c0004t0009g0072a0001c0004t0045g0104a0002c0001t0001g0086others(2): Show | 5 | HG02145.hp2 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-34819_142-3481 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17744461 | ||||||
| chr4:17744463
|
A | T | 1 | a0001c0003t0018g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-34819T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17744463 | ||||||
| chr4:17744486
|
CACACCAC others(1): Show |
C | 2 | a0001c0003t0023g0122a0002c0016t0001g0221 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.142-34850_142-3484 others(12): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17744486 | ||||||
| chr4:17744488
|
CACCA | C | 14 | a0001c0003t0019g0095a0001c0008t0068g0234a0001c0015t0029g0164others(11): Show | 14 | HG00423.hp1 HG01109.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-34848_142-3484 others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17744488 | ||||||
| chr4:17744489
|
A | C | 1 | a0001c0006t0003g0182 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.142-34845T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17744489 | ||||||
| chr4:17744489
|
AC | A | 4 | a0003c0009t0005g0009a0005c0036t0053g0233a0008c0039t0015g0016others(1): Show | 4 | HG02559.hp1 HG03041.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-34846delG | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17744489 | ||||||
| chr4:17744490
|
C | A | 1 | a0001c0006t0003g0182 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.142-34846G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17744490 | ||||||
| chr4:17744490
|
C | CA | 12 | a0001c0003t0067g0238a0001c0012t0026g0092a0001c0021t0018g0068others(9): Show | 12 | HG00544.hp2 HG01891.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.142-34847_142-3484 others(5): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17744490 | ||||||
| chr4:17744490
|
C | CACA | 2 | a0002c0001t0001g0156a0002c0002t0001g0180 | 2 | HG03831.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.142-34847_142-3484 others(7): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17744490 | ||||||
| chr4:17744490
|
C | CACCA | 11 | a0001c0006t0003g0026a0001c0006t0003g0028a0001c0006t0003g0029others(8): Show | 11 | HG02886.hp1 HG03579.hp2 HG04199.hp2 others(8): Show |
intron_variant | MODIFIER | c.142-34847_142-3484 others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17744490 | ||||||
| chr4:17744490
|
CCA | C | 12 | a0001c0003t0002g0158a0001c0003t0044g0159a0001c0005t0014g0170others(9): Show | 12 | HG01243.hp2 HG02145.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.142-34848_142-3484 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17744490 | ||||||
| chr4:17744491
|
C | A | 83 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(80): Show |
intron_variant | MODIFIER | c.142-34847G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17744491 | ||||||
| chr4:17744492
|
A | AC | 10 | a0001c0003t0067g0238a0001c0012t0026g0092a0001c0021t0018g0068others(7): Show | 10 | HG00544.hp2 HG01891.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-34849dupG | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17744492 | ||||||
| chr4:17744492
|
A | C | 83 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(80): Show |
intron_variant | MODIFIER | c.142-34848T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17744492 | ||||||
| chr4:17744493
|
CA | C | 4 | a0003c0009t0005g0009a0005c0036t0053g0233a0008c0039t0015g0016others(1): Show | 4 | HG02559.hp1 HG03041.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-34850delT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17744493 | ||||||
| chr4:17744565
|
C | T | 8 | a0001c0003t0007g0220a0001c0004t0009g0017a0001c0004t0009g0072others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.142-34921G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17744565 | ||||||
| chr4:17744654
|
A | T | 3 | a0001c0005t0007g0125a0001c0005t0007g0140a0004c0035t0006g0139 | 3 | HG02895.hp2 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.142-35010T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17744654 | ||||||
| chr4:17744706
|
C | T | 2 | a0002c0002t0001g0228a0023c0053t0012g0080 | 2 | HG02615.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.142-35062G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17744706 | ||||||
| chr4:17744730
|
A | AT | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-35087_142-3508 others(5): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17744730 | ||||||
| chr4:17745086
|
G | C | 5 | a0001c0005t0014g0170a0001c0012t0026g0092a0005c0042t0006g0093others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-35442C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17745086 | ||||||
| chr4:17745200
|
G | C | 1 | a0001c0015t0029g0164 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.142-35556C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17745200 | ||||||
| chr4:17745400
|
T | C | 154 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.142-35756A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17745400 | ||||||
| chr4:17745578
|
C | T | 1 | a0013c0058t0022g0174 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.141+35581G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17745578 | ||||||
| chr4:17745758
|
C | T | 5 | a0001c0005t0014g0170a0001c0012t0026g0092a0005c0042t0006g0093others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+35401G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17745758 | ||||||
| chr4:17745782
|
T | A | 5 | a0001c0005t0014g0170a0001c0012t0026g0092a0005c0042t0006g0093others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+35377A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17745782 | ||||||
| chr4:17745998
|
G | A | 2 | a0009c0011t0001g0081a0009c0011t0056g0084 | 2 | HG02717.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.141+35161C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17745998 | ||||||
| chr4:17746051
|
A | T | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.141+35108T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17746051 | ||||||
| chr4:17746418
|
T | C | 21 | a0001c0003t0007g0220a0001c0003t0018g0006a0001c0004t0009g0017others(18): Show | 21 | HG01891.hp1 HG01891.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.141+34741A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17746418 | ||||||
| chr4:17746592
|
C | T | 4 | a0002c0001t0001g0082a0002c0001t0001g0090a0002c0001t0001g0152others(1): Show | 4 | HG02129.hp1 NA18950.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+34567G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17746592 | ||||||
| chr4:17746667
|
G | A | 1 | a0001c0007t0020g0060 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.141+34492C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17746667 | ||||||
| chr4:17746724
|
A | T | 52 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(49): Show | 52 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.141+34435T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17746724 | ||||||
| chr4:17746725
|
C | T | 55 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(52): Show | 55 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.141+34434G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17746725 | ||||||
| chr4:17746731
|
C | CA | 20 | a0001c0003t0007g0220a0001c0003t0019g0095a0001c0004t0009g0017others(17): Show | 20 | HG01891.hp1 HG01891.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.141+34427dupT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17746731 | ||||||
| chr4:17746732
|
A | C | 1 | a0001c0015t0029g0164 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.141+34427T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17746732 | ||||||
| chr4:17746746
|
G | A | 13 | a0001c0003t0018g0006a0001c0005t0014g0170a0001c0012t0026g0092others(10): Show | 13 | HG01891.hp2 HG02145.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.141+34413C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17746746 | ||||||
| chr4:17746830
|
G | C | 5 | a0001c0005t0014g0170a0001c0012t0026g0092a0005c0042t0006g0093others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+34329C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17746830 | ||||||
| chr4:17747014
|
C | T | 2 | a0002c0001t0017g0091a0002c0001t0017g0137 | 2 | HG02698.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.141+34145G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17747014 | ||||||
| chr4:17747044
|
C | CA | 20 | a0001c0003t0002g0069a0001c0003t0002g0149a0001c0003t0002g0158others(17): Show | 20 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.141+34114dupT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17747044 | ||||||
| chr4:17747044
|
C | CAA | 5 | a0001c0005t0014g0170a0001c0012t0026g0092a0005c0042t0006g0093others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+34113_141+3411 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17747044 | ||||||
| chr4:17747044
|
CA | C | 71 | a0001c0003t0004g0057a0001c0003t0008g0216a0001c0003t0011g0166others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.141+34114delT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17747044 | ||||||
| chr4:17747445
|
T | C | 5 | a0001c0003t0007g0220a0001c0004t0009g0017a0001c0004t0026g0073others(2): Show | 5 | HG01891.hp1 HG02145.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+33714A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17747445 | ||||||
| chr4:17747556
|
C | G | 15 | a0001c0003t0018g0006a0001c0008t0068g0234a0001c0015t0029g0164others(12): Show | 15 | HG00423.hp1 HG02071.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.141+33603G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17747556 | ||||||
| chr4:17747649
|
C | T | 1 | a0001c0007t0019g0143 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.141+33510G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17747649 | ||||||
| chr4:17747714
|
G | A | 2 | a0017c0026t0038g0098a0017c0026t0041g0160 | 2 | HG01081.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.141+33445C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17747714 | ||||||
| chr4:17747755
|
A | C | 1 | a0001c0006t0003g0030 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.141+33404T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17747755 | ||||||
| chr4:17747777
|
C | T | 1 | a0001c0021t0064g0005 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.141+33382G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17747777 | ||||||
| chr4:17747783
|
A | T | 1 | a0001c0021t0064g0005 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.141+33376T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17747783 | ||||||
| chr4:17747792
|
G | A | 1 | a0001c0021t0064g0005 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.141+33367C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17747792 | ||||||
| chr4:17747920
|
C | CA | 35 | a0001c0003t0004g0169a0001c0003t0018g0006a0001c0004t0042g0108others(32): Show | 35 | HG00609.hp2 HG00642.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.141+33238dupT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17747920 | ||||||
| chr4:17747920
|
C | CAA | 65 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(62): Show | 65 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.141+33237_141+3323 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17747920 | ||||||
| chr4:17747920
|
C | CAAA | 44 | a0001c0003t0002g0069a0001c0003t0002g0227a0001c0003t0004g0018others(41): Show | 44 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.141+33236_141+3323 others(7): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17747920 | ||||||
| chr4:17747920
|
CA | C | 17 | a0001c0003t0007g0220a0001c0004t0009g0017a0001c0004t0026g0073others(14): Show | 17 | HG00609.hp1 HG00673.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.141+33238delT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17747920 | ||||||
| chr4:17747920
|
CAAA | C | 6 | a0001c0003t0019g0095a0001c0004t0009g0022a0001c0004t0025g0023others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+33236_141+3323 others(7): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17747920 | ||||||
| chr4:17747920
|
CAAAAAA | C | 5 | a0001c0005t0014g0170a0001c0012t0026g0092a0005c0042t0006g0093others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+33233_141+3323 others(10): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17747920 | ||||||
| chr4:17748037
|
G | C | 1 | a0002c0002t0001g0228 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.141+33122C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17748037 | ||||||
| chr4:17748094
|
A | G | 2 | a0002c0001t0001g0086a0002c0001t0001g0129 | 2 | HG03704.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.141+33065T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17748094 | ||||||
| chr4:17748103
|
G | GA | 113 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(110): Show | 113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.141+33055dupT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17748103 | ||||||
| chr4:17748103
|
G | GAA | 13 | a0001c0003t0007g0220a0001c0003t0019g0095a0001c0003t0037g0219others(10): Show | 13 | HG00597.hp1 HG02145.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.141+33054_141+3305 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17748103 | ||||||
| chr4:17748103
|
G | GAAA | 11 | a0001c0006t0003g0030a0001c0012t0026g0092a0005c0042t0006g0093others(8): Show | 11 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.141+33053_141+3305 others(7): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17748103 | ||||||
| chr4:17748119
|
A | AG | 8 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0032g0236others(5): Show | 8 | HG00423.hp1 HG02071.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.141+33039_141+3304 others(5): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17748119 | ||||||
| chr4:17748119
|
A | G | 1 | a0002c0001t0001g0131 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.141+33040T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17748119 | ||||||
| chr4:17748120
|
A | G | 1 | a0001c0015t0029g0164 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.141+33039T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17748120 | ||||||
| chr4:17748415
|
C | T | 2 | a0002c0002t0001g0228a0023c0053t0012g0080 | 2 | HG02615.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.141+32744G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17748415 | ||||||
| chr4:17748494
|
C | T | 1 | a0022c0045t0001g0061 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.141+32665G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17748494 | ||||||
| chr4:17748505
|
A | AT | 62 | a0001c0004t0009g0072a0001c0004t0042g0108a0001c0004t0045g0104others(59): Show | 62 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.141+32653dupA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17748505 | ||||||
| chr4:17748505
|
A | ATT | 23 | a0001c0005t0014g0118a0001c0005t0027g0111a0001c0007t0019g0143others(20): Show | 23 | HG00639.hp2 HG00642.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.141+32652_141+3265 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17748505 | ||||||
| chr4:17748505
|
AT | A | 53 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(50): Show | 53 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.141+32653delA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17748505 | ||||||
| chr4:17748505
|
ATT | A | 7 | a0002c0002t0001g0043a0002c0002t0001g0228a0003c0009t0005g0133others(4): Show | 7 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(4): Show |
intron_variant | MODIFIER | c.141+32652_141+3265 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17748505 | ||||||
| chr4:17748505
|
ATTTTTTT | A | 46 | a0001c0003t0004g0057a0001c0003t0008g0216a0001c0003t0011g0166others(43): Show | 46 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.141+32647_141+3265 others(11): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17748505 | ||||||
| chr4:17748505
|
ATTTTTTT others(3): Show |
A | 1 | a0003c0009t0005g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.141+32644_141+3265 others(14): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17748505 | ||||||
| chr4:17748505
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0007t0020g0060 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.141+32642_141+3265 others(16): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17748505 | ||||||
| chr4:17748510
|
T | G | 10 | a0001c0003t0007g0220a0001c0003t0019g0095a0001c0004t0009g0017others(7): Show | 10 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.141+32649A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17748510 | ||||||
| chr4:17748752
|
A | C | 2 | a0002c0001t0001g0152a0002c0001t0001g0156 | 2 | NA18950.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.141+32407T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17748752 | ||||||
| chr4:17748780
|
G | A | 1 | a0025c0056t0061g0078 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.141+32379C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17748780 | ||||||
| chr4:17748853
|
G | A | 3 | a0001c0015t0013g0106a0004c0010t0006g0107a0004c0010t0006g0109 | 3 | HG02451.hp1 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.141+32306C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17748853 | ||||||
| chr4:17748854
|
G | T | 3 | a0001c0015t0013g0106a0004c0010t0006g0107a0004c0010t0006g0109 | 3 | HG02451.hp1 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.141+32305C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17748854 | ||||||
| chr4:17748930
|
G | A | 1 | a0002c0001t0001g0002 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.141+32229C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17748930 | ||||||
| chr4:17748993
|
A | AT | 38 | a0001c0003t0002g0069a0001c0003t0023g0122a0001c0005t0014g0170others(35): Show | 38 | HG01074.hp2 HG01109.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.141+32165dupA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17748993 | ||||||
| chr4:17748993
|
AT | A | 56 | a0001c0003t0004g0057a0001c0003t0008g0216a0001c0003t0011g0166others(53): Show | 56 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.141+32165delA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17748993 | ||||||
| chr4:17748993
|
ATTT | A | 6 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0069g0235others(3): Show | 6 | HG00423.hp1 HG02071.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.141+32163_141+3216 others(7): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17748993 | ||||||
| chr4:17749104
|
G | T | 3 | a0002c0020t0001g0079a0007c0050t0012g0004a0008c0049t0034g0112 | 3 | HG01243.hp2 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.141+32055C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17749104 | ||||||
| chr4:17749205
|
C | T | 7 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0032g0236others(4): Show | 7 | HG00423.hp1 HG02071.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.141+31954G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17749205 | ||||||
| chr4:17749243
|
C | G | 17 | a0001c0006t0003g0026a0001c0006t0003g0028a0001c0006t0003g0029others(14): Show | 17 | HG02559.hp1 HG02886.hp1 HG03041.hp2 others(14): Show |
intron_variant | MODIFIER | c.141+31916G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17749243 | ||||||
| chr4:17749290
|
C | T | 8 | a0001c0004t0025g0023a0001c0008t0068g0234a0002c0002t0001g0134others(5): Show | 8 | HG00423.hp1 HG02071.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.141+31869G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17749290 | ||||||
| chr4:17749303
|
C | T | 1 | a0024c0037t0052g0094 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.141+31856G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17749303 | ||||||
| chr4:17749419
|
TAA | T | 6 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0032g0236others(3): Show | 6 | HG00423.hp1 HG02071.hp1 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.141+31738_141+3173 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17749419 | ||||||
| chr4:17749588
|
G | A | 154 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.141+31571C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17749588 | ||||||
| chr4:17749623
|
A | C | 1 | a0001c0006t0003g0030 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.141+31536T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17749623 | ||||||
| chr4:17749909
|
TGTAA | T | 63 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(60): Show | 63 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.141+31246_141+3124 others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17749909 | ||||||
| chr4:17750079
|
A | G | 2 | a0001c0003t0018g0006a0001c0015t0029g0164 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.141+31080T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17750079 | ||||||
| chr4:17750086
|
A | T | 1 | a0001c0006t0003g0030 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.141+31073T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17750086 | ||||||
| chr4:17750139
|
G | A | 1 | a0008c0034t0051g0010 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.141+31020C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17750139 | ||||||
| chr4:17750181
|
T | G | 3 | a0001c0005t0007g0125a0001c0005t0007g0140a0004c0035t0006g0139 | 3 | HG02895.hp2 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.141+30978A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17750181 | ||||||
| chr4:17750195
|
C | T | 1 | a0002c0001t0001g0190 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.141+30964G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17750195 | ||||||
| chr4:17750480
|
G | A | 1 | a0001c0003t0008g0163 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.141+30679C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17750480 | ||||||
| chr4:17750531
|
A | C | 1 | a0031c0027t0001g0088 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.141+30628T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17750531 | ||||||
| chr4:17750805
|
A | G | 2 | a0001c0003t0023g0122a0002c0016t0001g0221 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.141+30354T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17750805 | ||||||
| chr4:17751165
|
G | A | 1 | a0001c0008t0019g0102 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.141+29994C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751165 | ||||||
| chr4:17751193
|
A | C | 1 | a0002c0002t0069g0235 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.141+29966T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751193 | ||||||
| chr4:17751306
|
C | CA | 12 | a0001c0012t0026g0092a0001c0015t0013g0003a0001c0047t0010g0113others(9): Show | 12 | HG00642.hp1 HG01891.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.141+29852dupT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751306 | ||||||
| chr4:17751306
|
CA | C | 13 | a0001c0003t0008g0216a0001c0003t0018g0006a0001c0004t0009g0022others(10): Show | 13 | HG00423.hp1 HG00558.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.141+29852delT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751306 | ||||||
| chr4:17751306
|
CAA | C | 42 | a0001c0003t0004g0057a0001c0003t0011g0166a0001c0003t0011g0167others(39): Show | 42 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.141+29851_141+2985 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751306 | ||||||
| chr4:17751306
|
CAAAA | C | 49 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(46): Show | 49 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.141+29849_141+2985 others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751306 | ||||||
| chr4:17751388
|
T | A | 1 | a0023c0053t0012g0080 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.141+29771A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751388 | ||||||
| chr4:17751486
|
C | G | 2 | a0001c0003t0023g0122a0002c0016t0001g0221 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.141+29673G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751486 | ||||||
| chr4:17751587
|
C | T | 1 | a0002c0020t0001g0079 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.141+29572G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751587 | ||||||
| chr4:17751672
|
C | G | 2 | a0001c0008t0019g0102a0013c0048t0022g0048 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.141+29487G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751672 | ||||||
| chr4:17751808
|
G | C | 6 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0032g0236others(3): Show | 6 | HG00423.hp1 HG02071.hp1 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.141+29351C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751808 | ||||||
| chr4:17751823
|
G | GCA | 6 | a0001c0003t0008g0208a0001c0005t0007g0013a0001c0029t0005g0115others(3): Show | 6 | HG02135.hp1 HG02897.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.141+29334_141+2933 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751823 | ||||||
| chr4:17751823
|
G | GCACA | 27 | a0001c0003t0008g0216a0001c0003t0047g0199a0001c0004t0009g0017others(24): Show | 27 | HG00099.hp1 HG00544.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.141+29332_141+2933 others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751823 | ||||||
| chr4:17751823
|
G | GCACACA | 27 | a0001c0003t0007g0220a0001c0003t0023g0122a0001c0004t0009g0072others(24): Show | 27 | HG00558.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.141+29330_141+2933 others(10): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751823 | ||||||
| chr4:17751823
|
G | GCACACAC others(1): Show |
20 | a0001c0003t0019g0095a0001c0007t0019g0143a0001c0007t0023g0123others(17): Show | 20 | HG00609.hp2 HG01361.hp1 HG01516.hp1 others(17): Show |
intron_variant | MODIFIER | c.141+29328_141+2933 others(12): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751823 | ||||||
| chr4:17751823
|
G | GCACACAC others(3): Show |
9 | a0001c0004t0045g0104a0001c0007t0039g0124a0002c0001t0001g0087others(6): Show | 9 | HG01109.hp1 HG02280.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.141+29326_141+2933 others(14): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751823 | ||||||
| chr4:17751823
|
G | GCACACAC others(5): Show |
15 | a0001c0003t0018g0006a0001c0003t0049g0099a0001c0008t0004g0037others(12): Show | 15 | HG00280.hp2 HG01099.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.141+29324_141+2933 others(16): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751823 | ||||||
| chr4:17751823
|
G | GCACACAC others(7): Show |
24 | a0001c0003t0011g0166a0001c0003t0011g0167a0001c0003t0011g0168others(21): Show | 24 | HG00597.hp2 HG00639.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.141+29322_141+2933 others(18): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751823 | ||||||
| chr4:17751823
|
G | GCACACAC others(9): Show |
10 | a0001c0003t0004g0057a0001c0003t0046g0059a0001c0008t0002g0045others(7): Show | 10 | HG00323.hp2 HG00423.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.141+29320_141+2933 others(20): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751823 | ||||||
| chr4:17751823
|
G | GCACACAC others(11): Show |
4 | a0002c0001t0001g0148a0002c0001t0001g0154a0029c0059t0036g0038others(1): Show | 4 | HG01074.hp2 HG02738.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+29318_141+2933 others(22): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751823 | ||||||
| chr4:17751823
|
G | GCACACAC others(13): Show |
2 | a0002c0001t0001g0090a0002c0002t0001g0114 | 2 | HG03017.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.141+29316_141+2933 others(24): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751823 | ||||||
| chr4:17751823
|
G | GCGCACAC others(3): Show |
2 | a0001c0033t0003g0200a0002c0022t0001g0151 | 2 | NA18998.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.141+29335_141+2933 others(14): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751823 | ||||||
| chr4:17751823
|
G | GCGCACAC others(7): Show |
1 | a0002c0022t0001g0085 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.141+29335_141+2933 others(18): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751823 | ||||||
| chr4:17751823
|
GCA | G | 32 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0004g0018others(29): Show | 32 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.141+29334_141+2933 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751823 | ||||||
| chr4:17751823
|
GCACA | G | 21 | a0001c0003t0002g0227a0001c0003t0008g0163a0001c0005t0014g0170others(18): Show | 21 | HG00140.hp1 HG00323.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.141+29332_141+2933 others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751823 | ||||||
| chr4:17751823
|
GCACACA | G | 5 | a0001c0006t0003g0132a0001c0006t0003g0182a0001c0006t0028g0014others(2): Show | 5 | HG03579.hp2 HG03831.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+29330_141+2933 others(10): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751823 | ||||||
| chr4:17751823
|
GCACACAC others(1): Show |
G | 3 | a0001c0004t0042g0108a0001c0047t0010g0113a0010c0013t0004g0232 | 3 | HG01175.hp2 HG02886.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.141+29328_141+2933 others(12): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751823 | ||||||
| chr4:17751829
|
A | G | 1 | a0010c0013t0024g0211 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.141+29330T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751829 | ||||||
| chr4:17751867
|
A | ACACACAC others(6): Show |
1 | a0002c0002t0001g0040 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.141+29291_141+2929 others(17): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751867 | ||||||
| chr4:17751868
|
A | C | 2 | a0015c0062t0035g0230a0015c0063t0054g0229 | 2 | HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.141+29291T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751868 | ||||||
| chr4:17751881
|
C | T | 1 | a0004c0010t0006g0077 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.141+29278G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751881 | ||||||
| chr4:17751882
|
G | A | 1 | a0002c0001t0001g0198 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.141+29277C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751882 | ||||||
| chr4:17751937
|
C | T | 2 | a0003c0009t0005g0133a0003c0009t0005g0195 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.141+29222G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751937 | ||||||
| chr4:17751971
|
G | GA | 5 | a0001c0005t0007g0194a0001c0005t0013g0185a0001c0006t0028g0014others(2): Show | 5 | HG02622.hp1 HG03453.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+29187dupT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17751971 | ||||||
| chr4:17752047
|
T | C | 3 | a0002c0001t0017g0091a0002c0001t0017g0137a0002c0001t0017g0138 | 3 | HG01123.hp2 HG02698.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.141+29112A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17752047 | ||||||
| chr4:17752218
|
T | C | 1 | a0002c0001t0001g0090 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.141+28941A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17752218 | ||||||
| chr4:17752337
|
G | A | 3 | a0001c0003t0018g0006a0001c0015t0029g0164a0023c0053t0012g0080 | 3 | HG02615.hp1 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.141+28822C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17752337 | ||||||
| chr4:17752337
|
G | C | 53 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(50): Show | 53 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.141+28822C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17752337 | ||||||
| chr4:17752796
|
C | G | 1 | a0001c0003t0018g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.141+28363G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17752796 | ||||||
| chr4:17752814
|
C | T | 3 | a0001c0003t0018g0006a0001c0015t0029g0164a0023c0053t0012g0080 | 3 | HG02615.hp1 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.141+28345G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17752814 | ||||||
| chr4:17752820
|
C | T | 63 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(60): Show | 63 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.141+28339G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17752820 | ||||||
| chr4:17752866
|
A | G | 1 | a0002c0020t0016g0089 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.141+28293T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17752866 | ||||||
| chr4:17753049
|
C | A | 1 | a0001c0006t0003g0132 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.141+28110G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17753049 | ||||||
| chr4:17753091
|
G | T | 53 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(50): Show | 53 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.141+28068C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17753091 | ||||||
| chr4:17753106
|
A | C | 66 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(63): Show | 66 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.141+28053T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17753106 | ||||||
| chr4:17753159
|
T | C | 236 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(233): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.141+28000A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17753159 | ||||||
| chr4:17753173
|
C | T | 4 | a0001c0005t0014g0170a0001c0012t0026g0092a0005c0042t0006g0093others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+27986G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17753173 | ||||||
| chr4:17753246
|
G | A | 4 | a0001c0005t0014g0170a0001c0012t0026g0092a0005c0042t0006g0093others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+27913C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17753246 | ||||||
| chr4:17753322
|
T | C | 1 | a0002c0001t0001g0214 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.141+27837A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17753322 | ||||||
| chr4:17753350
|
T | G | 3 | a0001c0004t0009g0072a0001c0004t0045g0104a0013c0058t0022g0174 | 3 | HG02630.hp2 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.141+27809A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17753350 | ||||||
| chr4:17753372
|
A | C | 3 | a0001c0004t0009g0072a0001c0004t0045g0104a0013c0058t0022g0174 | 3 | HG02630.hp2 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.141+27787T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17753372 | ||||||
| chr4:17753405
|
AT | A | 2 | a0001c0021t0064g0005a0025c0056t0061g0078 | 2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.141+27753delA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17753405 | ||||||
| chr4:17753471
|
A | G | 7 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0032g0236others(4): Show | 7 | HG00423.hp1 HG02071.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.141+27688T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17753471 | ||||||
| chr4:17753738
|
G | C | 1 | a0001c0007t0008g0157 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.141+27421C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17753738 | ||||||
| chr4:17753931
|
A | C | 2 | a0001c0003t0023g0122a0002c0016t0001g0221 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.141+27228T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17753931 | ||||||
| chr4:17754101
|
G | A | 1 | a0001c0003t0060g0215 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.141+27058C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17754101 | ||||||
| chr4:17754341
|
C | T | 1 | a0025c0056t0061g0078 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.141+26818G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17754341 | ||||||
| chr4:17754367
|
C | T | 1 | a0013c0058t0022g0174 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.141+26792G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17754367 | ||||||
| chr4:17754394
|
A | C | 2 | a0015c0062t0035g0230a0015c0063t0054g0229 | 2 | HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.141+26765T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17754394 | ||||||
| chr4:17754419
|
C | T | 7 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0032g0236others(4): Show | 7 | HG00423.hp1 HG02071.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.141+26740G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17754419 | ||||||
| chr4:17754551
|
CAG | C | 45 | a0001c0003t0002g0019a0001c0003t0002g0149a0001c0003t0002g0158others(42): Show | 45 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.141+26606_141+2660 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17754551 | ||||||
| chr4:17754552
|
AG | A | 5 | a0001c0003t0018g0006a0001c0003t0037g0219a0001c0015t0029g0164others(2): Show | 5 | HG00597.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+26606delC | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17754552 | ||||||
| chr4:17754553
|
G | A | 3 | a0001c0004t0009g0072a0001c0004t0045g0104a0013c0058t0022g0174 | 3 | HG02630.hp2 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.141+26606C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17754553 | ||||||
| chr4:17754553
|
GA | G | 21 | a0001c0004t0042g0108a0001c0006t0003g0026a0001c0006t0003g0028others(18): Show | 21 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.141+26605delT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17754553 | ||||||
| chr4:17754568
|
A | C | 7 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0032g0236others(4): Show | 7 | HG00423.hp1 HG02071.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.141+26591T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17754568 | ||||||
| chr4:17754582
|
GA | G | 16 | a0001c0003t0002g0069a0001c0003t0007g0220a0001c0003t0019g0095others(13): Show | 16 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.141+26576delT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17754582 | ||||||
| chr4:17754650
|
G | A | 154 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.141+26509C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17754650 | ||||||
| chr4:17754786
|
T | A | 7 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0032g0236others(4): Show | 7 | HG00423.hp1 HG02071.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.141+26373A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17754786 | ||||||
| chr4:17754921
|
C | A | 1 | a0010c0013t0004g0232 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.141+26238G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17754921 | ||||||
| chr4:17755384
|
G | C | 12 | a0001c0003t0002g0069a0001c0003t0007g0220a0001c0004t0009g0017others(9): Show | 12 | HG01891.hp1 HG02145.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.141+25775C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17755384 | ||||||
| chr4:17755518
|
G | A | 1 | a0010c0013t0004g0232 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.141+25641C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17755518 | ||||||
| chr4:17755601
|
G | A | 1 | a0002c0001t0001g0142 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.141+25558C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17755601 | ||||||
| chr4:17755949
|
C | T | 4 | a0003c0009t0005g0009a0005c0036t0053g0233a0008c0039t0015g0016others(1): Show | 4 | HG02559.hp1 HG03041.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.141+25210G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17755949 | ||||||
| chr4:17755989
|
G | A | 2 | a0001c0017t0010g0175a0013c0058t0022g0174 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.141+25170C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17755989 | ||||||
| chr4:17756024
|
A | G | 1 | a0002c0001t0001g0090 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.141+25135T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17756024 | ||||||
| chr4:17756217
|
A | G | 4 | a0001c0021t0018g0068a0005c0036t0053g0233a0008c0039t0015g0016others(1): Show | 4 | HG03041.hp2 HG03486.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.141+24942T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17756217 | ||||||
| chr4:17756275
|
G | A | 1 | a0002c0001t0001g0131 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.141+24884C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17756275 | ||||||
| chr4:17756498
|
C | T | 17 | a0001c0003t0002g0069a0001c0003t0007g0220a0001c0004t0009g0022others(14): Show | 17 | HG01891.hp1 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.141+24661G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17756498 | ||||||
| chr4:17756863
|
G | A | 2 | a0001c0003t0018g0006a0001c0021t0064g0005 | 2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.141+24296C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17756863 | ||||||
| chr4:17756910
|
G | A | 1 | a0002c0002t0001g0065 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.141+24249C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17756910 | ||||||
| chr4:17756981
|
G | C | 1 | a0032c0061t0030g0007 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.141+24178C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17756981 | ||||||
| chr4:17757048
|
C | G | 14 | a0001c0003t0018g0006a0001c0004t0045g0104a0001c0005t0007g0013others(11): Show | 14 | HG02615.hp1 HG02630.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.141+24111G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17757048 | ||||||
| chr4:17757315
|
T | C | 1 | a0001c0005t0007g0013 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.141+23844A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17757315 | ||||||
| chr4:17757333
|
G | A | 92 | a0001c0003t0002g0019a0001c0003t0002g0158a0001c0003t0002g0206others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.141+23826C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17757333 | ||||||
| chr4:17757348
|
A | T | 20 | a0001c0003t0002g0069a0001c0003t0007g0220a0001c0004t0009g0022others(17): Show | 20 | HG01891.hp1 HG01891.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.141+23811T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17757348 | ||||||
| chr4:17757382
|
A | G | 13 | a0001c0003t0018g0006a0001c0005t0007g0013a0001c0008t0018g0020others(10): Show | 13 | HG02615.hp1 HG02630.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.141+23777T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17757382 | ||||||
| chr4:17757420
|
A | T | 1 | a0001c0004t0045g0104 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.141+23739T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17757420 | ||||||
| chr4:17757461
|
AT | A | 5 | a0001c0008t0018g0020a0001c0021t0018g0068a0005c0036t0053g0233others(2): Show | 5 | HG03041.hp2 HG03471.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+23697delA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17757461 | ||||||
| chr4:17757566
|
A | ATTC | 3 | a0001c0004t0009g0022a0001c0004t0025g0023a0001c0004t0025g0024 | 3 | HG02258.hp1 HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.141+23592_141+2359 others(7): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17757566 | ||||||
| chr4:17757567
|
A | T | 3 | a0001c0004t0009g0022a0001c0004t0025g0023a0001c0004t0025g0024 | 3 | HG02258.hp1 HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.141+23592T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17757567 | ||||||
| chr4:17757597
|
G | A | 13 | a0001c0003t0018g0006a0001c0005t0007g0013a0001c0008t0018g0020others(10): Show | 13 | HG02615.hp1 HG02630.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.141+23562C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17757597 | ||||||
| chr4:17757688
|
G | A | 3 | a0010c0013t0002g0231a0010c0013t0004g0232a0010c0013t0024g0211 | 3 | HG01169.hp1 HG01175.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.141+23471C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17757688 | ||||||
| chr4:17757692
|
C | T | 3 | a0010c0013t0002g0231a0010c0013t0004g0232a0010c0013t0024g0211 | 3 | HG01169.hp1 HG01175.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.141+23467G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17757692 | ||||||
| chr4:17757727
|
T | TGAAATTT others(316): Show |
1 | a0019c0040t0065g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.141+23431_141+2343 others(327): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17757727 | ||||||
| chr4:17757727
|
T | TGAAATTT others(317): Show |
2 | a0005c0036t0053g0233a0008c0039t0015g0016 | 2 | HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.141+23431_141+2343 others(328): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17757727 | ||||||
| chr4:17757727
|
T | TGAAATTT others(317): Show |
2 | a0001c0008t0018g0020a0001c0021t0018g0068 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.141+23431_141+2343 others(328): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17757727 | ||||||
| chr4:17757758
|
A | C | 2 | a0001c0015t0013g0003a0007c0050t0012g0004 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.141+23401T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17757758 | ||||||
| chr4:17758135
|
G | A | 1 | a0008c0049t0034g0112 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.141+23024C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17758135 | ||||||
| chr4:17758226
|
T | C | 5 | a0001c0008t0018g0020a0001c0021t0018g0068a0005c0036t0053g0233others(2): Show | 5 | HG03041.hp2 HG03471.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+22933A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17758226 | ||||||
| chr4:17758238
|
A | G | 20 | a0001c0003t0002g0069a0001c0003t0007g0220a0001c0004t0009g0022others(17): Show | 20 | HG01891.hp1 HG01891.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.141+22921T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17758238 | ||||||
| chr4:17758631
|
G | A | 2 | a0001c0003t0002g0227a0001c0003t0008g0163 | 2 | HG00140.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.141+22528C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17758631 | ||||||
| chr4:17758640
|
A | T | 1 | a0002c0002t0016g0039 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.141+22519T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17758640 | ||||||
| chr4:17758718
|
G | A | 2 | a0001c0003t0018g0006a0001c0021t0064g0005 | 2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.141+22441C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17758718 | ||||||
| chr4:17758730
|
G | C | 1 | a0001c0003t0018g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.141+22429C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17758730 | ||||||
| chr4:17758806
|
A | G | 1 | a0008c0039t0015g0016 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.141+22353T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17758806 | ||||||
| chr4:17758868
|
G | C | 18 | a0001c0004t0042g0108a0001c0006t0003g0026a0001c0006t0003g0028others(15): Show | 18 | HG01243.hp2 HG02451.hp1 HG02886.hp1 others(15): Show |
intron_variant | MODIFIER | c.141+22291C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17758868 | ||||||
| chr4:17758884
|
C | G | 4 | a0002c0001t0001g0120a0002c0001t0001g0121a0002c0001t0001g0222others(1): Show | 4 | HG00639.hp2 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+22275G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17758884 | ||||||
| chr4:17759007
|
T | A | 10 | a0001c0005t0007g0013a0001c0008t0018g0020a0001c0017t0010g0175others(7): Show | 10 | HG02615.hp1 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.141+22152A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17759007 | ||||||
| chr4:17759112
|
A | T | 8 | a0001c0003t0007g0220a0001c0004t0009g0072a0001c0004t0026g0073others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.141+22047T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17759112 | ||||||
| chr4:17759114
|
A | G | 1 | a0001c0003t0019g0095 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.141+22045T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17759114 | ||||||
| chr4:17759340
|
A | G | 1 | a0001c0007t0020g0060 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.141+21819T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17759340 | ||||||
| chr4:17759402
|
C | T | 1 | a0001c0003t0040g0201 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.141+21757G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17759402 | ||||||
| chr4:17759492
|
TTTTTTTC others(7): Show |
T | 4 | a0001c0008t0018g0020a0001c0021t0018g0068a0008c0039t0015g0016others(1): Show | 4 | HG03471.hp1 HG03486.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.141+21653_141+2166 others(18): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17759492 | ||||||
| chr4:17759522
|
A | G | 7 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0032g0236others(4): Show | 7 | HG00423.hp1 HG02071.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.141+21637T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17759522 | ||||||
| chr4:17759910
|
C | T | 1 | a0031c0027t0001g0088 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.141+21249G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17759910 | ||||||
| chr4:17759934
|
G | C | 1 | a0002c0001t0001g0188 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.141+21225C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17759934 | ||||||
| chr4:17760044
|
TC | T | 19 | a0001c0003t0002g0069a0001c0003t0007g0220a0001c0004t0009g0022others(16): Show | 19 | HG01891.hp1 HG01891.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.141+21114delG | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17760044 | ||||||
| chr4:17760065
|
T | A | 1 | a0009c0011t0056g0084 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.141+21094A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17760065 | ||||||
| chr4:17760335
|
G | A | 5 | a0001c0004t0045g0104a0001c0012t0026g0092a0002c0016t0001g0074others(2): Show | 5 | HG01891.hp2 HG02717.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+20824C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17760335 | ||||||
| chr4:17760352
|
T | C | 2 | a0001c0005t0014g0110a0001c0005t0027g0111 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.141+20807A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17760352 | ||||||
| chr4:17760469
|
C | CA | 26 | a0001c0003t0007g0220a0001c0004t0009g0072a0001c0004t0026g0073others(23): Show | 26 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.141+20689dupT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17760469 | ||||||
| chr4:17760487
|
A | C | 2 | a0002c0002t0001g0134a0014c0024t0001g0183 | 2 | NA18972.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.141+20672T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17760487 | ||||||
| chr4:17760489
|
C | A | 2 | a0002c0002t0001g0134a0014c0024t0001g0183 | 2 | NA18972.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.141+20670G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17760489 | ||||||
| chr4:17760497
|
CAAACAAA | C | 5 | a0001c0008t0068g0234a0002c0002t0032g0236a0002c0002t0069g0235others(2): Show | 5 | HG00423.hp1 HG02071.hp1 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+20655_141+2066 others(11): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17760497 | ||||||
| chr4:17760683
|
T | C | 7 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0032g0236others(4): Show | 7 | HG00423.hp1 HG02071.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.141+20476A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17760683 | ||||||
| chr4:17760815
|
G | A | 3 | a0016c0025t0021g0224a0016c0025t0021g0225a0033c0064t0057g0223 | 3 | HG01109.hp2 HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.141+20344C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17760815 | ||||||
| chr4:17760863
|
T | G | 1 | a0002c0020t0001g0079 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.141+20296A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17760863 | ||||||
| chr4:17760872
|
G | C | 1 | a0001c0003t0046g0059 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.141+20287C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17760872 | ||||||
| chr4:17760878
|
G | A | 4 | a0001c0008t0018g0020a0001c0021t0018g0068a0008c0039t0015g0016others(1): Show | 4 | HG03471.hp1 HG03486.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.141+20281C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17760878 | ||||||
| chr4:17760982
|
C | A | 2 | a0002c0001t0001g0086a0002c0001t0001g0129 | 2 | HG03704.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.141+20177G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17760982 | ||||||
| chr4:17761611
|
T | C | 18 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0005t0007g0013others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.141+19548A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17761611 | ||||||
| chr4:17762019
|
A | ATTTTGTT others(8): Show |
6 | a0001c0005t0007g0013a0001c0017t0010g0175a0001c0021t0018g0068others(3): Show | 6 | HG02630.hp2 HG02647.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.141+19125_141+1913 others(19): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17762019 | ||||||
| chr4:17762019
|
ATTTTGTT others(3): Show |
A | 7 | a0001c0003t0019g0095a0001c0015t0029g0164a0016c0025t0021g0224others(4): Show | 7 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.141+19130_141+1913 others(14): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17762019 | ||||||
| chr4:17762034
|
G | GTTTTGTT others(8): Show |
3 | a0001c0008t0018g0020a0008c0039t0015g0016a0019c0040t0065g0012 | 3 | HG03471.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.141+19124_141+1912 others(19): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17762034 | ||||||
| chr4:17762044
|
G | T | 3 | a0016c0025t0021g0224a0016c0025t0021g0225a0033c0064t0057g0223 | 3 | HG01109.hp2 HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.141+19115C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17762044 | ||||||
| chr4:17762073
|
TTCTC | T | 3 | a0001c0005t0007g0013a0015c0062t0035g0230a0015c0063t0054g0229 | 3 | HG02897.hp2 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.141+19082_141+1908 others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17762073 | ||||||
| chr4:17762120
|
G | A | 3 | a0001c0012t0026g0092a0005c0042t0006g0093a0007c0043t0012g0105 | 3 | HG01891.hp2 HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.141+19039C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17762120 | ||||||
| chr4:17762387
|
G | A | 18 | a0001c0004t0042g0108a0001c0006t0003g0026a0001c0006t0003g0028others(15): Show | 18 | HG01243.hp2 HG02451.hp1 HG02886.hp1 others(15): Show |
intron_variant | MODIFIER | c.141+18772C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17762387 | ||||||
| chr4:17762419
|
T | A | 9 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0015t0029g0164others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.141+18740A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17762419 | ||||||
| chr4:17762473
|
G | T | 3 | a0016c0025t0021g0224a0016c0025t0021g0225a0033c0064t0057g0223 | 3 | HG01109.hp2 HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.141+18686C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17762473 | ||||||
| chr4:17762595
|
C | T | 3 | a0001c0005t0007g0013a0015c0062t0035g0230a0015c0063t0054g0229 | 3 | HG02897.hp2 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.141+18564G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17762595 | ||||||
| chr4:17762776
|
C | T | 1 | a0001c0003t0040g0201 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.141+18383G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17762776 | ||||||
| chr4:17762949
|
C | T | 1 | a0032c0061t0030g0007 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.141+18210G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17762949 | ||||||
| chr4:17763146
|
A | T | 1 | a0002c0002t0001g0025 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.141+18013T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17763146 | ||||||
| chr4:17763331
|
G | A | 2 | a0001c0017t0010g0175a0013c0058t0022g0174 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.141+17828C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17763331 | ||||||
| chr4:17763405
|
A | AAC | 29 | a0001c0003t0002g0069a0001c0003t0007g0220a0001c0003t0018g0006others(26): Show | 29 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.141+17752_141+1775 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17763405 | ||||||
| chr4:17763572
|
G | A | 1 | a0003c0009t0005g0162 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.141+17587C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17763572 | ||||||
| chr4:17763573
|
T | TGAAAA | 152 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0158others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.141+17585_141+1758 others(9): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17763573 | ||||||
| chr4:17763689
|
T | C | 5 | a0001c0004t0009g0022a0001c0004t0025g0023a0001c0004t0025g0024others(2): Show | 5 | HG02258.hp1 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+17470A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17763689 | ||||||
| chr4:17763924
|
T | C | 1 | a0002c0002t0001g0114 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.141+17235A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17763924 | ||||||
| chr4:17763939
|
T | C | 1 | a0001c0008t0018g0020 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.141+17220A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17763939 | ||||||
| chr4:17763955
|
G | A | 1 | a0011c0023t0024g0209 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.141+17204C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17763955 | ||||||
| chr4:17763999
|
C | T | 50 | a0001c0003t0004g0057a0001c0003t0008g0216a0001c0003t0011g0166others(47): Show | 50 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.141+17160G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17763999 | ||||||
| chr4:17764087
|
C | G | 3 | a0001c0003t0002g0069a0001c0017t0010g0070a0002c0016t0001g0071 | 3 | HG02647.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.141+17072G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17764087 | ||||||
| chr4:17764356
|
T | G | 1 | a0001c0003t0002g0149 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.141+16803A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17764356 | ||||||
| chr4:17764358
|
C | T | 3 | a0016c0025t0021g0224a0016c0025t0021g0225a0033c0064t0057g0223 | 3 | HG01109.hp2 HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.141+16801G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17764358 | ||||||
| chr4:17764581
|
A | G | 1 | a0002c0002t0001g0046 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.141+16578T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17764581 | ||||||
| chr4:17764670
|
A | C | 1 | a0002c0001t0001g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.141+16489T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17764670 | ||||||
| chr4:17764791
|
G | A | 1 | a0002c0002t0001g0176 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.141+16368C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17764791 | ||||||
| chr4:17764813
|
T | TCAGCACT others(708): Show |
4 | a0001c0008t0018g0020a0001c0021t0018g0068a0008c0039t0015g0016others(1): Show | 4 | HG03471.hp1 HG03486.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.141+16345_141+1634 others(719): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17764813 | ||||||
| chr4:17764813
|
T | TCAGCACT others(708): Show |
2 | a0001c0017t0010g0175a0013c0058t0022g0174 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.141+16345_141+1634 others(719): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17764813 | ||||||
| chr4:17764879
|
A | G | 1 | a0001c0015t0029g0164 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.141+16280T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17764879 | ||||||
| chr4:17764980
|
C | A | 1 | a0002c0020t0001g0079 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.141+16179G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17764980 | ||||||
| chr4:17765078
|
A | G | 3 | a0004c0010t0006g0077a0007c0041t0012g0011a0025c0056t0061g0078 | 3 | HG01891.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.141+16081T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17765078 | ||||||
| chr4:17765251
|
A | G | 5 | a0001c0008t0018g0020a0001c0021t0018g0068a0004c0010t0006g0165others(2): Show | 5 | HG03098.hp2 HG03471.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+15908T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17765251 | ||||||
| chr4:17765286
|
C | G | 2 | a0001c0003t0018g0006a0001c0021t0064g0005 | 2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.141+15873G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17765286 | ||||||
| chr4:17765289
|
A | G | 7 | a0001c0008t0018g0020a0001c0017t0010g0175a0001c0021t0018g0068others(4): Show | 7 | HG02630.hp2 HG02647.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.141+15870T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17765289 | ||||||
| chr4:17765331
|
G | A | 1 | a0025c0056t0061g0078 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.141+15828C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17765331 | ||||||
| chr4:17765359
|
T | G | 2 | a0001c0003t0049g0099a0006c0019t0001g0100 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.141+15800A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17765359 | ||||||
| chr4:17765531
|
C | CTTAG | 19 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0005t0007g0013others(16): Show | 19 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.141+15624_141+1562 others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17765531 | ||||||
| chr4:17765532
|
T | TTAGC | 20 | a0001c0003t0002g0069a0001c0003t0007g0220a0001c0004t0009g0022others(17): Show | 20 | HG01891.hp1 HG01891.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.141+15623_141+1562 others(8): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17765532 | ||||||
| chr4:17765558
|
A | G | 1 | a0002c0020t0001g0079 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.141+15601T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17765558 | ||||||
| chr4:17765581
|
A | C | 5 | a0001c0008t0018g0020a0001c0021t0018g0068a0004c0010t0006g0165others(2): Show | 5 | HG03098.hp2 HG03471.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+15578T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17765581 | ||||||
| chr4:17765641
|
C | T | 18 | a0001c0004t0042g0108a0001c0006t0003g0026a0001c0006t0003g0028others(15): Show | 18 | HG01243.hp2 HG02451.hp1 HG02886.hp1 others(15): Show |
intron_variant | MODIFIER | c.141+15518G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17765641 | ||||||
| chr4:17765646
|
A | C | 48 | a0001c0003t0004g0057a0001c0003t0008g0216a0001c0003t0011g0166others(45): Show | 48 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.141+15513T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17765646 | ||||||
| chr4:17765667
|
T | C | 1 | a0005c0036t0053g0233 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.141+15492A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17765667 | ||||||
| chr4:17765761
|
C | T | 1 | a0013c0048t0022g0048 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.141+15398G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17765761 | ||||||
| chr4:17765830
|
G | A | 1 | a0001c0005t0007g0013 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.141+15329C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17765830 | ||||||
| chr4:17765893
|
G | A | 2 | a0001c0003t0023g0122a0002c0016t0001g0221 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.141+15266C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17765893 | ||||||
| chr4:17765930
|
G | C | 1 | a0001c0004t0045g0104 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.141+15229C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17765930 | ||||||
| chr4:17765970
|
A | G | 39 | a0001c0003t0002g0069a0001c0003t0007g0220a0001c0003t0018g0006others(36): Show | 39 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.141+15189T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17765970 | ||||||
| chr4:17765982
|
C | T | 1 | a0001c0004t0045g0104 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.141+15177G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17765982 | ||||||
| chr4:17765992
|
A | G | 13 | a0001c0006t0003g0026a0001c0006t0003g0028a0001c0006t0003g0029others(10): Show | 13 | HG01243.hp2 HG03471.hp2 HG03579.hp2 others(10): Show |
intron_variant | MODIFIER | c.141+15167T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17765992 | ||||||
| chr4:17766033
|
C | T | 35 | a0001c0003t0002g0019a0001c0003t0002g0158a0001c0003t0002g0206others(32): Show | 35 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.141+15126G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17766033 | ||||||
| chr4:17766049
|
CATAAAGG others(7): Show |
C | 1 | a0002c0002t0001g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.141+15096_141+1510 others(18): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17766049 | ||||||
| chr4:17766075
|
T | G | 5 | a0001c0008t0018g0020a0001c0021t0018g0068a0004c0010t0006g0165others(2): Show | 5 | HG03098.hp2 HG03471.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+15084A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17766075 | ||||||
| chr4:17766085
|
G | A | 8 | a0001c0007t0020g0060a0002c0001t0001g0120a0002c0001t0001g0121others(5): Show | 8 | HG00558.hp2 HG00609.hp1 HG00639.hp2 others(5): Show |
intron_variant | MODIFIER | c.141+15074C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17766085 | ||||||
| chr4:17766110
|
T | C | 39 | a0001c0003t0002g0069a0001c0003t0007g0220a0001c0003t0018g0006others(36): Show | 39 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.141+15049A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17766110 | ||||||
| chr4:17766128
|
A | G | 7 | a0001c0008t0018g0020a0001c0017t0010g0175a0001c0021t0018g0068others(4): Show | 7 | HG02630.hp2 HG02647.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.141+15031T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17766128 | ||||||
| chr4:17766135
|
C | T | 2 | a0001c0017t0010g0175a0013c0058t0022g0174 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.141+15024G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17766135 | ||||||
| chr4:17766178
|
A | C | 19 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0005t0007g0013others(16): Show | 19 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.141+14981T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17766178 | ||||||
| chr4:17766254
|
T | G | 31 | a0001c0003t0002g0019a0001c0003t0002g0158a0001c0003t0002g0206others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.141+14905A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17766254 | ||||||
| chr4:17766276
|
G | A | 1 | a0001c0003t0047g0199 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.141+14883C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17766276 | ||||||
| chr4:17766298
|
A | C | 5 | a0001c0003t0008g0216a0001c0003t0049g0099a0006c0014t0001g0042others(2): Show | 5 | HG01358.hp1 HG01516.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+14861T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17766298 | ||||||
| chr4:17766302
|
A | C | 50 | a0001c0003t0004g0057a0001c0003t0008g0216a0001c0003t0011g0166others(47): Show | 50 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.141+14857T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17766302 | ||||||
| chr4:17766360
|
A | G | 3 | a0001c0005t0007g0013a0015c0062t0035g0230a0015c0063t0054g0229 | 3 | HG02897.hp2 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.141+14799T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17766360 | ||||||
| chr4:17766442
|
A | G | 20 | a0001c0003t0002g0069a0001c0003t0007g0220a0001c0004t0009g0022others(17): Show | 20 | HG01891.hp1 HG01891.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.141+14717T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17766442 | ||||||
| chr4:17766495
|
C | T | 1 | a0002c0002t0001g0046 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.141+14664G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17766495 | ||||||
| chr4:17766496
|
G | A | 14 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0005t0007g0013others(11): Show | 14 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.141+14663C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17766496 | ||||||
| chr4:17766497
|
C | G | 3 | a0001c0005t0007g0013a0015c0062t0035g0230a0015c0063t0054g0229 | 3 | HG02897.hp2 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.141+14662G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17766497 | ||||||
| chr4:17766612
|
G | C | 2 | a0001c0003t0049g0099a0006c0019t0001g0100 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.141+14547C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17766612 | ||||||
| chr4:17766617
|
A | T | 3 | a0001c0005t0007g0013a0015c0062t0035g0230a0015c0063t0054g0229 | 3 | HG02897.hp2 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.141+14542T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17766617 | ||||||
| chr4:17766740
|
G | A | 1 | a0001c0004t0042g0108 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.141+14419C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17766740 | ||||||
| chr4:17766751
|
A | T | 10 | a0001c0005t0007g0013a0001c0008t0018g0020a0001c0017t0010g0175others(7): Show | 10 | HG02630.hp2 HG02647.hp1 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.141+14408T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17766751 | ||||||
| chr4:17766764
|
G | A | 1 | a0001c0021t0018g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.141+14395C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17766764 | ||||||
| chr4:17766776
|
G | A | 1 | a0001c0003t0066g0150 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.141+14383C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17766776 | ||||||
| chr4:17766942
|
G | A | 2 | a0001c0005t0029g0184a0003c0018t0005g0196 | 2 | HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.141+14217C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17766942 | ||||||
| chr4:17766952
|
G | A | 34 | a0001c0003t0002g0019a0001c0003t0002g0158a0001c0003t0002g0206others(31): Show | 34 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(31): Show |
intron_variant | MODIFIER | c.141+14207C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17766952 | ||||||
| chr4:17766992
|
C | T | 3 | a0001c0005t0007g0013a0015c0062t0035g0230a0015c0063t0054g0229 | 3 | HG02897.hp2 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.141+14167G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17766992 | ||||||
| chr4:17766999
|
G | A | 18 | a0001c0004t0042g0108a0001c0006t0003g0026a0001c0006t0003g0028others(15): Show | 18 | HG01243.hp2 HG02451.hp1 HG02886.hp1 others(15): Show |
intron_variant | MODIFIER | c.141+14160C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17766999 | ||||||
| chr4:17767011
|
C | T | 1 | a0001c0008t0002g0045 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.141+14148G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17767011 | ||||||
| chr4:17767094
|
C | A | 1 | a0025c0056t0061g0078 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.141+14065G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17767094 | ||||||
| chr4:17767121
|
C | T | 1 | a0001c0004t0045g0104 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.141+14038G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17767121 | ||||||
| chr4:17767207
|
G | A | 1 | a0002c0016t0001g0221 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.141+13952C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17767207 | ||||||
| chr4:17767218
|
C | T | 41 | a0001c0003t0002g0019a0001c0003t0002g0158a0001c0003t0002g0206others(38): Show | 41 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.141+13941G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17767218 | ||||||
| chr4:17767245
|
G | A | 2 | a0001c0017t0010g0175a0013c0058t0022g0174 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.141+13914C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17767245 | ||||||
| chr4:17767251
|
C | T | 1 | a0002c0001t0001g0087 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.141+13908G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17767251 | ||||||
| chr4:17767276
|
G | A | 1 | a0017c0026t0041g0160 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.141+13883C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17767276 | ||||||
| chr4:17767615
|
G | A | 48 | a0001c0003t0004g0057a0001c0003t0008g0216a0001c0003t0011g0166others(45): Show | 48 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.141+13544C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17767615 | ||||||
| chr4:17767641
|
G | T | 1 | a0017c0026t0038g0098 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.141+13518C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17767641 | ||||||
| chr4:17767701
|
C | A | 3 | a0001c0005t0007g0013a0015c0062t0035g0230a0015c0063t0054g0229 | 3 | HG02897.hp2 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.141+13458G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17767701 | ||||||
| chr4:17767705
|
G | C | 1 | a0002c0001t0001g0131 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.141+13454C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17767705 | ||||||
| chr4:17767705
|
G | GC | 54 | a0001c0003t0002g0019a0001c0003t0002g0227a0001c0003t0011g0168others(51): Show | 54 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.141+13453dupG | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17767705 | ||||||
| chr4:17767705
|
G | GCC | 8 | a0001c0003t0004g0018a0001c0003t0060g0215a0001c0015t0029g0164others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.141+13452_141+1345 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17767705 | ||||||
| chr4:17767712
|
A | C | 6 | a0001c0004t0009g0022a0001c0006t0003g0026a0001c0006t0028g0014others(3): Show | 6 | HG01109.hp2 HG01243.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+13447T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17767712 | ||||||
| chr4:17767775
|
A | G | 1 | a0001c0029t0005g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.141+13384T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17767775 | ||||||
| chr4:17767804
|
A | T | 12 | a0002c0001t0001g0101a0002c0001t0001g0181a0002c0001t0001g0186others(9): Show | 12 | HG00597.hp2 HG00673.hp1 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.141+13355T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17767804 | ||||||
| chr4:17767819
|
T | A | 2 | a0001c0017t0010g0175a0013c0058t0022g0174 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.141+13340A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17767819 | ||||||
| chr4:17767945
|
A | C | 3 | a0001c0005t0007g0013a0015c0062t0035g0230a0015c0063t0054g0229 | 3 | HG02897.hp2 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.141+13214T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17767945 | ||||||
| chr4:17768150
|
T | G | 1 | a0002c0001t0058g0173 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.141+13009A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17768150 | ||||||
| chr4:17768279
|
C | T | 1 | a0001c0005t0013g0185 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.141+12880G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17768279 | ||||||
| chr4:17768384
|
C | T | 10 | a0001c0005t0007g0013a0001c0008t0068g0234a0002c0002t0001g0134others(7): Show | 10 | HG00423.hp1 HG02071.hp1 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.141+12775G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17768384 | ||||||
| chr4:17768397
|
CCAGAGTA others(16): Show |
C | 3 | a0001c0005t0007g0013a0015c0062t0035g0230a0015c0063t0054g0229 | 3 | HG02897.hp2 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.141+12739_141+1276 others(27): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17768397 | ||||||
| chr4:17768447
|
G | A | 3 | a0001c0005t0007g0013a0015c0062t0035g0230a0015c0063t0054g0229 | 3 | HG02897.hp2 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.141+12712C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17768447 | ||||||
| chr4:17768487
|
C | T | 1 | a0002c0001t0017g0091 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.141+12672G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17768487 | ||||||
| chr4:17768580
|
C | T | 1 | a0002c0002t0001g0114 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.141+12579G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17768580 | ||||||
| chr4:17768672
|
G | A | 3 | a0001c0005t0007g0013a0015c0062t0035g0230a0015c0063t0054g0229 | 3 | HG02897.hp2 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.141+12487C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17768672 | ||||||
| chr4:17768809
|
C | CT | 10 | a0001c0006t0003g0026a0001c0006t0003g0028a0001c0006t0003g0029others(7): Show | 10 | HG03831.hp2 HG04199.hp2 NA18955.hp1 others(7): Show |
intron_variant | MODIFIER | c.141+12349dupA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17768809 | ||||||
| chr4:17768809
|
CT | C | 9 | a0001c0005t0007g0013a0001c0005t0014g0118a0001c0008t0018g0020others(6): Show | 9 | HG02809.hp1 HG02897.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.141+12349delA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17768809 | ||||||
| chr4:17768991
|
C | T | 1 | a0001c0008t0019g0102 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.141+12168G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17768991 | ||||||
| chr4:17769015
|
C | A | 9 | a0001c0003t0019g0095a0001c0005t0014g0170a0001c0015t0029g0164others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.141+12144G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17769015 | ||||||
| chr4:17769046
|
A | G | 63 | a0001c0003t0004g0057a0001c0003t0008g0216a0001c0003t0011g0166others(60): Show | 63 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.141+12113T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17769046 | ||||||
| chr4:17769067
|
T | G | 2 | a0001c0017t0010g0175a0013c0058t0022g0174 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.141+12092A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17769067 | ||||||
| chr4:17769146
|
C | A | 5 | a0001c0008t0018g0020a0001c0021t0018g0068a0004c0010t0006g0165others(2): Show | 5 | HG03098.hp2 HG03471.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+12013G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17769146 | ||||||
| chr4:17769151
|
AAC | A | 18 | a0001c0004t0042g0108a0001c0006t0003g0026a0001c0006t0003g0028others(15): Show | 18 | HG01243.hp2 HG02451.hp1 HG02886.hp1 others(15): Show |
intron_variant | MODIFIER | c.141+12006_141+1200 others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17769151 | ||||||
| chr4:17769596
|
C | T | 1 | a0001c0004t0045g0104 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.141+11563G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17769596 | ||||||
| chr4:17769694
|
G | C | 95 | a0001c0003t0002g0069a0001c0003t0004g0057a0001c0003t0007g0220others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.141+11465C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17769694 | ||||||
| chr4:17769872
|
T | C | 6 | a0001c0006t0003g0026a0001c0006t0003g0028a0001c0006t0003g0029others(3): Show | 6 | NA18955.hp1 NA18956.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.141+11287A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17769872 | ||||||
| chr4:17769947
|
C | T | 1 | a0010c0013t0002g0231 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.141+11212G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17769947 | ||||||
| chr4:17769948
|
G | A | 52 | a0001c0003t0004g0057a0001c0003t0008g0216a0001c0003t0011g0166others(49): Show | 52 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(49): Show |
intron_variant | MODIFIER | c.141+11211C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17769948 | ||||||
| chr4:17770043
|
C | A | 1 | a0005c0036t0053g0233 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.141+11116G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17770043 | ||||||
| chr4:17770106
|
A | T | 5 | a0001c0005t0007g0125a0001c0005t0007g0140a0002c0001t0001g0141others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+11053T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17770106 | ||||||
| chr4:17770367
|
A | C | 2 | a0009c0011t0001g0081a0009c0011t0056g0084 | 2 | HG02717.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.141+10792T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17770367 | ||||||
| chr4:17770436
|
A | AGTT | 10 | a0001c0005t0029g0184a0001c0007t0004g0097a0001c0007t0008g0157others(7): Show | 10 | HG00642.hp1 HG01081.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.141+10720_141+1072 others(7): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17770436 | ||||||
| chr4:17770436
|
AGTT | A | 67 | a0001c0003t0004g0057a0001c0003t0008g0216a0001c0003t0011g0166others(64): Show | 67 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.141+10720_141+1072 others(7): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17770436 | ||||||
| chr4:17770436
|
AGTTGTT | A | 79 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0158others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.141+10717_141+1072 others(10): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17770436 | ||||||
| chr4:17770436
|
AGTTGTTG others(5): Show |
A | 7 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0032g0236others(4): Show | 7 | HG00423.hp1 HG02071.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.141+10711_141+1072 others(16): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17770436 | ||||||
| chr4:17770443
|
G | T | 54 | a0001c0003t0004g0057a0001c0003t0008g0216a0001c0003t0011g0166others(51): Show | 54 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.141+10716C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17770443 | ||||||
| chr4:17770446
|
G | T | 17 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0005t0014g0170others(14): Show | 17 | HG00099.hp2 HG01109.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.141+10713C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17770446 | ||||||
| chr4:17770549
|
C | T | 3 | a0001c0012t0026g0092a0005c0042t0006g0093a0007c0043t0012g0105 | 3 | HG01891.hp2 HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.141+10610G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17770549 | ||||||
| chr4:17770589
|
G | A | 52 | a0001c0003t0004g0057a0001c0003t0008g0216a0001c0003t0011g0166others(49): Show | 52 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(49): Show |
intron_variant | MODIFIER | c.141+10570C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17770589 | ||||||
| chr4:17770655
|
G | A | 1 | a0002c0001t0001g0197 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.141+10504C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17770655 | ||||||
| chr4:17770656
|
G | A | 1 | a0005c0036t0053g0233 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.141+10503C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17770656 | ||||||
| chr4:17770658
|
G | A | 3 | a0001c0012t0026g0092a0005c0042t0006g0093a0007c0043t0012g0105 | 3 | HG01891.hp2 HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.141+10501C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17770658 | ||||||
| chr4:17770662
|
C | T | 1 | a0002c0002t0001g0040 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.141+10497G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17770662 | ||||||
| chr4:17770756
|
G | A | 1 | a0002c0001t0001g0198 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.141+10403C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17770756 | ||||||
| chr4:17770962
|
C | G | 10 | a0001c0003t0007g0220a0001c0004t0009g0072a0001c0004t0026g0073others(7): Show | 10 | HG01891.hp1 HG02145.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.141+10197G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17770962 | ||||||
| chr4:17771702
|
C | G | 1 | a0002c0001t0001g0136 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.141+9457G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17771702 | ||||||
| chr4:17771725
|
C | G | 4 | a0001c0005t0007g0013a0001c0005t0014g0118a0015c0062t0035g0230others(1): Show | 4 | HG02809.hp1 HG02897.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+9434G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17771725 | ||||||
| chr4:17771736
|
T | C | 39 | a0001c0003t0002g0069a0001c0003t0007g0220a0001c0003t0018g0006others(36): Show | 39 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.141+9423A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17771736 | ||||||
| chr4:17771737
|
G | A | 2 | a0001c0017t0010g0175a0013c0058t0022g0174 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.141+9422C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17771737 | ||||||
| chr4:17771819
|
G | A | 53 | a0001c0003t0004g0057a0001c0003t0008g0216a0001c0003t0011g0166others(50): Show | 53 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(50): Show |
intron_variant | MODIFIER | c.141+9340C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17771819 | ||||||
| chr4:17771862
|
A | G | 75 | a0001c0003t0004g0057a0001c0003t0008g0216a0001c0003t0011g0166others(72): Show | 75 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.141+9297T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17771862 | ||||||
| chr4:17771916
|
A | G | 2 | a0001c0003t0018g0006a0001c0021t0064g0005 | 2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.141+9243T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17771916 | ||||||
| chr4:17772161
|
G | C | 2 | a0001c0017t0010g0175a0013c0058t0022g0174 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.141+8998C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17772161 | ||||||
| chr4:17772234
|
T | C | 2 | a0001c0006t0028g0014a0001c0006t0028g0015 | 2 | HG03831.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.141+8925A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17772234 | ||||||
| chr4:17772247
|
T | C | 21 | a0001c0003t0002g0069a0001c0003t0007g0220a0001c0004t0009g0022others(18): Show | 21 | HG01891.hp1 HG01891.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.141+8912A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17772247 | ||||||
| chr4:17772440
|
G | A | 9 | a0001c0003t0019g0095a0001c0005t0014g0170a0001c0015t0029g0164others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.141+8719C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17772440 | ||||||
| chr4:17772690
|
T | G | 1 | a0002c0001t0017g0091 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.141+8469A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17772690 | ||||||
| chr4:17772719
|
G | A | 5 | a0001c0008t0018g0020a0001c0021t0018g0068a0004c0010t0006g0165others(2): Show | 5 | HG03098.hp2 HG03471.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+8440C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17772719 | ||||||
| chr4:17772796
|
C | T | 1 | a0001c0003t0002g0227 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.141+8363G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17772796 | ||||||
| chr4:17772810
|
G | A | 9 | a0001c0003t0019g0095a0001c0005t0014g0170a0001c0015t0029g0164others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.141+8349C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17772810 | ||||||
| chr4:17772838
|
A | C | 1 | a0002c0001t0001g0135 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.141+8321T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17772838 | ||||||
| chr4:17772839
|
C | G | 5 | a0001c0008t0018g0020a0001c0021t0018g0068a0004c0010t0006g0165others(2): Show | 5 | HG03098.hp2 HG03471.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+8320G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17772839 | ||||||
| chr4:17773043
|
G | C | 3 | a0001c0012t0026g0092a0005c0042t0006g0093a0007c0043t0012g0105 | 3 | HG01891.hp2 HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.141+8116C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17773043 | ||||||
| chr4:17773173
|
T | A | 5 | a0001c0008t0018g0020a0001c0021t0018g0068a0004c0010t0006g0165others(2): Show | 5 | HG03098.hp2 HG03471.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+7986A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17773173 | ||||||
| chr4:17773187
|
A | G | 6 | a0001c0003t0007g0220a0001c0004t0009g0072a0001c0004t0026g0073others(3): Show | 6 | HG02145.hp2 HG02818.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+7972T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17773187 | ||||||
| chr4:17773242
|
G | T | 1 | a0002c0001t0001g0126 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.141+7917C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17773242 | ||||||
| chr4:17773394
|
A | G | 20 | a0001c0003t0019g0095a0001c0005t0007g0013a0001c0005t0014g0118others(17): Show | 20 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.141+7765T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17773394 | ||||||
| chr4:17773425
|
T | C | 7 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0032g0236others(4): Show | 7 | HG00423.hp1 HG02071.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.141+7734A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17773425 | ||||||
| chr4:17773453
|
C | T | 5 | a0001c0003t0008g0216a0001c0003t0049g0099a0006c0014t0001g0042others(2): Show | 5 | HG01358.hp1 HG01516.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+7706G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17773453 | ||||||
| chr4:17773460
|
G | A | 2 | a0001c0017t0010g0175a0013c0058t0022g0174 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.141+7699C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17773460 | ||||||
| chr4:17773600
|
G | A | 2 | a0001c0017t0010g0175a0013c0058t0022g0174 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.141+7559C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17773600 | ||||||
| chr4:17773789
|
C | G | 1 | a0001c0003t0002g0227 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.141+7370G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17773789 | ||||||
| chr4:17774142
|
T | C | 13 | a0001c0003t0019g0095a0001c0005t0007g0013a0001c0005t0014g0118others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.141+7017A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17774142 | ||||||
| chr4:17774157
|
T | G | 22 | a0001c0003t0018g0006a0001c0003t0019g0095a0001c0005t0007g0013others(19): Show | 22 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.141+7002A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17774157 | ||||||
| chr4:17774205
|
C | G | 1 | a0001c0033t0003g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.141+6954G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17774205 | ||||||
| chr4:17774371
|
GACAA | G | 22 | a0001c0003t0019g0095a0001c0005t0007g0013a0001c0005t0014g0118others(19): Show | 22 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.141+6784_141+6787d others(6): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17774371 | ||||||
| chr4:17774419
|
G | A | 9 | a0001c0003t0019g0095a0001c0005t0014g0170a0001c0015t0029g0164others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.141+6740C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17774419 | ||||||
| chr4:17774508
|
C | A | 2 | a0001c0017t0010g0175a0013c0058t0022g0174 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.141+6651G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17774508 | ||||||
| chr4:17774543
|
A | G | 13 | a0001c0003t0019g0095a0001c0005t0007g0013a0001c0005t0014g0118others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.141+6616T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17774543 | ||||||
| chr4:17774698
|
T | A | 7 | a0001c0008t0068g0234a0002c0002t0001g0134a0002c0002t0032g0236others(4): Show | 7 | HG00423.hp1 HG02071.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.141+6461A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17774698 | ||||||
| chr4:17774936
|
T | C | 3 | a0001c0012t0026g0092a0005c0042t0006g0093a0007c0043t0012g0105 | 3 | HG01891.hp2 HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.141+6223A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17774936 | ||||||
| chr4:17774992
|
C | CT | 51 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0158others(48): Show | 51 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.141+6166dupA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17774992 | ||||||
| chr4:17774992
|
C | CTT | 5 | a0001c0003t0004g0018a0002c0001t0001g0116a0013c0058t0022g0174others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+6165_141+6166d others(4): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17774992 | ||||||
| chr4:17774992
|
CT | C | 72 | a0001c0003t0002g0149a0001c0003t0018g0006a0001c0003t0066g0150others(69): Show | 72 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.141+6166delA | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17774992 | ||||||
| chr4:17774997
|
T | C | 3 | a0001c0012t0026g0092a0005c0042t0006g0093a0007c0043t0012g0105 | 3 | HG01891.hp2 HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.141+6162A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17774997 | ||||||
| chr4:17775050
|
G | GCAGTGGT others(7): Show |
4 | a0001c0005t0007g0013a0001c0005t0014g0118a0015c0062t0035g0230others(1): Show | 4 | HG02809.hp1 HG02897.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+6095_141+6108d others(16): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17775050 | ||||||
| chr4:17775085
|
C | A | 9 | a0001c0003t0019g0095a0001c0005t0014g0170a0001c0015t0029g0164others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.141+6074G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17775085 | ||||||
| chr4:17775117
|
C | T | 1 | a0001c0005t0007g0125 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.141+6042G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17775117 | ||||||
| chr4:17775138
|
A | G | 54 | a0001c0003t0004g0057a0001c0003t0008g0216a0001c0003t0011g0166others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(51): Show |
intron_variant | MODIFIER | c.141+6021T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17775138 | ||||||
| chr4:17775192
|
A | T | 18 | a0001c0003t0019g0095a0001c0003t0047g0199a0001c0005t0007g0013others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.141+5967T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17775192 | ||||||
| chr4:17775288
|
C | T | 52 | a0001c0003t0004g0057a0001c0003t0008g0216a0001c0003t0011g0166others(49): Show | 52 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(49): Show |
intron_variant | MODIFIER | c.141+5871G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17775288 | ||||||
| chr4:17775310
|
C | T | 4 | a0001c0005t0007g0013a0001c0005t0014g0118a0015c0062t0035g0230others(1): Show | 4 | HG02809.hp1 HG02897.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+5849G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17775310 | ||||||
| chr4:17775328
|
G | A | 2 | a0001c0017t0010g0175a0013c0058t0022g0174 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.141+5831C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17775328 | ||||||
| chr4:17775494
|
A | T | 236 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(233): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.141+5665T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17775494 | ||||||
| chr4:17775632
|
G | A | 9 | a0001c0003t0019g0095a0001c0005t0014g0170a0001c0015t0029g0164others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.141+5527C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17775632 | ||||||
| chr4:17776024
|
C | A | 4 | a0001c0003t0019g0095a0001c0015t0029g0164a0024c0037t0052g0094others(1): Show | 4 | HG02257.hp1 HG03139.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+5135G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17776024 | ||||||
| chr4:17776128
|
C | T | 1 | a0002c0002t0001g0228 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.141+5031G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17776128 | ||||||
| chr4:17776137
|
A | G | 4 | a0001c0005t0007g0013a0001c0005t0014g0118a0015c0062t0035g0230others(1): Show | 4 | HG02809.hp1 HG02897.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+5022T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17776137 | ||||||
| chr4:17776203
|
C | A | 2 | a0001c0007t0004g0097a0001c0007t0008g0157 | 2 | HG01081.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.141+4956G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17776203 | ||||||
| chr4:17776214
|
T | A | 5 | a0001c0008t0018g0020a0001c0021t0018g0068a0004c0010t0006g0165others(2): Show | 5 | HG03098.hp2 HG03471.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+4945A>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17776214 | ||||||
| chr4:17776307
|
A | T | 5 | a0001c0005t0014g0170a0002c0002t0001g0228a0016c0025t0021g0224others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+4852T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17776307 | ||||||
| chr4:17776358
|
G | A | 5 | a0001c0008t0018g0020a0001c0021t0018g0068a0004c0010t0006g0165others(2): Show | 5 | HG03098.hp2 HG03471.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+4801C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17776358 | ||||||
| chr4:17776411
|
G | A | 6 | a0001c0003t0023g0122a0001c0005t0007g0013a0001c0005t0014g0118others(3): Show | 6 | HG02723.hp1 HG02809.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.141+4748C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17776411 | ||||||
| chr4:17776451
|
C | T | 11 | a0001c0003t0023g0122a0001c0005t0007g0013a0001c0005t0014g0118others(8): Show | 11 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.141+4708G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17776451 | ||||||
| chr4:17776481
|
C | T | 5 | a0001c0008t0018g0020a0001c0021t0018g0068a0004c0010t0006g0165others(2): Show | 5 | HG03098.hp2 HG03471.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+4678G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17776481 | ||||||
| chr4:17776533
|
T | C | 5 | a0001c0008t0018g0020a0001c0021t0018g0068a0004c0010t0006g0165others(2): Show | 5 | HG03098.hp2 HG03471.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+4626A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17776533 | ||||||
| chr4:17776538
|
A | G | 20 | a0001c0003t0002g0069a0001c0003t0007g0220a0001c0004t0009g0072others(17): Show | 20 | HG02145.hp2 HG02572.hp1 HG02615.hp1 others(17): Show |
intron_variant | MODIFIER | c.141+4621T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17776538 | ||||||
| chr4:17776545
|
T | C | 5 | a0001c0008t0018g0020a0001c0021t0018g0068a0004c0010t0006g0165others(2): Show | 5 | HG03098.hp2 HG03471.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+4614A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17776545 | ||||||
| chr4:17776554
|
AATT | A | 5 | a0001c0008t0018g0020a0001c0021t0018g0068a0004c0010t0006g0165others(2): Show | 5 | HG03098.hp2 HG03471.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+4602_141+4604d others(5): Show |
FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17776554 | ||||||
| chr4:17776563
|
C | T | 5 | a0001c0008t0018g0020a0001c0021t0018g0068a0004c0010t0006g0165others(2): Show | 5 | HG03098.hp2 HG03471.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+4596G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17776563 | ||||||
| chr4:17776712
|
G | C | 52 | a0001c0003t0004g0057a0001c0003t0008g0216a0001c0003t0011g0166others(49): Show | 52 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(49): Show |
intron_variant | MODIFIER | c.141+4447C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17776712 | ||||||
| chr4:17776724
|
T | C | 33 | a0001c0003t0002g0019a0001c0003t0002g0158a0001c0003t0002g0206others(30): Show | 33 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.141+4435A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17776724 | ||||||
| chr4:17776820
|
G | T | 1 | a0001c0005t0014g0170 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.141+4339C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17776820 | ||||||
| chr4:17776822
|
A | T | 2 | a0001c0017t0010g0175a0013c0058t0022g0174 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.141+4337T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17776822 | ||||||
| chr4:17777239
|
G | T | 2 | a0001c0003t0018g0006a0001c0021t0064g0005 | 2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.141+3920C>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17777239 | ||||||
| chr4:17777314
|
T | G | 169 | a0001c0003t0002g0019a0001c0003t0002g0069a0001c0003t0002g0149others(166): Show | 169 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.141+3845A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17777314 | ||||||
| chr4:17777321
|
G | C | 80 | a0001c0003t0002g0019a0001c0003t0002g0206a0001c0003t0002g0227others(77): Show | 80 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.141+3838C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17777321 | ||||||
| chr4:17777416
|
A | T | 20 | a0001c0004t0009g0022a0001c0004t0025g0023a0001c0004t0025g0024others(17): Show | 20 | HG01243.hp2 HG02258.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.141+3743T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17777416 | ||||||
| chr4:17777672
|
A | T | 53 | a0001c0003t0002g0019a0001c0003t0002g0206a0001c0003t0004g0018others(50): Show | 53 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.141+3487T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17777672 | ||||||
| chr4:17777687
|
A | T | 1 | a0001c0029t0005g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.141+3472T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17777687 | ||||||
| chr4:17777841
|
T | C | 4 | a0001c0005t0014g0170a0002c0002t0001g0228a0015c0062t0035g0230others(1): Show | 4 | HG02145.hp1 HG02965.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.141+3318A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17777841 | ||||||
| chr4:17777882
|
G | C | 1 | a0001c0004t0045g0104 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.141+3277C>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17777882 | ||||||
| chr4:17777913
|
C | T | 1 | a0001c0015t0029g0164 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.141+3246G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17777913 | ||||||
| chr4:17778074
|
GA | G | 5 | a0002c0001t0058g0173a0002c0002t0001g0114a0007c0041t0012g0011others(2): Show | 5 | HG01891.hp1 HG02135.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+3084delT | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17778074 | ||||||
| chr4:17778127
|
C | A | 1 | a0007c0041t0012g0011 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.141+3032G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17778127 | ||||||
| chr4:17778185
|
G | A | 1 | a0007c0041t0012g0011 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.141+2974C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17778185 | ||||||
| chr4:17778410
|
A | G | 17 | a0001c0003t0067g0238a0001c0004t0042g0108a0001c0005t0007g0013others(14): Show | 17 | HG00423.hp1 HG00544.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.141+2749T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17778410 | ||||||
| chr4:17778472
|
C | A | 65 | a0001c0003t0002g0206a0001c0003t0002g0227a0001c0003t0004g0169others(62): Show | 65 | HG00323.hp1 HG00597.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.141+2687G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17778472 | ||||||
| chr4:17778588
|
G | A | 64 | a0001c0003t0002g0206a0001c0003t0002g0227a0001c0003t0004g0169others(61): Show | 64 | HG00323.hp1 HG00597.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.141+2571C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17778588 | ||||||
| chr4:17778868
|
C | T | 5 | a0001c0003t0067g0238a0001c0008t0068g0234a0002c0002t0032g0236others(2): Show | 5 | HG00423.hp1 HG00544.hp2 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+2291G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17778868 | ||||||
| chr4:17778908
|
A | G | 1 | a0019c0040t0065g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.141+2251T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17778908 | ||||||
| chr4:17778945
|
T | C | 1 | a0007c0043t0012g0105 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.141+2214A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17778945 | ||||||
| chr4:17779093
|
T | G | 81 | a0001c0003t0002g0206a0001c0003t0002g0227a0001c0003t0004g0169others(78): Show | 81 | HG00323.hp1 HG00423.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.141+2066A>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17779093 | ||||||
| chr4:17779108
|
C | G | 2 | a0001c0006t0028g0014a0001c0006t0028g0015 | 2 | HG03831.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.141+2051G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17779108 | ||||||
| chr4:17779116
|
A | G | 1 | a0019c0040t0065g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.141+2043T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17779116 | ||||||
| chr4:17779152
|
A | G | 1 | a0001c0005t0007g0013 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.141+2007T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17779152 | ||||||
| chr4:17779159
|
A | G | 5 | a0001c0003t0067g0238a0001c0008t0068g0234a0002c0002t0032g0236others(2): Show | 5 | HG00423.hp1 HG00544.hp2 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+2000T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17779159 | ||||||
| chr4:17779309
|
G | A | 57 | a0001c0003t0002g0149a0001c0003t0002g0158a0001c0003t0008g0163others(54): Show | 57 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.141+1850C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17779309 | ||||||
| chr4:17779398
|
A | T | 1 | a0002c0002t0001g0171 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.141+1761T>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17779398 | ||||||
| chr4:17779406
|
C | T | 2 | a0001c0005t0014g0170a0019c0040t0065g0012 | 2 | HG02145.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.141+1753G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17779406 | ||||||
| chr4:17779586
|
C | T | 65 | a0001c0003t0002g0206a0001c0003t0002g0227a0001c0003t0004g0169others(62): Show | 65 | HG00323.hp1 HG00597.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.141+1573G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17779586 | ||||||
| chr4:17779612
|
T | C | 1 | a0001c0015t0029g0164 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.141+1547A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17779612 | ||||||
| chr4:17779624
|
A | C | 1 | a0001c0003t0004g0169 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.141+1535T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17779624 | ||||||
| chr4:17779634
|
A | G | 2 | a0003c0009t0005g0009a0008c0034t0051g0010 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.141+1525T>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17779634 | ||||||
| chr4:17779855
|
A | C | 3 | a0002c0001t0001g0002a0006c0014t0001g0008a0032c0061t0030g0007 | 3 | HG02735.hp2 NA18939.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.141+1304T>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17779855 | ||||||
| chr4:17779900
|
C | T | 2 | a0001c0003t0018g0006a0001c0021t0064g0005 | 2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.141+1259G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17779900 | ||||||
| chr4:17779995
|
C | T | 2 | a0001c0015t0013g0003a0007c0050t0012g0004 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.141+1164G>A | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17779995 | ||||||
| chr4:17780571
|
G | A | 1 | a0005c0036t0053g0233 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.141+588C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17780571 | ||||||
| chr4:17780641
|
T | C | 66 | a0001c0003t0002g0206a0001c0003t0002g0227a0001c0003t0004g0169others(63): Show | 66 | HG00323.hp1 HG00597.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.141+518A>G | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17780641 | ||||||
| chr4:17780801
|
C | A | 3 | a0001c0003t0011g0166a0001c0003t0011g0167a0001c0003t0011g0168 | 3 | HG03704.hp2 HG04199.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.141+358G>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17780801 | ||||||
| chr4:17781082
|
G | A | 65 | a0001c0003t0002g0206a0001c0003t0002g0227a0001c0003t0004g0169others(62): Show | 65 | HG00323.hp1 HG00597.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.141+77C>T | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17781082 | ||||||
| chr4:17781141
|
C | G | 1 | a0002c0001t0001g0002 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.141+18G>C | FAM184B | ENSG00000047662.5 | transcript | ENST00000265018.4 | protein_coding | 1/17 | chr4 | 17781141 |