Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 79632 |
|---|---|
| ensemblid | ENSG00000111879.20 |
| hgncid | 20991 |
| symbol | FAM184A |
| name | family with sequence similarity 184 member A |
| refseq_nuc | NM_024581.6 |
| refseq_prot | NP_078857.5 |
| ensembl_nuc | ENST00000338891.12 |
| ensembl_prot | ENSP00000342604.7 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 118959763 |
| end | 119078664 |
| strand | - |
| ver | v1.2 |
| region | chr6:118959763-119078664 |
| region5000 | chr6:118954763-119083664 |
| regionname0 | FAM184A_chr6_118959763_119078664 |
| regionname5000 | FAM184A_chr6_118954763_119083664 |
| 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 | 1/1 | 1140 | 259 | 80 | 56 | 94 | 7 | 20 | 72 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0002 | 0/0 | 1140 | 17 | 3 | 5 | 4 | 1 | 4 | 2 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0003 | 0/0 | 1140 | 5 | 0 | 5 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0004 | 0/0 | 1140 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0005 | 0/0 | 1140 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0006 | 0/0 | 1140 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0007 | 0/0 | 1140 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0008 | 0/0 | 1140 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| 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 | 1/1 | 3423 | 250 | 72 | 55 | 94 | 7 | 20 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| c0002 | 0/0 | 3423 | 17 | 3 | 5 | 4 | 1 | 4 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| c0003 | 0/0 | 3423 | 8 | 7 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| c0004 | 0/0 | 3423 | 5 | 0 | 5 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| c0005 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| c0006 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| c0007 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| c0008 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| c0009 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| c0010 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| 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 | 709 | 222 | 60 | 52 | 84 | 7 | 18 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| t0002 | 1/0 | 706 | 26 | 9 | 7 | 3 | 1 | 5 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| t0003 | 0/0 | 709 | 13 | 0 | 6 | 7 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| t0004 | 0/0 | 709 | 10 | 10 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| t0005 | 0/0 | 709 | 7 | 7 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| t0006 | 0/0 | 709 | 2 | 1 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| t0007 | 0/0 | 709 | 2 | 0 | 0 | 2 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| t0008 | 0/0 | 709 | 2 | 0 | 0 | 2 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| t0009 | 0/0 | 709 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| t0010 | 0/0 | 709 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| 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 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0049 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0053 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3423 | 250 | 72 | 55 | 94 | 7 | 20 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0001c0003 | 0/0 | 3423 | 8 | 7 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0001c0006 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0002c0002 | 0/0 | 3423 | 17 | 3 | 5 | 4 | 1 | 4 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0003c0004 | 0/0 | 3423 | 5 | 0 | 5 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0004c0008 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0005c0009 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0006c0007 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0007c0010 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0008c0005 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4131 | 206 | 51 | 46 | 83 | 7 | 18 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0001c0001t0002 | 1/0 | 4128 | 10 | 6 | 2 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0001c0001t0003 | 0/0 | 4131 | 13 | 0 | 6 | 7 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0001c0001t0004 | 0/0 | 4131 | 8 | 8 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0001c0001t0005 | 0/0 | 4131 | 5 | 5 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0001c0001t0006 | 0/0 | 4131 | 2 | 1 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0001c0001t0007 | 0/0 | 4131 | 2 | 0 | 0 | 2 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0001c0001t0008 | 0/0 | 4131 | 2 | 0 | 0 | 2 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0001c0001t0009 | 0/0 | 4131 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0001c0001t0010 | 0/0 | 4131 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0001c0003t0001 | 0/0 | 4131 | 7 | 6 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0001c0003t0005 | 0/0 | 4131 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0001c0006t0005 | 0/0 | 4131 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0002c0002t0001 | 0/0 | 4131 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0002c0002t0002 | 0/0 | 4128 | 16 | 3 | 5 | 3 | 1 | 4 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0003c0004t0001 | 0/0 | 4131 | 5 | 0 | 5 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0004c0008t0001 | 0/0 | 4131 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0005c0009t0004 | 0/0 | 4131 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0006c0007t0001 | 0/0 | 4131 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0007c0010t0004 | 0/0 | 4131 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| a0008c0005t0001 | 0/0 | 4131 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | copy fasta | chr6 | 118954763 | 119083664 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0053 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0002g0049 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0004g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0004g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0006g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0007g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0007g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0008g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0008g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0009g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0010g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0003t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0003t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0003t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0003t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0006t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0003c0004t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0003c0004t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0003c0004t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0003c0004t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0003c0004t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0004c0008t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0005c0009t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0006c0007t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0007c0010t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0008c0005t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0223 | EUR | GBR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | GBR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0208 | EAS | CHS | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00639 | hp1 | a0001 | c0003 | t0001 | g0133 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0236 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00738 | hp2 | a0003 | c0004 | t0001 | g0093 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0185 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0033 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0232 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0221 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0231 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01433 | hp1 | a0003 | c0004 | t0001 | g0091 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01496 | hp1 | a0003 | c0004 | t0001 | g0141 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | IBS | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0243 | EUR | IBS | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01884 | hp1 | a0001 | c0006 | t0005 | g0028 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01891 | hp1 | a0007 | c0010 | t0004 | g0004 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01891 | hp2 | a0004 | c0008 | t0001 | g0062 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | PEL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PEL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02004 | hp1 | a0003 | c0004 | t0001 | g0092 | AMR | PEL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0238 | EAS | KHV | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | CDX | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CDX | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02273 | hp2 | a0003 | c0004 | t0001 | g0101 | AMR | PEL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0139 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0031 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02572 | hp2 | a0005 | c0009 | t0004 | g0005 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0025 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02615 | hp2 | a0001 | c0001 | t0010 | g0284 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0029 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02698 | hp1 | a0001 | c0001 | t0009 | g0001 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02717 | hp1 | a0001 | c0003 | t0001 | g0262 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0136 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0026 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0046 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ESN | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | ESN | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | ESN | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0140 | AFR | ESN | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | MSL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | MSL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0032 | AFR | MSL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0211 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0212 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03516 | hp2 | a0002 | c0002 | t0002 | g0121 | AFR | ESN | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03540 | hp2 | a0006 | c0007 | t0001 | g0242 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0224 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0217 | SAS | BEB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | STU | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | STU | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | STU | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | STU | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18612 | hp2 | a0001 | c0001 | t0008 | g0285 | EAS | CHB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | YRI | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | YRI | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0189 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18986 | hp1 | a0001 | c0001 | t0007 | g0283 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0264 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19002 | hp1 | a0001 | c0001 | t0008 | g0286 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19030 | hp1 | a0002 | c0002 | t0002 | g0129 | AFR | LWK | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | LWK | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19043 | hp1 | a0001 | c0003 | t0005 | g0030 | AFR | LWK | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19055 | hp2 | a0001 | c0001 | t0007 | g0282 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0268 | AFR | ASW | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | ASW | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0267 | EUR | TSI | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0073 | EUR | TSI | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA20805 | hp1 | a0002 | c0002 | t0002 | g0143 | EUR | TSI | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0194 | EUR | TSI | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | GIH | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | GIH | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0142 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | USA | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | USA | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | USA | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA20300 | hp2 | a0008 | c0005 | t0001 | g0034 | AFR | USA | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | LWK | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | LWK | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0053 | REF | REF | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0049 | REF | REF | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:118974486
|
C | A | 1 | a0004 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.2857G>T | p.Ala953Ser | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/18 | 3222/4128 | 2857/3423 | 953/1140 | chr6 | 118974486 | ||
| chr6:118975978
|
T | A | 1 | a0003 | 5 | HG00738.hp2 HG01433.hp1 HG01496.hp1 others(2): Show |
missense_variant | MODERATE | c.2522A>T | p.His841Leu | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 12/18 | 2887/4128 | 2522/3423 | 841/1140 | chr6 | 118975978 | ||
| chr6:119002985
|
T | C | 1 | a0005 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.2002A>G | p.Met668Val | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/18 | 2367/4128 | 2002/3423 | 668/1140 | chr6 | 119002985 | ||
| chr6:119006467
|
C | T | 1 | a0002 | 17 | HG00597.hp1 HG00735.hp2 HG01081.hp2 others(14): Show |
missense_variant | MODERATE | c.1795G>A | p.Asp599Asn | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/18 | 2160/4128 | 1795/3423 | 599/1140 | chr6 | 119006467 | ||
| chr6:119006589
|
A | G | 1 | a0006 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.1673T>C | p.Met558Thr | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/18 | 2038/4128 | 1673/3423 | 558/1140 | chr6 | 119006589 | ||
| chr6:119016749
|
T | C | 1 | a0007 | 1 | HG01891.hp1 | missense_variant&splice_region_variant | MODERATE | c.1528A>G | p.Met510Val | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/18 | 1893/4128 | 1528/3423 | 510/1140 | chr6 | 119016749 | ||
| chr6:119078220
|
G | T | 1 | a0008 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.80C>A | p.Ala27Glu | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/18 | 445/4128 | 80/3423 | 27/1140 | chr6 | 119078220 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:119024243
|
G | A | 1 | a0001c0003 | 8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
synonymous_variant | LOW | c.730C>T | p.Leu244Leu | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/18 | 1095/4128 | 730/3423 | 244/1140 | chr6 | 119024243 | ||
| chr6:119024373
|
C | T | 1 | a0001c0006 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.600G>A | p.Glu200Glu | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/18 | 965/4128 | 600/3423 | 200/1140 | chr6 | 119024373 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:118959824
|
G | GCAT | 19 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(16): Show | 260 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(257): Show |
3_prime_UTR_variant | MODIFIER | c.*276_*278dupATG | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 18/18 | 278 | chr6 | 118959824 | |||||
| chr6:119078324
|
C | T | 1 | a0001c0001t0006 | 2 | HG01243.hp1 HG03486.hp2 |
5_prime_UTR_variant | MODIFIER | c.-25G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/18 | 25 | chr6 | 119078324 | |||||
| chr6:119078343
|
A | T | 3 | a0001c0001t0005a0001c0003t0005a0001c0006t0005 | 7 | HG01884.hp1 HG02451.hp2 HG02615.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-44T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/18 | 44 | chr6 | 119078343 | |||||
| chr6:119078432
|
G | A | 1 | a0001c0001t0007 | 2 | NA18986.hp1 NA19055.hp2 |
5_prime_UTR_variant | MODIFIER | c.-133C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/18 | 133 | chr6 | 119078432 | |||||
| chr6:119078454
|
C | T | 1 | a0001c0001t0003 | 13 | HG01081.hp1 HG01167.hp2 HG01243.hp2 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-155G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/18 | 155 | chr6 | 119078454 | |||||
| chr6:119078496
|
C | T | 3 | a0001c0001t0004a0005c0009t0004a0007c0010t0004 | 10 | HG01891.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-197G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/18 | 197 | chr6 | 119078496 | |||||
| chr6:119078556
|
G | A | 1 | a0001c0001t0010 | 1 | HG02615.hp2 | 5_prime_UTR_variant | MODIFIER | c.-257C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/18 | 257 | chr6 | 119078556 | |||||
| chr6:119078570
|
T | C | 1 | a0001c0001t0008 | 2 | NA18612.hp2 NA19002.hp1 |
5_prime_UTR_variant | MODIFIER | c.-271A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/18 | 271 | chr6 | 119078570 | |||||
| chr6:119078614
|
C | T | 1 | a0001c0001t0009 | 1 | HG02698.hp1 | 5_prime_UTR_variant | MODIFIER | c.-315G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/18 | 315 | chr6 | 119078614 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:118960257
|
A | G | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | NA18959.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.3342-73T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 17/17 | chr6 | 118960257 | ||||||
| chr6:118960534
|
C | G | 1 | a0002c0002t0002g0208 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3342-350G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 17/17 | chr6 | 118960534 | ||||||
| chr6:118960552
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3342-368C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 17/17 | chr6 | 118960552 | ||||||
| chr6:118960673
|
A | G | 1 | a0001c0001t0008g0286 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3342-489T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 17/17 | chr6 | 118960673 | ||||||
| chr6:118961324
|
C | CAT | 4 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(1): Show | 4 | HG01106.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.3341+435_3341+436d others(4): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 17/17 | chr6 | 118961324 | ||||||
| chr6:118961333
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3341+428T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 17/17 | chr6 | 118961333 | ||||||
| chr6:118961637
|
G | T | 1 | a0001c0001t0001g0061 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3341+124C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 17/17 | chr6 | 118961637 | ||||||
| chr6:118961667
|
GGTT | G | 7 | a0001c0001t0001g0130a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.3341+91_3341+93del others(3): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 17/17 | chr6 | 118961667 | ||||||
| chr6:118961753
|
G | C | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG03491.hp2 HG03492.hp2 |
splice_region_variant&intron_variant | LOW | c.3341+8C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 17/17 | chr6 | 118961753 | ||||||
| chr6:118962131
|
G | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3139-168C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118962131 | ||||||
| chr6:118962557
|
T | C | 1 | a0002c0002t0002g0208 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3139-594A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118962557 | ||||||
| chr6:118962903
|
A | C | 1 | a0001c0001t0001g0246 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3139-940T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118962903 | ||||||
| chr6:118963263
|
A | G | 4 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0131others(1): Show | 4 | HG02145.hp1 HG02572.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3139-1300T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118963263 | ||||||
| chr6:118963361
|
T | G | 7 | a0001c0001t0001g0130a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.3138+1306A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118963361 | ||||||
| chr6:118963414
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3138+1253T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118963414 | ||||||
| chr6:118963719
|
A | G | 94 | a0001c0001t0001g0044a0001c0001t0001g0047a0001c0001t0001g0050others(91): Show | 94 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.3138+948T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118963719 | ||||||
| chr6:118963735
|
A | G | 11 | a0001c0001t0001g0110a0001c0001t0001g0130a0001c0001t0001g0201others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.3138+932T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118963735 | ||||||
| chr6:118963776
|
G | A | 3 | a0001c0001t0001g0186a0001c0001t0001g0249a0001c0001t0001g0250 | 3 | HG00408.hp1 NA18952.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.3138+891C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118963776 | ||||||
| chr6:118964166
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3138+501T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118964166 | ||||||
| chr6:118964279
|
G | C | 4 | a0001c0001t0001g0110a0001c0001t0004g0003a0005c0009t0004g0005others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3138+388C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118964279 | ||||||
| chr6:118964307
|
G | A | 1 | a0002c0002t0002g0236 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3138+360C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118964307 | ||||||
| chr6:118964356
|
G | A | 1 | a0002c0002t0002g0232 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.3138+311C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118964356 | ||||||
| chr6:118964416
|
C | T | 259 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(256): Show | 259 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.3138+251G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118964416 | ||||||
| chr6:118964514
|
T | C | 5 | a0003c0004t0001g0091a0003c0004t0001g0092a0003c0004t0001g0093others(2): Show | 5 | HG00738.hp2 HG01433.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.3138+153A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118964514 | ||||||
| chr6:118964526
|
A | G | 53 | a0001c0001t0001g0044a0001c0001t0001g0047a0001c0001t0001g0083others(50): Show | 53 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.3138+141T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118964526 | ||||||
| chr6:118964526
|
A | T | 1 | a0001c0001t0001g0248 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.3138+141T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118964526 | ||||||
| chr6:118964529
|
AGTTT | A | 8 | a0001c0003t0001g0046a0001c0003t0001g0133a0001c0003t0001g0136others(5): Show | 8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3138+134_3138+137d others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118964529 | ||||||
| chr6:118964623
|
A | C | 1 | a0002c0002t0002g0208 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3138+44T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118964623 | ||||||
| chr6:118964637
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3138+30A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118964637 | ||||||
| chr6:118965057
|
G | C | 1 | a0001c0001t0001g0159 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3034-286C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118965057 | ||||||
| chr6:118965086
|
G | T | 1 | a0001c0001t0004g0009 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3034-315C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118965086 | ||||||
| chr6:118965155
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3034-384A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118965155 | ||||||
| chr6:118965205
|
G | GT | 248 | a0001c0001t0001g0036a0001c0001t0001g0041a0001c0001t0001g0042others(245): Show | 248 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.3034-435dupA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118965205 | ||||||
| chr6:118965205
|
G | GTT | 10 | a0001c0001t0001g0035a0001c0001t0001g0068a0001c0001t0001g0075others(7): Show | 10 | HG00735.hp1 HG01192.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.3034-436_3034-435d others(4): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118965205 | ||||||
| chr6:118965205
|
G | T | 1 | a0001c0001t0001g0061 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3034-434C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118965205 | ||||||
| chr6:118965208
|
T | TG | 20 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(17): Show | 20 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.3034-438_3034-437i others(3): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118965208 | ||||||
| chr6:118965211
|
T | G | 5 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(2): Show | 5 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.3034-440A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118965211 | ||||||
| chr6:118965212
|
T | G | 7 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0109others(4): Show | 7 | HG01106.hp2 HG01515.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.3034-441A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118965212 | ||||||
| chr6:118965580
|
C | T | 4 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0131others(1): Show | 4 | HG02145.hp1 HG02572.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3034-809G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118965580 | ||||||
| chr6:118965866
|
C | G | 1 | a0001c0001t0001g0150 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3033+969G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118965866 | ||||||
| chr6:118966012
|
C | G | 4 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0009others(1): Show | 4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.3033+823G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118966012 | ||||||
| chr6:118966444
|
C | A | 255 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(252): Show | 255 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.3033+391G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118966444 | ||||||
| chr6:118966634
|
G | A | 3 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203 | 3 | HG02109.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3033+201C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118966634 | ||||||
| chr6:118966694
|
T | A | 1 | a0001c0001t0001g0041 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3033+141A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118966694 | ||||||
| chr6:118966750
|
C | T | 4 | a0001c0001t0001g0110a0001c0001t0004g0003a0005c0009t0004g0005others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3033+85G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118966750 | ||||||
| chr6:118967428
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2916-476G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118967428 | ||||||
| chr6:118967444
|
T | A | 1 | a0001c0001t0001g0043 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2916-492A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118967444 | ||||||
| chr6:118967500
|
AT | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0004g0006 | 3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2916-549delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118967500 | ||||||
| chr6:118967635
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | NA18939.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.2916-683G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118967635 | ||||||
| chr6:118967816
|
CAT | C | 7 | a0001c0001t0001g0130a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2916-866_2916-865d others(4): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118967816 | ||||||
| chr6:118968113
|
G | A | 4 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0009others(1): Show | 4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2916-1161C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118968113 | ||||||
| chr6:118968174
|
G | T | 1 | a0002c0002t0002g0224 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2916-1222C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118968174 | ||||||
| chr6:118968370
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2916-1418C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118968370 | ||||||
| chr6:118968463
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2916-1511A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118968463 | ||||||
| chr6:118968545
|
A | G | 5 | a0001c0001t0001g0230a0001c0001t0001g0279a0001c0001t0001g0280others(2): Show | 5 | HG01934.hp1 HG02273.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.2916-1593T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118968545 | ||||||
| chr6:118968670
|
C | A | 231 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0041others(228): Show | 231 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.2916-1718G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118968670 | ||||||
| chr6:118968836
|
AAT | A | 255 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(252): Show | 255 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.2916-1886_2916-188 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118968836 | ||||||
| chr6:118969300
|
G | A | 10 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(7): Show | 10 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.2916-2348C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969300 | ||||||
| chr6:118969708
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2916-2756G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969708 | ||||||
| chr6:118969798
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2916-2846C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969798 | ||||||
| chr6:118969804
|
C | A | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2916-2852G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969804 | ||||||
| chr6:118969805
|
A | AC | 91 | a0001c0001t0001g0047a0001c0001t0001g0050a0001c0001t0001g0051others(88): Show | 91 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.2916-2854dupG | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969805 | ||||||
| chr6:118969810
|
G | C | 269 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(266): Show | 269 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.2916-2858C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969810 | ||||||
| chr6:118969827
|
G | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2916-2875C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969827 | ||||||
| chr6:118969861
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2916-2909A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969861 | ||||||
| chr6:118969992
|
T | TATAA | 141 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0041others(138): Show | 141 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.2916-3041_2916-304 others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969992 | ||||||
| chr6:118969992
|
T | TATATAA | 3 | a0001c0001t0001g0186a0001c0001t0001g0249a0001c0001t0001g0250 | 3 | HG00408.hp1 NA18952.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.2916-3041_2916-304 others(10): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969992 | ||||||
| chr6:118969992
|
TA | T | 3 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0010 | 3 | HG02109.hp1 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2916-3041delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969992 | ||||||
| chr6:118969993
|
A | ATAAAATA others(1): Show |
7 | a0001c0003t0001g0046a0001c0003t0001g0133a0001c0003t0001g0136others(4): Show | 7 | HG00639.hp1 HG02559.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATAAAATA others(5): Show |
7 | a0001c0001t0001g0061a0001c0001t0001g0074a0001c0001t0001g0086others(4): Show | 7 | HG00642.hp2 HG01123.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(16): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATAAAATA others(7): Show |
2 | a0001c0001t0001g0230a0001c0001t0003g0024 | 2 | HG02293.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(18): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATAAAATA others(9): Show |
14 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(11): Show | 14 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(20): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATAAAATA others(11): Show |
1 | a0001c0001t0001g0099 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2916-3042_2916-304 others(22): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATAAAATA others(15): Show |
3 | a0001c0001t0001g0161a0001c0001t0001g0202a0001c0001t0001g0203 | 3 | HG02109.hp2 NA18747.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(26): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATAAAATA others(17): Show |
1 | a0001c0001t0006g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2916-3042_2916-304 others(28): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATAAAATA others(19): Show |
5 | a0001c0001t0001g0084a0001c0001t0001g0170a0001c0001t0001g0281others(2): Show | 5 | HG02135.hp2 HG02683.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(30): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATAAAATA others(57): Show |
1 | a0004c0008t0001g0062 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2916-3042_2916-304 others(68): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATAAAATA others(21): Show |
1 | a0001c0001t0006g0032 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2916-3042_2916-304 others(32): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATAAAATA others(28): Show |
1 | a0001c0003t0001g0139 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2916-3042_2916-304 others(39): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATAAAATA others(23): Show |
1 | a0001c0001t0001g0167 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2916-3042_2916-304 others(34): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATAAAATA others(48): Show |
1 | a0001c0001t0001g0159 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2916-3042_2916-304 others(59): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATAAAATA others(25): Show |
3 | a0001c0001t0001g0047a0001c0001t0001g0107a0001c0001t0001g0255 | 3 | HG02280.hp1 HG02280.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(36): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATAAAATA others(62): Show |
1 | a0005c0009t0004g0005 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2916-3042_2916-304 others(73): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATAAAATA others(44): Show |
1 | a0001c0001t0001g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2916-3042_2916-304 others(55): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATAAAATA others(68): Show |
1 | a0001c0001t0003g0021 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2916-3042_2916-304 others(79): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATAAAATA others(27): Show |
2 | a0001c0001t0001g0103a0001c0001t0005g0029 | 2 | HG01515.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(38): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATAAAATA others(29): Show |
2 | a0001c0001t0001g0043a0001c0001t0001g0115 | 2 | HG01346.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(40): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATAAAATA others(31): Show |
11 | a0001c0001t0001g0051a0001c0001t0001g0104a0001c0001t0001g0108others(8): Show | 11 | HG00733.hp1 HG01106.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(42): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATAAAATA others(33): Show |
7 | a0001c0001t0001g0097a0001c0001t0001g0106a0001c0001t0001g0114others(4): Show | 7 | HG01081.hp1 HG02135.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(44): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATAAAATA others(35): Show |
2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(46): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATAAAATA others(37): Show |
4 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0105others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(48): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATAAAATA others(39): Show |
3 | a0001c0001t0001g0209a0001c0001t0001g0214a0001c0001t0003g0012 | 3 | NA18947.hp1 NA18968.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(50): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATAAAATA others(41): Show |
5 | a0001c0001t0001g0109a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | HG01978.hp1 HG02155.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(52): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATAAAATA others(43): Show |
4 | a0001c0001t0001g0210a0001c0001t0001g0246a0001c0001t0003g0016others(1): Show | 4 | HG01243.hp2 NA18943.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(54): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATAAAATA others(49): Show |
1 | a0001c0001t0001g0225 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2916-3042_2916-304 others(60): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATAAAATA others(33): Show |
1 | a0001c0001t0001g0219 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2916-3042_2916-304 others(44): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATAATATA others(35): Show |
1 | a0001c0001t0001g0171 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2916-3042_2916-304 others(46): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATACAATA others(3): Show |
3 | a0001c0001t0001g0130a0001c0001t0001g0277a0001c0001t0001g0278 | 3 | HG02055.hp2 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(14): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATATAAAA others(15): Show |
2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | NA18959.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(26): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969993
|
A | ATATAAAA others(17): Show |
2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(28): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | ||||||
| chr6:118969995
|
T | A | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2916-3043A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969995 | ||||||
| chr6:118970006
|
A | T | 19 | a0001c0001t0001g0043a0001c0001t0001g0084a0001c0001t0001g0163others(16): Show | 19 | HG01081.hp1 HG01243.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.2916-3054T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970006 | ||||||
| chr6:118970008
|
A | ATATATAA others(46): Show |
1 | a0001c0001t0001g0110 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(57): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(46): Show |
2 | a0001c0001t0004g0003a0007c0010t0004g0004 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(57): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(47): Show |
1 | a0002c0002t0001g0238 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(58): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(57): Show |
1 | a0001c0001t0001g0206 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(68): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(66): Show |
1 | a0001c0001t0001g0218 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(77): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(82): Show |
1 | a0001c0001t0001g0254 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(93): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(86): Show |
1 | a0001c0001t0001g0274 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(97): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(49): Show |
1 | a0001c0001t0001g0200 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(60): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(44): Show |
1 | a0001c0001t0001g0204 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(55): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(41): Show |
1 | a0001c0001t0001g0036 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(52): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(43): Show |
1 | a0001c0001t0001g0187 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(54): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(44): Show |
1 | a0001c0001t0001g0250 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(55): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(41): Show |
1 | a0001c0001t0008g0285 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(52): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(36): Show |
2 | a0001c0001t0001g0191a0001c0001t0001g0269 | 2 | NA18961.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(47): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(37): Show |
3 | a0001c0001t0001g0190a0001c0001t0001g0247a0001c0001t0001g0261 | 3 | HG02080.hp2 HG03017.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(48): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(39): Show |
1 | a0001c0001t0001g0279 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(50): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(48): Show |
2 | a0001c0001t0001g0188a0001c0001t0001g0273 | 2 | HG00597.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(59): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(34): Show |
1 | a0001c0001t0001g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(45): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(35): Show |
2 | a0001c0001t0001g0237a0001c0001t0003g0023 | 2 | HG01167.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(46): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(36): Show |
2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(47): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(38): Show |
1 | a0001c0001t0001g0249 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(49): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(39): Show |
2 | a0001c0001t0001g0207a0001c0001t0001g0280 | 2 | HG02273.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(50): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(32): Show |
1 | a0001c0001t0001g0042 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(43): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(34): Show |
1 | a0001c0001t0001g0272 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(45): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(35): Show |
1 | a0001c0001t0001g0243 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(46): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(36): Show |
1 | a0006c0007t0001g0242 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(47): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(37): Show |
3 | a0001c0001t0001g0192a0001c0001t0001g0235a0001c0001t0001g0271 | 3 | HG02071.hp1 HG02698.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(48): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(38): Show |
2 | a0001c0001t0004g0002a0001c0001t0005g0025 | 2 | HG02258.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(49): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(42): Show |
1 | a0001c0001t0002g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(53): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(30): Show |
1 | a0001c0001t0001g0134 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(41): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0220 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(44): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(35): Show |
2 | a0001c0001t0001g0186a0001c0001t0003g0015 | 2 | HG00408.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(46): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(37): Show |
1 | a0001c0001t0001g0195 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(48): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(39): Show |
1 | a0001c0001t0002g0197 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(50): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(28): Show |
2 | a0001c0001t0001g0111a0001c0001t0003g0022 | 2 | HG01361.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(39): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(29): Show |
1 | a0001c0001t0003g0014 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(40): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(30): Show |
1 | a0001c0001t0001g0223 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(41): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(31): Show |
3 | a0001c0001t0001g0228a0001c0001t0001g0245a0001c0001t0001g0251 | 3 | HG01496.hp2 NA18747.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(42): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(33): Show |
5 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0241others(2): Show | 5 | HG01358.hp1 HG02083.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(44): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(34): Show |
1 | a0001c0001t0001g0035 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(45): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(29): Show |
2 | a0001c0001t0001g0081a0001c0001t0001g0149 | 2 | HG01074.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(40): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(33): Show |
2 | a0001c0001t0001g0148a0001c0001t0001g0215 | 2 | NA19012.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(44): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(38): Show |
1 | a0001c0001t0002g0198 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(49): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(24): Show |
1 | a0001c0001t0001g0184 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(35): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(25): Show |
1 | a0001c0001t0001g0089 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(36): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(26): Show |
1 | a0001c0001t0001g0041 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(37): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0244 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(38): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(29): Show |
1 | a0001c0001t0001g0265 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(40): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(30): Show |
1 | a0001c0001t0001g0275 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(41): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(31): Show |
1 | a0001c0001t0001g0131 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(42): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(32): Show |
1 | a0001c0001t0001g0173 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(43): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0222 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(44): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0096 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(32): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0156 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(33): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(24): Show |
3 | a0001c0001t0001g0080a0001c0001t0001g0090a0001c0001t0001g0100 | 3 | HG01168.hp1 HG01192.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(35): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(26): Show |
1 | a0003c0004t0001g0141 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(37): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(29): Show |
1 | a0001c0001t0001g0205 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(40): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(32): Show |
1 | a0001c0001t0001g0229 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(43): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(20): Show |
2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | NA18975.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(31): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(22): Show |
1 | a0003c0004t0001g0091 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(33): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(25): Show |
1 | a0001c0001t0001g0266 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(36): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(29): Show |
1 | a0001c0001t0004g0006 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(40): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(30): Show |
1 | a0008c0005t0001g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(41): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(35): Show |
1 | a0001c0001t0004g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(46): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(18): Show |
4 | a0001c0001t0001g0147a0001c0001t0001g0155a0001c0001t0001g0172others(1): Show | 4 | HG02083.hp2 HG02523.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(29): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0078 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(32): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(22): Show |
8 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0124others(5): Show | 8 | HG00738.hp2 HG01981.hp2 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(33): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(24): Show |
2 | a0001c0001t0001g0073a0001c0001t0001g0260 | 2 | HG06807.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(35): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(26): Show |
1 | a0001c0001t0001g0082 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(37): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(28): Show |
1 | a0001c0001t0001g0079 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(39): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(32): Show |
1 | a0001c0001t0001g0137 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(43): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(16): Show |
5 | a0001c0001t0001g0144a0001c0001t0001g0177a0001c0001t0001g0181others(2): Show | 5 | HG00408.hp2 HG01071.hp1 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(27): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(20): Show |
10 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(7): Show | 10 | HG00140.hp2 HG00642.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(31): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(22): Show |
5 | a0001c0001t0001g0076a0001c0001t0001g0138a0001c0001t0005g0026others(2): Show | 5 | HG00733.hp2 HG02451.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(33): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0075 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(34): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(28): Show |
1 | a0001c0001t0001g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(39): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(14): Show |
12 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0145others(9): Show | 12 | HG01192.hp2 HG03195.hp2 HG03225.hp2 others(9): Show |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(25): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0146 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(26): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0175 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(27): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(30): Show |
1 | a0001c0001t0001g0048 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(41): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(14): Show |
8 | a0001c0001t0001g0094a0001c0001t0001g0151a0001c0001t0001g0152others(5): Show | 8 | HG00609.hp2 HG02080.hp1 HG03490.hp2 others(5): Show |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(25): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(28): Show |
1 | a0001c0001t0001g0045 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(39): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(25): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATTT | 28 | a0001c0001t0001g0047a0001c0001t0001g0103a0001c0001t0001g0104others(25): Show | 28 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.2916-3059_2916-305 others(7): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0002g0199 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2916-3067_2916-305 others(15): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970008
|
A | T | 33 | a0001c0001t0001g0043a0001c0001t0001g0066a0001c0001t0001g0069others(30): Show | 33 | HG00423.hp2 HG00609.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.2916-3056T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | ||||||
| chr6:118970009
|
T | TA | 7 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(4): Show | 7 | HG01168.hp2 HG01169.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.2916-3058_2916-305 others(5): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970009 | ||||||
| chr6:118970010
|
T | A | 13 | a0001c0001t0001g0067a0001c0001t0001g0132a0001c0001t0004g0009others(10): Show | 13 | HG00639.hp1 HG01358.hp2 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.2916-3058A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970010 | ||||||
| chr6:118970011
|
T | A | 3 | a0001c0001t0001g0130a0001c0001t0001g0277a0001c0001t0001g0278 | 3 | HG02055.hp2 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2916-3059A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970011 | ||||||
| chr6:118970012
|
T | A | 8 | a0001c0001t0004g0009a0001c0003t0001g0046a0001c0003t0001g0133others(5): Show | 8 | HG00639.hp1 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.2916-3060A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970012 | ||||||
| chr6:118970017
|
T | A | 4 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0009others(1): Show | 4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2916-3065A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970017 | ||||||
| chr6:118970036
|
T | C | 260 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(257): Show | 260 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.2916-3084A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970036 | ||||||
| chr6:118970106
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2916-3154G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970106 | ||||||
| chr6:118970246
|
C | T | 13 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(10): Show | 13 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.2916-3294G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970246 | ||||||
| chr6:118970247
|
G | A | 11 | a0001c0001t0001g0110a0001c0001t0001g0130a0001c0001t0001g0201others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2916-3295C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970247 | ||||||
| chr6:118970255
|
C | T | 122 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(119): Show | 122 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(119): Show |
intron_variant | MODIFIER | c.2916-3303G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970255 | ||||||
| chr6:118970259
|
C | G | 2 | a0001c0001t0006g0032a0001c0001t0006g0033 | 2 | HG01243.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2916-3307G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970259 | ||||||
| chr6:118970580
|
G | A | 4 | a0001c0001t0001g0110a0001c0001t0004g0003a0005c0009t0004g0005others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2916-3628C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970580 | ||||||
| chr6:118970764
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2915+3664G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970764 | ||||||
| chr6:118970782
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2915+3646T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970782 | ||||||
| chr6:118970853
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2915+3575C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970853 | ||||||
| chr6:118971451
|
AT | A | 17 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(14): Show | 17 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.2915+2976delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118971451 | ||||||
| chr6:118971548
|
T | TA | 101 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(98): Show | 101 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.2915+2879dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118971548 | ||||||
| chr6:118971720
|
A | C | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0128 | 3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2915+2708T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118971720 | ||||||
| chr6:118971860
|
C | A | 1 | a0001c0001t0003g0023 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2915+2568G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118971860 | ||||||
| chr6:118971860
|
C | CAGA | 188 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0041others(185): Show | 188 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.2915+2565_2915+256 others(7): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118971860 | ||||||
| chr6:118971863
|
A | AAGC | 5 | a0001c0001t0001g0081a0001c0001t0001g0205a0001c0001t0001g0243others(2): Show | 5 | HG01074.hp2 HG01109.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.2915+2562_2915+256 others(7): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118971863 | ||||||
| chr6:118972269
|
T | A | 258 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(255): Show | 258 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.2915+2159A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118972269 | ||||||
| chr6:118972300
|
G | A | 2 | a0002c0002t0002g0211a0002c0002t0002g0212 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2915+2128C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118972300 | ||||||
| chr6:118972637
|
G | C | 1 | a0001c0001t0001g0252 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2915+1791C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118972637 | ||||||
| chr6:118972864
|
C | T | 2 | a0001c0001t0006g0032a0001c0001t0006g0033 | 2 | HG01243.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2915+1564G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118972864 | ||||||
| chr6:118973049
|
A | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0187a0001c0001t0003g0015 | 3 | NA18954.hp2 NA18978.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.2915+1379T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118973049 | ||||||
| chr6:118973058
|
A | C | 7 | a0001c0001t0001g0130a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2915+1370T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118973058 | ||||||
| chr6:118973078
|
A | C | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2915+1350T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118973078 | ||||||
| chr6:118973412
|
C | T | 91 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(88): Show | 91 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.2915+1016G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118973412 | ||||||
| chr6:118973502
|
G | A | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2915+926C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118973502 | ||||||
| chr6:118974125
|
T | G | 1 | a0001c0001t0001g0149 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2915+303A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118974125 | ||||||
| chr6:118974252
|
C | A | 1 | a0001c0001t0001g0061 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2915+176G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118974252 | ||||||
| chr6:118974640
|
T | C | 4 | a0001c0001t0001g0110a0001c0001t0004g0003a0005c0009t0004g0005others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2769-66A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 13/17 | chr6 | 118974640 | ||||||
| chr6:118974642
|
C | T | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2769-68G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 13/17 | chr6 | 118974642 | ||||||
| chr6:118974706
|
G | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0004g0006 | 3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2769-132C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 13/17 | chr6 | 118974706 | ||||||
| chr6:118975213
|
T | TA | 56 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(53): Show | 56 | HG00597.hp1 HG00639.hp1 HG00642.hp2 others(53): Show |
splice_region_variant&intron_variant | LOW | c.2584-6dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 12/17 | chr6 | 118975213 | ||||||
| chr6:118975378
|
C | A | 8 | a0001c0003t0001g0046a0001c0003t0001g0133a0001c0003t0001g0136others(5): Show | 8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2584-170G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 12/17 | chr6 | 118975378 | ||||||
| chr6:118975572
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2583+345A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 12/17 | chr6 | 118975572 | ||||||
| chr6:118975607
|
G | A | 8 | a0001c0003t0001g0046a0001c0003t0001g0133a0001c0003t0001g0136others(5): Show | 8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2583+310C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 12/17 | chr6 | 118975607 | ||||||
| chr6:118975751
|
C | A | 14 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(11): Show | 14 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.2583+166G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 12/17 | chr6 | 118975751 | ||||||
| chr6:118975857
|
A | G | 2 | a0001c0001t0001g0226a0001c0001t0001g0227 | 2 | NA18951.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.2583+60T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 12/17 | chr6 | 118975857 | ||||||
| chr6:118976220
|
C | T | 43 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(40): Show | 43 | HG00597.hp1 HG00639.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.2456-176G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118976220 | ||||||
| chr6:118976390
|
C | T | 9 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(6): Show | 9 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2456-346G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118976390 | ||||||
| chr6:118976577
|
T | G | 7 | a0001c0001t0001g0130a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2456-533A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118976577 | ||||||
| chr6:118976663
|
CAAAA | C | 36 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(33): Show | 36 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.2456-623_2456-620d others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118976663 | ||||||
| chr6:118976952
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2456-908T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118976952 | ||||||
| chr6:118977145
|
C | T | 1 | a0002c0002t0002g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2456-1101G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118977145 | ||||||
| chr6:118977266
|
A | C | 1 | a0001c0001t0001g0191 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2456-1222T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118977266 | ||||||
| chr6:118977504
|
C | T | 2 | a0001c0001t0001g0207a0001c0001t0001g0251 | 2 | NA18964.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2456-1460G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118977504 | ||||||
| chr6:118977609
|
GATTTC | G | 4 | a0001c0001t0001g0110a0001c0001t0004g0003a0005c0009t0004g0005others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2456-1570_2456-156 others(9): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118977609 | ||||||
| chr6:118977665
|
G | A | 1 | a0002c0002t0002g0232 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2456-1621C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118977665 | ||||||
| chr6:118977672
|
G | T | 91 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(88): Show | 91 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.2456-1628C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118977672 | ||||||
| chr6:118977701
|
T | G | 1 | a0001c0001t0001g0276 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2456-1657A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118977701 | ||||||
| chr6:118977986
|
A | G | 46 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(43): Show | 46 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.2455+1379T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118977986 | ||||||
| chr6:118978121
|
G | A | 1 | a0001c0001t0010g0284 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2455+1244C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118978121 | ||||||
| chr6:118978191
|
G | A | 13 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(10): Show | 13 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.2455+1174C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118978191 | ||||||
| chr6:118978278
|
G | A | 149 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(146): Show | 149 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.2455+1087C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118978278 | ||||||
| chr6:118978418
|
C | G | 149 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(146): Show | 149 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.2455+947G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118978418 | ||||||
| chr6:118978430
|
T | G | 1 | a0001c0001t0001g0154 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2455+935A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118978430 | ||||||
| chr6:118978582
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2455+783T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118978582 | ||||||
| chr6:118978593
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2455+772C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118978593 | ||||||
| chr6:118978921
|
A | C | 1 | a0002c0002t0002g0143 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2455+444T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118978921 | ||||||
| chr6:118979263
|
G | A | 3 | a0001c0001t0001g0061a0001c0001t0001g0279a0001c0001t0001g0280 | 3 | HG01934.hp1 HG02273.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2455+102C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118979263 | ||||||
| chr6:118979312
|
A | G | 95 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(92): Show | 95 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.2455+53T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118979312 | ||||||
| chr6:118979788
|
A | G | 4 | a0001c0001t0001g0110a0001c0001t0004g0003a0005c0009t0004g0005others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2302-270T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 10/17 | chr6 | 118979788 | ||||||
| chr6:118979879
|
C | CA | 95 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0061others(92): Show | 95 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.2301+258dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 10/17 | chr6 | 118979879 | ||||||
| chr6:118979910
|
C | T | 4 | a0001c0001t0001g0204a0001c0001t0001g0209a0001c0001t0001g0269others(1): Show | 4 | NA18612.hp2 NA18947.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.2301+228G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 10/17 | chr6 | 118979910 | ||||||
| chr6:118980066
|
T | A | 1 | a0001c0001t0001g0256 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2301+72A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 10/17 | chr6 | 118980066 | ||||||
| chr6:118980499
|
T | TA | 6 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0098others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2089-150dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118980499 | ||||||
| chr6:118980588
|
A | G | 4 | a0001c0001t0002g0119a0001c0001t0002g0197a0001c0001t0002g0198others(1): Show | 4 | HG00642.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2089-238T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118980588 | ||||||
| chr6:118980682
|
A | C | 7 | a0001c0001t0001g0130a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-332T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118980682 | ||||||
| chr6:118981161
|
CTTAAAA | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2089-817_2089-812d others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118981161 | ||||||
| chr6:118981192
|
A | T | 1 | a0001c0001t0001g0104 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2089-842T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118981192 | ||||||
| chr6:118981430
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2089-1080C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118981430 | ||||||
| chr6:118981896
|
A | G | 36 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0128others(33): Show | 36 | HG00597.hp1 HG00642.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.2089-1546T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118981896 | ||||||
| chr6:118982170
|
C | T | 49 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(46): Show | 49 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.2089-1820G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118982170 | ||||||
| chr6:118982171
|
G | A | 49 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(46): Show | 49 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.2089-1821C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118982171 | ||||||
| chr6:118982185
|
G | A | 36 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(33): Show | 36 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.2089-1835C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118982185 | ||||||
| chr6:118982216
|
T | C | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0128 | 3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2089-1866A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118982216 | ||||||
| chr6:118982317
|
C | G | 36 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(33): Show | 36 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.2089-1967G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118982317 | ||||||
| chr6:118982324
|
T | C | 1 | a0001c0001t0001g0173 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2089-1974A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118982324 | ||||||
| chr6:118982397
|
T | C | 16 | a0002c0002t0002g0121a0002c0002t0002g0129a0002c0002t0002g0143others(13): Show | 16 | HG00597.hp1 HG00735.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.2089-2047A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118982397 | ||||||
| chr6:118982624
|
A | G | 2 | a0001c0001t0001g0207a0001c0001t0001g0251 | 2 | NA18964.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2089-2274T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118982624 | ||||||
| chr6:118982723
|
G | A | 1 | a0004c0008t0001g0062 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2089-2373C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118982723 | ||||||
| chr6:118982753
|
C | T | 7 | a0001c0001t0001g0130a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-2403G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118982753 | ||||||
| chr6:118983034
|
G | C | 1 | a0001c0003t0001g0046 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2089-2684C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118983034 | ||||||
| chr6:118983166
|
G | C | 25 | a0001c0001t0002g0060a0001c0001t0002g0072a0001c0001t0002g0119others(22): Show | 25 | HG00597.hp1 HG00642.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.2089-2816C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118983166 | ||||||
| chr6:118983244
|
T | C | 7 | a0001c0001t0001g0130a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-2894A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118983244 | ||||||
| chr6:118983388
|
C | A | 3 | a0001c0001t0002g0120a0001c0001t0002g0122a0001c0001t0002g0123 | 3 | HG02818.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2089-3038G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118983388 | ||||||
| chr6:118983433
|
A | G | 5 | a0001c0001t0001g0190a0001c0001t0001g0207a0001c0001t0001g0220others(2): Show | 5 | HG00423.hp1 NA18747.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.2089-3083T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118983433 | ||||||
| chr6:118983460
|
T | A | 152 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(149): Show | 152 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.2089-3110A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118983460 | ||||||
| chr6:118983563
|
A | C | 7 | a0001c0001t0001g0130a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-3213T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118983563 | ||||||
| chr6:118983718
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2089-3368C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118983718 | ||||||
| chr6:118983834
|
A | G | 1 | a0001c0001t0002g0120 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2089-3484T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118983834 | ||||||
| chr6:118983870
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2089-3520G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118983870 | ||||||
| chr6:118983953
|
G | A | 7 | a0001c0001t0001g0130a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-3603C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118983953 | ||||||
| chr6:118983994
|
C | CA | 7 | a0001c0001t0001g0130a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-3645dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118983994 | ||||||
| chr6:118984018
|
C | T | 8 | a0001c0003t0001g0046a0001c0003t0001g0133a0001c0003t0001g0136others(5): Show | 8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2089-3668G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984018 | ||||||
| chr6:118984022
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2089-3672G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984022 | ||||||
| chr6:118984023
|
G | A | 8 | a0001c0003t0001g0046a0001c0003t0001g0133a0001c0003t0001g0136others(5): Show | 8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2089-3673C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984023 | ||||||
| chr6:118984149
|
T | A | 1 | a0001c0001t0001g0047 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2089-3799A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984149 | ||||||
| chr6:118984149
|
T | TAA | 92 | a0001c0001t0001g0036a0001c0001t0001g0081a0001c0001t0001g0117others(89): Show | 92 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.2089-3801_2089-380 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984149 | ||||||
| chr6:118984149
|
TAA | T | 8 | a0001c0001t0001g0130a0001c0001t0001g0201a0001c0001t0001g0202others(5): Show | 8 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2089-3801_2089-380 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984149 | ||||||
| chr6:118984150
|
A | T | 1 | a0008c0005t0001g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2089-3800T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984150 | ||||||
| chr6:118984156
|
A | T | 16 | a0001c0001t0001g0061a0001c0001t0001g0074a0001c0001t0001g0076others(13): Show | 16 | HG00733.hp2 HG00738.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.2089-3806T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984156 | ||||||
| chr6:118984158
|
A | AAAT | 7 | a0001c0001t0001g0048a0001c0001t0001g0186a0001c0001t0001g0188others(4): Show | 7 | HG00408.hp1 HG01255.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-3809_2089-380 others(7): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984158 | ||||||
| chr6:118984158
|
A | AAT | 21 | a0001c0001t0001g0035a0001c0001t0001g0064a0001c0001t0001g0067others(18): Show | 21 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.2089-3810_2089-380 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984158 | ||||||
| chr6:118984158
|
A | ATAT | 4 | a0001c0001t0001g0045a0001c0001t0001g0104a0001c0001t0001g0132others(1): Show | 4 | HG02486.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2089-3809_2089-380 others(7): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984158 | ||||||
| chr6:118984158
|
A | T | 45 | a0001c0001t0001g0043a0001c0001t0001g0053a0001c0001t0001g0054others(42): Show | 45 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.2089-3808T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984158 | ||||||
| chr6:118984158
|
AAT | A | 7 | a0001c0003t0001g0046a0001c0003t0001g0133a0001c0003t0001g0136others(4): Show | 7 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-3810_2089-380 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984158 | ||||||
| chr6:118984159
|
AT | A | 18 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(15): Show | 18 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.2089-3810delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984159 | ||||||
| chr6:118984159
|
ATATATAT others(4): Show |
A | 1 | a0001c0001t0001g0261 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2089-3820_2089-381 others(15): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984159 | ||||||
| chr6:118984160
|
T | A | 33 | a0001c0001t0001g0069a0001c0001t0001g0117a0001c0001t0001g0169others(30): Show | 33 | HG00597.hp1 HG00735.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.2089-3810A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984160 | ||||||
| chr6:118984162
|
T | A | 24 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(21): Show | 24 | HG00639.hp1 HG00733.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.2089-3812A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984162 | ||||||
| chr6:118984177
|
A | T | 3 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0004g0006 | 3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2089-3827T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984177 | ||||||
| chr6:118984179
|
T | A | 4 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0261others(1): Show | 4 | HG02145.hp1 HG02965.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.2089-3829A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984179 | ||||||
| chr6:118984179
|
T | TTA | 5 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(2): Show | 5 | HG01884.hp2 HG02572.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2089-3831_2089-383 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984179 | ||||||
| chr6:118984191
|
TTATATTT others(3): Show |
T | 7 | a0001c0001t0001g0130a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-3851_2089-384 others(14): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984191 | ||||||
| chr6:118984247
|
T | TTA | 5 | a0001c0001t0001g0138a0001c0001t0001g0260a0001c0001t0005g0026others(2): Show | 5 | HG02451.hp2 HG02895.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2089-3899_2089-389 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984247 | ||||||
| chr6:118984376
|
C | G | 22 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0128others(19): Show | 22 | HG00597.hp1 HG00735.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.2089-4026G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984376 | ||||||
| chr6:118984429
|
C | T | 7 | a0001c0001t0001g0130a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-4079G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984429 | ||||||
| chr6:118984519
|
TA | T | 91 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(88): Show | 91 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.2089-4170delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984519 | ||||||
| chr6:118984520
|
A | G | 7 | a0001c0001t0001g0130a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-4170T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984520 | ||||||
| chr6:118984713
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2089-4363T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984713 | ||||||
| chr6:118984779
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2089-4429A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984779 | ||||||
| chr6:118984998
|
C | T | 7 | a0001c0001t0001g0130a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-4648G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984998 | ||||||
| chr6:118985034
|
A | G | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2089-4684T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118985034 | ||||||
| chr6:118985095
|
G | A | 7 | a0001c0003t0001g0046a0001c0003t0001g0133a0001c0003t0001g0136others(4): Show | 7 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-4745C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118985095 | ||||||
| chr6:118985128
|
T | C | 233 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(230): Show | 233 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.2089-4778A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118985128 | ||||||
| chr6:118985247
|
T | C | 94 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(91): Show | 94 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.2089-4897A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118985247 | ||||||
| chr6:118985426
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2089-5076C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118985426 | ||||||
| chr6:118985467
|
G | A | 1 | a0001c0001t0003g0024 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2089-5117C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118985467 | ||||||
| chr6:118985593
|
G | GTC | 8 | a0001c0003t0001g0046a0001c0003t0001g0133a0001c0003t0001g0136others(5): Show | 8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2089-5245_2089-524 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118985593 | ||||||
| chr6:118985603
|
T | C | 7 | a0001c0001t0001g0130a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-5253A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118985603 | ||||||
| chr6:118985618
|
C | T | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2089-5268G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118985618 | ||||||
| chr6:118985817
|
G | T | 4 | a0001c0001t0001g0110a0001c0001t0004g0003a0005c0009t0004g0005others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2089-5467C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118985817 | ||||||
| chr6:118985873
|
A | C | 9 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(6): Show | 9 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2089-5523T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118985873 | ||||||
| chr6:118985894
|
C | T | 1 | a0001c0001t0010g0284 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2089-5544G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118985894 | ||||||
| chr6:118985939
|
T | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0048 | 2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2089-5589A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118985939 | ||||||
| chr6:118986109
|
C | T | 2 | a0001c0001t0004g0002a0006c0007t0001g0242 | 2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2089-5759G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118986109 | ||||||
| chr6:118986322
|
C | T | 1 | a0001c0001t0005g0025 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2089-5972G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118986322 | ||||||
| chr6:118986608
|
T | G | 7 | a0001c0001t0001g0130a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-6258A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118986608 | ||||||
| chr6:118986644
|
T | C | 151 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(148): Show | 151 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.2089-6294A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118986644 | ||||||
| chr6:118986933
|
T | C | 4 | a0001c0001t0001g0110a0001c0001t0004g0003a0005c0009t0004g0005others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2089-6583A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118986933 | ||||||
| chr6:118986958
|
ATGC | A | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2089-6611_2089-660 others(7): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118986958 | ||||||
| chr6:118987008
|
G | T | 8 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(5): Show | 8 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2089-6658C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118987008 | ||||||
| chr6:118987027
|
G | GT | 6 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0098others(3): Show | 6 | HG02559.hp1 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2089-6678dupA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118987027 | ||||||
| chr6:118987032
|
A | C | 3 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0004g0006 | 3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2089-6682T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118987032 | ||||||
| chr6:118987049
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2089-6699A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118987049 | ||||||
| chr6:118987127
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2089-6777G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118987127 | ||||||
| chr6:118987566
|
A | G | 2 | a0001c0003t0001g0046a0001c0003t0001g0262 | 2 | HG02717.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2089-7216T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118987566 | ||||||
| chr6:118987574
|
T | G | 1 | a0001c0001t0010g0284 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2089-7224A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118987574 | ||||||
| chr6:118987972
|
A | C | 4 | a0001c0001t0002g0119a0001c0001t0002g0197a0001c0001t0002g0198others(1): Show | 4 | HG00642.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2089-7622T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118987972 | ||||||
| chr6:118988099
|
A | G | 1 | a0008c0005t0001g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2089-7749T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118988099 | ||||||
| chr6:118988420
|
A | T | 1 | a0001c0001t0001g0130 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2089-8070T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118988420 | ||||||
| chr6:118988512
|
G | A | 4 | a0001c0001t0002g0119a0001c0001t0002g0197a0001c0001t0002g0198others(1): Show | 4 | HG00642.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2089-8162C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118988512 | ||||||
| chr6:118988597
|
G | C | 7 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-8247C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118988597 | ||||||
| chr6:118988698
|
C | T | 8 | a0001c0003t0001g0046a0001c0003t0001g0133a0001c0003t0001g0136others(5): Show | 8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2089-8348G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118988698 | ||||||
| chr6:118988725
|
T | A | 1 | a0001c0001t0001g0096 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2089-8375A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118988725 | ||||||
| chr6:118988859
|
A | T | 232 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(229): Show | 232 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.2089-8509T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118988859 | ||||||
| chr6:118988917
|
GA | G | 4 | a0001c0001t0001g0110a0001c0001t0004g0003a0005c0009t0004g0005others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2089-8568delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118988917 | ||||||
| chr6:118988954
|
A | AT | 115 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0040others(112): Show | 115 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.2089-8605dupA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118988954 | ||||||
| chr6:118988954
|
A | ATT | 44 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(41): Show | 44 | HG00597.hp1 HG00639.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.2089-8606_2089-860 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118988954 | ||||||
| chr6:118989119
|
G | A | 5 | a0003c0004t0001g0091a0003c0004t0001g0092a0003c0004t0001g0093others(2): Show | 5 | HG00738.hp2 HG01433.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.2089-8769C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989119 | ||||||
| chr6:118989197
|
G | A | 5 | a0001c0001t0002g0060a0001c0001t0002g0072a0001c0001t0002g0120others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.2089-8847C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989197 | ||||||
| chr6:118989227
|
CT | C | 151 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(148): Show | 151 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.2089-8878delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989227 | ||||||
| chr6:118989253
|
C | T | 2 | a0001c0001t0001g0192a0001c0001t0001g0214 | 2 | HG04115.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.2089-8903G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989253 | ||||||
| chr6:118989428
|
A | G | 5 | a0001c0001t0001g0204a0001c0001t0001g0209a0001c0001t0001g0269others(2): Show | 5 | NA18612.hp2 NA18947.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.2089-9078T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989428 | ||||||
| chr6:118989498
|
A | AGTGACAC others(54): Show |
18 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(15): Show | 18 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.2089-9209_2089-914 others(65): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989498 | ||||||
| chr6:118989525
|
T | C | 1 | a0001c0001t0004g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2089-9175A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989525 | ||||||
| chr6:118989650
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2089-9300A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989650 | ||||||
| chr6:118989787
|
T | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2089-9437A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989787 | ||||||
| chr6:118989801
|
C | CATTT | 79 | a0001c0001t0001g0036a0001c0001t0001g0051a0001c0001t0001g0063others(76): Show | 79 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.2089-9455_2089-945 others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989801 | ||||||
| chr6:118989801
|
C | CATTTATT others(1): Show |
24 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(21): Show | 24 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.2089-9459_2089-945 others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989801 | ||||||
| chr6:118989801
|
C | CATTTATT others(5): Show |
2 | a0001c0001t0004g0007a0001c0001t0004g0010 | 2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2089-9463_2089-945 others(16): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989801 | ||||||
| chr6:118989801
|
CATTT | C | 24 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(21): Show | 24 | HG00597.hp1 HG00639.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.2089-9455_2089-945 others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989801 | ||||||
| chr6:118989801
|
CATTTATT others(1): Show |
C | 32 | a0001c0001t0001g0061a0001c0001t0001g0111a0001c0001t0001g0130others(29): Show | 32 | HG00735.hp2 HG00741.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.2089-9459_2089-945 others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989801 | ||||||
| chr6:118989801
|
CATTTATT others(9): Show |
C | 1 | a0001c0001t0002g0197 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2089-9467_2089-945 others(20): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989801 | ||||||
| chr6:118989953
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2089-9603G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989953 | ||||||
| chr6:118989982
|
C | T | 7 | a0001c0001t0001g0130a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-9632G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989982 | ||||||
| chr6:118989985
|
T | C | 232 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(229): Show | 232 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.2089-9635A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989985 | ||||||
| chr6:118990197
|
T | C | 5 | a0001c0001t0001g0155a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | NA18954.hp1 NA18975.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.2089-9847A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118990197 | ||||||
| chr6:118990245
|
G | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0048 | 2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2089-9895C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118990245 | ||||||
| chr6:118990400
|
C | T | 1 | a0001c0001t0003g0017 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2089-10050G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118990400 | ||||||
| chr6:118990491
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2089-10141C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118990491 | ||||||
| chr6:118990507
|
T | C | 2 | a0001c0001t0001g0225a0001c0001t0001g0234 | 2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.2089-10157A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118990507 | ||||||
| chr6:118990589
|
C | CCAG | 151 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(148): Show | 151 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.2089-10240_2089-10 others(9): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118990589 | ||||||
| chr6:118990590
|
A | G | 151 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(148): Show | 151 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.2089-10240T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118990590 | ||||||
| chr6:118990664
|
G | A | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0128 | 3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2089-10314C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118990664 | ||||||
| chr6:118990686
|
C | T | 1 | a0001c0001t0004g0009 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2089-10336G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118990686 | ||||||
| chr6:118990720
|
C | CA | 24 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(21): Show | 24 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.2089-10371dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118990720 | ||||||
| chr6:118990924
|
T | C | 8 | a0001c0003t0001g0046a0001c0003t0001g0133a0001c0003t0001g0136others(5): Show | 8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2089-10574A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118990924 | ||||||
| chr6:118990924
|
T | G | 1 | a0001c0001t0001g0191 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2089-10574A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118990924 | ||||||
| chr6:118991159
|
T | C | 1 | a0002c0002t0002g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2089-10809A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991159 | ||||||
| chr6:118991163
|
AT | A | 7 | a0001c0001t0001g0039a0001c0001t0001g0050a0001c0001t0001g0103others(4): Show | 7 | HG01169.hp1 HG01515.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-10814delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991163 | ||||||
| chr6:118991225
|
C | T | 16 | a0002c0002t0002g0121a0002c0002t0002g0129a0002c0002t0002g0143others(13): Show | 16 | HG00597.hp1 HG00735.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.2089-10875G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991225 | ||||||
| chr6:118991426
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2089-11076C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991426 | ||||||
| chr6:118991441
|
G | A | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2089-11091C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991441 | ||||||
| chr6:118991445
|
G | T | 4 | a0001c0001t0001g0110a0001c0001t0004g0003a0005c0009t0004g0005others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2089-11095C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991445 | ||||||
| chr6:118991484
|
T | C | 2 | a0001c0001t0006g0032a0001c0001t0006g0033 | 2 | HG01243.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2089-11134A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991484 | ||||||
| chr6:118991711
|
G | A | 232 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(229): Show | 232 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.2088+11188C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991711 | ||||||
| chr6:118991751
|
C | CT | 16 | a0001c0001t0001g0084a0001c0001t0001g0146a0001c0001t0001g0158others(13): Show | 16 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.2088+11147dupA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991751 | ||||||
| chr6:118991751
|
C | CTTT | 7 | a0001c0001t0002g0060a0001c0001t0002g0119a0001c0001t0002g0120others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2088+11145_2088+11 others(9): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991751 | ||||||
| chr6:118991751
|
C | CTTTT | 12 | a0001c0001t0001g0271a0001c0001t0002g0072a0001c0001t0002g0199others(9): Show | 12 | HG00642.hp2 HG00741.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.2088+11144_2088+11 others(10): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991751 | ||||||
| chr6:118991751
|
CT | C | 47 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(44): Show | 47 | HG00140.hp2 HG00423.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.2088+11147delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991751 | ||||||
| chr6:118991751
|
CTT | C | 133 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(130): Show | 133 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.2088+11146_2088+11 others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991751 | ||||||
| chr6:118991751
|
CTTT | C | 6 | a0001c0001t0001g0039a0001c0001t0001g0059a0001c0001t0001g0100others(3): Show | 6 | HG00741.hp2 HG01168.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.2088+11145_2088+11 others(9): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991751 | ||||||
| chr6:118991751
|
CTTTTTTT others(7): Show |
C | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0128 | 3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2088+11134_2088+11 others(20): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991751 | ||||||
| chr6:118991780
|
T | G | 7 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2088+11119A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991780 | ||||||
| chr6:118991908
|
G | A | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2088+10991C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991908 | ||||||
| chr6:118991948
|
T | A | 13 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(10): Show | 13 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.2088+10951A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991948 | ||||||
| chr6:118992120
|
T | A | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG01934.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.2088+10779A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118992120 | ||||||
| chr6:118992140
|
A | G | 1 | a0001c0001t0002g0060 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2088+10759T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118992140 | ||||||
| chr6:118992258
|
T | C | 232 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(229): Show | 232 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.2088+10641A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118992258 | ||||||
| chr6:118992352
|
A | T | 147 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(144): Show | 147 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.2088+10547T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118992352 | ||||||
| chr6:118992410
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2088+10489A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118992410 | ||||||
| chr6:118992468
|
A | G | 148 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(145): Show | 148 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.2088+10431T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118992468 | ||||||
| chr6:118992496
|
A | G | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2088+10403T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118992496 | ||||||
| chr6:118993020
|
C | A | 1 | a0008c0005t0001g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2088+9879G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118993020 | ||||||
| chr6:118993034
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2088+9865T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118993034 | ||||||
| chr6:118993227
|
G | T | 7 | a0001c0001t0001g0130a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2088+9672C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118993227 | ||||||
| chr6:118993429
|
A | G | 1 | a0001c0001t0004g0009 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2088+9470T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118993429 | ||||||
| chr6:118993513
|
CT | C | 22 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0128others(19): Show | 22 | HG00597.hp1 HG00735.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.2088+9385delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118993513 | ||||||
| chr6:118993517
|
T | G | 148 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(145): Show | 148 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.2088+9382A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118993517 | ||||||
| chr6:118993610
|
T | C | 148 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(145): Show | 148 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.2088+9289A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118993610 | ||||||
| chr6:118993668
|
C | A | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2088+9231G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118993668 | ||||||
| chr6:118993728
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2088+9171C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118993728 | ||||||
| chr6:118993780
|
T | C | 1 | a0001c0001t0001g0187 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2088+9119A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118993780 | ||||||
| chr6:118993959
|
T | G | 148 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(145): Show | 148 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.2088+8940A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118993959 | ||||||
| chr6:118993981
|
C | A | 13 | a0001c0001t0001g0061a0001c0001t0001g0110a0001c0001t0004g0003others(10): Show | 13 | HG00639.hp1 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.2088+8918G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118993981 | ||||||
| chr6:118994330
|
A | AAAAT | 94 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(91): Show | 94 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.2088+8565_2088+856 others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994330 | ||||||
| chr6:118994368
|
G | C | 5 | a0001c0001t0001g0104a0001c0001t0004g0007a0001c0001t0004g0008others(2): Show | 5 | HG02109.hp1 HG02486.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2088+8531C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994368 | ||||||
| chr6:118994540
|
G | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG02572.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2088+8359C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994540 | ||||||
| chr6:118994557
|
G | A | 20 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0050others(17): Show | 20 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.2088+8342C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994557 | ||||||
| chr6:118994596
|
G | A | 1 | a0001c0001t0003g0022 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2088+8303C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994596 | ||||||
| chr6:118994685
|
C | CAAAA | 16 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0096others(13): Show | 16 | HG00609.hp2 HG01243.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.2088+8213_2088+821 others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994685 | ||||||
| chr6:118994685
|
C | CAAAATAA others(1): Show |
5 | a0001c0001t0001g0138a0001c0001t0001g0146a0001c0001t0001g0164others(2): Show | 5 | HG03041.hp2 HG03490.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.2088+8213_2088+821 others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994685 | ||||||
| chr6:118994685
|
CTAAA | C | 68 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(65): Show | 68 | HG00140.hp2 HG00423.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.2088+8210_2088+821 others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994685 | ||||||
| chr6:118994685
|
CTAAATAA others(1): Show |
C | 81 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(78): Show | 81 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2088+8206_2088+821 others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994685 | ||||||
| chr6:118994685
|
CTAAATAA others(5): Show |
C | 9 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0201others(6): Show | 9 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2088+8202_2088+821 others(16): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994685 | ||||||
| chr6:118994685
|
CTAAATAA others(9): Show |
C | 12 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(9): Show | 12 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2088+8198_2088+821 others(20): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994685 | ||||||
| chr6:118994686
|
T | A | 94 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(91): Show | 94 | HG00408.hp2 HG00597.hp1 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.2088+8213A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994686 | ||||||
| chr6:118994690
|
T | A | 67 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(64): Show | 67 | HG00140.hp2 HG00423.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.2088+8209A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994690 | ||||||
| chr6:118994694
|
T | A | 81 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(78): Show | 81 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2088+8205A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994694 | ||||||
| chr6:118994698
|
T | A | 9 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0201others(6): Show | 9 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2088+8201A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994698 | ||||||
| chr6:118994702
|
T | A | 12 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(9): Show | 12 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2088+8197A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994702 | ||||||
| chr6:118994726
|
TAAATAAA others(5): Show |
T | 2 | a0001c0001t0001g0097a0001c0001t0001g0109 | 2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2088+8161_2088+817 others(16): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994726 | ||||||
| chr6:118994730
|
TAAATAAA others(1): Show |
T | 8 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(5): Show | 8 | HG00733.hp1 HG01106.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.2088+8161_2088+816 others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994730 | ||||||
| chr6:118994732
|
A | G | 1 | a0001c0003t0001g0046 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2088+8167T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994732 | ||||||
| chr6:118994733
|
A | C | 1 | a0001c0003t0001g0046 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2088+8166T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994733 | ||||||
| chr6:118994734
|
TAAAA | T | 8 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(5): Show | 8 | HG01069.hp2 HG01071.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2088+8161_2088+816 others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994734 | ||||||
| chr6:118994736
|
A | G | 144 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(141): Show | 144 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.2088+8163T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994736 | ||||||
| chr6:118994737
|
A | ATAAATAG others(1): Show |
3 | a0001c0001t0002g0120a0002c0002t0002g0208a0006c0007t0001g0242 | 3 | HG00597.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2088+8161_2088+816 others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994737 | ||||||
| chr6:118994737
|
A | ATAGC | 4 | a0001c0001t0001g0040a0001c0003t0001g0142a0001c0003t0001g0262others(1): Show | 4 | HG02559.hp2 HG02717.hp1 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.2088+8161_2088+816 others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994737 | ||||||
| chr6:118994737
|
A | C | 144 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(141): Show | 144 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.2088+8162T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994737 | ||||||
| chr6:118995005
|
A | G | 2 | a0001c0001t0001g0137a0001c0001t0004g0011 | 2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2088+7894T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118995005 | ||||||
| chr6:118995215
|
G | A | 1 | a0008c0005t0001g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2088+7684C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118995215 | ||||||
| chr6:118995555
|
C | T | 8 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(5): Show | 8 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2088+7344G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118995555 | ||||||
| chr6:118995681
|
T | C | 1 | a0008c0005t0001g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2088+7218A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118995681 | ||||||
| chr6:118995825
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2088+7074A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118995825 | ||||||
| chr6:118995976
|
A | G | 2 | a0001c0001t0001g0170a0001c0001t0001g0178 | 2 | HG02135.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.2088+6923T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118995976 | ||||||
| chr6:118996257
|
T | G | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0128 | 3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2088+6642A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118996257 | ||||||
| chr6:118996413
|
T | C | 3 | a0001c0001t0002g0120a0001c0001t0002g0122a0001c0001t0002g0123 | 3 | HG02818.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2088+6486A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118996413 | ||||||
| chr6:118996678
|
T | C | 152 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(149): Show | 152 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.2088+6221A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118996678 | ||||||
| chr6:118996684
|
A | G | 1 | a0008c0005t0001g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2088+6215T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118996684 | ||||||
| chr6:118996776
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2088+6123C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118996776 | ||||||
| chr6:118996881
|
A | AT | 13 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(10): Show | 13 | HG01069.hp1 HG02622.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.2088+6017dupA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118996881 | ||||||
| chr6:118996881
|
A | ATT | 7 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2088+6016_2088+601 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118996881 | ||||||
| chr6:118997003
|
C | T | 1 | a0001c0001t0005g0027 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2088+5896G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997003 | ||||||
| chr6:118997008
|
G | GAAGAC | 101 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0044others(98): Show | 101 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.2088+5890_2088+589 others(9): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997008 | ||||||
| chr6:118997010
|
C | CTGTGGGA others(1): Show |
101 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0044others(98): Show | 101 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.2088+5888_2088+588 others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997010 | ||||||
| chr6:118997011
|
A | T | 101 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0044others(98): Show | 101 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.2088+5888T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997011 | ||||||
| chr6:118997012
|
C | A | 101 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0044others(98): Show | 101 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.2088+5887G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997012 | ||||||
| chr6:118997217
|
G | A | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2088+5682C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997217 | ||||||
| chr6:118997245
|
T | C | 201 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(198): Show | 201 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.2088+5654A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997245 | ||||||
| chr6:118997282
|
C | G | 1 | a0001c0006t0005g0028 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2088+5617G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997282 | ||||||
| chr6:118997304
|
G | A | 1 | a0004c0008t0001g0062 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2088+5595C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997304 | ||||||
| chr6:118997324
|
CA | C | 181 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(178): Show | 181 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.2088+5574delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997324 | ||||||
| chr6:118997356
|
A | T | 2 | a0001c0001t0004g0002a0006c0007t0001g0242 | 2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2088+5543T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997356 | ||||||
| chr6:118997368
|
G | A | 18 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(15): Show | 18 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.2088+5531C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997368 | ||||||
| chr6:118997455
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2088+5444G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997455 | ||||||
| chr6:118997611
|
C | T | 1 | a0001c0001t0005g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2088+5288G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997611 | ||||||
| chr6:118997634
|
T | G | 1 | a0001c0001t0001g0132 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2088+5265A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997634 | ||||||
| chr6:118997843
|
C | T | 1 | a0001c0001t0003g0016 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2088+5056G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997843 | ||||||
| chr6:118997887
|
C | G | 89 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(86): Show | 89 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.2088+5012G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997887 | ||||||
| chr6:118997920
|
G | T | 1 | a0001c0001t0010g0284 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2088+4979C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997920 | ||||||
| chr6:118998028
|
T | C | 1 | a0008c0005t0001g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2088+4871A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118998028 | ||||||
| chr6:118998047
|
CTA | C | 4 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0009others(1): Show | 4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2088+4850_2088+485 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118998047 | ||||||
| chr6:118998216
|
C | A | 1 | a0001c0001t0008g0285 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2088+4683G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118998216 | ||||||
| chr6:118998359
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2088+4540T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118998359 | ||||||
| chr6:118998518
|
CA | C | 8 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(5): Show | 8 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2088+4380delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118998518 | ||||||
| chr6:118998676
|
G | A | 8 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(5): Show | 8 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2088+4223C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118998676 | ||||||
| chr6:118998707
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2088+4192C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118998707 | ||||||
| chr6:118998829
|
C | G | 7 | a0001c0001t0001g0130a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2088+4070G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118998829 | ||||||
| chr6:118998841
|
G | C | 4 | a0001c0001t0001g0110a0001c0001t0004g0003a0005c0009t0004g0005others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2088+4058C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118998841 | ||||||
| chr6:118999109
|
T | C | 1 | a0002c0002t0002g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2088+3790A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118999109 | ||||||
| chr6:118999146
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2088+3753C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118999146 | ||||||
| chr6:118999148
|
A | G | 152 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(149): Show | 152 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.2088+3751T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118999148 | ||||||
| chr6:118999578
|
T | C | 7 | a0001c0001t0001g0130a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2088+3321A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118999578 | ||||||
| chr6:118999617
|
A | G | 30 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0128others(27): Show | 30 | HG00597.hp1 HG00642.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.2088+3282T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118999617 | ||||||
| chr6:118999669
|
A | T | 8 | a0001c0003t0001g0046a0001c0003t0001g0133a0001c0003t0001g0136others(5): Show | 8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2088+3230T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118999669 | ||||||
| chr6:118999815
|
C | T | 1 | a0001c0001t0001g0191 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2088+3084G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118999815 | ||||||
| chr6:119000040
|
C | T | 1 | a0007c0010t0004g0004 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2088+2859G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119000040 | ||||||
| chr6:119000166
|
G | T | 1 | a0001c0001t0001g0201 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2088+2733C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119000166 | ||||||
| chr6:119000305
|
A | G | 4 | a0001c0001t0001g0110a0001c0001t0004g0003a0005c0009t0004g0005others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2088+2594T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119000305 | ||||||
| chr6:119000314
|
G | A | 26 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0128others(23): Show | 26 | HG00597.hp1 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.2088+2585C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119000314 | ||||||
| chr6:119000386
|
T | C | 94 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(91): Show | 94 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.2088+2513A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119000386 | ||||||
| chr6:119000529
|
T | C | 4 | a0001c0001t0001g0193a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG00741.hp2 NA18995.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.2088+2370A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119000529 | ||||||
| chr6:119000575
|
G | A | 2 | a0001c0001t0002g0122a0001c0001t0002g0123 | 2 | HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2088+2324C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119000575 | ||||||
| chr6:119000608
|
T | C | 1 | a0002c0002t0002g0224 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2088+2291A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119000608 | ||||||
| chr6:119000720
|
G | A | 1 | a0001c0003t0001g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2088+2179C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119000720 | ||||||
| chr6:119000928
|
G | T | 2 | a0002c0002t0001g0238a0002c0002t0002g0189 | 2 | HG02071.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.2088+1971C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119000928 | ||||||
| chr6:119001257
|
G | T | 152 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(149): Show | 152 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.2088+1642C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119001257 | ||||||
| chr6:119001303
|
T | C | 152 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(149): Show | 152 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.2088+1596A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119001303 | ||||||
| chr6:119001391
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2088+1508G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119001391 | ||||||
| chr6:119001536
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2088+1363T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119001536 | ||||||
| chr6:119001548
|
T | C | 1 | a0001c0001t0001g0073 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2088+1351A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119001548 | ||||||
| chr6:119001661
|
C | T | 30 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0128others(27): Show | 30 | HG00597.hp1 HG00642.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.2088+1238G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119001661 | ||||||
| chr6:119001719
|
T | G | 36 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(33): Show | 36 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.2088+1180A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119001719 | ||||||
| chr6:119001827
|
C | T | 88 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(85): Show | 88 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.2088+1072G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119001827 | ||||||
| chr6:119001895
|
G | T | 6 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG00738.hp1 HG01358.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.2088+1004C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119001895 | ||||||
| chr6:119002271
|
G | T | 1 | a0001c0001t0005g0027 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2088+628C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119002271 | ||||||
| chr6:119002384
|
A | G | 1 | a0001c0001t0003g0013 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2088+515T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119002384 | ||||||
| chr6:119002665
|
TA | T | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2088+233delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119002665 | ||||||
| chr6:119002822
|
A | T | 90 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(87): Show | 90 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.2088+77T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119002822 | ||||||
| chr6:119003343
|
C | T | 8 | a0001c0003t0001g0046a0001c0003t0001g0133a0001c0003t0001g0136others(5): Show | 8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1937+158G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 8/17 | chr6 | 119003343 | ||||||
| chr6:119003348
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1937+153C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 8/17 | chr6 | 119003348 | ||||||
| chr6:119003438
|
T | A | 1 | a0001c0001t0001g0074 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1937+63A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 8/17 | chr6 | 119003438 | ||||||
| chr6:119003658
|
T | G | 13 | a0001c0001t0001g0061a0001c0001t0001g0110a0001c0001t0004g0003others(10): Show | 13 | HG00639.hp1 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1816-36A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119003658 | ||||||
| chr6:119003711
|
C | T | 4 | a0001c0001t0001g0110a0001c0001t0004g0003a0005c0009t0004g0005others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1816-89G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119003711 | ||||||
| chr6:119003798
|
A | G | 4 | a0001c0001t0002g0119a0001c0001t0002g0197a0001c0001t0002g0198others(1): Show | 4 | HG00642.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1816-176T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119003798 | ||||||
| chr6:119003822
|
T | G | 2 | a0001c0001t0001g0090a0001c0001t0001g0100 | 2 | HG01168.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1816-200A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119003822 | ||||||
| chr6:119003870
|
A | G | 13 | a0001c0001t0001g0061a0001c0001t0001g0110a0001c0001t0004g0003others(10): Show | 13 | HG00639.hp1 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1816-248T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119003870 | ||||||
| chr6:119004128
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1816-506A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119004128 | ||||||
| chr6:119004255
|
A | G | 1 | a0008c0005t0001g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1816-633T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119004255 | ||||||
| chr6:119004536
|
T | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.1816-914A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119004536 | ||||||
| chr6:119004567
|
G | C | 1 | a0002c0002t0002g0236 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1816-945C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119004567 | ||||||
| chr6:119004753
|
G | C | 152 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(149): Show | 152 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.1816-1131C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119004753 | ||||||
| chr6:119004947
|
C | G | 1 | a0001c0001t0001g0192 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1816-1325G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119004947 | ||||||
| chr6:119005020
|
C | A | 4 | a0001c0001t0002g0119a0001c0001t0002g0197a0001c0001t0002g0198others(1): Show | 4 | HG00642.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1816-1398G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119005020 | ||||||
| chr6:119005171
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1815+1276G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119005171 | ||||||
| chr6:119005210
|
T | C | 28 | a0001c0001t0001g0271a0001c0001t0002g0060a0001c0001t0002g0072others(25): Show | 28 | HG00597.hp1 HG00642.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1815+1237A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119005210 | ||||||
| chr6:119005273
|
T | G | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0128 | 3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1815+1174A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119005273 | ||||||
| chr6:119005408
|
G | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.1815+1039C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119005408 | ||||||
| chr6:119005521
|
C | T | 13 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(10): Show | 13 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1815+926G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119005521 | ||||||
| chr6:119005845
|
CAG | C | 5 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0111others(2): Show | 5 | HG02055.hp1 HG02280.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1815+600_1815+601d others(4): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119005845 | ||||||
| chr6:119005931
|
C | T | 7 | a0001c0001t0001g0130a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1815+516G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119005931 | ||||||
| chr6:119005947
|
G | A | 152 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(149): Show | 152 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.1815+500C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119005947 | ||||||
| chr6:119006192
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1815+255T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119006192 | ||||||
| chr6:119006366
|
G | C | 1 | a0001c0001t0001g0228 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1815+81C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119006366 | ||||||
| chr6:119006627
|
C | T | 4 | a0001c0001t0001g0110a0001c0001t0004g0003a0005c0009t0004g0005others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1654-19G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119006627 | ||||||
| chr6:119006635
|
A | G | 4 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0009others(1): Show | 4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1654-27T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119006635 | ||||||
| chr6:119006743
|
G | A | 8 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(5): Show | 8 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1654-135C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119006743 | ||||||
| chr6:119007313
|
T | C | 1 | a0001c0003t0005g0030 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1654-705A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119007313 | ||||||
| chr6:119007352
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1654-744C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119007352 | ||||||
| chr6:119007400
|
C | T | 1 | a0002c0002t0002g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1654-792G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119007400 | ||||||
| chr6:119007434
|
G | A | 152 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(149): Show | 152 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.1654-826C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119007434 | ||||||
| chr6:119007460
|
G | C | 1 | a0001c0001t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1654-852C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119007460 | ||||||
| chr6:119007667
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1654-1059C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119007667 | ||||||
| chr6:119007668
|
C | T | 1 | a0001c0001t0001g0190 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1654-1060G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119007668 | ||||||
| chr6:119007770
|
G | A | 1 | a0001c0001t0002g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1654-1162C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119007770 | ||||||
| chr6:119007802
|
G | A | 5 | a0001c0001t0001g0080a0001c0001t0001g0089a0001c0001t0001g0090others(2): Show | 5 | HG00639.hp2 HG01168.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1654-1194C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119007802 | ||||||
| chr6:119007813
|
C | T | 7 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1654-1205G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119007813 | ||||||
| chr6:119007866
|
G | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.1654-1258C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119007866 | ||||||
| chr6:119007889
|
G | A | 1 | a0008c0005t0001g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1654-1281C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119007889 | ||||||
| chr6:119007941
|
G | GA | 9 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(6): Show | 9 | HG00741.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1654-1334dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119007941 | ||||||
| chr6:119008222
|
G | A | 90 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(87): Show | 90 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.1654-1614C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119008222 | ||||||
| chr6:119008243
|
C | T | 7 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1654-1635G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119008243 | ||||||
| chr6:119008295
|
G | T | 17 | a0001c0001t0001g0150a0001c0001t0001g0230a0001c0001t0001g0279others(14): Show | 17 | HG01081.hp1 HG01167.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.1654-1687C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119008295 | ||||||
| chr6:119008336
|
G | A | 1 | a0003c0004t0001g0093 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1654-1728C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119008336 | ||||||
| chr6:119008344
|
G | T | 2 | a0001c0001t0001g0223a0001c0001t0001g0272 | 2 | HG00140.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1654-1736C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119008344 | ||||||
| chr6:119008393
|
C | T | 160 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(157): Show | 160 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.1654-1785G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119008393 | ||||||
| chr6:119008474
|
A | G | 8 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(5): Show | 8 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1654-1866T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119008474 | ||||||
| chr6:119008604
|
G | A | 13 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(10): Show | 13 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1654-1996C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119008604 | ||||||
| chr6:119008779
|
A | G | 6 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG00738.hp1 HG01358.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.1654-2171T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119008779 | ||||||
| chr6:119008800
|
A | G | 1 | a0001c0001t0001g0152 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1654-2192T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119008800 | ||||||
| chr6:119008837
|
T | C | 152 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(149): Show | 152 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.1654-2229A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119008837 | ||||||
| chr6:119009014
|
T | C | 15 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(12): Show | 15 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.1653+2295A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119009014 | ||||||
| chr6:119009077
|
C | G | 1 | a0001c0001t0001g0266 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1653+2232G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119009077 | ||||||
| chr6:119009103
|
T | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.1653+2206A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119009103 | ||||||
| chr6:119009139
|
G | T | 36 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0128others(33): Show | 36 | HG00597.hp1 HG00642.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.1653+2170C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119009139 | ||||||
| chr6:119009258
|
G | C | 1 | a0008c0005t0001g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1653+2051C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119009258 | ||||||
| chr6:119009643
|
T | G | 1 | a0001c0001t0001g0234 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1653+1666A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119009643 | ||||||
| chr6:119009813
|
C | T | 5 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0131others(2): Show | 5 | HG02145.hp1 HG02572.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1653+1496G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119009813 | ||||||
| chr6:119009905
|
T | G | 4 | a0001c0001t0002g0119a0001c0001t0002g0197a0001c0001t0002g0198others(1): Show | 4 | HG00642.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1653+1404A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119009905 | ||||||
| chr6:119009949
|
A | G | 233 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(230): Show | 233 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.1653+1360T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119009949 | ||||||
| chr6:119010025
|
A | G | 1 | a0001c0001t0001g0126 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1653+1284T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119010025 | ||||||
| chr6:119010219
|
C | T | 3 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0061 | 3 | HG01168.hp2 HG01169.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1653+1090G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119010219 | ||||||
| chr6:119010236
|
G | C | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1653+1073C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119010236 | ||||||
| chr6:119010402
|
A | G | 1 | a0001c0001t0001g0254 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1653+907T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119010402 | ||||||
| chr6:119010723
|
T | A | 105 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0079others(102): Show | 105 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1653+586A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119010723 | ||||||
| chr6:119010939
|
T | A | 93 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(90): Show | 93 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.1653+370A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119010939 | ||||||
| chr6:119010995
|
G | A | 8 | a0001c0003t0001g0046a0001c0003t0001g0133a0001c0003t0001g0136others(5): Show | 8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1653+314C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119010995 | ||||||
| chr6:119011292
|
G | T | 4 | a0001c0001t0001g0204a0001c0001t0001g0209a0001c0001t0001g0269others(1): Show | 4 | NA18612.hp2 NA18947.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.1653+17C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119011292 | ||||||
| chr6:119011452
|
A | G | 1 | a0001c0001t0001g0214 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1531-21T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119011452 | ||||||
| chr6:119011484
|
T | C | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048 | 3 | HG01884.hp2 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1531-53A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119011484 | ||||||
| chr6:119011553
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0001g0135 | 2 | HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1531-122G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119011553 | ||||||
| chr6:119011608
|
A | C | 8 | a0001c0003t0001g0046a0001c0003t0001g0133a0001c0003t0001g0136others(5): Show | 8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1531-177T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119011608 | ||||||
| chr6:119011765
|
T | C | 3 | a0001c0001t0004g0003a0005c0009t0004g0005a0007c0010t0004g0004 | 3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1531-334A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119011765 | ||||||
| chr6:119011791
|
G | A | 233 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(230): Show | 233 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.1531-360C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119011791 | ||||||
| chr6:119012035
|
C | T | 3 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0004g0006 | 3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1531-604G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119012035 | ||||||
| chr6:119012109
|
C | T | 2 | a0001c0001t0001g0254a0001c0001t0001g0274 | 2 | NA19056.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1531-678G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119012109 | ||||||
| chr6:119012260
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1531-829C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119012260 | ||||||
| chr6:119012273
|
A | T | 105 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(102): Show | 105 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1531-842T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119012273 | ||||||
| chr6:119012332
|
G | A | 1 | a0008c0005t0001g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1531-901C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119012332 | ||||||
| chr6:119012356
|
G | T | 3 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0004g0006 | 3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1531-925C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119012356 | ||||||
| chr6:119012406
|
G | T | 1 | a0002c0002t0002g0208 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1531-975C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119012406 | ||||||
| chr6:119012539
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1531-1108G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119012539 | ||||||
| chr6:119012607
|
C | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0082 | 2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1531-1176G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119012607 | ||||||
| chr6:119012643
|
A | G | 15 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0128others(12): Show | 15 | HG00642.hp2 HG00741.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1531-1212T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119012643 | ||||||
| chr6:119012693
|
T | G | 1 | a0001c0001t0003g0021 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1531-1262A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119012693 | ||||||
| chr6:119012964
|
G | A | 20 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(17): Show | 20 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1531-1533C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119012964 | ||||||
| chr6:119013107
|
TA | T | 233 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(230): Show | 233 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.1531-1677delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119013107 | ||||||
| chr6:119013193
|
G | A | 3 | a0001c0003t0001g0133a0001c0003t0001g0136a0001c0003t0001g0142 | 3 | HG00639.hp1 HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1531-1762C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119013193 | ||||||
| chr6:119013261
|
A | T | 1 | a0004c0008t0001g0062 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1531-1830T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119013261 | ||||||
| chr6:119013360
|
G | A | 8 | a0001c0003t0001g0046a0001c0003t0001g0133a0001c0003t0001g0136others(5): Show | 8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1531-1929C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119013360 | ||||||
| chr6:119013716
|
T | C | 1 | a0001c0001t0001g0035 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1531-2285A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119013716 | ||||||
| chr6:119013767
|
T | G | 1 | a0001c0001t0001g0099 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1531-2336A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119013767 | ||||||
| chr6:119014079
|
T | A | 8 | a0001c0003t0001g0046a0001c0003t0001g0133a0001c0003t0001g0136others(5): Show | 8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1531-2648A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119014079 | ||||||
| chr6:119014117
|
A | G | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.1530+2630T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119014117 | ||||||
| chr6:119014237
|
C | G | 1 | a0001c0006t0005g0028 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1530+2510G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119014237 | ||||||
| chr6:119014670
|
A | C | 233 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(230): Show | 233 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.1530+2077T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119014670 | ||||||
| chr6:119014684
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1530+2063T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119014684 | ||||||
| chr6:119014700
|
A | G | 105 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(102): Show | 105 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1530+2047T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119014700 | ||||||
| chr6:119014724
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1530+2023T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119014724 | ||||||
| chr6:119014786
|
C | T | 105 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(102): Show | 105 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1530+1961G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119014786 | ||||||
| chr6:119014853
|
G | T | 3 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0240 | 3 | HG02630.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1530+1894C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119014853 | ||||||
| chr6:119015063
|
C | CA | 21 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(18): Show | 21 | HG00639.hp1 HG02257.hp2 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.1530+1683dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015063 | ||||||
| chr6:119015156
|
T | C | 229 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(226): Show | 229 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.1530+1591A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015156 | ||||||
| chr6:119015194
|
G | A | 6 | a0001c0001t0001g0035a0001c0001t0002g0060a0001c0001t0002g0072others(3): Show | 6 | HG00741.hp1 HG02818.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1530+1553C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015194 | ||||||
| chr6:119015258
|
G | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1530+1489C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015258 | ||||||
| chr6:119015294
|
C | T | 1 | a0008c0005t0001g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1530+1453G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015294 | ||||||
| chr6:119015295
|
G | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0004g0006 | 3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1530+1452C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015295 | ||||||
| chr6:119015301
|
C | A | 100 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(97): Show | 100 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1530+1446G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015301 | ||||||
| chr6:119015355
|
C | T | 1 | a0001c0001t0001g0180 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1530+1392G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015355 | ||||||
| chr6:119015356
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1530+1391C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015356 | ||||||
| chr6:119015369
|
G | A | 5 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0131others(2): Show | 5 | HG02145.hp1 HG02572.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1530+1378C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015369 | ||||||
| chr6:119015480
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1530+1267G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015480 | ||||||
| chr6:119015688
|
C | T | 110 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(107): Show | 110 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.1530+1059G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015688 | ||||||
| chr6:119015692
|
C | T | 5 | a0003c0004t0001g0091a0003c0004t0001g0092a0003c0004t0001g0093others(2): Show | 5 | HG00738.hp2 HG01433.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.1530+1055G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015692 | ||||||
| chr6:119015753
|
G | A | 1 | a0001c0001t0010g0284 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1530+994C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015753 | ||||||
| chr6:119015816
|
T | C | 6 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0098others(3): Show | 6 | HG02559.hp1 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1530+931A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015816 | ||||||
| chr6:119015894
|
C | A | 1 | a0001c0001t0003g0018 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1530+853G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015894 | ||||||
| chr6:119015895
|
A | T | 1 | a0001c0001t0003g0018 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1530+852T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015895 | ||||||
| chr6:119015962
|
C | G | 105 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(102): Show | 105 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1530+785G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015962 | ||||||
| chr6:119015967
|
A | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0082 | 2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1530+780T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015967 | ||||||
| chr6:119016050
|
T | C | 100 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(97): Show | 100 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1530+697A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119016050 | ||||||
| chr6:119016093
|
C | T | 9 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0192others(6): Show | 9 | HG00738.hp1 HG01358.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.1530+654G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119016093 | ||||||
| chr6:119016108
|
T | C | 1 | a0001c0001t0006g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1530+639A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119016108 | ||||||
| chr6:119016148
|
A | C | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG01934.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1530+599T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119016148 | ||||||
| chr6:119016160
|
G | A | 1 | a0008c0005t0001g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1530+587C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119016160 | ||||||
| chr6:119016219
|
C | T | 11 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(8): Show | 11 | HG00735.hp1 HG00741.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.1530+528G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119016219 | ||||||
| chr6:119016233
|
G | A | 1 | a0001c0001t0010g0284 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1530+514C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119016233 | ||||||
| chr6:119016331
|
C | T | 13 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(10): Show | 13 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1530+416G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119016331 | ||||||
| chr6:119016333
|
A | C | 2 | a0001c0001t0001g0050a0001c0001t0001g0052 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1530+414T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119016333 | ||||||
| chr6:119016443
|
C | A | 5 | a0001c0001t0001g0138a0001c0001t0001g0260a0001c0001t0005g0026others(2): Show | 5 | HG02451.hp2 HG02895.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1530+304G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119016443 | ||||||
| chr6:119016445
|
G | A | 120 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0079others(117): Show | 120 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1530+302C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119016445 | ||||||
| chr6:119016459
|
A | G | 2 | a0001c0001t0001g0144a0001c0001t0001g0158 | 2 | HG01192.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1530+288T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119016459 | ||||||
| chr6:119016467
|
C | T | 5 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0131others(2): Show | 5 | HG02145.hp1 HG02572.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1530+280G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119016467 | ||||||
| chr6:119016567
|
C | T | 5 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(2): Show | 5 | HG00140.hp2 HG00642.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.1530+180G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119016567 | ||||||
| chr6:119017007
|
T | G | 1 | a0001c0001t0001g0061 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1333-63A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119017007 | ||||||
| chr6:119017019
|
A | G | 1 | a0001c0006t0005g0028 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1333-75T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119017019 | ||||||
| chr6:119017358
|
C | T | 3 | a0001c0001t0004g0003a0005c0009t0004g0005a0007c0010t0004g0004 | 3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1333-414G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119017358 | ||||||
| chr6:119017420
|
A | C | 122 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(119): Show | 122 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.1333-476T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119017420 | ||||||
| chr6:119017429
|
CAG | C | 8 | a0001c0003t0001g0046a0001c0003t0001g0133a0001c0003t0001g0136others(5): Show | 8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1333-487_1333-486d others(4): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119017429 | ||||||
| chr6:119017497
|
CA | C | 16 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(13): Show | 16 | HG00639.hp1 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1333-554delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119017497 | ||||||
| chr6:119017546
|
A | C | 3 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0004g0006 | 3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1333-602T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119017546 | ||||||
| chr6:119017582
|
T | A | 1 | a0007c0010t0004g0004 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1333-638A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119017582 | ||||||
| chr6:119017670
|
T | C | 15 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0128others(12): Show | 15 | HG00642.hp2 HG00741.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1333-726A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119017670 | ||||||
| chr6:119017672
|
G | C | 1 | a0001c0001t0003g0023 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1333-728C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119017672 | ||||||
| chr6:119017899
|
C | A | 3 | a0001c0001t0001g0108a0001c0001t0001g0112a0001c0001t0001g0113 | 3 | HG00733.hp1 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1333-955G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119017899 | ||||||
| chr6:119017900
|
A | T | 1 | a0002c0002t0002g0185 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1333-956T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119017900 | ||||||
| chr6:119017917
|
C | T | 20 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(17): Show | 20 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1333-973G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119017917 | ||||||
| chr6:119018131
|
C | T | 13 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(10): Show | 13 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1333-1187G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119018131 | ||||||
| chr6:119018340
|
A | G | 1 | a0004c0008t0001g0062 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1333-1396T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119018340 | ||||||
| chr6:119018472
|
G | C | 7 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1332+1506C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119018472 | ||||||
| chr6:119018510
|
A | C | 1 | a0001c0001t0001g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1332+1468T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119018510 | ||||||
| chr6:119018516
|
G | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0126 | 3 | HG02970.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1332+1462C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119018516 | ||||||
| chr6:119018570
|
T | C | 2 | a0001c0001t0001g0074a0001c0001t0001g0086 | 2 | HG01123.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1332+1408A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119018570 | ||||||
| chr6:119018643
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1332+1335A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119018643 | ||||||
| chr6:119018741
|
C | T | 5 | a0001c0001t0001g0155a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | NA18954.hp1 NA18975.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.1332+1237G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119018741 | ||||||
| chr6:119018893
|
TAGAC | T | 20 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(17): Show | 20 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1332+1081_1332+108 others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119018893 | ||||||
| chr6:119018949
|
A | G | 116 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(113): Show | 116 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(113): Show |
intron_variant | MODIFIER | c.1332+1029T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119018949 | ||||||
| chr6:119018980
|
T | A | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.1332+998A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119018980 | ||||||
| chr6:119019002
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1332+976T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119019002 | ||||||
| chr6:119019098
|
G | A | 1 | a0001c0001t0003g0022 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1332+880C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119019098 | ||||||
| chr6:119019145
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1332+833G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119019145 | ||||||
| chr6:119019254
|
T | C | 3 | a0001c0001t0004g0003a0005c0009t0004g0005a0007c0010t0004g0004 | 3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1332+724A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119019254 | ||||||
| chr6:119019423
|
T | C | 229 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(226): Show | 229 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.1332+555A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119019423 | ||||||
| chr6:119019716
|
T | C | 122 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(119): Show | 122 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.1332+262A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119019716 | ||||||
| chr6:119019751
|
A | G | 12 | a0001c0003t0001g0046a0001c0003t0001g0133a0001c0003t0001g0136others(9): Show | 12 | HG00639.hp1 HG01433.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.1332+227T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119019751 | ||||||
| chr6:119019773
|
T | C | 50 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(47): Show | 50 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1332+205A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119019773 | ||||||
| chr6:119019783
|
A | G | 3 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203 | 3 | HG02109.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1332+195T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119019783 | ||||||
| chr6:119020169
|
A | C | 3 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0004g0006 | 3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1151-10T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119020169 | ||||||
| chr6:119020343
|
G | A | 11 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0128others(8): Show | 11 | HG00741.hp1 HG01099.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1151-184C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119020343 | ||||||
| chr6:119020419
|
G | T | 229 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(226): Show | 229 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.1151-260C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119020419 | ||||||
| chr6:119020630
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1151-471C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119020630 | ||||||
| chr6:119020735
|
G | A | 3 | a0001c0001t0001g0041a0001c0001t0001g0098a0001c0001t0001g0259 | 3 | HG02559.hp1 HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1151-576C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119020735 | ||||||
| chr6:119020835
|
G | A | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0128 | 3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1151-676C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119020835 | ||||||
| chr6:119020840
|
C | G | 97 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(94): Show | 97 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1151-681G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119020840 | ||||||
| chr6:119021012
|
G | C | 2 | a0001c0001t0001g0222a0001c0001t0001g0229 | 2 | NA18949.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1151-853C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119021012 | ||||||
| chr6:119021069
|
C | T | 105 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(102): Show | 105 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1151-910G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119021069 | ||||||
| chr6:119021239
|
CTGA | C | 3 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0004g0006 | 3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1151-1083_1151-108 others(7): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119021239 | ||||||
| chr6:119021325
|
T | C | 1 | a0002c0002t0002g0208 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1151-1166A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119021325 | ||||||
| chr6:119021342
|
C | T | 13 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(10): Show | 13 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1151-1183G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119021342 | ||||||
| chr6:119021679
|
C | A | 1 | a0001c0001t0001g0191 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1150+1266G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119021679 | ||||||
| chr6:119021805
|
G | A | 5 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.1150+1140C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119021805 | ||||||
| chr6:119021934
|
C | A | 1 | a0001c0001t0001g0252 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1150+1011G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119021934 | ||||||
| chr6:119022050
|
T | G | 1 | a0001c0001t0001g0047 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1150+895A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119022050 | ||||||
| chr6:119022053
|
C | CT | 19 | a0001c0001t0001g0064a0001c0001t0001g0067a0001c0001t0001g0068others(16): Show | 19 | HG00639.hp2 HG00735.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.1150+891dupA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119022053 | ||||||
| chr6:119022053
|
CT | C | 122 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(119): Show | 122 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.1150+891delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119022053 | ||||||
| chr6:119022053
|
CTT | C | 9 | a0001c0001t0001g0039a0001c0001t0001g0117a0001c0001t0001g0118others(6): Show | 9 | HG01099.hp2 HG01884.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1150+890_1150+891d others(4): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119022053 | ||||||
| chr6:119022261
|
G | A | 5 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0131others(2): Show | 5 | HG02145.hp1 HG02572.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1150+684C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119022261 | ||||||
| chr6:119022374
|
G | A | 2 | a0001c0001t0006g0032a0001c0001t0006g0033 | 2 | HG01243.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+571C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119022374 | ||||||
| chr6:119022382
|
T | C | 3 | a0001c0001t0001g0132a0001c0001t0001g0270a0001c0001t0001g0271 | 3 | HG02004.hp2 HG02698.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1150+563A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119022382 | ||||||
| chr6:119022507
|
G | A | 2 | a0004c0008t0001g0062a0008c0005t0001g0034 | 2 | HG01891.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1150+438C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119022507 | ||||||
| chr6:119022693
|
G | A | 1 | a0001c0003t0005g0030 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1150+252C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119022693 | ||||||
| chr6:119022825
|
C | T | 8 | a0001c0003t0001g0046a0001c0003t0001g0133a0001c0003t0001g0136others(5): Show | 8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1150+120G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119022825 | ||||||
| chr6:119022855
|
C | T | 48 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(45): Show | 48 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.1150+90G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119022855 | ||||||
| chr6:119022899
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1150+46C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119022899 | ||||||
| chr6:119023091
|
T | A | 1 | a0001c0001t0001g0159 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1015-11A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023091 | ||||||
| chr6:119023292
|
C | A | 1 | a0001c0001t0004g0009 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1015-212G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023292 | ||||||
| chr6:119023343
|
A | G | 1 | a0008c0005t0001g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1015-263T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023343 | ||||||
| chr6:119023364
|
C | T | 127 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(124): Show | 127 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.1015-284G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023364 | ||||||
| chr6:119023381
|
A | C | 92 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(89): Show | 92 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1015-301T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023381 | ||||||
| chr6:119023552
|
T | TC | 3 | a0001c0001t0001g0045a0002c0002t0002g0129a0007c0010t0004g0004 | 3 | HG01891.hp1 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1014+406dupG | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023552 | ||||||
| chr6:119023553
|
CCG | C | 76 | a0001c0001t0001g0035a0001c0001t0001g0050a0001c0001t0001g0051others(73): Show | 76 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1014+404_1014+405d others(4): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023553 | ||||||
| chr6:119023554
|
CG | C | 112 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0039others(109): Show | 112 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.1014+404delC | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023554 | ||||||
| chr6:119023555
|
G | C | 45 | a0001c0001t0001g0037a0001c0001t0001g0044a0001c0001t0001g0045others(42): Show | 45 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1014+404C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023555 | ||||||
| chr6:119023555
|
G | GC | 14 | a0001c0001t0001g0084a0001c0001t0001g0154a0001c0001t0001g0156others(11): Show | 14 | HG01069.hp1 HG01192.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1014+403dupG | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023555 | ||||||
| chr6:119023562
|
C | G | 15 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(12): Show | 15 | HG00639.hp1 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1014+397G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023562 | ||||||
| chr6:119023563
|
C | A | 6 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0131others(3): Show | 6 | HG02145.hp1 HG02572.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1014+396G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023563 | ||||||
| chr6:119023564
|
C | G | 53 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(50): Show | 53 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1014+395G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023564 | ||||||
| chr6:119023565
|
C | G | 1 | a0004c0008t0001g0062 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1014+394G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023565 | ||||||
| chr6:119023672
|
G | A | 2 | a0002c0002t0002g0121a0002c0002t0002g0129 | 2 | HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1014+287C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023672 | ||||||
| chr6:119023822
|
T | TA | 8 | a0001c0001t0001g0128a0001c0001t0001g0145a0001c0001t0001g0252others(5): Show | 8 | HG02615.hp2 HG02630.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1014+136dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023822 | ||||||
| chr6:119023822
|
TA | T | 81 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0053others(78): Show | 81 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.1014+136delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023822 | ||||||
| chr6:119023822
|
TAA | T | 10 | a0001c0001t0001g0044a0001c0001t0001g0056a0001c0001t0001g0132others(7): Show | 10 | HG02293.hp1 HG02451.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1014+135_1014+136d others(4): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023822 | ||||||
| chr6:119023823
|
A | T | 1 | a0001c0001t0004g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1014+136T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023823 | ||||||
| chr6:119024820
|
G | C | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | HG01167.hp1 HG01169.hp2 |
splice_region_variant&intron_variant | LOW | c.160-7C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119024820 | ||||||
| chr6:119024839
|
G | A | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-26C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119024839 | ||||||
| chr6:119024845
|
T | C | 108 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(105): Show | 108 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.160-32A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119024845 | ||||||
| chr6:119024963
|
T | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-150A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119024963 | ||||||
| chr6:119025030
|
A | C | 1 | a0001c0001t0001g0042 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.160-217T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119025030 | ||||||
| chr6:119025134
|
A | G | 1 | a0001c0001t0001g0246 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.160-321T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119025134 | ||||||
| chr6:119025283
|
T | C | 2 | a0001c0001t0001g0235a0001c0001t0001g0241 | 2 | HG02071.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.160-470A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119025283 | ||||||
| chr6:119025553
|
C | A | 1 | a0001c0001t0001g0131 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.160-740G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119025553 | ||||||
| chr6:119025554
|
C | A | 1 | a0001c0001t0001g0131 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.160-741G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119025554 | ||||||
| chr6:119025652
|
G | A | 1 | a0008c0005t0001g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.160-839C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119025652 | ||||||
| chr6:119025681
|
C | G | 1 | a0001c0001t0001g0255 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.160-868G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119025681 | ||||||
| chr6:119025741
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.160-928C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119025741 | ||||||
| chr6:119025747
|
G | A | 113 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0041others(110): Show | 113 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.160-934C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119025747 | ||||||
| chr6:119025921
|
A | G | 2 | a0001c0001t0001g0081a0001c0001t0001g0243 | 2 | HG01074.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.160-1108T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119025921 | ||||||
| chr6:119025925
|
A | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0079a0001c0001t0001g0082others(1): Show | 4 | HG02145.hp1 HG02717.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-1112T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119025925 | ||||||
| chr6:119026186
|
T | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0082 | 2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.160-1373A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119026186 | ||||||
| chr6:119026288
|
A | G | 1 | a0001c0001t0001g0152 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.160-1475T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119026288 | ||||||
| chr6:119026366
|
C | G | 1 | a0001c0001t0001g0215 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.160-1553G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119026366 | ||||||
| chr6:119026412
|
C | T | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(4): Show | 7 | HG01258.hp2 HG01358.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-1599G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119026412 | ||||||
| chr6:119026498
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.160-1685C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119026498 | ||||||
| chr6:119026508
|
AC | A | 7 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-1696delG | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119026508 | ||||||
| chr6:119026574
|
G | A | 3 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0010 | 3 | HG02109.hp1 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.160-1761C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119026574 | ||||||
| chr6:119026636
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.160-1823C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119026636 | ||||||
| chr6:119026646
|
C | T | 1 | a0001c0001t0004g0006 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.160-1833G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119026646 | ||||||
| chr6:119026648
|
C | A | 7 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-1835G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119026648 | ||||||
| chr6:119026691
|
CA | C | 3 | a0001c0001t0004g0003a0005c0009t0004g0005a0007c0010t0004g0004 | 3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.160-1879delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119026691 | ||||||
| chr6:119027102
|
C | A | 104 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(101): Show | 104 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.160-2289G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119027102 | ||||||
| chr6:119027419
|
T | G | 239 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(236): Show | 239 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.160-2606A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119027419 | ||||||
| chr6:119027436
|
T | C | 113 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(110): Show | 113 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.160-2623A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119027436 | ||||||
| chr6:119027437
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.160-2624T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119027437 | ||||||
| chr6:119027551
|
A | G | 23 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0154others(20): Show | 23 | HG00408.hp2 HG01192.hp2 HG02135.hp2 others(20): Show |
intron_variant | MODIFIER | c.160-2738T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119027551 | ||||||
| chr6:119027560
|
C | T | 23 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0154others(20): Show | 23 | HG00408.hp2 HG01192.hp2 HG02135.hp2 others(20): Show |
intron_variant | MODIFIER | c.160-2747G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119027560 | ||||||
| chr6:119027634
|
A | G | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0126 | 3 | HG02970.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.160-2821T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119027634 | ||||||
| chr6:119027690
|
A | G | 20 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(17): Show | 20 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.160-2877T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119027690 | ||||||
| chr6:119027951
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.160-3138C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119027951 | ||||||
| chr6:119028255
|
T | C | 3 | a0001c0001t0004g0003a0005c0009t0004g0005a0007c0010t0004g0004 | 3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.160-3442A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119028255 | ||||||
| chr6:119028273
|
T | A | 239 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(236): Show | 239 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.160-3460A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119028273 | ||||||
| chr6:119028295
|
T | C | 1 | a0001c0001t0003g0018 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.160-3482A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119028295 | ||||||
| chr6:119028371
|
G | A | 87 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(84): Show | 87 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.160-3558C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119028371 | ||||||
| chr6:119028407
|
T | C | 1 | a0002c0002t0002g0189 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.160-3594A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119028407 | ||||||
| chr6:119028575
|
G | A | 3 | a0001c0001t0001g0137a0001c0001t0004g0011a0001c0003t0001g0136 | 3 | HG02723.hp1 HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.160-3762C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119028575 | ||||||
| chr6:119028649
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.160-3836T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119028649 | ||||||
| chr6:119028662
|
C | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048 | 3 | HG01884.hp2 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.160-3849G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119028662 | ||||||
| chr6:119028685
|
C | A | 2 | a0001c0001t0001g0223a0001c0001t0001g0272 | 2 | HG00140.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.160-3872G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119028685 | ||||||
| chr6:119028860
|
T | C | 239 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(236): Show | 239 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.160-4047A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119028860 | ||||||
| chr6:119028871
|
G | C | 1 | a0002c0002t0002g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.160-4058C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119028871 | ||||||
| chr6:119029017
|
C | A | 239 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(236): Show | 239 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.160-4204G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119029017 | ||||||
| chr6:119029031
|
T | G | 2 | a0001c0001t0001g0254a0001c0001t0001g0274 | 2 | NA19056.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.160-4218A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119029031 | ||||||
| chr6:119029350
|
A | G | 4 | a0001c0001t0001g0130a0001c0001t0001g0277a0001c0001t0001g0278others(1): Show | 4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-4537T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119029350 | ||||||
| chr6:119029386
|
G | A | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0126 | 3 | HG02970.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.160-4573C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119029386 | ||||||
| chr6:119029472
|
A | G | 6 | a0001c0001t0001g0061a0001c0001t0001g0079a0001c0001t0001g0082others(3): Show | 6 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-4659T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119029472 | ||||||
| chr6:119029529
|
A | C | 1 | a0001c0001t0001g0214 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.160-4716T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119029529 | ||||||
| chr6:119029584
|
C | G | 221 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(218): Show | 221 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.160-4771G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119029584 | ||||||
| chr6:119029614
|
C | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048 | 3 | HG01884.hp2 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.160-4801G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119029614 | ||||||
| chr6:119029623
|
T | C | 6 | a0001c0001t0001g0061a0001c0001t0001g0079a0001c0001t0001g0082others(3): Show | 6 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-4810A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119029623 | ||||||
| chr6:119029769
|
G | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.160-4956C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119029769 | ||||||
| chr6:119029788
|
C | G | 54 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(51): Show | 54 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.160-4975G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119029788 | ||||||
| chr6:119030289
|
T | G | 8 | a0001c0003t0001g0046a0001c0003t0001g0133a0001c0003t0001g0136others(5): Show | 8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-5476A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119030289 | ||||||
| chr6:119030554
|
A | G | 13 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(10): Show | 13 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.160-5741T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119030554 | ||||||
| chr6:119030555
|
C | T | 2 | a0001c0001t0006g0032a0001c0001t0006g0033 | 2 | HG01243.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.160-5742G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119030555 | ||||||
| chr6:119030644
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.160-5831G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119030644 | ||||||
| chr6:119030828
|
A | G | 225 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(222): Show | 225 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.160-6015T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119030828 | ||||||
| chr6:119030894
|
A | AATTTCAT others(24): Show |
1 | a0001c0001t0001g0280 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.160-6112_160-6082d others(33): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119030894 | ||||||
| chr6:119031143
|
C | G | 1 | a0002c0002t0002g0143 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.160-6330G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119031143 | ||||||
| chr6:119031225
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.160-6412A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119031225 | ||||||
| chr6:119031417
|
T | C | 3 | a0001c0001t0004g0003a0005c0009t0004g0005a0007c0010t0004g0004 | 3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.160-6604A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119031417 | ||||||
| chr6:119031549
|
C | T | 104 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(101): Show | 104 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.160-6736G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119031549 | ||||||
| chr6:119031597
|
T | C | 4 | a0001c0001t0001g0061a0001c0001t0001g0079a0001c0001t0001g0082others(1): Show | 4 | HG02145.hp1 HG02717.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-6784A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119031597 | ||||||
| chr6:119031600
|
A | G | 7 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-6787T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119031600 | ||||||
| chr6:119031705
|
T | C | 20 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(17): Show | 20 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.160-6892A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119031705 | ||||||
| chr6:119031801
|
T | C | 1 | a0002c0002t0002g0217 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.160-6988A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119031801 | ||||||
| chr6:119031853
|
A | T | 96 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(93): Show | 96 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.160-7040T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119031853 | ||||||
| chr6:119031861
|
G | A | 1 | a0007c0010t0004g0004 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.160-7048C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119031861 | ||||||
| chr6:119031879
|
G | A | 1 | a0002c0002t0002g0268 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.160-7066C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119031879 | ||||||
| chr6:119032047
|
G | A | 104 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(101): Show | 104 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.160-7234C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119032047 | ||||||
| chr6:119032092
|
C | T | 1 | a0001c0001t0001g0228 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.160-7279G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119032092 | ||||||
| chr6:119032096
|
A | T | 15 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0128others(12): Show | 15 | HG00642.hp2 HG00741.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.160-7283T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119032096 | ||||||
| chr6:119032143
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.160-7330C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119032143 | ||||||
| chr6:119032352
|
A | G | 117 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(114): Show | 117 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.160-7539T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119032352 | ||||||
| chr6:119032466
|
C | A | 1 | a0001c0001t0005g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.160-7653G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119032466 | ||||||
| chr6:119032523
|
G | A | 1 | a0001c0001t0001g0040 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.160-7710C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119032523 | ||||||
| chr6:119032524
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.160-7711T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119032524 | ||||||
| chr6:119032524
|
AAGAGGG | A | 6 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0098others(3): Show | 6 | HG02559.hp1 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.160-7717_160-7712d others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119032524 | ||||||
| chr6:119032567
|
A | C | 1 | a0001c0001t0001g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.160-7754T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119032567 | ||||||
| chr6:119032574
|
G | C | 5 | a0001c0001t0002g0060a0001c0001t0002g0072a0001c0001t0002g0120others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-7761C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119032574 | ||||||
| chr6:119032723
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.160-7910T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119032723 | ||||||
| chr6:119032885
|
G | C | 1 | a0001c0001t0001g0205 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.160-8072C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119032885 | ||||||
| chr6:119032930
|
T | C | 1 | a0002c0002t0002g0224 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.160-8117A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119032930 | ||||||
| chr6:119033028
|
A | G | 1 | a0001c0006t0005g0028 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.160-8215T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033028 | ||||||
| chr6:119033093
|
T | A | 7 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-8280A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033093 | ||||||
| chr6:119033184
|
C | T | 3 | a0001c0001t0004g0003a0005c0009t0004g0005a0007c0010t0004g0004 | 3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.160-8371G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033184 | ||||||
| chr6:119033262
|
T | C | 2 | a0001c0001t0001g0226a0001c0001t0001g0227 | 2 | NA18951.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.160-8449A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033262 | ||||||
| chr6:119033269
|
A | C | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG02004.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.160-8456T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033269 | ||||||
| chr6:119033292
|
T | A | 20 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(17): Show | 20 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.160-8479A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033292 | ||||||
| chr6:119033525
|
C | T | 12 | a0001c0001t0002g0060a0001c0001t0002g0072a0001c0001t0002g0119others(9): Show | 12 | HG00642.hp2 HG00741.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.160-8712G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033525 | ||||||
| chr6:119033571
|
C | A | 239 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(236): Show | 239 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.160-8758G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033571 | ||||||
| chr6:119033586
|
A | G | 41 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0186others(38): Show | 41 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.160-8773T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033586 | ||||||
| chr6:119033664
|
C | CA | 20 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(17): Show | 20 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.160-8852dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033664 | ||||||
| chr6:119033664
|
C | CAA | 21 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0097others(18): Show | 21 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.160-8853_160-8852d others(4): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033664 | ||||||
| chr6:119033677
|
AAG | A | 8 | a0001c0003t0001g0046a0001c0003t0001g0133a0001c0003t0001g0136others(5): Show | 8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-8866_160-8865d others(4): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033677 | ||||||
| chr6:119033690
|
A | T | 1 | a0001c0001t0003g0014 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.160-8877T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033690 | ||||||
| chr6:119033703
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.160-8890G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033703 | ||||||
| chr6:119033720
|
G | A | 7 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0110others(4): Show | 7 | HG00408.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.160-8907C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033720 | ||||||
| chr6:119033864
|
C | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048 | 3 | HG01884.hp2 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.160-9051G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033864 | ||||||
| chr6:119033905
|
T | C | 4 | a0001c0001t0001g0130a0001c0001t0001g0277a0001c0001t0001g0278others(1): Show | 4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-9092A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033905 | ||||||
| chr6:119033939
|
C | T | 1 | a0001c0003t0001g0262 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.160-9126G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033939 | ||||||
| chr6:119033990
|
CA | C | 19 | a0001c0001t0001g0157a0001c0001t0001g0159a0001c0001t0001g0171others(16): Show | 19 | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.160-9178delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033990 | ||||||
| chr6:119033990
|
CAAAAAAA | C | 7 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0066others(4): Show | 7 | HG00423.hp2 HG00741.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.160-9184_160-9178d others(9): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033990 | ||||||
| chr6:119033990
|
CAAAAAAA others(3): Show |
C | 4 | a0001c0001t0002g0072a0001c0001t0002g0120a0001c0001t0002g0122others(1): Show | 4 | HG00741.hp1 HG02818.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.160-9187_160-9178d others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033990 | ||||||
| chr6:119033990
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0043a0001c0001t0002g0060 | 2 | HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.160-9188_160-9178d others(13): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033990 | ||||||
| chr6:119034009
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0001g0042 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.160-9208_160-9197d others(14): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034009 | ||||||
| chr6:119034010
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0001g0134 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.160-9208_160-9198d others(13): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034010 | ||||||
| chr6:119034010
|
AAAAAAAA others(6): Show |
A | 4 | a0001c0001t0001g0041a0001c0001t0001g0098a0001c0001t0001g0135others(1): Show | 4 | HG02559.hp1 HG02818.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.160-9210_160-9198d others(15): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034010 | ||||||
| chr6:119034011
|
AAAAAAAA others(5): Show |
A | 2 | a0001c0001t0001g0067a0001c0001t0001g0103 | 2 | HG01515.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.160-9210_160-9199d others(14): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034011 | ||||||
| chr6:119034012
|
AAAAAAAA others(4): Show |
A | 3 | a0001c0001t0001g0064a0001c0001t0001g0068a0001c0001t0001g0070 | 3 | HG00735.hp1 HG01978.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.160-9210_160-9200d others(13): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034012 | ||||||
| chr6:119034013
|
AAAAAAAA others(3): Show |
A | 2 | a0001c0001t0001g0256a0001c0001t0001g0258 | 2 | NA18995.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.160-9210_160-9201d others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034013 | ||||||
| chr6:119034013
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0001g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.160-9212_160-9201d others(14): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034013 | ||||||
| chr6:119034014
|
AAAAAAAT others(4): Show |
A | 5 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0108others(2): Show | 5 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-9212_160-9202d others(13): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034014 | ||||||
| chr6:119034015
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.160-9203_160-9202i others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034015 | ||||||
| chr6:119034015
|
AAAAAAT | A | 6 | a0001c0001t0001g0111a0001c0001t0001g0132a0001c0003t0001g0046others(3): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.160-9208_160-9203d others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034015 | ||||||
| chr6:119034015
|
AAAAAATA others(3): Show |
A | 3 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0003t0001g0136 | 3 | HG02723.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.160-9212_160-9203d others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034015 | ||||||
| chr6:119034016
|
AAAAATAT others(4): Show |
A | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0126 | 3 | HG02970.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.160-9214_160-9204d others(13): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034016 | ||||||
| chr6:119034017
|
A | T | 3 | a0001c0001t0001g0044a0001c0001t0002g0122a0001c0001t0002g0123 | 3 | HG02965.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.160-9204T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034017 | ||||||
| chr6:119034018
|
AAAT | A | 12 | a0001c0001t0001g0053a0001c0001t0001g0058a0001c0001t0001g0059others(9): Show | 12 | HG01099.hp2 HG01433.hp1 HG02273.hp1 others(9): Show |
intron_variant | MODIFIER | c.160-9208_160-9206d others(5): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034018 | ||||||
| chr6:119034018
|
AAATAT | A | 21 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0073others(18): Show | 21 | HG00140.hp2 HG00639.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.160-9210_160-9206d others(7): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034018 | ||||||
| chr6:119034019
|
A | AT | 3 | a0001c0001t0002g0198a0001c0001t0006g0032a0001c0001t0006g0033 | 3 | HG01243.hp1 HG03486.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.160-9207_160-9206i others(3): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034019 | ||||||
| chr6:119034019
|
A | T | 26 | a0001c0001t0001g0039a0001c0001t0001g0044a0001c0001t0001g0100others(23): Show | 26 | HG00140.hp1 HG00741.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.160-9206T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034019 | ||||||
| chr6:119034019
|
AAT | A | 11 | a0001c0001t0001g0152a0001c0001t0001g0158a0001c0001t0001g0175others(8): Show | 11 | HG00408.hp2 HG01192.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.160-9208_160-9207d others(4): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034019 | ||||||
| chr6:119034020
|
AT | A | 20 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0085others(17): Show | 20 | HG00609.hp2 HG02080.hp1 HG02155.hp1 others(17): Show |
intron_variant | MODIFIER | c.160-9208delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034020 | ||||||
| chr6:119034020
|
ATAT | A | 3 | a0001c0001t0001g0078a0001c0001t0001g0130a0001c0001t0001g0201 | 3 | HG01934.hp2 HG02922.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.160-9210_160-9208d others(5): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034020 | ||||||
| chr6:119034021
|
T | A | 28 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0094others(25): Show | 28 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.160-9208A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034021 | ||||||
| chr6:119034023
|
T | A | 3 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0096 | 3 | HG02622.hp2 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.160-9210A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034023 | ||||||
| chr6:119034025
|
T | A | 1 | a0001c0001t0001g0096 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.160-9212A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034025 | ||||||
| chr6:119034035
|
T | A | 1 | a0001c0001t0001g0039 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.160-9222A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034035 | ||||||
| chr6:119034035
|
TATATATA others(3): Show |
T | 1 | a0001c0001t0004g0008 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.160-9232_160-9223d others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034035 | ||||||
| chr6:119034035
|
TATATATA others(11): Show |
T | 2 | a0001c0001t0001g0100a0001c0001t0005g0026 | 2 | HG01168.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.160-9240_160-9223d others(20): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034035 | ||||||
| chr6:119034037
|
T | A | 3 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0040 | 3 | HG01167.hp1 HG01169.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.160-9224A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034037 | ||||||
| chr6:119034037
|
T | G | 3 | a0001c0001t0001g0145a0001c0001t0001g0173a0001c0001t0001g0176 | 3 | NA18959.hp2 NA19002.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.160-9224A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034037 | ||||||
| chr6:119034037
|
TATATAG | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0253a0001c0001t0001g0273 | 3 | HG00597.hp2 HG02109.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.160-9230_160-9225d others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034037 | ||||||
| chr6:119034037
|
TATATAGA others(3): Show |
T | 2 | a0001c0001t0004g0006a0001c0001t0004g0007 | 2 | HG02145.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.160-9234_160-9225d others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034037 | ||||||
| chr6:119034037
|
TATATAGA others(9): Show |
T | 1 | a0001c0001t0001g0125 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.160-9240_160-9225d others(18): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034037 | ||||||
| chr6:119034039
|
T | G | 18 | a0001c0001t0001g0117a0001c0001t0001g0128a0001c0001t0001g0144others(15): Show | 18 | HG01099.hp2 HG02523.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.160-9226A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034039 | ||||||
| chr6:119034039
|
TATAGAGA others(1): Show |
T | 9 | a0001c0001t0001g0149a0001c0001t0001g0215a0001c0001t0001g0247others(6): Show | 9 | HG00735.hp2 HG01361.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.160-9234_160-9227d others(10): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034039 | ||||||
| chr6:119034039
|
TATAGAGA others(5): Show |
T | 4 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0094others(1): Show | 4 | HG02622.hp2 HG03225.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.160-9238_160-9227d others(14): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034039 | ||||||
| chr6:119034039
|
TATAGAGA others(9): Show |
T | 1 | a0001c0001t0001g0054 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.160-9242_160-9227d others(18): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034039 | ||||||
| chr6:119034041
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.160-9228A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034041 | ||||||
| chr6:119034041
|
T | G | 46 | a0001c0001t0001g0069a0001c0001t0001g0117a0001c0001t0001g0128others(43): Show | 46 | HG00408.hp2 HG00609.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.160-9228A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034041 | ||||||
| chr6:119034041
|
T | TAGAGAGA others(5): Show |
1 | a0005c0009t0004g0005 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.160-9240_160-9229d others(14): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034041 | ||||||
| chr6:119034041
|
TAGAG | T | 23 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0066others(20): Show | 23 | HG00423.hp2 HG00741.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.160-9232_160-9229d others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034041 | ||||||
| chr6:119034041
|
TAGAGAG | T | 38 | a0001c0001t0001g0036a0001c0001t0001g0106a0001c0001t0001g0107others(35): Show | 38 | HG00597.hp1 HG00609.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.160-9234_160-9229d others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034041 | ||||||
| chr6:119034041
|
TAGAGAGA others(1): Show |
T | 62 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(59): Show | 62 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.160-9236_160-9229d others(10): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034041 | ||||||
| chr6:119034041
|
TAGAGAGA others(3): Show |
T | 11 | a0001c0001t0001g0039a0001c0001t0001g0042a0001c0001t0001g0043others(8): Show | 11 | HG00733.hp2 HG01258.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.160-9238_160-9229d others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034041 | ||||||
| chr6:119034041
|
TAGAGAGA others(5): Show |
T | 23 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0073others(20): Show | 23 | HG00140.hp2 HG00639.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.160-9240_160-9229d others(14): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034041 | ||||||
| chr6:119034041
|
TAGAGAGA others(7): Show |
T | 4 | a0001c0001t0001g0053a0001c0001t0001g0058a0001c0001t0001g0059others(1): Show | 4 | HG01433.hp1 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.160-9242_160-9229d others(16): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034041 | ||||||
| chr6:119034041
|
TAGAGAGA others(9): Show |
T | 1 | a0001c0001t0001g0205 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.160-9244_160-9229d others(18): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034041 | ||||||
| chr6:119034041
|
TAGAGAGA others(11): Show |
T | 4 | a0001c0001t0001g0081a0001c0001t0001g0243a0001c0001t0001g0244others(1): Show | 4 | HG01074.hp2 HG01433.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.160-9246_160-9229d others(20): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034041 | ||||||
| chr6:119034043
|
G | T | 29 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0050others(26): Show | 29 | HG00642.hp2 HG00733.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.160-9230C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034043 | ||||||
| chr6:119034045
|
G | T | 1 | a0001c0001t0001g0045 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.160-9232C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034045 | ||||||
| chr6:119034047
|
G | T | 11 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0071others(8): Show | 11 | HG02071.hp1 HG02083.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.160-9234C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034047 | ||||||
| chr6:119034049
|
G | T | 33 | a0001c0001t0001g0036a0001c0001t0001g0187a0001c0001t0001g0188others(30): Show | 33 | HG00597.hp1 HG00609.hp1 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.160-9236C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034049 | ||||||
| chr6:119034051
|
G | T | 61 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(58): Show | 61 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.160-9238C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034051 | ||||||
| chr6:119034053
|
G | T | 18 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.160-9240C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034053 | ||||||
| chr6:119034055
|
G | T | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-9242C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034055 | ||||||
| chr6:119034059
|
G | T | 1 | a0001c0001t0001g0205 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.160-9246C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034059 | ||||||
| chr6:119034212
|
G | A | 41 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.160-9399C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034212 | ||||||
| chr6:119034384
|
T | C | 1 | a0001c0001t0001g0253 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.160-9571A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034384 | ||||||
| chr6:119034533
|
AGTC | A | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-9723_160-9721d others(5): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034533 | ||||||
| chr6:119034566
|
G | GT | 15 | a0001c0001t0001g0137a0001c0001t0002g0060a0001c0001t0002g0072others(12): Show | 15 | HG00642.hp2 HG00741.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.160-9754dupA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034566 | ||||||
| chr6:119034568
|
T | TG | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048 | 3 | HG01884.hp2 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.160-9756_160-9755i others(3): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034568 | ||||||
| chr6:119034578
|
T | A | 32 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(29): Show | 32 | HG00423.hp2 HG00733.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.160-9765A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034578 | ||||||
| chr6:119034579
|
T | A | 47 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(44): Show | 47 | HG00423.hp2 HG00639.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.160-9766A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034579 | ||||||
| chr6:119034579
|
T | TA | 23 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(20): Show | 23 | HG00140.hp2 HG00642.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.160-9767_160-9766i others(3): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034579 | ||||||
| chr6:119034580
|
T | A | 129 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(126): Show | 129 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.160-9767A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034580 | ||||||
| chr6:119034580
|
T | TA | 136 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0041others(133): Show | 136 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.160-9768dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034580 | ||||||
| chr6:119034581
|
A | T | 3 | a0001c0001t0001g0137a0001c0001t0002g0072a0001c0001t0004g0011 | 3 | HG00741.hp1 HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.160-9768T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034581 | ||||||
| chr6:119034727
|
C | T | 4 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0009others(1): Show | 4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-9914G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034727 | ||||||
| chr6:119034732
|
T | C | 1 | a0001c0001t0001g0210 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.160-9919A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034732 | ||||||
| chr6:119035036
|
T | C | 108 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(105): Show | 108 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.160-10223A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119035036 | ||||||
| chr6:119035080
|
C | T | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-10267G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119035080 | ||||||
| chr6:119035170
|
A | T | 123 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(120): Show | 123 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.160-10357T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119035170 | ||||||
| chr6:119035181
|
A | G | 168 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0053others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.160-10368T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119035181 | ||||||
| chr6:119035222
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.160-10409G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119035222 | ||||||
| chr6:119035230
|
CTTGGCCA others(6): Show |
C | 4 | a0001c0001t0001g0137a0001c0001t0004g0002a0001c0001t0004g0011others(1): Show | 4 | HG02258.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.160-10430_160-1041 others(17): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119035230 | ||||||
| chr6:119035246
|
C | A | 1 | a0001c0001t0002g0120 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.160-10433G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119035246 | ||||||
| chr6:119035266
|
T | G | 1 | a0001c0001t0001g0276 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.160-10453A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119035266 | ||||||
| chr6:119035396
|
G | A | 4 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0009others(1): Show | 4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-10583C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119035396 | ||||||
| chr6:119035668
|
A | G | 47 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(44): Show | 47 | HG00423.hp2 HG00639.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.160-10855T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119035668 | ||||||
| chr6:119035686
|
C | G | 1 | a0001c0001t0001g0219 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.160-10873G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119035686 | ||||||
| chr6:119035726
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.160-10913C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119035726 | ||||||
| chr6:119035891
|
T | C | 7 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-11078A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119035891 | ||||||
| chr6:119035909
|
C | T | 6 | a0001c0001t0001g0061a0001c0001t0001g0079a0001c0001t0001g0082others(3): Show | 6 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-11096G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119035909 | ||||||
| chr6:119036020
|
C | A | 1 | a0001c0006t0005g0028 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.160-11207G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119036020 | ||||||
| chr6:119036161
|
A | ATAGTTCA others(3): Show |
1 | a0001c0001t0001g0255 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.160-11349_160-1134 others(14): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119036161 | ||||||
| chr6:119036205
|
C | T | 230 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(227): Show | 230 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.160-11392G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119036205 | ||||||
| chr6:119036216
|
C | CT | 237 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(234): Show | 237 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.160-11404dupA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119036216 | ||||||
| chr6:119036540
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.160-11727C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119036540 | ||||||
| chr6:119036686
|
T | C | 1 | a0001c0001t0001g0190 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.160-11873A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119036686 | ||||||
| chr6:119036702
|
T | G | 1 | a0001c0001t0001g0210 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.160-11889A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119036702 | ||||||
| chr6:119037033
|
A | G | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048 | 3 | HG01884.hp2 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.160-12220T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119037033 | ||||||
| chr6:119037051
|
A | T | 1 | a0001c0001t0001g0097 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.160-12238T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119037051 | ||||||
| chr6:119037320
|
G | T | 4 | a0001c0001t0001g0130a0001c0001t0001g0277a0001c0001t0001g0278others(1): Show | 4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-12507C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119037320 | ||||||
| chr6:119037334
|
T | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-12521A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119037334 | ||||||
| chr6:119037354
|
C | G | 2 | a0001c0001t0001g0206a0001c0001t0001g0218 | 2 | HG01123.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.160-12541G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119037354 | ||||||
| chr6:119037372
|
C | A | 1 | a0001c0001t0001g0207 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.160-12559G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119037372 | ||||||
| chr6:119037402
|
A | C | 2 | a0001c0001t0001g0099a0001c0001t0001g0281 | 2 | HG02683.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.160-12589T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119037402 | ||||||
| chr6:119037457
|
C | T | 6 | a0001c0001t0001g0061a0001c0001t0001g0079a0001c0001t0001g0082others(3): Show | 6 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-12644G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119037457 | ||||||
| chr6:119037628
|
A | T | 3 | a0001c0001t0004g0003a0005c0009t0004g0005a0007c0010t0004g0004 | 3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.160-12815T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119037628 | ||||||
| chr6:119037986
|
CAAG | C | 8 | a0001c0001t0002g0060a0001c0001t0002g0072a0001c0001t0002g0120others(5): Show | 8 | HG00741.hp1 HG02615.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-13176_160-1317 others(7): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119037986 | ||||||
| chr6:119038089
|
G | A | 39 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(36): Show | 39 | HG00423.hp2 HG00733.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.160-13276C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119038089 | ||||||
| chr6:119038261
|
G | A | 8 | a0001c0003t0001g0046a0001c0003t0001g0133a0001c0003t0001g0136others(5): Show | 8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-13448C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119038261 | ||||||
| chr6:119038389
|
A | G | 1 | a0001c0001t0003g0017 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.160-13576T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119038389 | ||||||
| chr6:119038392
|
T | A | 4 | a0001c0001t0001g0204a0001c0001t0001g0209a0001c0001t0001g0269others(1): Show | 4 | NA18612.hp2 NA18947.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-13579A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119038392 | ||||||
| chr6:119038533
|
G | A | 2 | a0002c0002t0001g0238a0002c0002t0002g0189 | 2 | HG02071.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.160-13720C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119038533 | ||||||
| chr6:119038624
|
G | A | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048 | 3 | HG01884.hp2 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.160-13811C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119038624 | ||||||
| chr6:119038668
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.160-13855G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119038668 | ||||||
| chr6:119038753
|
G | A | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-13940C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119038753 | ||||||
| chr6:119038783
|
G | A | 239 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(236): Show | 239 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.160-13970C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119038783 | ||||||
| chr6:119038799
|
G | A | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0126 | 3 | HG02970.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.160-13986C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119038799 | ||||||
| chr6:119038808
|
G | A | 3 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0276 | 3 | HG01069.hp1 HG01071.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.160-13995C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119038808 | ||||||
| chr6:119038861
|
G | A | 8 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(5): Show | 8 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.160-14048C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119038861 | ||||||
| chr6:119039102
|
T | C | 1 | a0001c0001t0008g0286 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.160-14289A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119039102 | ||||||
| chr6:119039413
|
G | T | 1 | a0001c0001t0001g0085 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.160-14600C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119039413 | ||||||
| chr6:119039473
|
A | G | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-14660T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119039473 | ||||||
| chr6:119039540
|
A | G | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-14727T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119039540 | ||||||
| chr6:119039815
|
A | C | 4 | a0001c0001t0001g0130a0001c0001t0001g0277a0001c0001t0001g0278others(1): Show | 4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-15002T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119039815 | ||||||
| chr6:119039817
|
G | A | 39 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(36): Show | 39 | HG00423.hp2 HG00733.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.160-15004C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119039817 | ||||||
| chr6:119039838
|
G | C | 2 | a0001c0001t0001g0074a0001c0001t0001g0086 | 2 | HG01123.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.160-15025C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119039838 | ||||||
| chr6:119039964
|
C | G | 6 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG00738.hp1 HG01358.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-15151G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119039964 | ||||||
| chr6:119040092
|
G | A | 33 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(30): Show | 33 | HG00423.hp2 HG00733.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.160-15279C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119040092 | ||||||
| chr6:119040169
|
CTGTT | C | 20 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(17): Show | 20 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.160-15360_160-1535 others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119040169 | ||||||
| chr6:119040445
|
A | G | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048 | 3 | HG01884.hp2 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.160-15632T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119040445 | ||||||
| chr6:119040486
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.160-15673A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119040486 | ||||||
| chr6:119040578
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.160-15765G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119040578 | ||||||
| chr6:119040731
|
C | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0127 | 2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.160-15918G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119040731 | ||||||
| chr6:119040832
|
T | A | 8 | a0001c0003t0001g0046a0001c0003t0001g0133a0001c0003t0001g0136others(5): Show | 8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-16019A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119040832 | ||||||
| chr6:119040888
|
G | A | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048 | 3 | HG01884.hp2 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.160-16075C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119040888 | ||||||
| chr6:119040894
|
G | A | 3 | a0001c0001t0004g0003a0005c0009t0004g0005a0007c0010t0004g0004 | 3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.160-16081C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119040894 | ||||||
| chr6:119040990
|
C | A | 239 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(236): Show | 239 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.160-16177G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119040990 | ||||||
| chr6:119041096
|
C | T | 4 | a0001c0001t0001g0130a0001c0001t0001g0277a0001c0001t0001g0278others(1): Show | 4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-16283G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119041096 | ||||||
| chr6:119041290
|
G | C | 164 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0053others(161): Show | 164 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.160-16477C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119041290 | ||||||
| chr6:119041477
|
G | A | 9 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(6): Show | 9 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.160-16664C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119041477 | ||||||
| chr6:119041685
|
G | A | 9 | a0001c0001t0001g0134a0001c0003t0001g0046a0001c0003t0001g0133others(6): Show | 9 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.160-16872C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119041685 | ||||||
| chr6:119041804
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.160-16991G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119041804 | ||||||
| chr6:119041908
|
G | A | 41 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.160-17095C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119041908 | ||||||
| chr6:119041998
|
C | T | 1 | a0001c0001t0001g0191 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.160-17185G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119041998 | ||||||
| chr6:119042160
|
C | G | 1 | a0001c0001t0001g0261 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.160-17347G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119042160 | ||||||
| chr6:119042236
|
G | T | 7 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(4): Show | 7 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.160-17423C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119042236 | ||||||
| chr6:119042348
|
G | A | 5 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(2): Show | 5 | HG00140.hp2 HG00642.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-17535C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119042348 | ||||||
| chr6:119042411
|
T | C | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.160-17598A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119042411 | ||||||
| chr6:119042470
|
C | CT | 164 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0053others(161): Show | 164 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.160-17658dupA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119042470 | ||||||
| chr6:119042478
|
T | G | 6 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-17665A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119042478 | ||||||
| chr6:119042535
|
G | A | 4 | a0001c0001t0001g0130a0001c0001t0001g0277a0001c0001t0001g0278others(1): Show | 4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-17722C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119042535 | ||||||
| chr6:119042752
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.160-17939A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119042752 | ||||||
| chr6:119042811
|
C | T | 164 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0053others(161): Show | 164 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.160-17998G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119042811 | ||||||
| chr6:119042862
|
CT | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-18050delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119042862 | ||||||
| chr6:119043076
|
T | TA | 9 | a0001c0001t0001g0134a0001c0003t0001g0046a0001c0003t0001g0133others(6): Show | 9 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.160-18264dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119043076 | ||||||
| chr6:119043082
|
T | A | 239 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(236): Show | 239 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.160-18269A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119043082 | ||||||
| chr6:119043125
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.160-18312A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119043125 | ||||||
| chr6:119043191
|
T | C | 9 | a0001c0001t0001g0134a0001c0003t0001g0046a0001c0003t0001g0133others(6): Show | 9 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.160-18378A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119043191 | ||||||
| chr6:119044278
|
C | G | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048 | 3 | HG01884.hp2 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.160-19465G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119044278 | ||||||
| chr6:119044364
|
C | T | 164 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0053others(161): Show | 164 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.160-19551G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119044364 | ||||||
| chr6:119044459
|
T | C | 6 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0087others(3): Show | 6 | HG01106.hp1 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.160-19646A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119044459 | ||||||
| chr6:119044496
|
T | C | 1 | a0008c0005t0001g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.160-19683A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119044496 | ||||||
| chr6:119044538
|
T | C | 1 | a0001c0001t0003g0012 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.160-19725A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119044538 | ||||||
| chr6:119044591
|
TA | T | 46 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0144others(43): Show | 46 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.160-19779delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119044591 | ||||||
| chr6:119044651
|
T | C | 3 | a0001c0001t0004g0003a0005c0009t0004g0005a0007c0010t0004g0004 | 3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.160-19838A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119044651 | ||||||
| chr6:119044731
|
T | A | 6 | a0001c0001t0001g0061a0001c0001t0001g0079a0001c0001t0001g0082others(3): Show | 6 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-19918A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119044731 | ||||||
| chr6:119044872
|
T | G | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048 | 3 | HG01884.hp2 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.160-20059A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119044872 | ||||||
| chr6:119044986
|
A | T | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0128 | 3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.160-20173T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119044986 | ||||||
| chr6:119045037
|
C | T | 59 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0130others(56): Show | 59 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.160-20224G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119045037 | ||||||
| chr6:119045038
|
G | A | 4 | a0001c0001t0001g0204a0001c0001t0001g0209a0001c0001t0001g0269others(1): Show | 4 | NA18612.hp2 NA18947.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-20225C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119045038 | ||||||
| chr6:119045228
|
T | C | 1 | a0001c0001t0001g0214 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.160-20415A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119045228 | ||||||
| chr6:119045291
|
A | AT | 21 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(18): Show | 21 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.160-20479dupA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119045291 | ||||||
| chr6:119045291
|
A | ATT | 223 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(220): Show | 223 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.160-20480_160-2047 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119045291 | ||||||
| chr6:119045291
|
A | ATTT | 20 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0047others(17): Show | 20 | HG01884.hp2 HG02280.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.160-20481_160-2047 others(7): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119045291 | ||||||
| chr6:119045475
|
C | T | 5 | a0001c0001t0001g0080a0001c0001t0001g0089a0001c0001t0001g0090others(2): Show | 5 | HG00639.hp2 HG01168.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.160-20662G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119045475 | ||||||
| chr6:119045521
|
C | G | 1 | a0001c0001t0009g0001 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.160-20708G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119045521 | ||||||
| chr6:119045548
|
T | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-20735A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119045548 | ||||||
| chr6:119045630
|
C | T | 9 | a0001c0001t0001g0134a0001c0003t0001g0046a0001c0003t0001g0133others(6): Show | 9 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.160-20817G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119045630 | ||||||
| chr6:119045644
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.160-20831G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119045644 | ||||||
| chr6:119045703
|
G | T | 1 | a0002c0002t0002g0217 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.160-20890C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119045703 | ||||||
| chr6:119045805
|
AT | A | 6 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-20993delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119045805 | ||||||
| chr6:119045806
|
T | A | 1 | a0001c0006t0005g0028 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.160-20993A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119045806 | ||||||
| chr6:119046226
|
CT | C | 35 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(32): Show | 35 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.160-21414delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119046226 | ||||||
| chr6:119046316
|
T | G | 3 | a0001c0001t0001g0188a0001c0001t0001g0210a0001c0001t0001g0273 | 3 | HG00597.hp2 HG01255.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.160-21503A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119046316 | ||||||
| chr6:119046423
|
C | T | 4 | a0001c0001t0001g0130a0001c0001t0001g0277a0001c0001t0001g0278others(1): Show | 4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-21610G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119046423 | ||||||
| chr6:119046453
|
A | G | 246 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(243): Show | 246 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.160-21640T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119046453 | ||||||
| chr6:119046495
|
T | A | 46 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0144others(43): Show | 46 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.160-21682A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119046495 | ||||||
| chr6:119046564
|
T | TA | 165 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0053others(162): Show | 165 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.160-21752dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119046564 | ||||||
| chr6:119046740
|
G | C | 4 | a0001c0001t0001g0130a0001c0001t0001g0277a0001c0001t0001g0278others(1): Show | 4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-21927C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119046740 | ||||||
| chr6:119046840
|
A | G | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-22027T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119046840 | ||||||
| chr6:119046872
|
T | C | 2 | a0001c0001t0004g0002a0006c0007t0001g0242 | 2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.160-22059A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119046872 | ||||||
| chr6:119047052
|
T | TA | 164 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0053others(161): Show | 164 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.160-22240dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119047052 | ||||||
| chr6:119047065
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.160-22252T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119047065 | ||||||
| chr6:119047121
|
TA | T | 46 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0144others(43): Show | 46 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.160-22309delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119047121 | ||||||
| chr6:119047129
|
T | G | 46 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0144others(43): Show | 46 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.160-22316A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119047129 | ||||||
| chr6:119047156
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.160-22343T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119047156 | ||||||
| chr6:119047248
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.160-22435A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119047248 | ||||||
| chr6:119047300
|
T | A | 1 | a0001c0001t0001g0187 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.160-22487A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119047300 | ||||||
| chr6:119047448
|
C | T | 164 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0053others(161): Show | 164 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.160-22635G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119047448 | ||||||
| chr6:119047777
|
C | T | 4 | a0001c0001t0004g0003a0001c0001t0010g0284a0005c0009t0004g0005others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.160-22964G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119047777 | ||||||
| chr6:119047790
|
C | T | 9 | a0001c0001t0001g0134a0001c0003t0001g0046a0001c0003t0001g0133others(6): Show | 9 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.160-22977G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119047790 | ||||||
| chr6:119048055
|
G | T | 1 | a0008c0005t0001g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.160-23242C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119048055 | ||||||
| chr6:119048057
|
G | A | 6 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-23244C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119048057 | ||||||
| chr6:119048351
|
T | A | 13 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(10): Show | 13 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.160-23538A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119048351 | ||||||
| chr6:119048353
|
C | A | 4 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0009others(1): Show | 4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-23540G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119048353 | ||||||
| chr6:119048491
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.160-23678C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119048491 | ||||||
| chr6:119048682
|
G | A | 9 | a0001c0001t0001g0134a0001c0003t0001g0046a0001c0003t0001g0133others(6): Show | 9 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.160-23869C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119048682 | ||||||
| chr6:119048796
|
G | A | 164 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0053others(161): Show | 164 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.160-23983C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119048796 | ||||||
| chr6:119048921
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.160-24108A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119048921 | ||||||
| chr6:119048936
|
A | T | 6 | a0001c0001t0001g0061a0001c0001t0001g0079a0001c0001t0001g0082others(3): Show | 6 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-24123T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119048936 | ||||||
| chr6:119049121
|
A | C | 6 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-24308T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119049121 | ||||||
| chr6:119049164
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.160-24351A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119049164 | ||||||
| chr6:119049166
|
C | G | 246 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(243): Show | 246 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.160-24353G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119049166 | ||||||
| chr6:119049222
|
C | T | 1 | a0001c0001t0001g0215 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.160-24409G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119049222 | ||||||
| chr6:119049246
|
G | A | 164 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0053others(161): Show | 164 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.160-24433C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119049246 | ||||||
| chr6:119049810
|
C | T | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0128 | 3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.160-24997G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119049810 | ||||||
| chr6:119049868
|
A | C | 3 | a0001c0001t0004g0003a0005c0009t0004g0005a0007c0010t0004g0004 | 3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.160-25055T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119049868 | ||||||
| chr6:119050203
|
A | G | 9 | a0001c0001t0001g0134a0001c0003t0001g0046a0001c0003t0001g0133others(6): Show | 9 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.160-25390T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050203 | ||||||
| chr6:119050378
|
G | C | 1 | a0001c0001t0001g0273 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.160-25565C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050378 | ||||||
| chr6:119050390
|
C | T | 1 | a0001c0001t0001g0182 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.160-25577G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050390 | ||||||
| chr6:119050415
|
A | G | 177 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0041others(174): Show | 177 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.160-25602T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050415 | ||||||
| chr6:119050438
|
T | C | 246 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(243): Show | 246 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.160-25625A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050438 | ||||||
| chr6:119050452
|
GT | G | 243 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(240): Show | 243 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.160-25640delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050452 | ||||||
| chr6:119050454
|
T | G | 5 | a0001c0001t0001g0081a0001c0001t0001g0205a0001c0001t0001g0243others(2): Show | 5 | HG01074.hp2 HG01109.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-25641A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050454 | ||||||
| chr6:119050462
|
T | A | 3 | a0001c0001t0004g0003a0005c0009t0004g0005a0007c0010t0004g0004 | 3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.160-25649A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050462 | ||||||
| chr6:119050504
|
T | TA | 169 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0053others(166): Show | 169 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.160-25692dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050504 | ||||||
| chr6:119050504
|
T | TAA | 8 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(5): Show | 8 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.160-25693_160-2569 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050504 | ||||||
| chr6:119050515
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.160-25702A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050515 | ||||||
| chr6:119050572
|
T | C | 2 | a0002c0002t0002g0121a0002c0002t0002g0129 | 2 | HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.160-25759A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050572 | ||||||
| chr6:119050663
|
G | T | 4 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0009others(1): Show | 4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-25850C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050663 | ||||||
| chr6:119050678
|
C | T | 4 | a0001c0001t0001g0130a0001c0001t0001g0277a0001c0001t0001g0278others(1): Show | 4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-25865G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050678 | ||||||
| chr6:119050698
|
G | A | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048 | 3 | HG01884.hp2 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.160-25885C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050698 | ||||||
| chr6:119050740
|
G | A | 2 | a0001c0001t0001g0193a0001c0001t0001g0258 | 2 | NA18995.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.160-25927C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050740 | ||||||
| chr6:119050811
|
C | CA | 50 | a0001c0001t0001g0047a0001c0001t0001g0098a0001c0001t0001g0099others(47): Show | 50 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.160-25999dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050811 | ||||||
| chr6:119050811
|
CA | C | 11 | a0001c0001t0001g0044a0001c0001t0001g0117a0001c0001t0001g0204others(8): Show | 11 | HG01099.hp2 HG01884.hp1 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.160-25999delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050811 | ||||||
| chr6:119050899
|
A | G | 239 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0041others(236): Show | 239 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.160-26086T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050899 | ||||||
| chr6:119051002
|
G | A | 162 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0053others(159): Show | 162 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.160-26189C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119051002 | ||||||
| chr6:119051116
|
AC | A | 49 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0144others(46): Show | 49 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.160-26304delG | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119051116 | ||||||
| chr6:119051118
|
T | A | 49 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0144others(46): Show | 49 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.160-26305A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119051118 | ||||||
| chr6:119051156
|
A | AAAAG | 245 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(242): Show | 245 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.160-26347_160-2634 others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119051156 | ||||||
| chr6:119051156
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.160-26343T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119051156 | ||||||
| chr6:119051182
|
A | G | 1 | a0008c0005t0001g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.160-26369T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119051182 | ||||||
| chr6:119051299
|
C | T | 7 | a0001c0001t0001g0130a0001c0001t0001g0277a0001c0001t0001g0278others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-26486G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119051299 | ||||||
| chr6:119051627
|
C | T | 13 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(10): Show | 13 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.159+26514G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119051627 | ||||||
| chr6:119051642
|
G | T | 4 | a0001c0001t0001g0130a0001c0001t0001g0277a0001c0001t0001g0278others(1): Show | 4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+26499C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119051642 | ||||||
| chr6:119051711
|
T | C | 7 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0138others(4): Show | 7 | HG02451.hp2 HG02895.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.159+26430A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119051711 | ||||||
| chr6:119051719
|
T | C | 3 | a0001c0001t0004g0003a0005c0009t0004g0005a0007c0010t0004g0004 | 3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.159+26422A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119051719 | ||||||
| chr6:119051756
|
G | A | 3 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153 | 3 | HG00609.hp2 HG02080.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.159+26385C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119051756 | ||||||
| chr6:119051849
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.159+26292C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119051849 | ||||||
| chr6:119051956
|
C | G | 1 | a0001c0001t0001g0205 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.159+26185G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119051956 | ||||||
| chr6:119052007
|
C | T | 165 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0041others(162): Show | 165 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.159+26134G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119052007 | ||||||
| chr6:119052034
|
C | T | 276 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(273): Show | 276 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(273): Show |
intron_variant | MODIFIER | c.159+26107G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119052034 | ||||||
| chr6:119052146
|
T | C | 3 | a0001c0001t0001g0182a0001c0001t0007g0282a0001c0001t0007g0283 | 3 | NA18986.hp1 NA19055.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.159+25995A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119052146 | ||||||
| chr6:119052413
|
C | T | 1 | a0001c0001t0004g0002 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.159+25728G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119052413 | ||||||
| chr6:119052667
|
C | G | 6 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.159+25474G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119052667 | ||||||
| chr6:119052669
|
A | T | 2 | a0002c0002t0002g0211a0002c0002t0002g0212 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.159+25472T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119052669 | ||||||
| chr6:119052746
|
C | G | 1 | a0001c0001t0001g0097 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.159+25395G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119052746 | ||||||
| chr6:119052747
|
T | G | 117 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0061others(114): Show | 117 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.159+25394A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119052747 | ||||||
| chr6:119052998
|
A | T | 46 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0144others(43): Show | 46 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.159+25143T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119052998 | ||||||
| chr6:119053493
|
A | G | 4 | a0001c0001t0002g0119a0001c0001t0002g0197a0001c0001t0002g0198others(1): Show | 4 | HG00642.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.159+24648T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119053493 | ||||||
| chr6:119053584
|
T | C | 106 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(103): Show | 106 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.159+24557A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119053584 | ||||||
| chr6:119053599
|
T | C | 1 | a0001c0001t0001g0102 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.159+24542A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119053599 | ||||||
| chr6:119053676
|
C | T | 13 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(10): Show | 13 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.159+24465G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119053676 | ||||||
| chr6:119053735
|
A | C | 1 | a0001c0001t0003g0016 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.159+24406T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119053735 | ||||||
| chr6:119053894
|
T | C | 3 | a0001c0001t0004g0003a0005c0009t0004g0005a0007c0010t0004g0004 | 3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.159+24247A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119053894 | ||||||
| chr6:119053966
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.159+24175C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119053966 | ||||||
| chr6:119053997
|
T | A | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+24144A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119053997 | ||||||
| chr6:119054085
|
GA | G | 271 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(268): Show | 271 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.159+24055delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119054085 | ||||||
| chr6:119054241
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.159+23900G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119054241 | ||||||
| chr6:119054392
|
G | C | 4 | a0001c0001t0001g0130a0001c0001t0001g0277a0001c0001t0001g0278others(1): Show | 4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+23749C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119054392 | ||||||
| chr6:119054705
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.159+23436G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119054705 | ||||||
| chr6:119054866
|
A | AT | 274 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(271): Show | 274 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(271): Show |
intron_variant | MODIFIER | c.159+23274dupA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119054866 | ||||||
| chr6:119054933
|
C | T | 6 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.159+23208G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119054933 | ||||||
| chr6:119055182
|
C | G | 159 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0047others(156): Show | 159 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.159+22959G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119055182 | ||||||
| chr6:119055368
|
A | C | 1 | a0001c0001t0001g0147 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.159+22773T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119055368 | ||||||
| chr6:119055547
|
A | T | 4 | a0001c0001t0001g0130a0001c0001t0001g0277a0001c0001t0001g0278others(1): Show | 4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+22594T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119055547 | ||||||
| chr6:119055711
|
T | C | 1 | a0001c0001t0001g0191 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.159+22430A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119055711 | ||||||
| chr6:119055736
|
C | T | 3 | a0001c0001t0002g0120a0001c0001t0002g0122a0001c0001t0002g0123 | 3 | HG02818.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.159+22405G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119055736 | ||||||
| chr6:119055931
|
T | TC | 21 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(18): Show | 21 | HG00642.hp2 HG00741.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.159+22209dupG | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119055931 | ||||||
| chr6:119056038
|
C | A | 4 | a0001c0001t0001g0080a0001c0001t0001g0089a0001c0001t0001g0090others(1): Show | 4 | HG01168.hp1 HG01192.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+22103G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119056038 | ||||||
| chr6:119056076
|
G | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.159+22065C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119056076 | ||||||
| chr6:119056211
|
T | C | 4 | a0001c0001t0001g0061a0001c0001t0001g0079a0001c0001t0001g0082others(1): Show | 4 | HG02145.hp1 HG02717.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+21930A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119056211 | ||||||
| chr6:119056334
|
T | C | 113 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0061others(110): Show | 113 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.159+21807A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119056334 | ||||||
| chr6:119056434
|
C | T | 2 | a0001c0001t0006g0032a0001c0001t0006g0033 | 2 | HG01243.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.159+21707G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119056434 | ||||||
| chr6:119056483
|
T | C | 43 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(40): Show | 43 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.159+21658A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119056483 | ||||||
| chr6:119056609
|
A | AAT | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048 | 3 | HG01884.hp2 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.159+21530_159+2153 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119056609 | ||||||
| chr6:119056904
|
G | A | 9 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(6): Show | 9 | HG01891.hp1 HG02257.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.159+21237C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119056904 | ||||||
| chr6:119056959
|
T | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+21182A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119056959 | ||||||
| chr6:119057417
|
A | C | 15 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(12): Show | 15 | HG00642.hp2 HG00741.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.159+20724T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119057417 | ||||||
| chr6:119057418
|
A | G | 3 | a0001c0001t0004g0003a0005c0009t0004g0005a0007c0010t0004g0004 | 3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.159+20723T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119057418 | ||||||
| chr6:119057521
|
C | T | 265 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(262): Show | 265 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.159+20620G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119057521 | ||||||
| chr6:119057692
|
G | A | 1 | a0008c0005t0001g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.159+20449C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119057692 | ||||||
| chr6:119057704
|
G | A | 1 | a0001c0001t0003g0024 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.159+20437C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119057704 | ||||||
| chr6:119057794
|
G | A | 4 | a0001c0001t0002g0119a0001c0001t0002g0197a0001c0001t0002g0198others(1): Show | 4 | HG00642.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.159+20347C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119057794 | ||||||
| chr6:119057843
|
GT | G | 245 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(242): Show | 245 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.159+20297delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119057843 | ||||||
| chr6:119057895
|
A | G | 2 | a0001c0001t0006g0032a0001c0001t0006g0033 | 2 | HG01243.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.159+20246T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119057895 | ||||||
| chr6:119057939
|
T | C | 1 | a0001c0001t0003g0014 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.159+20202A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119057939 | ||||||
| chr6:119057953
|
G | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0187a0001c0001t0001g0246others(1): Show | 4 | HG02080.hp2 NA18954.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+20188C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119057953 | ||||||
| chr6:119057972
|
TA | T | 154 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(151): Show | 154 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.159+20168delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119057972 | ||||||
| chr6:119057973
|
A | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0126 | 3 | HG02970.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.159+20168T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119057973 | ||||||
| chr6:119058012
|
G | T | 1 | a0002c0002t0002g0208 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.159+20129C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119058012 | ||||||
| chr6:119058052
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.159+20089T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119058052 | ||||||
| chr6:119058154
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.159+19987T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119058154 | ||||||
| chr6:119058175
|
C | CT | 30 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(27): Show | 30 | HG00423.hp2 HG00735.hp1 HG01975.hp1 others(27): Show |
intron_variant | MODIFIER | c.159+19965dupA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119058175 | ||||||
| chr6:119058175
|
CT | C | 74 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(71): Show | 74 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.159+19965delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119058175 | ||||||
| chr6:119058349
|
C | T | 46 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0144others(43): Show | 46 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.159+19792G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119058349 | ||||||
| chr6:119058479
|
A | C | 1 | a0001c0001t0001g0080 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.159+19662T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119058479 | ||||||
| chr6:119058594
|
C | G | 15 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(12): Show | 15 | HG00642.hp2 HG00741.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.159+19547G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119058594 | ||||||
| chr6:119058889
|
G | GCTTTATT others(1): Show |
3 | a0001c0001t0004g0003a0005c0009t0004g0005a0007c0010t0004g0004 | 3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.159+19251_159+1925 others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119058889 | ||||||
| chr6:119059029
|
C | T | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+19112G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119059029 | ||||||
| chr6:119059228
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.159+18913G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119059228 | ||||||
| chr6:119059249
|
G | A | 15 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(12): Show | 15 | HG00642.hp2 HG00741.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.159+18892C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119059249 | ||||||
| chr6:119059571
|
G | T | 1 | a0003c0004t0001g0093 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.159+18570C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119059571 | ||||||
| chr6:119059597
|
T | G | 2 | a0001c0001t0001g0063a0001c0001t0001g0071 | 2 | NA18980.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.159+18544A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119059597 | ||||||
| chr6:119059720
|
T | C | 19 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(16): Show | 19 | HG00642.hp2 HG00741.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.159+18421A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119059720 | ||||||
| chr6:119059921
|
T | C | 3 | a0001c0001t0004g0003a0005c0009t0004g0005a0007c0010t0004g0004 | 3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.159+18220A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119059921 | ||||||
| chr6:119059937
|
T | C | 4 | a0001c0001t0001g0130a0001c0001t0001g0277a0001c0001t0001g0278others(1): Show | 4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+18204A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119059937 | ||||||
| chr6:119060173
|
G | A | 9 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0002g0060others(6): Show | 9 | HG00741.hp1 HG01884.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.159+17968C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119060173 | ||||||
| chr6:119060297
|
T | A | 3 | a0001c0001t0001g0186a0001c0001t0001g0249a0001c0001t0001g0250 | 3 | HG00408.hp1 NA18952.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.159+17844A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119060297 | ||||||
| chr6:119060337
|
T | C | 244 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.159+17804A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119060337 | ||||||
| chr6:119060540
|
G | A | 1 | a0003c0004t0001g0093 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.159+17601C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119060540 | ||||||
| chr6:119060855
|
CCT | C | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0128 | 3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.159+17284_159+1728 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119060855 | ||||||
| chr6:119060882
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.159+17259C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119060882 | ||||||
| chr6:119060936
|
T | C | 106 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0132others(103): Show | 106 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.159+17205A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119060936 | ||||||
| chr6:119061186
|
C | T | 105 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0148others(102): Show | 105 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.159+16955G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061186 | ||||||
| chr6:119061299
|
T | C | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.159+16842A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061299 | ||||||
| chr6:119061335
|
G | C | 1 | a0002c0002t0002g0208 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.159+16806C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061335 | ||||||
| chr6:119061337
|
G | A | 1 | a0008c0005t0001g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.159+16804C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061337 | ||||||
| chr6:119061485
|
A | G | 1 | a0002c0002t0002g0268 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.159+16656T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061485 | ||||||
| chr6:119061531
|
C | CT | 24 | a0001c0001t0001g0036a0001c0001t0001g0041a0001c0001t0001g0043others(21): Show | 24 | HG00597.hp1 HG00597.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.159+16609dupA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061531 | ||||||
| chr6:119061531
|
C | CTT | 58 | a0001c0001t0001g0042a0001c0001t0001g0063a0001c0001t0001g0065others(55): Show | 58 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.159+16608_159+1660 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061531 | ||||||
| chr6:119061531
|
C | CTTT | 16 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0064others(13): Show | 16 | HG00741.hp2 HG01978.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.159+16607_159+1660 others(7): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061531 | ||||||
| chr6:119061531
|
CT | C | 42 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(39): Show | 42 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.159+16609delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061531 | ||||||
| chr6:119061532
|
T | C | 4 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0009others(1): Show | 4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+16609A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061532 | ||||||
| chr6:119061583
|
GC | G | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0128 | 3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.159+16557delG | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061583 | ||||||
| chr6:119061873
|
G | A | 13 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(10): Show | 13 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.159+16268C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061873 | ||||||
| chr6:119061875
|
A | G | 4 | a0001c0001t0001g0130a0001c0001t0001g0277a0001c0001t0001g0278others(1): Show | 4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+16266T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061875 | ||||||
| chr6:119061915
|
AGAAAAAA others(4): Show |
A | 1 | a0001c0001t0001g0036 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.159+16215_159+1622 others(15): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061915 | ||||||
| chr6:119061934
|
G | A | 5 | a0003c0004t0001g0091a0003c0004t0001g0092a0003c0004t0001g0093others(2): Show | 5 | HG00738.hp2 HG01433.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.159+16207C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061934 | ||||||
| chr6:119061989
|
G | C | 4 | a0001c0001t0001g0130a0001c0001t0001g0277a0001c0001t0001g0278others(1): Show | 4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+16152C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061989 | ||||||
| chr6:119062025
|
T | C | 46 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0144others(43): Show | 46 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.159+16116A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119062025 | ||||||
| chr6:119062291
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.159+15850G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119062291 | ||||||
| chr6:119062394
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.159+15747A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119062394 | ||||||
| chr6:119062552
|
G | A | 13 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(10): Show | 13 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.159+15589C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119062552 | ||||||
| chr6:119062572
|
T | C | 13 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(10): Show | 13 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.159+15569A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119062572 | ||||||
| chr6:119062614
|
C | T | 46 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0144others(43): Show | 46 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.159+15527G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119062614 | ||||||
| chr6:119062655
|
A | G | 1 | a0001c0001t0004g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.159+15486T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119062655 | ||||||
| chr6:119062710
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.159+15431A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119062710 | ||||||
| chr6:119062817
|
G | C | 101 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0148others(98): Show | 101 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.159+15324C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119062817 | ||||||
| chr6:119063523
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.159+14618A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119063523 | ||||||
| chr6:119063543
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.159+14598C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119063543 | ||||||
| chr6:119063711
|
G | A | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0128 | 3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.159+14430C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119063711 | ||||||
| chr6:119063757
|
T | TA | 11 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(8): Show | 11 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.159+14383dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119063757 | ||||||
| chr6:119063891
|
C | T | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+14250G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119063891 | ||||||
| chr6:119063938
|
T | C | 1 | a0001c0001t0005g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.159+14203A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119063938 | ||||||
| chr6:119063963
|
T | C | 2 | a0001c0001t0001g0254a0001c0001t0001g0274 | 2 | NA19056.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.159+14178A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119063963 | ||||||
| chr6:119064013
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.159+14128A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119064013 | ||||||
| chr6:119064069
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.159+14072A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119064069 | ||||||
| chr6:119064303
|
G | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | NA18959.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.159+13838C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119064303 | ||||||
| chr6:119064351
|
T | C | 1 | a0001c0001t0001g0255 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.159+13790A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119064351 | ||||||
| chr6:119064421
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.159+13720G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119064421 | ||||||
| chr6:119064879
|
G | T | 46 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0144others(43): Show | 46 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.159+13262C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119064879 | ||||||
| chr6:119064908
|
C | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0131a0001c0001t0004g0006others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+13233G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119064908 | ||||||
| chr6:119065011
|
T | G | 4 | a0001c0001t0001g0130a0001c0001t0001g0277a0001c0001t0001g0278others(1): Show | 4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+13130A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119065011 | ||||||
| chr6:119065019
|
C | A | 106 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0132others(103): Show | 106 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.159+13122G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119065019 | ||||||
| chr6:119065114
|
T | G | 1 | a0001c0001t0001g0196 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.159+13027A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119065114 | ||||||
| chr6:119065138
|
C | T | 110 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(107): Show | 110 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.159+13003G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119065138 | ||||||
| chr6:119065175
|
G | A | 13 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(10): Show | 13 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.159+12966C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119065175 | ||||||
| chr6:119065345
|
A | G | 1 | a0001c0001t0001g0200 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.159+12796T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119065345 | ||||||
| chr6:119065563
|
T | C | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0128 | 3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.159+12578A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119065563 | ||||||
| chr6:119065623
|
C | T | 3 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153 | 3 | HG00609.hp2 HG02080.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.159+12518G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119065623 | ||||||
| chr6:119065661
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.159+12480G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119065661 | ||||||
| chr6:119065703
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.159+12438C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119065703 | ||||||
| chr6:119065809
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.159+12332G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119065809 | ||||||
| chr6:119065900
|
C | T | 2 | a0001c0001t0006g0032a0001c0001t0006g0033 | 2 | HG01243.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.159+12241G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119065900 | ||||||
| chr6:119065991
|
C | A | 13 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(10): Show | 13 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.159+12150G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119065991 | ||||||
| chr6:119066447
|
G | C | 54 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0099others(51): Show | 54 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.159+11694C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119066447 | ||||||
| chr6:119066582
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.159+11559C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119066582 | ||||||
| chr6:119066626
|
C | G | 3 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199 | 3 | HG00642.hp2 HG02486.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.159+11515G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119066626 | ||||||
| chr6:119066879
|
C | A | 1 | a0002c0002t0002g0264 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.159+11262G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119066879 | ||||||
| chr6:119067149
|
A | G | 8 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0194others(5): Show | 8 | HG00738.hp1 HG01358.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+10992T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119067149 | ||||||
| chr6:119067304
|
T | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.159+10837A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119067304 | ||||||
| chr6:119067304
|
T | C | 5 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(2): Show | 5 | HG02622.hp2 HG03209.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.159+10837A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119067304 | ||||||
| chr6:119067313
|
G | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.159+10828C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119067313 | ||||||
| chr6:119067326
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.159+10815T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119067326 | ||||||
| chr6:119067394
|
T | C | 4 | a0001c0001t0001g0175a0001c0001t0001g0177a0001c0001t0001g0181others(1): Show | 4 | HG00408.hp2 NA18947.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+10747A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119067394 | ||||||
| chr6:119067707
|
T | C | 1 | a0001c0001t0001g0190 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.159+10434A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119067707 | ||||||
| chr6:119067723
|
C | T | 17 | a0001c0001t0001g0132a0001c0001t0001g0134a0001c0001t0001g0137others(14): Show | 17 | HG00639.hp1 HG01884.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.159+10418G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119067723 | ||||||
| chr6:119067733
|
G | C | 1 | a0004c0008t0001g0062 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.159+10408C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119067733 | ||||||
| chr6:119067783
|
C | T | 5 | a0001c0001t0004g0002a0001c0001t0004g0003a0001c0001t0004g0006others(2): Show | 5 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+10358G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119067783 | ||||||
| chr6:119067987
|
TAAAC | T | 8 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(5): Show | 8 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+10150_159+1015 others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119067987 | ||||||
| chr6:119068030
|
TG | T | 3 | a0001c0001t0005g0029a0001c0003t0005g0030a0001c0006t0005g0028 | 3 | HG01884.hp1 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.159+10110delC | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119068030 | ||||||
| chr6:119068047
|
GT | G | 63 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(60): Show | 63 | HG00408.hp2 HG00609.hp2 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.159+10093delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119068047 | ||||||
| chr6:119068047
|
GTT | G | 200 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(197): Show | 200 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.159+10092_159+1009 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119068047 | ||||||
| chr6:119068108
|
G | A | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0128 | 3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.159+10033C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119068108 | ||||||
| chr6:119068111
|
A | G | 45 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(42): Show | 45 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.159+10030T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119068111 | ||||||
| chr6:119068181
|
G | C | 2 | a0001c0001t0001g0098a0001c0001t0010g0284 | 2 | HG02615.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.159+9960C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119068181 | ||||||
| chr6:119068344
|
T | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+9797A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119068344 | ||||||
| chr6:119068405
|
G | C | 1 | a0001c0001t0001g0099 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.159+9736C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119068405 | ||||||
| chr6:119068474
|
T | C | 1 | a0001c0001t0001g0177 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.159+9667A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119068474 | ||||||
| chr6:119068493
|
T | C | 13 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(10): Show | 13 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.159+9648A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119068493 | ||||||
| chr6:119068845
|
AG | A | 57 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(54): Show | 57 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.159+9295delC | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119068845 | ||||||
| chr6:119068895
|
C | T | 1 | a0001c0001t0010g0284 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.159+9246G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119068895 | ||||||
| chr6:119068942
|
T | C | 10 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(7): Show | 10 | HG00423.hp2 HG00735.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.159+9199A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119068942 | ||||||
| chr6:119069098
|
G | C | 1 | a0001c0001t0010g0284 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.159+9043C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119069098 | ||||||
| chr6:119069296
|
A | AAC | 15 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0003g0012others(12): Show | 15 | HG01081.hp1 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.159+8843_159+8844d others(4): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119069296 | ||||||
| chr6:119069486
|
G | A | 11 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(8): Show | 11 | HG00423.hp2 HG00735.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.159+8655C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119069486 | ||||||
| chr6:119069550
|
C | T | 12 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0130others(9): Show | 12 | HG00741.hp1 HG02055.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.159+8591G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119069550 | ||||||
| chr6:119070016
|
A | G | 280 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(277): Show | 280 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.159+8125T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119070016 | ||||||
| chr6:119070041
|
A | G | 57 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(54): Show | 57 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.159+8100T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119070041 | ||||||
| chr6:119070300
|
C | T | 1 | a0001c0001t0001g0191 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.159+7841G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119070300 | ||||||
| chr6:119070558
|
T | C | 1 | a0001c0003t0005g0030 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.159+7583A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119070558 | ||||||
| chr6:119070605
|
TTTTC | T | 45 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(42): Show | 45 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.159+7532_159+7535d others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119070605 | ||||||
| chr6:119070784
|
G | C | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0128 | 3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.159+7357C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119070784 | ||||||
| chr6:119070844
|
A | G | 1 | a0001c0001t0002g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.159+7297T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119070844 | ||||||
| chr6:119070910
|
T | TA | 57 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(54): Show | 57 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.159+7230dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119070910 | ||||||
| chr6:119070910
|
TA | T | 44 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(41): Show | 44 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.159+7230delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119070910 | ||||||
| chr6:119070938
|
A | T | 3 | a0001c0001t0001g0061a0001c0001t0002g0060a0004c0008t0001g0062 | 3 | HG01891.hp2 HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.159+7203T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119070938 | ||||||
| chr6:119071189
|
T | C | 41 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.159+6952A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119071189 | ||||||
| chr6:119071210
|
G | A | 1 | a0002c0002t0002g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.159+6931C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119071210 | ||||||
| chr6:119071286
|
T | C | 45 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(42): Show | 45 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.159+6855A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119071286 | ||||||
| chr6:119071296
|
A | T | 1 | a0001c0001t0001g0073 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.159+6845T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119071296 | ||||||
| chr6:119071402
|
C | T | 103 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(100): Show | 103 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.159+6739G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119071402 | ||||||
| chr6:119071752
|
T | C | 5 | a0001c0001t0004g0002a0001c0001t0004g0003a0001c0001t0004g0006others(2): Show | 5 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+6389A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119071752 | ||||||
| chr6:119071778
|
A | G | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+6363T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119071778 | ||||||
| chr6:119071860
|
C | CT | 126 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0041others(123): Show | 126 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.159+6280dupA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119071860 | ||||||
| chr6:119071860
|
C | CTT | 10 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(7): Show | 10 | HG00597.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+6279_159+6280d others(4): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119071860 | ||||||
| chr6:119071860
|
CT | C | 11 | a0001c0001t0001g0048a0001c0001t0001g0100a0001c0001t0001g0126others(8): Show | 11 | HG00408.hp2 HG01168.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.159+6280delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119071860 | ||||||
| chr6:119071868
|
T | C | 1 | a0002c0002t0002g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.159+6273A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119071868 | ||||||
| chr6:119071912
|
C | A | 1 | a0001c0001t0001g0102 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.159+6229G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119071912 | ||||||
| chr6:119072008
|
C | T | 41 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.159+6133G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119072008 | ||||||
| chr6:119072012
|
C | T | 4 | a0001c0001t0001g0130a0001c0001t0001g0277a0001c0001t0001g0278others(1): Show | 4 | HG00741.hp1 HG02055.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+6129G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119072012 | ||||||
| chr6:119072290
|
C | T | 3 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043 | 3 | HG02257.hp2 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.159+5851G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119072290 | ||||||
| chr6:119072300
|
T | C | 1 | a0001c0001t0001g0273 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.159+5841A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119072300 | ||||||
| chr6:119072571
|
T | G | 10 | a0001c0001t0001g0132a0001c0001t0001g0134a0001c0001t0001g0135others(7): Show | 10 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+5570A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119072571 | ||||||
| chr6:119072638
|
ATGAC | A | 3 | a0001c0001t0001g0130a0001c0001t0001g0277a0001c0001t0001g0278 | 3 | HG02055.hp2 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.159+5499_159+5502d others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119072638 | ||||||
| chr6:119072672
|
G | C | 15 | a0001c0001t0001g0132a0001c0001t0001g0134a0001c0001t0001g0135others(12): Show | 15 | HG00639.hp1 HG02109.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.159+5469C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119072672 | ||||||
| chr6:119072883
|
A | ATACAATT others(308): Show |
2 | a0001c0003t0001g0139a0001c0003t0001g0140 | 2 | HG02451.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.159+5257_159+5258i others(317): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119072883 | ||||||
| chr6:119072883
|
A | ATACAATT others(328): Show |
3 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0003t0001g0136 | 3 | HG02723.hp1 HG03041.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.159+5257_159+5258i others(337): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119072883 | ||||||
| chr6:119072883
|
A | ATACAATT others(329): Show |
4 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0003t0001g0133others(1): Show | 4 | HG00639.hp1 HG02559.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+5257_159+5258i others(338): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119072883 | ||||||
| chr6:119072883
|
A | ATACAATT others(330): Show |
4 | a0001c0001t0001g0132a0001c0001t0004g0009a0001c0001t0004g0010others(1): Show | 4 | HG02486.hp1 HG02809.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.159+5257_159+5258i others(339): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119072883 | ||||||
| chr6:119072883
|
A | ATACAATT others(331): Show |
2 | a0001c0001t0004g0007a0001c0001t0004g0008 | 2 | HG02109.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.159+5257_159+5258i others(340): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119072883 | ||||||
| chr6:119072892
|
C | T | 22 | a0001c0001t0001g0132a0001c0001t0001g0134a0001c0001t0001g0135others(19): Show | 22 | HG00639.hp1 HG01884.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.159+5249G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119072892 | ||||||
| chr6:119072971
|
C | T | 11 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(8): Show | 11 | HG00423.hp2 HG00735.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.159+5170G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119072971 | ||||||
| chr6:119073053
|
C | A | 1 | a0001c0001t0001g0131 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.159+5088G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119073053 | ||||||
| chr6:119073070
|
AAAAC | A | 3 | a0001c0001t0001g0182a0001c0001t0007g0282a0001c0001t0007g0283 | 3 | NA18986.hp1 NA19055.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.159+5067_159+5070d others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119073070 | ||||||
| chr6:119073448
|
A | T | 1 | a0001c0001t0001g0186 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.159+4693T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119073448 | ||||||
| chr6:119073619
|
G | T | 1 | a0001c0003t0001g0142 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.159+4522C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119073619 | ||||||
| chr6:119073639
|
G | T | 1 | a0001c0001t0001g0145 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.159+4502C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119073639 | ||||||
| chr6:119073717
|
G | A | 15 | a0001c0001t0001g0132a0001c0001t0001g0134a0001c0001t0001g0135others(12): Show | 15 | HG00639.hp1 HG02109.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.159+4424C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119073717 | ||||||
| chr6:119073802
|
G | T | 1 | a0002c0002t0002g0185 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.159+4339C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119073802 | ||||||
| chr6:119073831
|
T | C | 5 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0009others(2): Show | 5 | HG02109.hp1 HG02486.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.159+4310A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119073831 | ||||||
| chr6:119074043
|
T | C | 22 | a0001c0001t0001g0132a0001c0001t0001g0134a0001c0001t0001g0135others(19): Show | 22 | HG00639.hp1 HG01884.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.159+4098A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119074043 | ||||||
| chr6:119074447
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.159+3694T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119074447 | ||||||
| chr6:119074549
|
C | A | 1 | a0003c0004t0001g0141 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.159+3592G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119074549 | ||||||
| chr6:119074603
|
C | CA | 45 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(42): Show | 45 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.159+3537dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119074603 | ||||||
| chr6:119074701
|
T | C | 1 | a0001c0003t0001g0142 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.159+3440A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119074701 | ||||||
| chr6:119074765
|
T | A | 1 | a0002c0002t0002g0143 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.159+3376A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119074765 | ||||||
| chr6:119074769
|
A | G | 1 | a0001c0001t0001g0144 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.159+3372T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119074769 | ||||||
| chr6:119074950
|
C | T | 5 | a0001c0001t0004g0002a0001c0001t0004g0003a0001c0001t0004g0006others(2): Show | 5 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+3191G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119074950 | ||||||
| chr6:119075034
|
A | G | 66 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(63): Show | 66 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.159+3107T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119075034 | ||||||
| chr6:119075046
|
T | C | 5 | a0001c0001t0004g0002a0001c0001t0004g0003a0001c0001t0004g0006others(2): Show | 5 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+3095A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119075046 | ||||||
| chr6:119075101
|
T | C | 45 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(42): Show | 45 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.159+3040A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119075101 | ||||||
| chr6:119075172
|
G | A | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.159+2969C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119075172 | ||||||
| chr6:119075277
|
C | A | 1 | a0001c0001t0001g0274 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.159+2864G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119075277 | ||||||
| chr6:119075344
|
T | C | 5 | a0001c0001t0004g0002a0001c0001t0004g0003a0001c0001t0004g0006others(2): Show | 5 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+2797A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119075344 | ||||||
| chr6:119075417
|
A | G | 7 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(4): Show | 7 | HG00140.hp2 HG00642.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.159+2724T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119075417 | ||||||
| chr6:119075458
|
G | T | 13 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(10): Show | 13 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.159+2683C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119075458 | ||||||
| chr6:119075494
|
T | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+2647A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119075494 | ||||||
| chr6:119075563
|
G | A | 8 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(5): Show | 8 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+2578C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119075563 | ||||||
| chr6:119075652
|
T | C | 2 | a0001c0001t0008g0285a0001c0001t0008g0286 | 2 | NA18612.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.159+2489A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119075652 | ||||||
| chr6:119075764
|
A | G | 3 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043 | 3 | HG02257.hp2 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.159+2377T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119075764 | ||||||
| chr6:119075934
|
T | G | 1 | a0001c0001t0001g0183 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.159+2207A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119075934 | ||||||
| chr6:119076052
|
C | T | 15 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0003g0012others(12): Show | 15 | HG01081.hp1 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.159+2089G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119076052 | ||||||
| chr6:119076080
|
T | C | 1 | a0001c0001t0010g0284 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.159+2061A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119076080 | ||||||
| chr6:119076183
|
T | G | 1 | a0001c0001t0001g0184 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.159+1958A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119076183 | ||||||
| chr6:119076210
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.159+1931C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119076210 | ||||||
| chr6:119076695
|
T | C | 95 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0186others(92): Show | 95 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.159+1446A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119076695 | ||||||
| chr6:119076748
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.159+1393C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119076748 | ||||||
| chr6:119076839
|
T | C | 282 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(279): Show | 282 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(279): Show |
intron_variant | MODIFIER | c.159+1302A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119076839 | ||||||
| chr6:119077131
|
C | T | 13 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(10): Show | 13 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.159+1010G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119077131 | ||||||
| chr6:119077198
|
C | T | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+943G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119077198 | ||||||
| chr6:119077214
|
A | G | 1 | a0008c0005t0001g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.159+927T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119077214 | ||||||
| chr6:119077294
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.159+847G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119077294 | ||||||
| chr6:119077501
|
A | G | 5 | a0001c0001t0004g0002a0001c0001t0004g0003a0001c0001t0004g0006others(2): Show | 5 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+640T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119077501 | ||||||
| chr6:119077582
|
T | C | 2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.159+559A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119077582 | ||||||
| chr6:119077877
|
T | C | 15 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0003g0012others(12): Show | 15 | HG01081.hp1 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.159+264A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119077877 | ||||||
| chr6:119077905
|
G | C | 1 | a0001c0001t0001g0281 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.159+236C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119077905 | ||||||
| chr6:119077933
|
C | A | 7 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(4): Show | 7 | HG01884.hp1 HG02451.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.159+208G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119077933 | ||||||
| chr6:119078105
|
C | G | 1 | a0001c0001t0001g0035 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.159+36G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119078105 |