| geneid | 10522 |
|---|---|
| ensemblid | ENSG00000177030.19 |
| hgncid | 14677 |
| symbol | DEAF1 |
| name | DEAF1 transcription factor |
| refseq_nuc | NM_021008.4 |
| refseq_prot | NP_066288.2 |
| ensembl_nuc | ENST00000382409.4 |
| ensembl_prot | ENSP00000371846.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 644233 |
| end | 695222 |
| strand | - |
| ver | v1.2 |
| region | chr11:644233-695222 |
| region5000 | chr11:639233-700222 |
| regionname0 | DEAF1_chr11_644233_695222 |
| regionname5000 | DEAF1_chr11_639233_700222 |
| 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 | 1/0 | 565 | 335 | 89 | 67 | 129 | 7 | 42 | 92 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0002 | 0/0 | 565 | 6 | 0 | 0 | 6 | 0 | 0 | 5 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0003 | 0/0 | 565 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0004 | 0/0 | 565 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0005 | 0/0 | 565 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| 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 | 1/0 | 1698 | 169 | 28 | 41 | 71 | 5 | 23 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| c0002 | 0/0 | 1698 | 91 | 47 | 11 | 22 | 1 | 10 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| c0003 | 0/0 | 1698 | 53 | 7 | 11 | 30 | 1 | 4 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| c0004 | 0/0 | 1698 | 10 | 0 | 3 | 2 | 0 | 5 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| c0005 | 0/0 | 1698 | 6 | 0 | 0 | 6 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| c0006 | 0/0 | 1698 | 5 | 5 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| c0007 | 0/0 | 1698 | 2 | 0 | 1 | 0 | 1 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| c0008 | 0/0 | 1698 | 2 | 2 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| c0009 | 0/0 | 1698 | 2 | 0 | 0 | 2 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| c0010 | 0/0 | 1698 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| c0011 | 0/0 | 1698 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| c0012 | 0/0 | 1698 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| c0013 | 0/0 | 1698 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| c0014 | 0/0 | 1698 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| 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 | 1/0 | 493 | 336 | 87 | 66 | 133 | 8 | 41 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| t0002 | 0/0 | 493 | 3 | 0 | 0 | 3 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| t0003 | 0/0 | 493 | 2 | 0 | 1 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| t0004 | 0/0 | 493 | 2 | 2 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| t0005 | 0/0 | 493 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| t0006 | 0/0 | 493 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| 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 | 2 | 0 | 0 | 2 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0281 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| 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 | 1/0 | 1698 | 169 | 28 | 41 | 71 | 5 | 23 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0001c0002 | 0/0 | 1698 | 91 | 47 | 11 | 22 | 1 | 10 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0001c0003 | 0/0 | 1698 | 53 | 7 | 11 | 30 | 1 | 4 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0001c0004 | 0/0 | 1698 | 10 | 0 | 3 | 2 | 0 | 5 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0001c0006 | 0/0 | 1698 | 5 | 5 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0001c0008 | 0/0 | 1698 | 2 | 2 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0001c0009 | 0/0 | 1698 | 2 | 0 | 0 | 2 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0001c0011 | 0/0 | 1698 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0001c0013 | 0/0 | 1698 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0001c0014 | 0/0 | 1698 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0002c0005 | 0/0 | 1698 | 6 | 0 | 0 | 6 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0003c0007 | 0/0 | 1698 | 2 | 0 | 1 | 0 | 1 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0004c0012 | 0/0 | 1698 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0005c0010 | 0/0 | 1698 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2190 | 160 | 25 | 39 | 68 | 5 | 22 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0001c0001t0002 | 0/0 | 2190 | 3 | 0 | 0 | 3 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0001c0001t0003 | 0/0 | 2190 | 2 | 0 | 1 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0001c0001t0004 | 0/0 | 2190 | 2 | 2 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0001c0001t0005 | 0/0 | 2190 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0001c0001t0006 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0001c0002t0001 | 0/0 | 2190 | 91 | 47 | 11 | 22 | 1 | 10 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0001c0003t0001 | 0/0 | 2190 | 53 | 7 | 11 | 30 | 1 | 4 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0001c0004t0001 | 0/0 | 2190 | 10 | 0 | 3 | 2 | 0 | 5 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0001c0006t0001 | 0/0 | 2190 | 5 | 5 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0001c0008t0001 | 0/0 | 2190 | 2 | 2 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0001c0009t0001 | 0/0 | 2190 | 2 | 0 | 0 | 2 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0001c0011t0001 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0001c0013t0001 | 0/0 | 2190 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0001c0014t0001 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0002c0005t0001 | 0/0 | 2190 | 6 | 0 | 0 | 6 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0003c0007t0001 | 0/0 | 2190 | 2 | 0 | 1 | 0 | 1 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0004c0012t0001 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| a0005c0010t0001 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | copy fasta | chr11 | 639233 | 700222 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0281 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0005g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0004t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0004t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0004t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0004t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0004t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0004t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0004t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0004t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0004t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0004t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0006t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0006t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0006t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0006t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0006t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0008t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0009t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0009t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0011t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0013t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0014t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0002c0005t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0002c0005t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0002c0005t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0002c0005t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0002c0005t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0002c0005t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0003c0007t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0003c0007t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0004c0012t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0005c0010t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0149 | EUR | GBR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | GBR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | FIN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0247 | EUR | FIN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0309 | EUR | FIN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | FIN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00423 | hp1 | a0001 | c0003 | t0001 | g0148 | EAS | CHS | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00438 | hp2 | a0001 | c0003 | t0001 | g0190 | EAS | CHS | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00558 | hp1 | a0001 | c0003 | t0001 | g0178 | EAS | CHS | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00597 | hp1 | a0002 | c0005 | t0001 | g0264 | EAS | CHS | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | CHS | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0211 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0207 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00673 | hp1 | a0001 | c0003 | t0001 | g0152 | EAS | CHS | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00673 | hp2 | a0001 | c0003 | t0001 | g0151 | EAS | CHS | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00735 | hp1 | a0001 | c0013 | t0001 | g0078 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0139 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01069 | hp2 | a0001 | c0003 | t0001 | g0310 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01070 | hp1 | a0001 | c0003 | t0001 | g0181 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01074 | hp1 | a0001 | c0003 | t0001 | g0161 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01106 | hp1 | a0003 | c0007 | t0001 | g0040 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01106 | hp2 | a0001 | c0004 | t0001 | g0022 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0328 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0203 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0300 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01255 | hp1 | a0001 | c0003 | t0001 | g0164 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0215 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0216 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01258 | hp2 | a0001 | c0003 | t0001 | g0188 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0157 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0238 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01346 | hp2 | a0001 | c0003 | t0001 | g0145 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01358 | hp1 | a0001 | c0001 | t0005 | g0290 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0213 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0248 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0214 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01496 | hp2 | a0001 | c0004 | t0001 | g0020 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | IBS | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01515 | hp2 | a0003 | c0007 | t0001 | g0039 | EUR | IBS | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01943 | hp1 | a0001 | c0003 | t0001 | g0056 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02004 | hp2 | a0001 | c0004 | t0001 | g0021 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02015 | hp1 | a0001 | c0003 | t0001 | g0173 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02040 | hp1 | a0001 | c0004 | t0001 | g0013 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0286 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0256 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02071 | hp2 | a0001 | c0003 | t0001 | g0156 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0227 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02074 | hp2 | a0001 | c0003 | t0001 | g0179 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02083 | hp2 | a0001 | c0004 | t0001 | g0014 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0228 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02132 | hp2 | a0001 | c0014 | t0001 | g0147 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0255 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0242 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02155 | hp1 | a0001 | c0003 | t0001 | g0180 | EAS | CDX | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | CDX | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02165 | hp1 | a0001 | c0011 | t0001 | g0085 | EAS | CDX | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | CDX | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02258 | hp1 | a0001 | c0006 | t0001 | g0105 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02273 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02293 | hp2 | a0001 | c0003 | t0001 | g0155 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02451 | hp1 | a0001 | c0006 | t0001 | g0019 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0249 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0329 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0187 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0194 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02615 | hp2 | a0004 | c0012 | t0001 | g0270 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0197 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0258 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0327 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0265 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0252 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0236 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0170 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0199 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0339 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02735 | hp2 | a0001 | c0004 | t0001 | g0028 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0266 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0332 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0195 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0259 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0169 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0257 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0330 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0171 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0334 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0287 | AFR | ESN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0232 | AFR | ESN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ESN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0301 | AFR | ESN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0219 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03017 | hp2 | a0001 | c0004 | t0001 | g0024 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0239 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0245 | AFR | MSL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0335 | AFR | MSL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0240 | AFR | ESN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0241 | AFR | ESN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0196 | AFR | ESN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | ESN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0304 | AFR | ESN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03195 | hp2 | a0001 | c0006 | t0001 | g0117 | AFR | ESN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0198 | AFR | MSL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03209 | hp2 | a0001 | c0008 | t0001 | g0003 | AFR | MSL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03225 | hp2 | a0001 | c0006 | t0001 | g0080 | AFR | MSL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0231 | AFR | MSL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03453 | hp2 | a0001 | c0008 | t0001 | g0003 | AFR | MSL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0331 | AFR | MSL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0271 | AFR | MSL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03490 | hp1 | a0001 | c0003 | t0001 | g0189 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0308 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0311 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0233 | AFR | ESN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0251 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0237 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0274 | AFR | MSL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0218 | SAS | STU | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | STU | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0140 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03710 | hp2 | a0001 | c0004 | t0001 | g0025 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03831 | hp2 | a0001 | c0003 | t0001 | g0146 | SAS | BEB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0210 | SAS | BEB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | STU | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0246 | SAS | STU | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | STU | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0182 | SAS | STU | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | STU | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0212 | SAS | STU | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG04228 | hp1 | a0001 | c0004 | t0001 | g0027 | SAS | STU | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | STU | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0244 | AFR | YRI | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0201 | AFR | YRI | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | CHB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18747 | hp1 | a0001 | c0003 | t0001 | g0165 | EAS | CHB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | CHB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | YRI | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0243 | AFR | YRI | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18947 | hp2 | a0001 | c0003 | t0001 | g0163 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18950 | hp2 | a0001 | c0003 | t0001 | g0144 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18952 | hp1 | a0001 | c0003 | t0001 | g0166 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18954 | hp1 | a0001 | c0003 | t0001 | g0177 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18962 | hp1 | a0001 | c0009 | t0001 | g0063 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18962 | hp2 | a0001 | c0003 | t0001 | g0183 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18964 | hp1 | a0001 | c0003 | t0001 | g0142 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18971 | hp1 | a0001 | c0003 | t0001 | g0176 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18971 | hp2 | a0001 | c0003 | t0001 | g0032 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18978 | hp1 | a0002 | c0005 | t0001 | g0260 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18978 | hp2 | a0001 | c0003 | t0001 | g0143 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18981 | hp2 | a0001 | c0009 | t0001 | g0137 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18982 | hp2 | a0001 | c0003 | t0001 | g0153 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18983 | hp2 | a0005 | c0010 | t0001 | g0084 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0340 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18994 | hp2 | a0001 | c0003 | t0001 | g0141 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19005 | hp2 | a0001 | c0003 | t0001 | g0160 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19009 | hp1 | a0001 | c0003 | t0001 | g0186 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0206 | AFR | LWK | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0337 | AFR | LWK | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0235 | AFR | LWK | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19055 | hp2 | a0002 | c0005 | t0001 | g0004 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19056 | hp1 | a0001 | c0003 | t0001 | g0162 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19064 | hp1 | a0002 | c0005 | t0001 | g0261 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19064 | hp2 | a0001 | c0003 | t0001 | g0168 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19065 | hp1 | a0001 | c0003 | t0001 | g0167 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19066 | hp2 | a0001 | c0003 | t0001 | g0154 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0342 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19074 | hp2 | a0001 | c0003 | t0001 | g0184 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19079 | hp1 | a0002 | c0005 | t0001 | g0005 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19079 | hp2 | a0001 | c0003 | t0001 | g0175 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19081 | hp1 | a0001 | c0003 | t0001 | g0185 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19081 | hp2 | a0002 | c0005 | t0001 | g0263 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0341 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ASW | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0234 | AFR | ASW | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA20905 | hp1 | a0001 | c0003 | t0001 | g0174 | SAS | GIH | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA20905 | hp2 | a0001 | c0004 | t0001 | g0026 | SAS | GIH | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0217 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0150 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0250 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0204 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0336 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02559 | hp1 | a0001 | c0006 | t0001 | g0106 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0269 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0172 | AFR | MSL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0267 | AFR | MSL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG06807 | hp1 | a0001 | c0003 | t0001 | g0159 | AFR | USA | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0333 | AFR | USA | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0268 | AFR | LWK | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0031 | AFR | LWK | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0281 | REF | REF | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:644568
|
C | G | 1 | a0002 | 6 | HG00597.hp1 NA18978.hp1 NA19055.hp2 others(3): Show |
missense_variant | MODERATE | c.1680G>C | p.Met560Ile | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 12/12 | 1855/2190 | 1680/1698 | 560/565 | chr11 | 644568 | ||
| chr11:644597
|
C | T | 1 | a0004 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.1651G>A | p.Asp551Asn | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 12/12 | 1826/2190 | 1651/1698 | 551/565 | chr11 | 644597 | ||
| chr11:644614
|
G | C | 1 | a0003 | 2 | HG01106.hp1 HG01515.hp2 |
missense_variant | MODERATE | c.1634C>G | p.Ala545Gly | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 12/12 | 1809/2190 | 1634/1698 | 545/565 | chr11 | 644614 | ||
| chr11:674733
|
C | T | 1 | a0005 | 1 | NA18983.hp2 | missense_variant | MODERATE | c.1306G>A | p.Ala436Thr | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/12 | 1481/2190 | 1306/1698 | 436/565 | chr11 | 674733 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:653968
|
T | C | 4 | a0001c0002a0001c0008a0002c0005others(1): Show | 100 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(97): Show |
synonymous_variant | LOW | c.1587A>G | p.Gln529Gln | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/12 | 1762/2190 | 1587/1698 | 529/565 | chr11 | 653968 | ||
| chr11:654043
|
G | A | 3 | a0001c0003a0001c0008a0001c0014 | 56 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(53): Show |
synonymous_variant | LOW | c.1512C>T | p.Cys504Cys | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/12 | 1687/2190 | 1512/1698 | 504/565 | chr11 | 654043 | ||
| chr11:674551
|
G | A | 1 | a0001c0006 | 5 | HG02258.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
synonymous_variant | LOW | c.1488C>T | p.Asp496Asp | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/12 | 1663/2190 | 1488/1698 | 496/565 | chr11 | 674551 | ||
| chr11:674638
|
C | T | 1 | a0001c0004 | 10 | HG01106.hp2 HG01496.hp2 HG02004.hp2 others(7): Show |
synonymous_variant | LOW | c.1401G>A | p.Ala467Ala | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/12 | 1576/2190 | 1401/1698 | 467/565 | chr11 | 674638 | ||
| chr11:674731
|
C | T | 1 | a0001c0011 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.1308G>A | p.Ala436Ala | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/12 | 1483/2190 | 1308/1698 | 436/565 | chr11 | 674731 | ||
| chr11:678812
|
G | A | 1 | a0001c0009 | 2 | NA18962.hp1 NA18981.hp2 |
synonymous_variant | LOW | c.1137C>T | p.Ala379Ala | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/12 | 1312/2190 | 1137/1698 | 379/565 | chr11 | 678812 | ||
| chr11:681078
|
G | C | 1 | a0001c0013 | 1 | HG00735.hp1 | synonymous_variant | LOW | c.882C>G | p.Val294Val | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 7/12 | 1057/2190 | 882/1698 | 294/565 | chr11 | 681078 | ||
| chr11:688365
|
G | A | 1 | a0001c0014 | 1 | HG02132.hp2 | synonymous_variant | LOW | c.483C>T | p.Thr161Thr | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 3/12 | 658/2190 | 483/1698 | 161/565 | chr11 | 688365 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:644302
|
A | C | 1 | a0001c0001t0003 | 2 | HG00738.hp2 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*248T>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 12/12 | 248 | chr11 | 644302 | |||||
| chr11:644325
|
G | A | 1 | a0001c0001t0005 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*225C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 12/12 | 225 | chr11 | 644325 | |||||
| chr11:644353
|
A | C | 1 | a0001c0001t0002 | 3 | NA18999.hp2 NA19065.hp2 NA19082.hp1 |
3_prime_UTR_variant | MODIFIER | c.*197T>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 12/12 | 197 | chr11 | 644353 | |||||
| chr11:644377
|
G | A | 1 | a0001c0001t0004 | 2 | HG02723.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*173C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 12/12 | 173 | chr11 | 644377 | |||||
| chr11:644529
|
C | A | 1 | a0001c0001t0006 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*21G>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 12/12 | 21 | chr11 | 644529 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:644748
|
C | G | 49 | a0001c0001t0001g0121a0001c0003t0001g0006a0001c0003t0001g0032others(46): Show | 49 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.1594-94G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 644748 | ||||||
| chr11:644835
|
C | T | 1 | a0001c0002t0001g0248 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1594-181G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 644835 | ||||||
| chr11:644946
|
T | C | 4 | a0001c0001t0001g0124a0001c0001t0001g0126a0001c0001t0001g0130others(1): Show | 4 | NA18954.hp2 NA18970.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.1594-292A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 644946 | ||||||
| chr11:644960
|
C | T | 6 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0030others(3): Show | 7 | HG02257.hp1 HG02622.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1594-306G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 644960 | ||||||
| chr11:645048
|
A | C | 1 | a0001c0001t0001g0068 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1594-394T>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 645048 | ||||||
| chr11:645057
|
G | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(199): Show | 205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1594-403C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 645057 | ||||||
| chr11:645060
|
A | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(199): Show | 205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1594-406T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 645060 | ||||||
| chr11:645067
|
G | T | 1 | a0001c0001t0001g0046 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1594-413C>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 645067 | ||||||
| chr11:645132
|
C | T | 5 | a0001c0002t0001g0231a0001c0002t0001g0232a0001c0002t0001g0233others(2): Show | 5 | HG02970.hp1 HG03453.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1594-478G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 645132 | ||||||
| chr11:645160
|
C | CA | 187 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(184): Show | 189 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.1594-507dupT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 645160 | ||||||
| chr11:645160
|
C | CAA | 8 | a0001c0001t0001g0118a0001c0002t0001g0210a0001c0002t0001g0219others(5): Show | 8 | HG00558.hp1 HG00673.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1594-508_1594-507d others(4): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 645160 | ||||||
| chr11:645336
|
G | A | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(143): Show | 148 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.1594-682C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 645336 | ||||||
| chr11:645393
|
C | G | 1 | a0001c0001t0001g0307 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1594-739G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 645393 | ||||||
| chr11:645393
|
CACG | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(139): Show | 144 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.1594-742_1594-740d others(5): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 645393 | ||||||
| chr11:645569
|
C | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(201): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1594-915G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 645569 | ||||||
| chr11:645669
|
T | G | 1 | a0001c0003t0001g0180 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1594-1015A>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 645669 | ||||||
| chr11:645751
|
C | A | 1 | a0001c0001t0001g0102 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1594-1097G>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 645751 | ||||||
| chr11:645859
|
C | T | 1 | a0001c0001t0001g0326 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1594-1205G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 645859 | ||||||
| chr11:645871
|
G | A | 1 | a0001c0002t0001g0252 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1594-1217C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 645871 | ||||||
| chr11:645875
|
A | T | 1 | a0001c0014t0001g0147 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1594-1221T>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 645875 | ||||||
| chr11:645881
|
CACAGAGC others(28): Show |
C | 1 | a0001c0002t0001g0195 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1594-1262_1594-122 others(39): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 645881 | ||||||
| chr11:645885
|
G | C | 1 | a0001c0003t0001g0155 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1594-1231C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 645885 | ||||||
| chr11:646051
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1594-1397C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 646051 | ||||||
| chr11:646232
|
G | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(201): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1594-1578C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 646232 | ||||||
| chr11:646239
|
T | A | 6 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0030others(3): Show | 7 | HG02257.hp1 HG02622.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1594-1585A>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 646239 | ||||||
| chr11:646252
|
C | CA | 34 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0029others(31): Show | 34 | HG00323.hp2 HG00735.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.1594-1599dupT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 646252 | ||||||
| chr11:646252
|
C | CAA | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(155): Show | 160 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1594-1600_1594-159 others(6): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 646252 | ||||||
| chr11:646252
|
C | CAAA | 15 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(12): Show | 15 | HG00438.hp1 HG01167.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.1594-1601_1594-159 others(7): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 646252 | ||||||
| chr11:646252
|
CA | C | 14 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0312others(11): Show | 15 | HG01257.hp2 HG01515.hp2 HG03209.hp2 others(12): Show |
intron_variant | MODIFIER | c.1594-1599delT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 646252 | ||||||
| chr11:646485
|
G | T | 1 | a0001c0002t0001g0237 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1594-1831C>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 646485 | ||||||
| chr11:646538
|
T | A | 2 | a0001c0002t0001g0201a0001c0002t0001g0267 | 2 | HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1594-1884A>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 646538 | ||||||
| chr11:646767
|
A | G | 1 | a0001c0003t0001g0180 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1594-2113T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 646767 | ||||||
| chr11:646888
|
C | T | 1 | a0001c0003t0001g0164 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1594-2234G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 646888 | ||||||
| chr11:646897
|
C | A | 1 | a0001c0001t0001g0091 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1594-2243G>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 646897 | ||||||
| chr11:646915
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1594-2261G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 646915 | ||||||
| chr11:646921
|
G | A | 4 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0066others(1): Show | 4 | HG01943.hp2 HG02258.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1594-2267C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 646921 | ||||||
| chr11:646923
|
T | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(200): Show | 206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1594-2269A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 646923 | ||||||
| chr11:646980
|
T | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(200): Show | 206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1594-2326A>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 646980 | ||||||
| chr11:646986
|
TAA | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(199): Show | 205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1594-2334_1594-233 others(6): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 646986 | ||||||
| chr11:647045
|
G | A | 4 | a0001c0002t0001g0241a0001c0002t0001g0327a0001c0002t0001g0335others(1): Show | 4 | HG02647.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1594-2391C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 647045 | ||||||
| chr11:647145
|
G | A | 83 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0093others(80): Show | 83 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.1594-2491C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 647145 | ||||||
| chr11:647355
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1594-2701A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 647355 | ||||||
| chr11:647395
|
C | T | 142 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(139): Show | 143 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.1594-2741G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 647395 | ||||||
| chr11:647404
|
A | G | 1 | a0001c0001t0001g0338 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1594-2750T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 647404 | ||||||
| chr11:647483
|
G | A | 1 | a0001c0003t0001g0056 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1594-2829C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 647483 | ||||||
| chr11:647580
|
C | T | 2 | a0001c0001t0006g0031a0001c0008t0001g0003 | 3 | HG03209.hp2 HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1594-2926G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 647580 | ||||||
| chr11:647669
|
G | A | 1 | a0001c0003t0001g0182 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1594-3015C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 647669 | ||||||
| chr11:647696
|
G | A | 16 | a0001c0001t0001g0017a0001c0001t0001g0049a0001c0001t0001g0060others(13): Show | 16 | HG00741.hp2 HG01106.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.1594-3042C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 647696 | ||||||
| chr11:647699
|
G | A | 1 | a0001c0002t0001g0301 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1594-3045C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 647699 | ||||||
| chr11:647806
|
A | AGTGCTGG others(28): Show |
4 | a0001c0001t0001g0089a0001c0001t0001g0307a0001c0008t0001g0003others(1): Show | 5 | HG00735.hp1 HG01069.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1594-3187_1594-315 others(39): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 647806 | ||||||
| chr11:647806
|
A | AGTGCTGG others(133): Show |
1 | a0001c0001t0001g0046 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1594-3292_1594-315 others(144): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 647806 | ||||||
| chr11:647806
|
AGTGCTGG others(28): Show |
A | 65 | a0001c0001t0001g0047a0001c0001t0001g0051a0001c0001t0001g0061others(62): Show | 65 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.1594-3187_1594-315 others(39): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 647806 | ||||||
| chr11:647806
|
AGTGCTGG others(63): Show |
A | 20 | a0001c0001t0001g0038a0001c0001t0001g0121a0001c0001t0001g0275others(17): Show | 20 | HG00438.hp2 HG00597.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.1594-3222_1594-315 others(74): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 647806 | ||||||
| chr11:647806
|
AGTGCTGG others(98): Show |
A | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(108): Show | 113 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1594-3257_1594-315 others(4): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 647806 | ||||||
| chr11:647806
|
AGTGCTGG others(133): Show |
A | 88 | a0001c0001t0001g0007a0001c0001t0001g0023a0001c0001t0001g0029others(85): Show | 88 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1594-3292_1594-315 others(4): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 647806 | ||||||
| chr11:647806
|
AGTGCTGG others(168): Show |
A | 20 | a0001c0001t0001g0035a0001c0001t0001g0045a0001c0001t0001g0052others(17): Show | 20 | HG01074.hp2 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1594-3327_1594-315 others(4): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 647806 | ||||||
| chr11:647806
|
AGTGCTGG others(203): Show |
A | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1594-3362_1594-315 others(4): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 647806 | ||||||
| chr11:647806
|
AGTGCTGG others(238): Show |
A | 1 | a0001c0002t0001g0247 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1594-3397_1594-315 others(4): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 647806 | ||||||
| chr11:647849
|
G | GAGCAGGT others(28): Show |
3 | a0001c0001t0001g0116a0001c0003t0001g0162a0001c0003t0001g0163 | 3 | NA18947.hp2 NA18994.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1594-3196_1594-319 others(39): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 647849 | ||||||
| chr11:647875
|
C | T | 1 | a0001c0003t0001g0179 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1594-3221G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 647875 | ||||||
| chr11:647884
|
G | C | 3 | a0001c0001t0001g0015a0001c0001t0001g0192a0001c0002t0001g0265 | 3 | HG02083.hp1 HG02683.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1594-3230C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 647884 | ||||||
| chr11:647919
|
G | C | 9 | a0001c0001t0001g0051a0001c0001t0001g0088a0001c0001t0001g0112others(6): Show | 9 | HG00558.hp2 HG02083.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.1594-3265C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 647919 | ||||||
| chr11:647938
|
ACCCAGGC others(29): Show |
A | 1 | a0001c0001t0001g0320 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1594-3320_1594-328 others(40): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 647938 | ||||||
| chr11:647954
|
G | C | 4 | a0001c0001t0001g0038a0001c0001t0001g0280a0001c0001t0001g0312others(1): Show | 4 | NA18906.hp1 NA18951.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.1594-3300C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 647954 | ||||||
| chr11:647954
|
G | GAGCAGGT others(98): Show |
1 | a0001c0001t0001g0116 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1594-3301_1594-330 others(109): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 647954 | ||||||
| chr11:647989
|
G | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(91): Show | 96 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1594-3335C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 647989 | ||||||
| chr11:647989
|
G | GAGCAGGT others(63): Show |
9 | a0001c0001t0001g0048a0001c0001t0001g0057a0001c0001t0001g0058others(6): Show | 9 | HG01167.hp2 HG02165.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.1594-3336_1594-333 others(74): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 647989 | ||||||
| chr11:648024
|
G | C | 7 | a0001c0002t0001g0220a0001c0002t0001g0256a0001c0004t0001g0013others(4): Show | 7 | HG01106.hp2 HG01496.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.1594-3370C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 648024 | ||||||
| chr11:648059
|
G | C | 6 | a0001c0001t0001g0035a0001c0001t0001g0052a0001c0001t0001g0119others(3): Show | 6 | HG01934.hp1 HG01975.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1594-3405C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 648059 | ||||||
| chr11:648137
|
G | A | 49 | a0001c0002t0001g0266a0001c0003t0001g0006a0001c0003t0001g0032others(46): Show | 49 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.1594-3483C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 648137 | ||||||
| chr11:648148
|
T | C | 5 | a0001c0002t0001g0201a0001c0002t0001g0241a0001c0002t0001g0267others(2): Show | 5 | HG01243.hp2 HG02976.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1594-3494A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 648148 | ||||||
| chr11:648175
|
A | C | 1 | a0001c0003t0001g0173 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1594-3521T>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 648175 | ||||||
| chr11:648196
|
C | CT | 14 | a0001c0001t0001g0015a0001c0001t0001g0103a0001c0001t0001g0272others(11): Show | 14 | HG00639.hp2 HG00741.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.1594-3543dupA | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 648196 | ||||||
| chr11:648196
|
C | CTT | 101 | a0001c0001t0001g0017a0001c0001t0001g0068a0001c0001t0001g0093others(98): Show | 102 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.1594-3544_1594-354 others(6): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 648196 | ||||||
| chr11:648196
|
C | CTTT | 33 | a0001c0002t0001g0204a0001c0002t0001g0207a0001c0002t0001g0208others(30): Show | 33 | HG00642.hp1 HG00642.hp2 HG01433.hp1 others(30): Show |
intron_variant | MODIFIER | c.1594-3545_1594-354 others(7): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 648196 | ||||||
| chr11:648245
|
A | T | 1 | a0001c0001t0003g0139 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1594-3591T>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 648245 | ||||||
| chr11:648250
|
T | A | 2 | a0001c0001t0001g0326a0001c0001t0003g0139 | 2 | HG00738.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1594-3596A>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 648250 | ||||||
| chr11:648251
|
G | C | 130 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(127): Show | 131 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.1594-3597C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 648251 | ||||||
| chr11:648256
|
A | G | 2 | a0001c0001t0001g0326a0001c0001t0003g0139 | 2 | HG00738.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1594-3602T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 648256 | ||||||
| chr11:648257
|
C | G | 1 | a0001c0001t0001g0326 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1594-3603G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 648257 | ||||||
| chr11:648257
|
C | T | 2 | a0001c0001t0003g0139a0001c0003t0001g0154 | 2 | HG00738.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1594-3603G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 648257 | ||||||
| chr11:648295
|
T | A | 1 | a0001c0001t0003g0139 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1594-3641A>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 648295 | ||||||
| chr11:648295
|
T | C | 3 | a0001c0002t0001g0223a0001c0002t0001g0340a0001c0002t0001g0342 | 3 | NA18993.hp1 NA19070.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1594-3641A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 648295 | ||||||
| chr11:648304
|
C | G | 116 | a0001c0001t0001g0093a0001c0002t0001g0196a0001c0002t0001g0201others(113): Show | 116 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1594-3650G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 648304 | ||||||
| chr11:648332
|
C | G | 1 | a0001c0001t0001g0104 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1594-3678G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 648332 | ||||||
| chr11:648363
|
T | C | 3 | a0001c0002t0001g0195a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1594-3709A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 648363 | ||||||
| chr11:648410
|
T | C | 4 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0066others(1): Show | 4 | HG01943.hp2 HG02258.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1594-3756A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 648410 | ||||||
| chr11:648474
|
C | T | 2 | a0001c0003t0001g0142a0001c0003t0001g0143 | 2 | NA18964.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.1594-3820G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 648474 | ||||||
| chr11:648476
|
T | G | 147 | a0001c0001t0001g0007a0001c0001t0001g0093a0001c0001t0001g0298others(144): Show | 148 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.1594-3822A>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 648476 | ||||||
| chr11:648486
|
T | C | 141 | a0001c0001t0001g0093a0001c0002t0001g0042a0001c0002t0001g0196others(138): Show | 142 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.1594-3832A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 648486 | ||||||
| chr11:648526
|
G | A | 3 | a0001c0002t0001g0195a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1594-3872C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 648526 | ||||||
| chr11:648715
|
C | A | 79 | a0001c0001t0001g0093a0001c0002t0001g0042a0001c0002t0001g0196others(76): Show | 79 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.1594-4061G>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 648715 | ||||||
| chr11:648776
|
TAAC | T | 3 | a0001c0002t0001g0195a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1594-4125_1594-412 others(7): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 648776 | ||||||
| chr11:648791
|
T | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0158 | 2 | HG00438.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1594-4137A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 648791 | ||||||
| chr11:648936
|
C | T | 1 | a0001c0003t0001g0151 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1594-4282G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 648936 | ||||||
| chr11:648980
|
G | A | 5 | a0001c0002t0001g0206a0001c0002t0001g0250a0001c0002t0001g0286others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1594-4326C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 648980 | ||||||
| chr11:649015
|
C | T | 4 | a0001c0002t0001g0327a0001c0002t0001g0335a0001c0002t0001g0336others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1594-4361G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 649015 | ||||||
| chr11:649111
|
C | T | 6 | a0001c0003t0001g0169a0001c0003t0001g0170a0001c0003t0001g0171others(3): Show | 6 | HG02572.hp2 HG02615.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1594-4457G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 649111 | ||||||
| chr11:649278
|
C | T | 1 | a0002c0005t0001g0004 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1594-4624G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 649278 | ||||||
| chr11:649279
|
G | A | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1594-4625C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 649279 | ||||||
| chr11:649411
|
G | C | 1 | a0001c0003t0001g0179 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1593+4551C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 649411 | ||||||
| chr11:649428
|
AAAAC | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(128): Show | 133 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.1593+4530_1593+453 others(8): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 649428 | ||||||
| chr11:649447
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1593+4515A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 649447 | ||||||
| chr11:649486
|
G | A | 54 | a0001c0003t0001g0006a0001c0003t0001g0032a0001c0003t0001g0056others(51): Show | 54 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.1593+4476C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 649486 | ||||||
| chr11:649506
|
G | T | 3 | a0001c0002t0001g0195a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1593+4456C>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 649506 | ||||||
| chr11:649579
|
G | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(44): Show | 48 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.1593+4383C>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 649579 | ||||||
| chr11:649639
|
A | G | 148 | a0001c0001t0001g0093a0001c0002t0001g0042a0001c0002t0001g0195others(145): Show | 149 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.1593+4323T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 649639 | ||||||
| chr11:649655
|
G | GGCTGCAG others(12): Show |
1 | a0001c0001t0002g0127 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1593+4288_1593+430 others(23): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 649655 | ||||||
| chr11:649657
|
C | G | 3 | a0001c0003t0001g0159a0001c0003t0001g0188a0001c0003t0001g0189 | 3 | HG01258.hp2 HG03490.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1593+4305G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 649657 | ||||||
| chr11:649696
|
G | C | 1 | a0001c0001t0001g0037 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1593+4266C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 649696 | ||||||
| chr11:649697
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1593+4265C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 649697 | ||||||
| chr11:649705
|
G | C | 1 | a0001c0001t0001g0104 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1593+4257C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 649705 | ||||||
| chr11:649797
|
G | A | 4 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0030others(1): Show | 4 | HG02257.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1593+4165C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 649797 | ||||||
| chr11:650022
|
AAAAAAC | A | 83 | a0001c0002t0001g0042a0001c0002t0001g0202a0001c0002t0001g0205others(80): Show | 83 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.1593+3934_1593+393 others(10): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 650022 | ||||||
| chr11:650022
|
AAAAAACA others(5): Show |
A | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(133): Show | 138 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.1593+3928_1593+393 others(16): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 650022 | ||||||
| chr11:650028
|
C | A | 3 | a0001c0002t0001g0195a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1593+3934G>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 650028 | ||||||
| chr11:650177
|
C | A | 1 | a0001c0002t0001g0218 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1593+3785G>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 650177 | ||||||
| chr11:650196
|
G | A | 3 | a0001c0002t0001g0195a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1593+3766C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 650196 | ||||||
| chr11:650202
|
C | T | 3 | a0001c0002t0001g0206a0001c0002t0001g0250a0001c0002t0001g0304 | 3 | HG02109.hp1 HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1593+3760G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 650202 | ||||||
| chr11:650373
|
C | CA | 14 | a0001c0001t0001g0048a0001c0001t0001g0067a0001c0001t0001g0074others(11): Show | 14 | HG00621.hp1 HG01167.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.1593+3588dupT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 650373 | ||||||
| chr11:650373
|
C | CAA | 15 | a0001c0001t0001g0029a0001c0001t0001g0200a0001c0001t0006g0031others(12): Show | 15 | HG01243.hp2 HG02886.hp2 HG02897.hp2 others(12): Show |
intron_variant | MODIFIER | c.1593+3587_1593+358 others(6): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 650373 | ||||||
| chr11:650373
|
C | CAAA | 55 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0093others(52): Show | 55 | HG00597.hp1 HG00642.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1593+3586_1593+358 others(7): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 650373 | ||||||
| chr11:650373
|
C | CAAAA | 25 | a0001c0002t0001g0042a0001c0002t0001g0195a0001c0002t0001g0197others(22): Show | 26 | HG00280.hp2 HG02015.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.1593+3585_1593+358 others(8): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 650373 | ||||||
| chr11:650373
|
C | CAAAAA | 8 | a0001c0002t0001g0212a0001c0002t0001g0213a0001c0002t0001g0214others(5): Show | 8 | HG01123.hp1 HG01255.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1593+3584_1593+358 others(9): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 650373 | ||||||
| chr11:650373
|
CA | C | 17 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0045others(14): Show | 17 | HG00423.hp1 HG00438.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.1593+3588delT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 650373 | ||||||
| chr11:650373
|
CAA | C | 40 | a0001c0003t0001g0006a0001c0003t0001g0032a0001c0003t0001g0142others(37): Show | 40 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1593+3587_1593+358 others(6): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 650373 | ||||||
| chr11:650373
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0003t0001g0154 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1593+3576_1593+358 others(17): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 650373 | ||||||
| chr11:650498
|
G | C | 1 | a0001c0001t0001g0131 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1593+3464C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 650498 | ||||||
| chr11:650672
|
G | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0116 | 3 | NA18960.hp2 NA18994.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1593+3290C>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 650672 | ||||||
| chr11:650713
|
G | C | 150 | a0001c0001t0001g0093a0001c0002t0001g0042a0001c0002t0001g0196others(147): Show | 151 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.1593+3249C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 650713 | ||||||
| chr11:650716
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1593+3246C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 650716 | ||||||
| chr11:650751
|
C | T | 5 | a0001c0001t0001g0049a0001c0001t0001g0062a0001c0001t0001g0073others(2): Show | 5 | HG00741.hp2 HG01099.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1593+3211G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 650751 | ||||||
| chr11:650836
|
G | A | 54 | a0001c0003t0001g0006a0001c0003t0001g0032a0001c0003t0001g0056others(51): Show | 54 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.1593+3126C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 650836 | ||||||
| chr11:650843
|
G | A | 1 | a0001c0008t0001g0003 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1593+3119C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 650843 | ||||||
| chr11:650904
|
A | G | 1 | a0001c0001t0006g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1593+3058T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 650904 | ||||||
| chr11:650994
|
G | A | 73 | a0001c0002t0001g0042a0001c0002t0001g0196a0001c0002t0001g0202others(70): Show | 73 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.1593+2968C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 650994 | ||||||
| chr11:651036
|
T | C | 3 | a0001c0002t0001g0268a0001c0002t0001g0269a0004c0012t0001g0270 | 3 | HG02559.hp2 HG02615.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1593+2926A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 651036 | ||||||
| chr11:651110
|
G | A | 1 | a0001c0002t0001g0254 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1593+2852C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 651110 | ||||||
| chr11:651112
|
G | A | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1593+2850C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 651112 | ||||||
| chr11:651139
|
T | C | 54 | a0001c0003t0001g0006a0001c0003t0001g0032a0001c0003t0001g0056others(51): Show | 54 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.1593+2823A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 651139 | ||||||
| chr11:651227
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1593+2735A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 651227 | ||||||
| chr11:651230
|
G | C | 1 | a0001c0003t0001g0056 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1593+2732C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 651230 | ||||||
| chr11:651414
|
GA | G | 149 | a0001c0001t0001g0015a0001c0001t0001g0309a0001c0001t0001g0316others(146): Show | 150 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1593+2547delT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 651414 | ||||||
| chr11:651415
|
A | G | 1 | a0002c0005t0001g0004 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1593+2547T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 651415 | ||||||
| chr11:651491
|
C | G | 94 | a0001c0002t0001g0042a0001c0002t0001g0196a0001c0002t0001g0201others(91): Show | 94 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.1593+2471G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 651491 | ||||||
| chr11:651593
|
A | T | 1 | a0001c0001t0001g0338 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1593+2369T>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 651593 | ||||||
| chr11:651681
|
T | C | 1 | a0001c0001t0001g0126 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1593+2281A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 651681 | ||||||
| chr11:651714
|
G | A | 3 | a0001c0002t0001g0195a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1593+2248C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 651714 | ||||||
| chr11:651768
|
C | G | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(131): Show | 136 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.1593+2194G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 651768 | ||||||
| chr11:651827
|
G | A | 30 | a0001c0002t0001g0042a0001c0002t0001g0202a0001c0002t0001g0205others(27): Show | 30 | HG00280.hp2 HG00597.hp1 HG02040.hp2 others(27): Show |
intron_variant | MODIFIER | c.1593+2135C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 651827 | ||||||
| chr11:651872
|
C | T | 3 | a0001c0002t0001g0195a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1593+2090G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 651872 | ||||||
| chr11:651882
|
T | C | 3 | a0001c0002t0001g0195a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1593+2080A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 651882 | ||||||
| chr11:651884
|
T | TCAAAAA | 3 | a0001c0002t0001g0195a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1593+2072_1593+207 others(10): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 651884 | ||||||
| chr11:652018
|
C | T | 1 | a0001c0002t0001g0211 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1593+1944G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 652018 | ||||||
| chr11:652029
|
T | G | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1593+1933A>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 652029 | ||||||
| chr11:652060
|
C | T | 1 | a0001c0008t0001g0003 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1593+1902G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 652060 | ||||||
| chr11:652102
|
C | A | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1593+1860G>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 652102 | ||||||
| chr11:652386
|
C | G | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1593+1576G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 652386 | ||||||
| chr11:652495
|
G | A | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1593+1467C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 652495 | ||||||
| chr11:652621
|
G | C | 3 | a0001c0002t0001g0195a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1593+1341C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 652621 | ||||||
| chr11:652656
|
G | A | 4 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0249others(1): Show | 4 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1593+1306C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 652656 | ||||||
| chr11:652747
|
C | A | 1 | a0001c0002t0001g0224 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1593+1215G>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 652747 | ||||||
| chr11:652900
|
G | A | 4 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0249others(1): Show | 4 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1593+1062C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 652900 | ||||||
| chr11:652964
|
A | G | 1 | a0001c0002t0001g0287 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1593+998T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 652964 | ||||||
| chr11:653083
|
C | CA | 8 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0070others(5): Show | 8 | HG01167.hp2 HG01261.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.1593+878dupT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653083 | ||||||
| chr11:653083
|
CA | C | 192 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(189): Show | 193 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1593+878delT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653083 | ||||||
| chr11:653083
|
CAA | C | 70 | a0001c0001t0001g0076a0001c0001t0001g0089a0001c0001t0001g0090others(67): Show | 70 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.1593+877_1593+878d others(4): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653083 | ||||||
| chr11:653083
|
CAAAAAAA others(3): Show |
C | 4 | a0001c0001t0001g0282a0001c0001t0001g0288a0001c0001t0001g0292others(1): Show | 4 | HG02735.hp1 HG03669.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1593+869_1593+878d others(12): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653083 | ||||||
| chr11:653083
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0200 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1593+867_1593+878d others(14): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653083 | ||||||
| chr11:653083
|
CAAAAAAA others(7): Show |
C | 2 | a0001c0002t0001g0308a0001c0002t0001g0311 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1593+865_1593+878d others(16): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653083 | ||||||
| chr11:653185
|
T | C | 150 | a0001c0001t0001g0284a0001c0002t0001g0042a0001c0002t0001g0196others(147): Show | 151 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.1593+777A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653185 | ||||||
| chr11:653218
|
G | A | 1 | a0001c0002t0001g0241 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1593+744C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653218 | ||||||
| chr11:653248
|
G | C | 154 | a0001c0001t0001g0284a0001c0002t0001g0042a0001c0002t0001g0195others(151): Show | 155 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.1593+714C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653248 | ||||||
| chr11:653253
|
T | G | 1 | a0001c0003t0001g0149 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1593+709A>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653253 | ||||||
| chr11:653289
|
T | C | 1 | a0001c0001t0001g0126 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1593+673A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653289 | ||||||
| chr11:653304
|
CAG | C | 6 | a0001c0002t0001g0195a0001c0002t0001g0197a0001c0002t0001g0198others(3): Show | 6 | HG02630.hp1 HG02818.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1593+656_1593+657d others(4): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653304 | ||||||
| chr11:653307
|
T | G | 6 | a0001c0002t0001g0195a0001c0002t0001g0197a0001c0002t0001g0198others(3): Show | 6 | HG02630.hp1 HG02818.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1593+655A>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653307 | ||||||
| chr11:653307
|
T | TCTCTCTC others(53): Show |
3 | a0001c0003t0001g0141a0001c0003t0001g0144a0001c0003t0001g0160 | 3 | NA18950.hp2 NA18994.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1593+595_1593+654d others(62): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653307 | ||||||
| chr11:653308
|
C | CTCTCTCT others(113): Show |
7 | a0001c0001t0001g0283a0001c0001t0001g0315a0001c0001t0001g0316others(4): Show | 7 | NA18963.hp1 NA18964.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.1593+534_1593+653d others(122): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653308 | ||||||
| chr11:653315
|
T | G | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1593+647A>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653315 | ||||||
| chr11:653367
|
G | A | 2 | a0001c0003t0001g0146a0001c0003t0001g0167 | 2 | HG03831.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1593+595C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653367 | ||||||
| chr11:653368
|
C | CTCTCTCT others(233): Show |
1 | a0001c0001t0001g0109 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1593+593_1593+594i others(242): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653368 | ||||||
| chr11:653368
|
C | CTCTCTCT others(233): Show |
1 | a0001c0001t0001g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1593+593_1593+594i others(242): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653368 | ||||||
| chr11:653368
|
C | G | 2 | a0001c0003t0001g0146a0001c0003t0001g0167 | 2 | HG03831.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1593+594G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653368 | ||||||
| chr11:653368
|
CTCTCTCT others(53): Show |
C | 2 | a0001c0001t0001g0328a0001c0003t0001g0182 | 2 | HG01109.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1593+534_1593+593d others(62): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653368 | ||||||
| chr11:653427
|
A | G | 6 | a0001c0003t0001g0141a0001c0003t0001g0144a0001c0003t0001g0146others(3): Show | 6 | HG01255.hp1 HG03831.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1593+535T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653427 | ||||||
| chr11:653428
|
G | C | 6 | a0001c0003t0001g0141a0001c0003t0001g0144a0001c0003t0001g0146others(3): Show | 6 | HG01255.hp1 HG03831.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1593+534C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653428 | ||||||
| chr11:653428
|
G | GTC | 3 | a0001c0002t0001g0195a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1593+532_1593+533d others(4): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653428 | ||||||
| chr11:653428
|
G | GTCTCTCT others(53): Show |
45 | a0001c0003t0001g0006a0001c0003t0001g0056a0001c0003t0001g0142others(42): Show | 45 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.1593+533_1593+534i others(62): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653428 | ||||||
| chr11:653428
|
G | GTCTCTCT others(173): Show |
1 | a0001c0003t0001g0032 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1593+533_1593+534i others(182): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653428 | ||||||
| chr11:653428
|
G | GTCTCTCT others(115): Show |
1 | a0001c0002t0001g0204 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1593+533_1593+534i others(124): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653428 | ||||||
| chr11:653436
|
C | CGCGTGGC others(115): Show |
2 | a0001c0004t0001g0020a0001c0004t0001g0021 | 2 | HG01496.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1593+525_1593+526i others(124): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653436 | ||||||
| chr11:653437
|
G | GCGTGGCT others(109): Show |
3 | a0001c0002t0001g0195a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1593+524_1593+525i others(118): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653437 | ||||||
| chr11:653439
|
G | A | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1593+523C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653439 | ||||||
| chr11:653465
|
C | CAATAATA others(113): Show |
8 | a0001c0004t0001g0013a0001c0004t0001g0014a0001c0004t0001g0022others(5): Show | 8 | HG01106.hp2 HG02040.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.1593+377_1593+496d others(122): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653465 | ||||||
| chr11:653465
|
C | G | 2 | a0001c0004t0001g0020a0001c0004t0001g0021 | 2 | HG01496.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1593+497G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653465 | ||||||
| chr11:653475
|
A | G | 4 | a0001c0002t0001g0195a0001c0002t0001g0197a0001c0002t0001g0198others(1): Show | 4 | HG02630.hp1 HG02818.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1593+487T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653475 | ||||||
| chr11:653475
|
AGAACTGT others(53): Show |
A | 1 | a0001c0001t0001g0324 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1593+427_1593+486d others(62): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653475 | ||||||
| chr11:653496
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1593+466G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653496 | ||||||
| chr11:653530
|
A | G | 48 | a0001c0003t0001g0006a0001c0003t0001g0032a0001c0003t0001g0056others(45): Show | 48 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.1593+432T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653530 | ||||||
| chr11:653556
|
T | C | 1 | a0001c0001t0001g0319 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1593+406A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653556 | ||||||
| chr11:653557
|
G | A | 1 | a0001c0001t0001g0319 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1593+405C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653557 | ||||||
| chr11:653585
|
G | C | 1 | a0001c0001t0001g0319 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1593+377C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653585 | ||||||
| chr11:653643
|
C | G | 1 | a0001c0003t0001g0175 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1593+319G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 11/11 | chr11 | 653643 | ||||||
| chr11:654091
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(128): Show | 133 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.1504-40C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 654091 | ||||||
| chr11:654109
|
A | G | 153 | a0001c0002t0001g0042a0001c0002t0001g0195a0001c0002t0001g0196others(150): Show | 154 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.1504-58T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 654109 | ||||||
| chr11:654122
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1504-71C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 654122 | ||||||
| chr11:654144
|
A | C | 1 | a0001c0002t0001g0248 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1504-93T>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 654144 | ||||||
| chr11:654147
|
T | G | 153 | a0001c0002t0001g0042a0001c0002t0001g0195a0001c0002t0001g0196others(150): Show | 154 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.1504-96A>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 654147 | ||||||
| chr11:654160
|
AC | A | 67 | a0001c0002t0001g0042a0001c0002t0001g0198a0001c0002t0001g0207others(64): Show | 67 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.1504-110delG | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 654160 | ||||||
| chr11:654160
|
ACC | A | 64 | a0001c0002t0001g0195a0001c0002t0001g0196a0001c0002t0001g0197others(61): Show | 64 | HG00280.hp2 HG01123.hp1 HG01243.hp1 others(61): Show |
intron_variant | MODIFIER | c.1504-111_1504-110d others(4): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 654160 | ||||||
| chr11:654160
|
ACCC | A | 5 | a0001c0002t0001g0201a0001c0002t0001g0204a0001c0002t0001g0224others(2): Show | 5 | HG02109.hp2 HG03098.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1504-112_1504-110d others(5): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 654160 | ||||||
| chr11:654163
|
C | T | 4 | a0001c0002t0001g0258a0001c0002t0001g0268a0001c0002t0001g0269others(1): Show | 4 | HG02559.hp2 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1504-112G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 654163 | ||||||
| chr11:654164
|
C | T | 28 | a0001c0002t0001g0042a0001c0002t0001g0207a0001c0002t0001g0209others(25): Show | 28 | HG00597.hp1 HG00642.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.1504-113G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 654164 | ||||||
| chr11:654164
|
CCT | C | 6 | a0001c0003t0001g0169a0001c0003t0001g0170a0001c0003t0001g0171others(3): Show | 6 | HG02572.hp2 HG02615.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1504-115_1504-114d others(4): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 654164 | ||||||
| chr11:654165
|
C | CT | 26 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(23): Show | 26 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1504-115dupA | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 654165 | ||||||
| chr11:654165
|
C | T | 98 | a0001c0002t0001g0042a0001c0002t0001g0196a0001c0002t0001g0198others(95): Show | 99 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.1504-114G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 654165 | ||||||
| chr11:654165
|
CT | C | 14 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(11): Show | 14 | HG00597.hp2 HG02523.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.1504-115delA | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 654165 | ||||||
| chr11:654166
|
T | C | 3 | a0001c0001t0001g0038a0001c0001t0001g0192a0001c0009t0001g0063 | 3 | HG02083.hp1 NA18962.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1504-115A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 654166 | ||||||
| chr11:654195
|
G | A | 1 | a0001c0002t0001g0257 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1504-144C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 654195 | ||||||
| chr11:654226
|
TGGTGCGA others(926): Show |
T | 3 | a0001c0002t0001g0195a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1504-1108_1504-176 others(3): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 654226 | ||||||
| chr11:654229
|
T | C | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(283): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1504-178A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 654229 | ||||||
| chr11:654230
|
G | A | 54 | a0001c0003t0001g0006a0001c0003t0001g0032a0001c0003t0001g0056others(51): Show | 55 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1504-179C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 654230 | ||||||
| chr11:654232
|
G | A | 53 | a0001c0003t0001g0006a0001c0003t0001g0032a0001c0003t0001g0056others(50): Show | 53 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.1504-181C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 654232 | ||||||
| chr11:654445
|
G | A | 1 | a0001c0003t0001g0181 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1504-394C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 654445 | ||||||
| chr11:654469
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1504-418A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 654469 | ||||||
| chr11:654511
|
G | A | 94 | a0001c0002t0001g0042a0001c0002t0001g0196a0001c0002t0001g0201others(91): Show | 94 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.1504-460C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 654511 | ||||||
| chr11:654856
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1504-805C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 654856 | ||||||
| chr11:654946
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1504-895C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 654946 | ||||||
| chr11:655048
|
A | AAAAC | 7 | a0001c0001t0001g0047a0001c0001t0001g0115a0001c0001t0001g0282others(4): Show | 7 | HG00621.hp1 HG01167.hp2 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.1504-1001_1504-998 others(7): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 655048 | ||||||
| chr11:655281
|
T | C | 3 | a0001c0002t0001g0195a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1504-1230A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 655281 | ||||||
| chr11:655302
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1504-1251A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 655302 | ||||||
| chr11:655357
|
G | C | 1 | a0001c0001t0001g0046 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1504-1306C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 655357 | ||||||
| chr11:655541
|
A | AGGC | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(284): Show | 290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1504-1491_1504-149 others(7): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 655541 | ||||||
| chr11:655598
|
G | A | 1 | a0001c0003t0001g0180 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1504-1547C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 655598 | ||||||
| chr11:655603
|
A | G | 113 | a0001c0001t0001g0017a0001c0001t0001g0049a0001c0001t0001g0060others(110): Show | 114 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(111): Show |
intron_variant | MODIFIER | c.1504-1552T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 655603 | ||||||
| chr11:655644
|
G | A | 94 | a0001c0001t0001g0280a0001c0002t0001g0042a0001c0002t0001g0201others(91): Show | 95 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.1504-1593C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 655644 | ||||||
| chr11:655723
|
T | TA | 4 | a0001c0002t0001g0195a0001c0002t0001g0196a0001c0002t0001g0197others(1): Show | 4 | HG02630.hp1 HG02818.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1504-1673dupT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 655723 | ||||||
| chr11:655822
|
T | C | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1504-1771A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 655822 | ||||||
| chr11:655828
|
TTTATTA | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(131): Show | 136 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.1504-1783_1504-177 others(10): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 655828 | ||||||
| chr11:655840
|
A | T | 5 | a0001c0002t0001g0232a0001c0002t0001g0233a0001c0002t0001g0234others(2): Show | 5 | HG02723.hp2 HG02970.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1504-1789T>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 655840 | ||||||
| chr11:655843
|
A | T | 100 | a0001c0001t0001g0328a0001c0002t0001g0042a0001c0002t0001g0195others(97): Show | 101 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.1504-1792T>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 655843 | ||||||
| chr11:655894
|
G | A | 2 | a0001c0002t0001g0300a0001c0002t0001g0301 | 2 | HG01243.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1504-1843C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 655894 | ||||||
| chr11:655989
|
G | A | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1504-1938C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 655989 | ||||||
| chr11:655998
|
A | AT | 54 | a0001c0003t0001g0006a0001c0003t0001g0032a0001c0003t0001g0056others(51): Show | 54 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.1504-1948dupA | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 655998 | ||||||
| chr11:656031
|
A | G | 5 | a0001c0001t0001g0328a0001c0002t0001g0195a0001c0002t0001g0196others(2): Show | 5 | HG01109.hp2 HG02630.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1504-1980T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 656031 | ||||||
| chr11:656116
|
G | A | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1504-2065C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 656116 | ||||||
| chr11:656158
|
C | CTCTT | 94 | a0001c0001t0001g0328a0001c0002t0001g0042a0001c0002t0001g0195others(91): Show | 95 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.1504-2108_1504-210 others(8): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 656158 | ||||||
| chr11:656357
|
T | A | 1 | a0001c0002t0001g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1504-2306A>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 656357 | ||||||
| chr11:656376
|
G | A | 94 | a0001c0002t0001g0042a0001c0002t0001g0201a0001c0002t0001g0202others(91): Show | 95 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.1504-2325C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 656376 | ||||||
| chr11:656523
|
C | T | 43 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(40): Show | 44 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.1504-2472G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 656523 | ||||||
| chr11:656547
|
G | A | 1 | a0001c0001t0001g0328 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1504-2496C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 656547 | ||||||
| chr11:656561
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1504-2510G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 656561 | ||||||
| chr11:656591
|
C | T | 1 | a0001c0003t0001g0176 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1504-2540G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 656591 | ||||||
| chr11:656772
|
C | T | 2 | a0001c0003t0001g0152a0001c0003t0001g0168 | 2 | HG00673.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1504-2721G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 656772 | ||||||
| chr11:656845
|
G | A | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(125): Show | 130 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1504-2794C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 656845 | ||||||
| chr11:656880
|
A | T | 1 | a0001c0002t0001g0256 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1504-2829T>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 656880 | ||||||
| chr11:656897
|
T | C | 6 | a0001c0003t0001g0169a0001c0003t0001g0170a0001c0003t0001g0171others(3): Show | 6 | HG02572.hp2 HG02615.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1504-2846A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 656897 | ||||||
| chr11:656940
|
G | A | 9 | a0001c0001t0001g0012a0001c0001t0001g0068a0001c0001t0001g0083others(6): Show | 9 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(6): Show |
intron_variant | MODIFIER | c.1504-2889C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 656940 | ||||||
| chr11:656973
|
G | T | 1 | a0001c0001t0001g0061 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1504-2922C>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 656973 | ||||||
| chr11:657005
|
CACAGGTG others(27): Show |
C | 3 | a0001c0003t0001g0145a0001c0003t0001g0155a0001c0003t0001g0181 | 3 | HG01070.hp1 HG01346.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1504-2988_1504-295 others(38): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 657005 | ||||||
| chr11:657106
|
G | A | 3 | a0001c0002t0001g0223a0001c0002t0001g0340a0001c0002t0001g0342 | 3 | NA18993.hp1 NA19070.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1504-3055C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 657106 | ||||||
| chr11:657107
|
GACCCACC others(4): Show |
G | 48 | a0001c0003t0001g0006a0001c0003t0001g0032a0001c0003t0001g0056others(45): Show | 48 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.1504-3067_1504-305 others(15): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 657107 | ||||||
| chr11:657202
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1504-3151G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 657202 | ||||||
| chr11:657204
|
C | T | 5 | a0001c0001t0001g0328a0001c0002t0001g0195a0001c0002t0001g0196others(2): Show | 5 | HG01109.hp2 HG02630.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1504-3153G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 657204 | ||||||
| chr11:657229
|
C | T | 1 | a0001c0002t0001g0202 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1504-3178G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 657229 | ||||||
| chr11:657374
|
G | A | 1 | a0001c0003t0001g0181 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1504-3323C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 657374 | ||||||
| chr11:657466
|
A | G | 1 | a0005c0010t0001g0084 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1504-3415T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 657466 | ||||||
| chr11:657477
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0296 | 2 | HG00735.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.1504-3426G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 657477 | ||||||
| chr11:657503
|
T | A | 1 | a0001c0001t0001g0328 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1504-3452A>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 657503 | ||||||
| chr11:657552
|
C | G | 7 | a0001c0001t0001g0282a0001c0001t0001g0288a0001c0001t0001g0291others(4): Show | 7 | HG01167.hp2 HG01358.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.1504-3501G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 657552 | ||||||
| chr11:657676
|
G | A | 5 | a0001c0001t0001g0328a0001c0002t0001g0195a0001c0002t0001g0196others(2): Show | 5 | HG01109.hp2 HG02630.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1504-3625C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 657676 | ||||||
| chr11:657713
|
A | G | 57 | a0001c0001t0001g0328a0001c0002t0001g0195a0001c0002t0001g0196others(54): Show | 57 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.1504-3662T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 657713 | ||||||
| chr11:658050
|
G | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(132): Show | 137 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1504-3999C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 658050 | ||||||
| chr11:658141
|
T | C | 1 | a0001c0002t0001g0239 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1504-4090A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 658141 | ||||||
| chr11:658151
|
G | A | 1 | a0001c0004t0001g0013 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1504-4100C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 658151 | ||||||
| chr11:658194
|
T | C | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(289): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.1504-4143A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 658194 | ||||||
| chr11:658244
|
C | T | 3 | a0001c0001t0001g0061a0001c0001t0001g0081a0001c0001t0001g0091 | 3 | HG01109.hp1 HG01496.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1504-4193G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 658244 | ||||||
| chr11:658354
|
A | G | 1 | a0001c0001t0001g0328 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1504-4303T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 658354 | ||||||
| chr11:658360
|
T | C | 5 | a0001c0001t0001g0328a0001c0002t0001g0195a0001c0002t0001g0196others(2): Show | 5 | HG01109.hp2 HG02630.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1504-4309A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 658360 | ||||||
| chr11:658385
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1504-4334G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 658385 | ||||||
| chr11:658430
|
A | G | 68 | a0001c0002t0001g0042a0001c0002t0001g0202a0001c0002t0001g0203others(65): Show | 68 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.1504-4379T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 658430 | ||||||
| chr11:658506
|
G | A | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(185): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1504-4455C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 658506 | ||||||
| chr11:658511
|
C | T | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(185): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1504-4460G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 658511 | ||||||
| chr11:658514
|
A | G | 294 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(291): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.1504-4463T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 658514 | ||||||
| chr11:658582
|
T | C | 5 | a0001c0001t0001g0328a0001c0002t0001g0195a0001c0002t0001g0196others(2): Show | 5 | HG01109.hp2 HG02630.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1504-4531A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 658582 | ||||||
| chr11:658599
|
G | A | 1 | a0001c0011t0001g0085 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1504-4548C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 658599 | ||||||
| chr11:658607
|
G | A | 1 | a0001c0001t0001g0328 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1504-4556C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 658607 | ||||||
| chr11:658618
|
C | T | 21 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0049others(18): Show | 21 | HG00741.hp2 HG01074.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1504-4567G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 658618 | ||||||
| chr11:658722
|
C | T | 1 | a0001c0003t0001g0180 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1504-4671G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 658722 | ||||||
| chr11:658723
|
G | A | 11 | a0001c0001t0001g0038a0001c0001t0001g0077a0001c0001t0001g0079others(8): Show | 11 | HG00558.hp2 HG00621.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.1504-4672C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 658723 | ||||||
| chr11:658749
|
C | T | 1 | a0001c0002t0001g0251 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1504-4698G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 658749 | ||||||
| chr11:658798
|
C | A | 1 | a0001c0001t0001g0055 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1504-4747G>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 658798 | ||||||
| chr11:658960
|
G | C | 1 | a0001c0001t0001g0046 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1504-4909C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 658960 | ||||||
| chr11:659032
|
C | T | 3 | a0001c0002t0001g0243a0001c0002t0001g0249a0001c0002t0001g0258 | 3 | HG02451.hp2 HG02630.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1504-4981G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 659032 | ||||||
| chr11:659179
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1504-5128G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 659179 | ||||||
| chr11:659228
|
C | CA | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0052others(3): Show | 6 | HG00741.hp2 HG02148.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1504-5178dupT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 659228 | ||||||
| chr11:659228
|
CA | C | 129 | a0001c0001t0001g0041a0001c0001t0001g0079a0001c0001t0001g0253others(126): Show | 130 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1504-5178delT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 659228 | ||||||
| chr11:659229
|
A | C | 4 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0030others(1): Show | 4 | HG02257.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1504-5178T>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 659229 | ||||||
| chr11:659266
|
C | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(119): Show | 124 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.1504-5215G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 659266 | ||||||
| chr11:659479
|
G | A | 7 | a0001c0001t0001g0282a0001c0001t0001g0288a0001c0001t0001g0291others(4): Show | 7 | HG01167.hp2 HG01358.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.1504-5428C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 659479 | ||||||
| chr11:659489
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1504-5438G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 659489 | ||||||
| chr11:659490
|
A | G | 101 | a0001c0001t0001g0253a0001c0001t0001g0328a0001c0002t0001g0042others(98): Show | 102 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.1504-5439T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 659490 | ||||||
| chr11:659516
|
C | T | 1 | a0001c0002t0001g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1504-5465G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 659516 | ||||||
| chr11:659545
|
C | T | 96 | a0001c0001t0001g0253a0001c0002t0001g0042a0001c0002t0001g0201others(93): Show | 97 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.1504-5494G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 659545 | ||||||
| chr11:659619
|
C | A | 53 | a0001c0003t0001g0006a0001c0003t0001g0032a0001c0003t0001g0141others(50): Show | 53 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.1504-5568G>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 659619 | ||||||
| chr11:659661
|
C | T | 5 | a0001c0001t0001g0328a0001c0002t0001g0195a0001c0002t0001g0196others(2): Show | 5 | HG01109.hp2 HG02630.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1504-5610G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 659661 | ||||||
| chr11:659707
|
C | T | 1 | a0001c0003t0001g0182 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1504-5656G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 659707 | ||||||
| chr11:659784
|
G | C | 1 | a0001c0001t0001g0328 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1504-5733C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 659784 | ||||||
| chr11:659889
|
C | A | 1 | a0001c0001t0001g0089 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1504-5838G>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 659889 | ||||||
| chr11:659906
|
C | T | 5 | a0001c0001t0001g0328a0001c0002t0001g0195a0001c0002t0001g0196others(2): Show | 5 | HG01109.hp2 HG02630.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1504-5855G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 659906 | ||||||
| chr11:659925
|
G | A | 1 | a0001c0003t0001g0172 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1504-5874C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 659925 | ||||||
| chr11:660058
|
A | G | 6 | a0001c0003t0001g0169a0001c0003t0001g0170a0001c0003t0001g0171others(3): Show | 6 | HG02572.hp2 HG02615.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1504-6007T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 660058 | ||||||
| chr11:660211
|
A | C | 11 | a0001c0001t0001g0038a0001c0001t0001g0077a0001c0001t0001g0079others(8): Show | 11 | HG00558.hp2 HG00621.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.1504-6160T>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 660211 | ||||||
| chr11:660266
|
G | A | 4 | a0001c0002t0001g0206a0001c0002t0001g0250a0001c0002t0001g0259others(1): Show | 4 | HG02109.hp1 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1504-6215C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 660266 | ||||||
| chr11:660456
|
G | A | 4 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(1): Show | 4 | HG01346.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1504-6405C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 660456 | ||||||
| chr11:660456
|
G | T | 53 | a0001c0003t0001g0006a0001c0003t0001g0032a0001c0003t0001g0141others(50): Show | 53 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.1504-6405C>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 660456 | ||||||
| chr11:660514
|
T | C | 154 | a0001c0001t0001g0253a0001c0001t0001g0328a0001c0002t0001g0042others(151): Show | 155 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.1504-6463A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 660514 | ||||||
| chr11:660597
|
C | T | 47 | a0001c0003t0001g0006a0001c0003t0001g0032a0001c0003t0001g0141others(44): Show | 47 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.1504-6546G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 660597 | ||||||
| chr11:660609
|
G | T | 95 | a0001c0001t0001g0253a0001c0002t0001g0042a0001c0002t0001g0201others(92): Show | 96 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.1504-6558C>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 660609 | ||||||
| chr11:660645
|
C | T | 26 | a0001c0002t0001g0201a0001c0002t0001g0206a0001c0002t0001g0236others(23): Show | 27 | HG01243.hp2 HG01346.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1504-6594G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 660645 | ||||||
| chr11:660739
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1504-6688C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 660739 | ||||||
| chr11:660888
|
T | TAA | 96 | a0001c0001t0001g0253a0001c0002t0001g0042a0001c0002t0001g0201others(93): Show | 97 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.1504-6838_1504-683 others(6): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 660888 | ||||||
| chr11:660891
|
G | A | 1 | a0001c0001t0001g0324 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1504-6840C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 660891 | ||||||
| chr11:660901
|
G | C | 1 | a0001c0001t0001g0328 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1504-6850C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 660901 | ||||||
| chr11:660964
|
G | A | 1 | a0001c0002t0001g0211 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1504-6913C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 660964 | ||||||
| chr11:661129
|
C | A | 5 | a0001c0001t0001g0328a0001c0002t0001g0195a0001c0002t0001g0196others(2): Show | 5 | HG01109.hp2 HG02630.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1504-7078G>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 661129 | ||||||
| chr11:661240
|
G | C | 1 | a0001c0001t0001g0038 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1504-7189C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 661240 | ||||||
| chr11:661261
|
T | C | 100 | a0001c0001t0001g0253a0001c0001t0001g0328a0001c0002t0001g0042others(97): Show | 101 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.1504-7210A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 661261 | ||||||
| chr11:661398
|
AT | A | 7 | a0001c0001t0001g0136a0001c0001t0001g0276a0001c0002t0001g0195others(4): Show | 7 | HG02630.hp1 HG02683.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1504-7348delA | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 661398 | ||||||
| chr11:661410
|
T | C | 4 | a0001c0002t0001g0195a0001c0002t0001g0196a0001c0002t0001g0197others(1): Show | 4 | HG02630.hp1 HG02818.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1504-7359A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 661410 | ||||||
| chr11:661412
|
T | A | 2 | a0001c0001t0001g0312a0001c0001t0001g0313 | 2 | NA18951.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1504-7361A>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 661412 | ||||||
| chr11:661439
|
G | A | 69 | a0001c0001t0001g0253a0001c0002t0001g0042a0001c0002t0001g0202others(66): Show | 69 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.1504-7388C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 661439 | ||||||
| chr11:661697
|
C | T | 2 | a0001c0002t0001g0214a0001c0002t0001g0216 | 2 | HG01257.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1504-7646G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 661697 | ||||||
| chr11:661754
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0111 | 2 | HG01167.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1504-7703C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 661754 | ||||||
| chr11:661905
|
T | A | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1504-7854A>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 661905 | ||||||
| chr11:662019
|
G | A | 96 | a0001c0001t0001g0253a0001c0002t0001g0042a0001c0002t0001g0201others(93): Show | 97 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.1504-7968C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 662019 | ||||||
| chr11:662169
|
C | G | 5 | a0001c0001t0001g0328a0001c0002t0001g0195a0001c0002t0001g0196others(2): Show | 5 | HG01109.hp2 HG02630.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1504-8118G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 662169 | ||||||
| chr11:662171
|
C | T | 5 | a0001c0001t0001g0328a0001c0002t0001g0195a0001c0002t0001g0196others(2): Show | 5 | HG01109.hp2 HG02630.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1504-8120G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 662171 | ||||||
| chr11:662202
|
C | G | 69 | a0001c0001t0001g0253a0001c0002t0001g0042a0001c0002t0001g0202others(66): Show | 69 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.1504-8151G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 662202 | ||||||
| chr11:662375
|
G | A | 53 | a0001c0003t0001g0006a0001c0003t0001g0032a0001c0003t0001g0141others(50): Show | 53 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.1504-8324C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 662375 | ||||||
| chr11:662407
|
G | A | 95 | a0001c0001t0001g0253a0001c0002t0001g0042a0001c0002t0001g0201others(92): Show | 96 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.1504-8356C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 662407 | ||||||
| chr11:662496
|
GACC | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 8 | HG01943.hp1 HG02148.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.1504-8448_1504-844 others(7): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 662496 | ||||||
| chr11:662799
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1504-8748G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 662799 | ||||||
| chr11:662811
|
C | T | 7 | a0001c0001t0001g0278a0001c0001t0001g0328a0001c0002t0001g0195others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1504-8760G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 662811 | ||||||
| chr11:662922
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1504-8871G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 662922 | ||||||
| chr11:662972
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1504-8921G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 662972 | ||||||
| chr11:663028
|
G | C | 6 | a0001c0002t0001g0329a0001c0002t0001g0330a0001c0002t0001g0331others(3): Show | 6 | HG02572.hp1 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1504-8977C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 663028 | ||||||
| chr11:663050
|
C | T | 3 | a0001c0002t0001g0223a0001c0002t0001g0340a0001c0002t0001g0342 | 3 | NA18993.hp1 NA19070.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1504-8999G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 663050 | ||||||
| chr11:663129
|
A | C | 148 | a0001c0001t0001g0253a0001c0001t0001g0328a0001c0002t0001g0042others(145): Show | 149 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.1504-9078T>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 663129 | ||||||
| chr11:663174
|
T | C | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(122): Show | 127 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.1504-9123A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 663174 | ||||||
| chr11:663203
|
T | C | 10 | a0001c0004t0001g0013a0001c0004t0001g0014a0001c0004t0001g0020others(7): Show | 10 | HG01106.hp2 HG01496.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.1504-9152A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 663203 | ||||||
| chr11:663243
|
T | C | 4 | a0001c0003t0001g0159a0001c0003t0001g0188a0001c0003t0001g0189others(1): Show | 4 | HG01069.hp2 HG01258.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1504-9192A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 663243 | ||||||
| chr11:663340
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(133): Show | 138 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.1504-9289G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 663340 | ||||||
| chr11:663358
|
C | G | 101 | a0001c0001t0001g0253a0001c0001t0001g0328a0001c0002t0001g0042others(98): Show | 102 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.1504-9307G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 663358 | ||||||
| chr11:663434
|
T | A | 3 | a0001c0002t0001g0240a0001c0002t0001g0244a0001c0002t0001g0245 | 3 | HG03098.hp1 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1504-9383A>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 663434 | ||||||
| chr11:663463
|
C | G | 95 | a0001c0001t0001g0253a0001c0002t0001g0042a0001c0002t0001g0201others(92): Show | 96 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.1504-9412G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 663463 | ||||||
| chr11:663591
|
C | T | 1 | a0001c0002t0001g0230 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1504-9540G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 663591 | ||||||
| chr11:663617
|
TCTCCTCA others(50): Show |
T | 7 | a0001c0002t0001g0208a0001c0002t0001g0209a0001c0002t0001g0222others(4): Show | 7 | HG02040.hp2 NA18943.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.1504-9623_1504-956 others(61): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 663617 | ||||||
| chr11:663834
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1504-9783G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 663834 | ||||||
| chr11:663868
|
G | A | 2 | a0001c0001t0001g0325a0001c0001t0001g0326 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1504-9817C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 663868 | ||||||
| chr11:663911
|
C | A | 1 | a0001c0002t0001g0268 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1504-9860G>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 663911 | ||||||
| chr11:663949
|
C | T | 1 | a0001c0004t0001g0024 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1504-9898G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 663949 | ||||||
| chr11:663981
|
G | C | 1 | a0001c0002t0001g0268 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1504-9930C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 663981 | ||||||
| chr11:663995
|
G | A | 5 | a0001c0001t0001g0328a0001c0002t0001g0195a0001c0002t0001g0196others(2): Show | 5 | HG01109.hp2 HG02630.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1504-9944C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 663995 | ||||||
| chr11:664230
|
G | GA | 11 | a0001c0001t0001g0058a0001c0001t0001g0282a0001c0001t0002g0033others(8): Show | 11 | HG01243.hp2 HG01433.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1504-10180dupT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 664230 | ||||||
| chr11:664366
|
G | C | 2 | a0001c0003t0001g0146a0001c0003t0001g0167 | 2 | HG03831.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1503+10170C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 664366 | ||||||
| chr11:664411
|
C | CCAGCTAT others(55): Show |
24 | a0001c0001t0001g0273a0001c0001t0001g0275a0001c0001t0001g0276others(21): Show | 24 | HG00597.hp2 HG01192.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.1503+10063_1503+10 others(68): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 664411 | ||||||
| chr11:664411
|
C | CCAGCTAT others(179): Show |
17 | a0001c0001t0001g0007a0001c0001t0001g0272a0001c0001t0001g0277others(14): Show | 17 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.1503+9939_1503+101 others(191): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 664411 | ||||||
| chr11:664411
|
C | CCAGCTAT others(303): Show |
6 | a0001c0002t0001g0208a0001c0002t0001g0209a0001c0002t0001g0222others(3): Show | 6 | HG02040.hp2 NA18943.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.1503+9815_1503+101 others(315): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 664411 | ||||||
| chr11:664411
|
C | CCAGCTAT others(613): Show |
1 | a0001c0001t0001g0046 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1503+10124_1503+10 others(626): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 664411 | ||||||
| chr11:664411
|
C | CCAGCTAT others(737): Show |
3 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0072 | 3 | HG01261.hp2 HG01515.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1503+10124_1503+10 others(750): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 664411 | ||||||
| chr11:664411
|
C | CCAGCTAT others(551): Show |
1 | a0001c0002t0001g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1503+9567_1503+101 others(563): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 664411 | ||||||
| chr11:664411
|
C | CCAGCTAT others(613): Show |
3 | a0001c0002t0001g0195a0001c0002t0001g0196a0001c0002t0001g0198 | 3 | HG02818.hp2 HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1503+9505_1503+101 others(625): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 664411 | ||||||
| chr11:664411
|
C | CCAGCTAT others(737): Show |
2 | a0001c0001t0001g0055a0001c0002t0001g0271 | 2 | HG03486.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1503+10124_1503+10 others(750): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 664411 | ||||||
| chr11:664411
|
C | CCAGCTAT others(923): Show |
1 | a0001c0001t0001g0328 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1503+10124_1503+10 others(936): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 664411 | ||||||
| chr11:664411
|
C | CCAGCTAT others(179): Show |
1 | a0001c0001t0001g0295 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1503+10124_1503+10 others(192): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 664411 | ||||||
| chr11:664411
|
C | CCAGCTAT others(365): Show |
3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0200 | 3 | HG02622.hp1 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1503+10124_1503+10 others(378): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 664411 | ||||||
| chr11:664411
|
C | CCAGCTAT others(180): Show |
1 | a0001c0002t0001g0242 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1503+10124_1503+10 others(193): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 664411 | ||||||
| chr11:664411
|
CCAGCTAT others(179): Show |
C | 52 | a0001c0003t0001g0006a0001c0003t0001g0032a0001c0003t0001g0141others(49): Show | 52 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.1503+9939_1503+101 others(5): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 664411 | ||||||
| chr11:664411
|
CCAGCTAT others(241): Show |
C | 9 | a0001c0001t0001g0282a0001c0001t0001g0288a0001c0001t0001g0291others(6): Show | 9 | HG01167.hp2 HG02735.hp1 HG03669.hp2 others(6): Show |
intron_variant | MODIFIER | c.1503+9877_1503+101 others(5): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 664411 | ||||||
| chr11:664466
|
T | A | 1 | a0001c0001t0001g0074 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1503+10070A>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 664466 | ||||||
| chr11:664550
|
G | GAGAGGAG others(365): Show |
1 | a0001c0001t0001g0074 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1503+9985_1503+998 others(376): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 664550 | ||||||
| chr11:664612
|
G | GAGAGGAG others(303): Show |
1 | a0001c0001t0001g0090 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1503+9923_1503+992 others(314): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 664612 | ||||||
| chr11:664673
|
C | CGAGAGGA others(55): Show |
1 | a0001c0002t0001g0339 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1503+9862_1503+986 others(66): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 664673 | ||||||
| chr11:664689
|
G | C | 1 | a0001c0003t0001g0157 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1503+9847C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 664689 | ||||||
| chr11:664811
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1503+9725G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 664811 | ||||||
| chr11:664817
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1503+9719C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 664817 | ||||||
| chr11:664860
|
G | GAGAGGAG others(55): Show |
1 | a0001c0001t0001g0070 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1503+9675_1503+967 others(66): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 664860 | ||||||
| chr11:664873
|
C | A | 3 | a0001c0002t0001g0265a0001c0002t0001g0308a0001c0002t0001g0311 | 3 | HG02683.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1503+9663G>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 664873 | ||||||
| chr11:664878
|
C | T | 1 | a0001c0001t0001g0010 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1503+9658G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 664878 | ||||||
| chr11:664922
|
G | C | 30 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0015others(27): Show | 30 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.1503+9614C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 664922 | ||||||
| chr11:665002
|
C | CGTCACAC others(303): Show |
16 | a0001c0002t0001g0042a0001c0002t0001g0202a0001c0002t0001g0205others(13): Show | 16 | HG00597.hp1 HG02056.hp1 HG02523.hp1 others(13): Show |
intron_variant | MODIFIER | c.1503+9533_1503+953 others(314): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665002 | ||||||
| chr11:665002
|
C | CGTCACAC others(241): Show |
1 | a0001c0002t0001g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1503+9533_1503+953 others(252): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665002 | ||||||
| chr11:665002
|
C | CGTCACAC others(179): Show |
4 | a0001c0002t0001g0220a0001c0002t0001g0227a0001c0002t0001g0228others(1): Show | 4 | HG00280.hp2 HG02074.hp1 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1503+9533_1503+953 others(190): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665002 | ||||||
| chr11:665002
|
C | T | 3 | a0001c0002t0001g0223a0001c0002t0001g0340a0001c0002t0001g0342 | 3 | NA18993.hp1 NA19070.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1503+9534G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665002 | ||||||
| chr11:665021
|
G | A | 3 | a0001c0002t0001g0223a0001c0002t0001g0340a0001c0002t0001g0342 | 3 | NA18993.hp1 NA19070.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1503+9515C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665021 | ||||||
| chr11:665021
|
G | GAGTCCTG others(551): Show |
1 | a0001c0002t0001g0259 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1503+9514_1503+951 others(562): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665021 | ||||||
| chr11:665021
|
G | GAGTCCTG others(675): Show |
4 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(1): Show | 4 | HG01346.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1503+9514_1503+951 others(686): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665021 | ||||||
| chr11:665021
|
G | GAGTCCTG others(551): Show |
10 | a0001c0002t0001g0327a0001c0002t0001g0329a0001c0002t0001g0330others(7): Show | 10 | HG02486.hp1 HG02572.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1503+9514_1503+951 others(562): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665021 | ||||||
| chr11:665021
|
G | GAGTCCTG others(489): Show |
3 | a0001c0002t0001g0206a0001c0002t0001g0250a0001c0002t0001g0304 | 3 | HG02109.hp1 HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1503+9514_1503+951 others(500): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665021 | ||||||
| chr11:665021
|
G | GAGTCCTG others(427): Show |
1 | a0001c0002t0001g0268 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1503+9514_1503+951 others(438): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665021 | ||||||
| chr11:665021
|
G | GAGTCCTG others(365): Show |
7 | a0001c0002t0001g0214a0001c0002t0001g0240a0001c0002t0001g0243others(4): Show | 7 | HG01433.hp2 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1503+9514_1503+951 others(376): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665021 | ||||||
| chr11:665021
|
G | GAGTCCTG others(303): Show |
21 | a0001c0001t0001g0253a0001c0002t0001g0203a0001c0002t0001g0204others(18): Show | 21 | HG01123.hp1 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.1503+9514_1503+951 others(314): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665021 | ||||||
| chr11:665021
|
G | GAGTCCTG others(241): Show |
12 | a0001c0002t0001g0201a0001c0002t0001g0207a0001c0002t0001g0211others(9): Show | 13 | HG00642.hp1 HG00642.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1503+9514_1503+951 others(252): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665021 | ||||||
| chr11:665021
|
G | GAGTCCTG others(117): Show |
1 | a0001c0002t0001g0242 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1503+9391_1503+951 others(128): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665021 | ||||||
| chr11:665021
|
G | GAGTCCTG others(303): Show |
1 | a0001c0002t0001g0251 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1503+9514_1503+951 others(314): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665021 | ||||||
| chr11:665046
|
G | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0158 | 2 | HG00438.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1503+9490C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665046 | ||||||
| chr11:665054
|
GAGGACAG others(121): Show |
G | 1 | a0001c0001t0001g0103 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1503+9354_1503+948 others(4): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665054 | ||||||
| chr11:665096
|
G | GCTATTCA others(303): Show |
3 | a0001c0002t0001g0221a0001c0002t0001g0224a0001c0002t0001g0341 | 3 | NA18945.hp2 NA19084.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1503+9439_1503+944 others(314): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665096 | ||||||
| chr11:665126
|
T | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(140): Show | 145 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.1503+9410A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665126 | ||||||
| chr11:665143
|
CTAAG | C | 7 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0046others(4): Show | 7 | HG00140.hp2 HG02622.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.1503+9389_1503+939 others(8): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665143 | ||||||
| chr11:665145
|
A | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(124): Show | 129 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.1503+9391T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665145 | ||||||
| chr11:665147
|
G | GTCCTGGC others(51): Show |
2 | a0001c0001t0001g0059a0001c0001t0001g0070 | 2 | HG04199.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1503+9388_1503+938 others(62): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665147 | ||||||
| chr11:665147
|
G | GTCCTGGC others(113): Show |
1 | a0001c0001t0001g0138 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1503+9388_1503+938 others(124): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665147 | ||||||
| chr11:665147
|
G | GTCCTGGC others(175): Show |
4 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0191others(1): Show | 4 | HG01167.hp1 HG01943.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.1503+9388_1503+938 others(186): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665147 | ||||||
| chr11:665147
|
G | GTCCTGGC others(671): Show |
1 | a0001c0001t0001g0097 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1503+9388_1503+938 others(682): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665147 | ||||||
| chr11:665147
|
G | GTCCTGGC others(485): Show |
2 | a0001c0004t0001g0014a0001c0004t0001g0027 | 2 | HG02083.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1503+9388_1503+938 others(496): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665147 | ||||||
| chr11:665147
|
G | GTCCTGGC others(547): Show |
8 | a0001c0004t0001g0013a0001c0004t0001g0020a0001c0004t0001g0021others(5): Show | 8 | HG01106.hp2 HG01496.hp2 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.1503+9388_1503+938 others(558): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665147 | ||||||
| chr11:665147
|
G | GTCCTGGC others(237): Show |
1 | a0001c0001t0001g0045 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1503+9388_1503+938 others(248): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665147 | ||||||
| chr11:665147
|
G | GTCCTGGC others(299): Show |
2 | a0001c0001t0001g0129a0001c0001t0001g0280 | 2 | NA18612.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1503+9388_1503+938 others(310): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665147 | ||||||
| chr11:665147
|
G | GTCCTGGC others(361): Show |
3 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0133 | 3 | HG02071.hp1 HG04184.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1503+9388_1503+938 others(372): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665147 | ||||||
| chr11:665147
|
G | GTCCTGGC others(485): Show |
4 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0125others(1): Show | 4 | HG00735.hp1 HG03688.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1503+9388_1503+938 others(496): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665147 | ||||||
| chr11:665147
|
G | GTCCTGGC others(609): Show |
9 | a0001c0001t0001g0012a0001c0001t0001g0037a0001c0001t0001g0068others(6): Show | 9 | HG00639.hp1 HG01106.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.1503+9388_1503+938 others(620): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665147 | ||||||
| chr11:665147
|
G | GTCCTGGC others(671): Show |
85 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(82): Show | 87 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1503+9388_1503+938 others(682): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665147 | ||||||
| chr11:665147
|
G | GTCCTGGC others(733): Show |
3 | a0001c0001t0001g0043a0001c0001t0001g0066a0001c0001t0001g0089 | 3 | HG01069.hp1 HG02132.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1503+9388_1503+938 others(744): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665147 | ||||||
| chr11:665147
|
G | GTCCTGGC others(857): Show |
1 | a0001c0001t0001g0048 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1503+9388_1503+938 others(868): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665147 | ||||||
| chr11:665147
|
G | GTCCTGGC others(981): Show |
1 | a0001c0001t0001g0279 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1503+9388_1503+938 others(992): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665147 | ||||||
| chr11:665149
|
A | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(130): Show | 135 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.1503+9387T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665149 | ||||||
| chr11:665173
|
C | T | 1 | a0001c0001t0001g0055 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1503+9363G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665173 | ||||||
| chr11:665182
|
A | G | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(141): Show | 146 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.1503+9354T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665182 | ||||||
| chr11:665213
|
G | C | 95 | a0001c0001t0001g0253a0001c0002t0001g0042a0001c0002t0001g0201others(92): Show | 96 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.1503+9323C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665213 | ||||||
| chr11:665239
|
T | C | 25 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0030others(22): Show | 25 | HG00741.hp2 HG01074.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.1503+9297A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665239 | ||||||
| chr11:665248
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0200 | 3 | HG02622.hp1 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1503+9288C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665248 | ||||||
| chr11:665279
|
C | G | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0200 | 3 | HG02622.hp1 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1503+9257G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665279 | ||||||
| chr11:665321
|
G | C | 1 | a0001c0001t0001g0046 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1503+9215C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665321 | ||||||
| chr11:665673
|
A | T | 6 | a0001c0003t0001g0169a0001c0003t0001g0170a0001c0003t0001g0171others(3): Show | 6 | HG02572.hp2 HG02615.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1503+8863T>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665673 | ||||||
| chr11:665995
|
T | TG | 16 | a0001c0001t0001g0007a0001c0001t0001g0272a0001c0001t0001g0289others(13): Show | 16 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1503+8540dupC | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665995 | ||||||
| chr11:665999
|
C | T | 1 | a0001c0003t0001g0141 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1503+8537G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 665999 | ||||||
| chr11:666049
|
C | CT | 53 | a0001c0003t0001g0006a0001c0003t0001g0032a0001c0003t0001g0141others(50): Show | 53 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.1503+8486dupA | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 666049 | ||||||
| chr11:666331
|
A | C | 4 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0200others(1): Show | 4 | HG02622.hp1 HG02970.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1503+8205T>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 666331 | ||||||
| chr11:666496
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1503+8040C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 666496 | ||||||
| chr11:666551
|
G | A | 101 | a0001c0001t0001g0253a0001c0001t0001g0328a0001c0002t0001g0042others(98): Show | 102 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.1503+7985C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 666551 | ||||||
| chr11:666677
|
C | A | 95 | a0001c0001t0001g0253a0001c0002t0001g0042a0001c0002t0001g0201others(92): Show | 96 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.1503+7859G>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 666677 | ||||||
| chr11:666873
|
C | CA | 48 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0047others(45): Show | 49 | HG00597.hp2 HG01106.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.1503+7662dupT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 666873 | ||||||
| chr11:666873
|
CA | C | 55 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0046others(52): Show | 55 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1503+7662delT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 666873 | ||||||
| chr11:666891
|
A | G | 1 | a0001c0001t0006g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1503+7645T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 666891 | ||||||
| chr11:666893
|
A | G | 1 | a0001c0002t0001g0242 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1503+7643T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 666893 | ||||||
| chr11:667094
|
G | T | 53 | a0001c0003t0001g0006a0001c0003t0001g0032a0001c0003t0001g0141others(50): Show | 53 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.1503+7442C>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 667094 | ||||||
| chr11:667104
|
G | A | 5 | a0001c0001t0001g0328a0001c0002t0001g0195a0001c0002t0001g0196others(2): Show | 5 | HG01109.hp2 HG02630.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1503+7432C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 667104 | ||||||
| chr11:667153
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1503+7383C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 667153 | ||||||
| chr11:667284
|
T | A | 1 | a0001c0001t0001g0280 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1503+7252A>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 667284 | ||||||
| chr11:667312
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1503+7224G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 667312 | ||||||
| chr11:667329
|
G | GA | 101 | a0001c0001t0001g0253a0001c0001t0001g0328a0001c0002t0001g0042others(98): Show | 102 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.1503+7206dupT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 667329 | ||||||
| chr11:667355
|
TGGAG | T | 95 | a0001c0001t0001g0253a0001c0002t0001g0042a0001c0002t0001g0201others(92): Show | 96 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.1503+7177_1503+718 others(8): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 667355 | ||||||
| chr11:667410
|
A | G | 95 | a0001c0001t0001g0253a0001c0002t0001g0042a0001c0002t0001g0201others(92): Show | 96 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.1503+7126T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 667410 | ||||||
| chr11:667424
|
A | G | 95 | a0001c0001t0001g0253a0001c0002t0001g0042a0001c0002t0001g0201others(92): Show | 96 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.1503+7112T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 667424 | ||||||
| chr11:667427
|
A | G | 95 | a0001c0001t0001g0253a0001c0002t0001g0042a0001c0002t0001g0201others(92): Show | 96 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.1503+7109T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 667427 | ||||||
| chr11:667435
|
G | A | 95 | a0001c0001t0001g0253a0001c0002t0001g0042a0001c0002t0001g0201others(92): Show | 96 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.1503+7101C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 667435 | ||||||
| chr11:667438
|
A | G | 95 | a0001c0001t0001g0253a0001c0002t0001g0042a0001c0002t0001g0201others(92): Show | 96 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.1503+7098T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 667438 | ||||||
| chr11:667440
|
G | A | 95 | a0001c0001t0001g0253a0001c0002t0001g0042a0001c0002t0001g0201others(92): Show | 96 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.1503+7096C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 667440 | ||||||
| chr11:667455
|
G | A | 95 | a0001c0001t0001g0253a0001c0002t0001g0042a0001c0002t0001g0201others(92): Show | 96 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.1503+7081C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 667455 | ||||||
| chr11:667659
|
A | C | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0200 | 3 | HG02622.hp1 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1503+6877T>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 667659 | ||||||
| chr11:667665
|
T | C | 101 | a0001c0001t0001g0253a0001c0001t0001g0328a0001c0002t0001g0042others(98): Show | 102 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.1503+6871A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 667665 | ||||||
| chr11:667837
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1503+6699G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 667837 | ||||||
| chr11:667980
|
C | T | 3 | a0001c0002t0001g0240a0001c0002t0001g0244a0001c0002t0001g0245 | 3 | HG03098.hp1 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1503+6556G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 667980 | ||||||
| chr11:667988
|
G | T | 96 | a0001c0001t0001g0253a0001c0002t0001g0042a0001c0002t0001g0201others(93): Show | 97 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.1503+6548C>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 667988 | ||||||
| chr11:668066
|
T | C | 97 | a0001c0001t0001g0023a0001c0001t0001g0253a0001c0002t0001g0042others(94): Show | 98 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.1503+6470A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 668066 | ||||||
| chr11:668118
|
A | T | 1 | a0001c0001t0001g0082 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1503+6418T>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 668118 | ||||||
| chr11:668233
|
C | G | 2 | a0001c0002t0001g0206a0001c0002t0001g0250 | 2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1503+6303G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 668233 | ||||||
| chr11:668770
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1503+5766G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 668770 | ||||||
| chr11:668773
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0057others(2): Show | 6 | HG02165.hp2 NA18944.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.1503+5763C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 668773 | ||||||
| chr11:668970
|
T | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(292): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1503+5566A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 668970 | ||||||
| chr11:668974
|
T | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(111): Show | 116 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.1503+5562A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 668974 | ||||||
| chr11:669053
|
C | T | 52 | a0001c0003t0001g0006a0001c0003t0001g0032a0001c0003t0001g0141others(49): Show | 52 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.1503+5483G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 669053 | ||||||
| chr11:669080
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0043 | 2 | HG02132.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1503+5456G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 669080 | ||||||
| chr11:669088
|
C | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(292): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1503+5448G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 669088 | ||||||
| chr11:669107
|
A | G | 14 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(11): Show | 14 | HG00597.hp2 HG02523.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.1503+5429T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 669107 | ||||||
| chr11:669109
|
G | C | 97 | a0001c0001t0001g0253a0001c0001t0001g0307a0001c0002t0001g0042others(94): Show | 98 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.1503+5427C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 669109 | ||||||
| chr11:669125
|
C | CT | 15 | a0001c0001t0001g0325a0001c0002t0001g0222a0001c0002t0001g0242others(12): Show | 15 | HG00597.hp1 HG01433.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.1503+5410dupA | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 669125 | ||||||
| chr11:669125
|
CT | C | 57 | a0001c0001t0001g0007a0001c0001t0001g0272a0001c0001t0001g0277others(54): Show | 58 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.1503+5410delA | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 669125 | ||||||
| chr11:669125
|
CTTT | C | 13 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0035others(10): Show | 13 | HG00621.hp1 HG01361.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1503+5408_1503+541 others(7): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 669125 | ||||||
| chr11:669125
|
CTTTT | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(128): Show | 133 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.1503+5407_1503+541 others(8): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 669125 | ||||||
| chr11:669125
|
CTTTTT | C | 54 | a0001c0001t0004g0199a0001c0001t0006g0031a0001c0002t0001g0195others(51): Show | 54 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.1503+5406_1503+541 others(9): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 669125 | ||||||
| chr11:669267
|
C | T | 1 | a0001c0002t0001g0304 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1503+5269G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 669267 | ||||||
| chr11:669293
|
A | G | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1503+5243T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 669293 | ||||||
| chr11:669317
|
G | C | 3 | a0001c0002t0001g0210a0001c0002t0001g0219a0001c0002t0001g0266 | 3 | HG02738.hp2 HG03017.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1503+5219C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 669317 | ||||||
| chr11:669327
|
T | A | 4 | a0001c0002t0001g0205a0001c0002t0001g0223a0001c0002t0001g0340others(1): Show | 4 | HG02523.hp1 NA18993.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.1503+5209A>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 669327 | ||||||
| chr11:669573
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1503+4963A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 669573 | ||||||
| chr11:669624
|
G | GA | 14 | a0001c0001t0001g0017a0001c0001t0001g0049a0001c0001t0001g0060others(11): Show | 14 | HG00741.hp2 HG01074.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1503+4911dupT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 669624 | ||||||
| chr11:669758
|
C | T | 1 | a0004c0012t0001g0270 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1503+4778G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 669758 | ||||||
| chr11:669770
|
A | C | 1 | a0001c0001t0001g0118 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1503+4766T>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 669770 | ||||||
| chr11:669905
|
G | C | 2 | a0001c0003t0001g0150a0001c0003t0001g0176 | 2 | HG01123.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1503+4631C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 669905 | ||||||
| chr11:669927
|
CAA | C | 13 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0060others(10): Show | 13 | HG00438.hp1 HG01358.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1503+4607_1503+460 others(6): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 669927 | ||||||
| chr11:669927
|
CAAA | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(125): Show | 130 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1503+4606_1503+460 others(7): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 669927 | ||||||
| chr11:669927
|
CAAAA | C | 85 | a0001c0001t0001g0023a0001c0001t0001g0109a0001c0001t0001g0253others(82): Show | 86 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.1503+4605_1503+460 others(8): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 669927 | ||||||
| chr11:669927
|
CAAAAAA | C | 61 | a0001c0002t0001g0208a0001c0002t0001g0209a0001c0002t0001g0220others(58): Show | 61 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.1503+4603_1503+460 others(10): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 669927 | ||||||
| chr11:669959
|
C | G | 2 | a0001c0002t0001g0224a0001c0002t0001g0341 | 2 | NA18945.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1503+4577G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 669959 | ||||||
| chr11:669974
|
A | G | 3 | a0001c0002t0001g0243a0001c0002t0001g0249a0001c0002t0001g0258 | 3 | HG02451.hp2 HG02630.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1503+4562T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 669974 | ||||||
| chr11:670081
|
GA | G | 225 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(222): Show | 227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.1503+4454delT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 670081 | ||||||
| chr11:670127
|
C | T | 1 | a0001c0001t0006g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1503+4409G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 670127 | ||||||
| chr11:670401
|
CT | C | 32 | a0001c0001t0001g0116a0001c0001t0001g0307a0001c0001t0001g0324others(29): Show | 33 | HG01069.hp2 HG01243.hp2 HG01346.hp1 others(30): Show |
intron_variant | MODIFIER | c.1503+4134delA | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 670401 | ||||||
| chr11:670401
|
CTT | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(260): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.1503+4133_1503+413 others(6): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 670401 | ||||||
| chr11:670419
|
T | A | 3 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0013t0001g0078 | 3 | HG00735.hp1 HG03688.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1503+4117A>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 670419 | ||||||
| chr11:670443
|
G | A | 2 | a0001c0001t0005g0290a0001c0002t0001g0271 | 2 | HG01358.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1503+4093C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 670443 | ||||||
| chr11:670493
|
T | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(133): Show | 138 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.1503+4043A>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 670493 | ||||||
| chr11:670754
|
ATTTCTTT | A | 70 | a0001c0001t0001g0253a0001c0002t0001g0042a0001c0002t0001g0202others(67): Show | 70 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.1503+3775_1503+378 others(11): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 670754 | ||||||
| chr11:670771
|
G | GTT | 5 | a0001c0001t0001g0328a0001c0001t0004g0199a0001c0002t0001g0195others(2): Show | 5 | HG01109.hp2 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1503+3763_1503+376 others(6): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 670771 | ||||||
| chr11:670775
|
TTG | T | 277 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(274): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.1503+3759_1503+376 others(6): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 670775 | ||||||
| chr11:670776
|
TG | T | 11 | a0001c0001t0001g0073a0001c0003t0001g0152a0001c0004t0001g0013others(8): Show | 11 | HG00673.hp1 HG01106.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.1503+3759delC | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 670776 | ||||||
| chr11:670777
|
G | T | 8 | a0001c0001t0001g0305a0001c0001t0001g0328a0001c0001t0004g0199others(5): Show | 8 | HG01109.hp2 HG02083.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1503+3759C>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 670777 | ||||||
| chr11:670779
|
T | C | 97 | a0001c0001t0001g0253a0001c0001t0001g0307a0001c0002t0001g0042others(94): Show | 98 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.1503+3757A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 670779 | ||||||
| chr11:670779
|
T | G | 1 | a0001c0004t0001g0014 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1503+3757A>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 670779 | ||||||
| chr11:670780
|
T | G | 11 | a0001c0001t0001g0073a0001c0003t0001g0152a0001c0004t0001g0013others(8): Show | 11 | HG00673.hp1 HG01106.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.1503+3756A>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 670780 | ||||||
| chr11:670781
|
T | G | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(176): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.1503+3755A>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 670781 | ||||||
| chr11:670800
|
C | T | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1503+3736G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 670800 | ||||||
| chr11:670931
|
G | GTTTTTT | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(163): Show | 168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1503+3599_1503+360 others(10): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 670931 | ||||||
| chr11:670931
|
G | GTTTTTTT | 47 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0049others(44): Show | 47 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1503+3598_1503+360 others(11): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 670931 | ||||||
| chr11:670931
|
G | GTTTTTTT others(1): Show |
59 | a0001c0001t0001g0253a0001c0002t0001g0042a0001c0002t0001g0195others(56): Show | 60 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.1503+3597_1503+360 others(12): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 670931 | ||||||
| chr11:670931
|
G | GTTTTTTT others(2): Show |
19 | a0001c0002t0001g0203a0001c0002t0001g0205a0001c0002t0001g0212others(16): Show | 19 | HG01243.hp1 HG01433.hp2 HG02074.hp1 others(16): Show |
intron_variant | MODIFIER | c.1503+3596_1503+360 others(13): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 670931 | ||||||
| chr11:670931
|
G | GTTTTTTT others(3): Show |
1 | a0001c0002t0001g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1503+3595_1503+360 others(14): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 670931 | ||||||
| chr11:670931
|
G | T | 1 | a0001c0001t0001g0103 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1503+3605C>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 670931 | ||||||
| chr11:671022
|
G | A | 1 | a0001c0002t0001g0248 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1503+3514C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 671022 | ||||||
| chr11:671090
|
G | A | 1 | a0001c0002t0001g0247 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1503+3446C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 671090 | ||||||
| chr11:671164
|
G | A | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1503+3372C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 671164 | ||||||
| chr11:671171
|
G | A | 1 | a0001c0001t0006g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1503+3365C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 671171 | ||||||
| chr11:671261
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1503+3275C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 671261 | ||||||
| chr11:671413
|
G | C | 1 | a0001c0003t0001g0153 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1503+3123C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 671413 | ||||||
| chr11:671509
|
A | G | 6 | a0001c0001t0001g0328a0001c0001t0004g0199a0001c0002t0001g0195others(3): Show | 6 | HG01109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1503+3027T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 671509 | ||||||
| chr11:671595
|
G | A | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1503+2941C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 671595 | ||||||
| chr11:671804
|
AAC | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(133): Show | 138 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.1503+2730_1503+273 others(6): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 671804 | ||||||
| chr11:671816
|
C | G | 1 | a0001c0001t0001g0328 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1503+2720G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 671816 | ||||||
| chr11:671826
|
TA | T | 42 | a0001c0001t0001g0007a0001c0001t0001g0272a0001c0001t0001g0277others(39): Show | 42 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.1503+2709delT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 671826 | ||||||
| chr11:671842
|
A | C | 1 | a0001c0001t0001g0023 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1503+2694T>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 671842 | ||||||
| chr11:671847
|
AAAG | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(118): Show | 123 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1503+2686_1503+268 others(7): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 671847 | ||||||
| chr11:671848
|
AAG | A | 61 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(58): Show | 61 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.1503+2686_1503+268 others(6): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 671848 | ||||||
| chr11:671849
|
AG | A | 78 | a0001c0001t0001g0043a0001c0001t0001g0253a0001c0001t0006g0031others(75): Show | 79 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.1503+2686delC | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 671849 | ||||||
| chr11:671850
|
G | A | 31 | a0001c0001t0001g0307a0001c0001t0004g0199a0001c0002t0001g0198others(28): Show | 31 | HG01346.hp1 HG02055.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.1503+2686C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 671850 | ||||||
| chr11:671852
|
A | C | 1 | a0001c0001t0001g0046 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1503+2684T>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 671852 | ||||||
| chr11:671864
|
A | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(189): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1503+2672T>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 671864 | ||||||
| chr11:671921
|
T | C | 96 | a0001c0001t0001g0253a0001c0001t0001g0307a0001c0002t0001g0042others(93): Show | 97 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.1503+2615A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 671921 | ||||||
| chr11:671923
|
G | A | 29 | a0001c0002t0001g0042a0001c0002t0001g0202a0001c0002t0001g0208others(26): Show | 29 | HG00280.hp2 HG00597.hp1 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.1503+2613C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 671923 | ||||||
| chr11:672161
|
G | A | 96 | a0001c0001t0001g0253a0001c0001t0001g0307a0001c0002t0001g0042others(93): Show | 97 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.1503+2375C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 672161 | ||||||
| chr11:672254
|
TGTTCATT others(67): Show |
T | 6 | a0001c0001t0001g0328a0001c0001t0004g0199a0001c0002t0001g0195others(3): Show | 6 | HG01109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1503+2208_1503+228 others(78): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 672254 | ||||||
| chr11:672310
|
ACCTGGGT others(67): Show |
A | 1 | a0001c0002t0001g0211 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1503+2152_1503+222 others(78): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 672310 | ||||||
| chr11:672315
|
G | C | 1 | a0001c0002t0001g0259 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1503+2221C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 672315 | ||||||
| chr11:672328
|
C | T | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(285): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.1503+2208G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 672328 | ||||||
| chr11:672356
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1503+2180G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 672356 | ||||||
| chr11:672357
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1503+2179G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 672357 | ||||||
| chr11:672402
|
C | T | 1 | a0001c0002t0001g0211 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1503+2134G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 672402 | ||||||
| chr11:672443
|
C | T | 52 | a0001c0003t0001g0006a0001c0003t0001g0032a0001c0003t0001g0141others(49): Show | 52 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.1503+2093G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 672443 | ||||||
| chr11:672457
|
G | A | 6 | a0001c0001t0001g0328a0001c0001t0004g0199a0001c0002t0001g0195others(3): Show | 6 | HG01109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1503+2079C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 672457 | ||||||
| chr11:672569
|
G | A | 1 | a0001c0001t0001g0076 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1503+1967C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 672569 | ||||||
| chr11:672645
|
A | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(292): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1503+1891T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 672645 | ||||||
| chr11:672715
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1503+1821C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 672715 | ||||||
| chr11:672858
|
A | T | 2 | a0001c0001t0001g0086a0001c0013t0001g0078 | 2 | HG00735.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1503+1678T>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 672858 | ||||||
| chr11:672905
|
T | G | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1503+1631A>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 672905 | ||||||
| chr11:672919
|
C | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(189): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1503+1617G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 672919 | ||||||
| chr11:672934
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(189): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1503+1602T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 672934 | ||||||
| chr11:673136
|
G | A | 1 | a0001c0001t0006g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1503+1400C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 673136 | ||||||
| chr11:673144
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1503+1392C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 673144 | ||||||
| chr11:673282
|
T | G | 4 | a0001c0002t0001g0205a0001c0002t0001g0223a0001c0002t0001g0340others(1): Show | 4 | HG02523.hp1 NA18993.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.1503+1254A>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 673282 | ||||||
| chr11:673443
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1503+1093C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 673443 | ||||||
| chr11:673446
|
G | A | 1 | a0001c0003t0001g0032 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1503+1090C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 673446 | ||||||
| chr11:673498
|
A | G | 1 | a0001c0014t0001g0147 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1503+1038T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 673498 | ||||||
| chr11:673507
|
G | A | 2 | a0001c0002t0001g0300a0001c0002t0001g0301 | 2 | HG01243.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1503+1029C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 673507 | ||||||
| chr11:673565
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0058 | 4 | NA18944.hp1 NA18960.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.1503+971C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 673565 | ||||||
| chr11:673637
|
C | T | 95 | a0001c0001t0001g0253a0001c0001t0001g0307a0001c0002t0001g0042others(92): Show | 95 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.1503+899G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 673637 | ||||||
| chr11:673644
|
G | T | 1 | a0001c0001t0001g0328 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1503+892C>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 673644 | ||||||
| chr11:673730
|
G | A | 1 | a0001c0002t0001g0304 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1503+806C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 673730 | ||||||
| chr11:673791
|
T | G | 2 | a0001c0002t0001g0212a0001c0002t0001g0213 | 2 | HG01361.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1503+745A>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 673791 | ||||||
| chr11:673925
|
G | C | 3 | a0001c0002t0001g0327a0001c0002t0001g0335a0001c0002t0001g0337 | 3 | HG02647.hp2 HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1503+611C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 673925 | ||||||
| chr11:674029
|
C | T | 2 | a0001c0002t0001g0308a0001c0002t0001g0311 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1503+507G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 674029 | ||||||
| chr11:674062
|
G | A | 2 | a0001c0002t0001g0212a0001c0002t0001g0213 | 2 | HG01361.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1503+474C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 674062 | ||||||
| chr11:674094
|
G | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(189): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1503+442C>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 674094 | ||||||
| chr11:674115
|
G | A | 1 | a0001c0002t0001g0195 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1503+421C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 674115 | ||||||
| chr11:674153
|
G | C | 1 | a0001c0001t0006g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1503+383C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 674153 | ||||||
| chr11:674180
|
T | C | 1 | a0002c0005t0001g0263 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1503+356A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 674180 | ||||||
| chr11:674198
|
C | G | 1 | a0001c0001t0001g0016 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1503+338G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 674198 | ||||||
| chr11:674206
|
A | C | 2 | a0001c0002t0001g0224a0001c0002t0001g0341 | 2 | NA18945.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1503+330T>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 674206 | ||||||
| chr11:674259
|
G | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(189): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1503+277C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 674259 | ||||||
| chr11:674380
|
C | CTTCATTT others(26): Show |
1 | a0001c0003t0001g0006 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1503+123_1503+155d others(35): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 674380 | ||||||
| chr11:674454
|
G | T | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(292): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1503+82C>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 674454 | ||||||
| chr11:674458
|
G | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(189): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1503+78C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 674458 | ||||||
| chr11:674499
|
G | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(189): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1503+37C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 10/11 | chr11 | 674499 | ||||||
| chr11:674800
|
G | A | 10 | a0001c0004t0001g0013a0001c0004t0001g0014a0001c0004t0001g0020others(7): Show | 10 | HG01106.hp2 HG01496.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.1256-17C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 674800 | ||||||
| chr11:674955
|
T | C | 15 | a0001c0002t0001g0201a0001c0002t0001g0241a0001c0002t0001g0267others(12): Show | 15 | HG02055.hp1 HG02486.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1256-172A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 674955 | ||||||
| chr11:675162
|
GCAA | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(195): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1256-382_1256-380d others(5): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 675162 | ||||||
| chr11:675349
|
C | T | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(292): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1256-566G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 675349 | ||||||
| chr11:675384
|
A | C | 341 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(338): Show | 344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1256-601T>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 675384 | ||||||
| chr11:675437
|
G | A | 1 | a0001c0003t0001g0173 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1256-654C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 675437 | ||||||
| chr11:675451
|
C | A | 1 | a0001c0002t0001g0248 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1256-668G>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 675451 | ||||||
| chr11:675462
|
G | A | 1 | a0001c0002t0001g0256 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1256-679C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 675462 | ||||||
| chr11:675489
|
A | G | 10 | a0001c0004t0001g0013a0001c0004t0001g0014a0001c0004t0001g0020others(7): Show | 10 | HG01106.hp2 HG01496.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.1256-706T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 675489 | ||||||
| chr11:675507
|
T | A | 1 | a0001c0002t0001g0243 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1256-724A>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 675507 | ||||||
| chr11:675693
|
G | A | 1 | a0001c0003t0001g0152 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1256-910C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 675693 | ||||||
| chr11:675749
|
G | C | 1 | a0001c0002t0001g0205 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1256-966C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 675749 | ||||||
| chr11:675815
|
A | C | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1256-1032T>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 675815 | ||||||
| chr11:675887
|
A | C | 1 | a0001c0001t0001g0036 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1256-1104T>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 675887 | ||||||
| chr11:675987
|
GGGCACCT others(10): Show |
G | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(188): Show | 193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.1256-1221_1256-120 others(21): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 675987 | ||||||
| chr11:675994
|
T | C | 1 | a0001c0001t0001g0059 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1256-1211A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 675994 | ||||||
| chr11:675996
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1256-1213C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 675996 | ||||||
| chr11:675996
|
G | GCACCCCA others(10): Show |
1 | a0001c0002t0001g0304 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1256-1214_1256-121 others(21): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 675996 | ||||||
| chr11:676003
|
C | A | 21 | a0001c0001t0001g0307a0001c0002t0001g0201a0001c0002t0001g0206others(18): Show | 22 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1256-1220G>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 676003 | ||||||
| chr11:676004
|
C | T | 96 | a0001c0001t0001g0253a0001c0001t0001g0307a0001c0002t0001g0042others(93): Show | 97 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.1256-1221G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 676004 | ||||||
| chr11:676005
|
G | A | 2 | a0001c0001t0001g0059a0001c0002t0001g0304 | 2 | HG03195.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1256-1222C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 676005 | ||||||
| chr11:676012
|
G | A | 1 | a0001c0002t0001g0255 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1256-1229C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 676012 | ||||||
| chr11:676028
|
C | T | 1 | a0001c0002t0001g0251 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1256-1245G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 676028 | ||||||
| chr11:676060
|
T | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(199): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1256-1277A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 676060 | ||||||
| chr11:676068
|
C | T | 4 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(1): Show | 4 | HG01346.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1256-1285G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 676068 | ||||||
| chr11:676118
|
C | T | 1 | a0001c0004t0001g0022 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1256-1335G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 676118 | ||||||
| chr11:676180
|
ACCTGACA others(15): Show |
A | 1 | a0001c0001t0004g0274 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1256-1419_1256-139 others(26): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 676180 | ||||||
| chr11:676226
|
ACCCCCAG others(11): Show |
A | 6 | a0001c0001t0001g0328a0001c0001t0004g0199a0001c0002t0001g0195others(3): Show | 6 | HG01109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1256-1461_1256-144 others(22): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 676226 | ||||||
| chr11:676229
|
C | T | 1 | a0001c0002t0001g0329 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1256-1446G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 676229 | ||||||
| chr11:676244
|
CCCCCCAG others(10): Show |
C | 2 | a0001c0002t0001g0286a0001c0002t0001g0287 | 2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1256-1478_1256-146 others(21): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 676244 | ||||||
| chr11:676264
|
C | T | 1 | a0001c0004t0001g0024 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1256-1481G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 676264 | ||||||
| chr11:676297
|
G | A | 3 | a0001c0001t0001g0307a0001c0002t0001g0206a0001c0002t0001g0250 | 3 | HG02055.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1256-1514C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 676297 | ||||||
| chr11:676317
|
TCCCCCCA others(12): Show |
T | 1 | a0001c0002t0001g0339 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1256-1553_1256-153 others(23): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 676317 | ||||||
| chr11:676330
|
C | T | 294 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(291): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.1256-1547G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 676330 | ||||||
| chr11:676335
|
TC | T | 294 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(291): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.1256-1553delG | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 676335 | ||||||
| chr11:676341
|
C | A | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(292): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1256-1558G>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 676341 | ||||||
| chr11:676543
|
C | T | 1 | a0001c0003t0001g0177 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1256-1760G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 676543 | ||||||
| chr11:676655
|
C | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0200others(1): Show | 4 | HG02622.hp1 HG02970.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1256-1872G>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 676655 | ||||||
| chr11:676668
|
C | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(189): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1256-1885G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 676668 | ||||||
| chr11:676768
|
C | T | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(292): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1255+1926G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 676768 | ||||||
| chr11:676795
|
C | T | 1 | a0001c0001t0001g0059 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1255+1899G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 676795 | ||||||
| chr11:677019
|
CA | C | 97 | a0001c0001t0001g0253a0001c0001t0001g0307a0001c0002t0001g0042others(94): Show | 98 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.1255+1674delT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 677019 | ||||||
| chr11:677126
|
C | CT | 11 | a0001c0001t0001g0012a0001c0001t0001g0053a0001c0001t0001g0054others(8): Show | 11 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.1255+1567dupA | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 677126 | ||||||
| chr11:677200
|
G | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(137): Show | 142 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.1255+1494C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 677200 | ||||||
| chr11:677230
|
A | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(292): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1255+1464T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 677230 | ||||||
| chr11:677316
|
CGGTGAAA others(447): Show |
C | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(195): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1255+924_1255+1377 others(3): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 677316 | ||||||
| chr11:677727
|
G | C | 3 | a0001c0001t0001g0307a0001c0002t0001g0206a0001c0002t0001g0250 | 3 | HG02055.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1255+967C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 677727 | ||||||
| chr11:677935
|
CCTGGGCG others(11): Show |
C | 6 | a0001c0001t0001g0328a0001c0001t0004g0199a0001c0002t0001g0195others(3): Show | 6 | HG01109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1255+741_1255+758d others(20): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 677935 | ||||||
| chr11:677962
|
C | CA | 150 | a0001c0001t0001g0130a0001c0001t0001g0307a0001c0001t0001g0328others(147): Show | 151 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.1255+731dupT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 677962 | ||||||
| chr11:677962
|
C | CAA | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(132): Show | 137 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1255+730_1255+731d others(4): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 677962 | ||||||
| chr11:677962
|
C | CAAA | 8 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0035others(5): Show | 8 | HG01975.hp1 HG01981.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.1255+729_1255+731d others(5): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 677962 | ||||||
| chr11:678011
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0200 | 3 | HG02622.hp1 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1255+683C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 678011 | ||||||
| chr11:678514
|
G | A | 1 | a0001c0003t0001g0179 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1255+180C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 678514 | ||||||
| chr11:678533
|
C | T | 2 | a0001c0001t0001g0283a0001c0001t0001g0284 | 2 | NA18966.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1255+161G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 678533 | ||||||
| chr11:678561
|
C | T | 46 | a0001c0001t0001g0007a0001c0001t0001g0272a0001c0001t0001g0273others(43): Show | 46 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.1255+133G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 9/11 | chr11 | 678561 | ||||||
| chr11:678973
|
C | T | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(241): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1127-151G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 8/11 | chr11 | 678973 | ||||||
| chr11:678989
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1127-167A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 8/11 | chr11 | 678989 | ||||||
| chr11:679104
|
A | G | 46 | a0001c0001t0001g0007a0001c0001t0001g0272a0001c0001t0001g0273others(43): Show | 46 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.1127-282T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 8/11 | chr11 | 679104 | ||||||
| chr11:679136
|
C | T | 5 | a0001c0001t0001g0124a0001c0001t0001g0126a0001c0001t0001g0128others(2): Show | 5 | NA18954.hp2 NA18970.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.1127-314G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 8/11 | chr11 | 679136 | ||||||
| chr11:679189
|
G | A | 1 | a0001c0002t0001g0304 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1127-367C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 8/11 | chr11 | 679189 | ||||||
| chr11:679301
|
C | G | 6 | a0001c0001t0001g0328a0001c0001t0004g0199a0001c0002t0001g0195others(3): Show | 6 | HG01109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1126+387G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 8/11 | chr11 | 679301 | ||||||
| chr11:679314
|
C | CA | 51 | a0001c0001t0001g0007a0001c0001t0001g0272a0001c0001t0001g0273others(48): Show | 51 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.1126+373dupT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 8/11 | chr11 | 679314 | ||||||
| chr11:679314
|
CA | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(139): Show | 144 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.1126+373delT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 8/11 | chr11 | 679314 | ||||||
| chr11:679380
|
A | T | 46 | a0001c0001t0001g0007a0001c0001t0001g0272a0001c0001t0001g0273others(43): Show | 46 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.1126+308T>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 8/11 | chr11 | 679380 | ||||||
| chr11:679436
|
G | C | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1126+252C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 8/11 | chr11 | 679436 | ||||||
| chr11:679494
|
G | A | 46 | a0001c0001t0001g0007a0001c0001t0001g0272a0001c0001t0001g0273others(43): Show | 46 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.1126+194C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 8/11 | chr11 | 679494 | ||||||
| chr11:679497
|
A | G | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(242): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1126+191T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 8/11 | chr11 | 679497 | ||||||
| chr11:679659
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1126+29G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 8/11 | chr11 | 679659 | ||||||
| chr11:679915
|
G | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(133): Show | 138 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.998-99C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 7/11 | chr11 | 679915 | ||||||
| chr11:680002
|
A | AACCAGGA others(2): Show |
198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(195): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.998-195_998-187dup others(9): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 7/11 | chr11 | 680002 | ||||||
| chr11:680096
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.998-280T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 7/11 | chr11 | 680096 | ||||||
| chr11:680254
|
G | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0298a0001c0001t0001g0299others(2): Show | 5 | HG01192.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.998-438C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 7/11 | chr11 | 680254 | ||||||
| chr11:680396
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.997+567T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 7/11 | chr11 | 680396 | ||||||
| chr11:680408
|
C | T | 46 | a0001c0001t0001g0007a0001c0001t0001g0272a0001c0001t0001g0273others(43): Show | 46 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.997+555G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 7/11 | chr11 | 680408 | ||||||
| chr11:680500
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.997+463G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 7/11 | chr11 | 680500 | ||||||
| chr11:680508
|
G | A | 3 | a0001c0001t0001g0307a0001c0002t0001g0206a0001c0002t0001g0250 | 3 | HG02055.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.997+455C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 7/11 | chr11 | 680508 | ||||||
| chr11:680614
|
C | T | 29 | a0001c0002t0001g0042a0001c0002t0001g0202a0001c0002t0001g0208others(26): Show | 29 | HG00280.hp2 HG00597.hp1 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.997+349G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 7/11 | chr11 | 680614 | ||||||
| chr11:680647
|
A | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(137): Show | 142 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.997+316T>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 7/11 | chr11 | 680647 | ||||||
| chr11:680748
|
C | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0052others(4): Show | 8 | HG01943.hp1 HG02148.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.997+215G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 7/11 | chr11 | 680748 | ||||||
| chr11:680866
|
A | G | 46 | a0001c0001t0001g0007a0001c0001t0001g0272a0001c0001t0001g0273others(43): Show | 46 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.997+97T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 7/11 | chr11 | 680866 | ||||||
| chr11:680877
|
C | A | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.997+86G>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 7/11 | chr11 | 680877 | ||||||
| chr11:681383
|
C | CA | 76 | a0001c0001t0001g0253a0001c0002t0001g0201a0001c0002t0001g0202others(73): Show | 76 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.871-295dupT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 681383 | ||||||
| chr11:681411
|
CT | C | 8 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0108others(5): Show | 8 | HG00597.hp1 HG02056.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.871-323delA | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 681411 | ||||||
| chr11:681411
|
CTT | C | 312 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(309): Show | 314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.871-324_871-323del others(2): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 681411 | ||||||
| chr11:681502
|
C | G | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(131): Show | 136 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.871-413G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 681502 | ||||||
| chr11:681579
|
G | T | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(321): Show | 326 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.871-490C>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 681579 | ||||||
| chr11:681623
|
G | C | 1 | a0001c0001t0001g0112 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.871-534C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 681623 | ||||||
| chr11:681674
|
T | G | 6 | a0001c0001t0001g0328a0001c0001t0004g0199a0001c0002t0001g0195others(3): Show | 6 | HG01109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.871-585A>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 681674 | ||||||
| chr11:681710
|
G | A | 1 | a0001c0002t0001g0265 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.871-621C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 681710 | ||||||
| chr11:681712
|
C | CT | 9 | a0001c0001t0001g0036a0001c0001t0001g0288a0001c0001t0001g0292others(6): Show | 9 | HG01109.hp2 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.871-624dupA | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 681712 | ||||||
| chr11:681722
|
T | A | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.871-633A>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 681722 | ||||||
| chr11:681872
|
G | A | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.871-783C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 681872 | ||||||
| chr11:681897
|
C | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0200others(1): Show | 4 | HG02622.hp1 HG02970.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-808G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 681897 | ||||||
| chr11:682054
|
C | T | 53 | a0001c0001t0001g0158a0001c0003t0001g0006a0001c0003t0001g0032others(50): Show | 53 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.871-965G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 682054 | ||||||
| chr11:682164
|
G | A | 1 | a0001c0002t0001g0246 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.871-1075C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 682164 | ||||||
| chr11:682373
|
C | T | 1 | a0001c0002t0001g0247 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.871-1284G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 682373 | ||||||
| chr11:682558
|
T | TA | 10 | a0001c0004t0001g0013a0001c0004t0001g0014a0001c0004t0001g0020others(7): Show | 10 | HG01106.hp2 HG01496.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.871-1470dupT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 682558 | ||||||
| chr11:682560
|
C | A | 6 | a0001c0001t0001g0328a0001c0001t0004g0199a0001c0002t0001g0195others(3): Show | 6 | HG01109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.871-1471G>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 682560 | ||||||
| chr11:682668
|
G | A | 1 | a0001c0001t0003g0139 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.871-1579C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 682668 | ||||||
| chr11:682671
|
T | G | 1 | a0001c0001t0001g0011 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.871-1582A>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 682671 | ||||||
| chr11:682712
|
T | A | 1 | a0001c0001t0001g0038 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.871-1623A>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 682712 | ||||||
| chr11:682795
|
A | C | 274 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(271): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.871-1706T>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 682795 | ||||||
| chr11:682973
|
T | C | 76 | a0001c0001t0001g0253a0001c0002t0001g0201a0001c0002t0001g0202others(73): Show | 76 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.871-1884A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 682973 | ||||||
| chr11:683022
|
C | T | 10 | a0001c0001t0001g0273a0001c0001t0001g0275a0001c0001t0001g0276others(7): Show | 10 | HG01192.hp2 HG01884.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.870+1876G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 683022 | ||||||
| chr11:683177
|
C | T | 10 | a0001c0001t0001g0273a0001c0001t0001g0275a0001c0001t0001g0276others(7): Show | 10 | HG01192.hp2 HG01884.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.870+1721G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 683177 | ||||||
| chr11:683298
|
T | C | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.870+1600A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 683298 | ||||||
| chr11:683403
|
A | G | 284 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(281): Show | 286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.870+1495T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 683403 | ||||||
| chr11:683443
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(198): Show | 203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.870+1455A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 683443 | ||||||
| chr11:683504
|
G | A | 1 | a0001c0001t0006g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.870+1394C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 683504 | ||||||
| chr11:683510
|
G | A | 1 | a0001c0002t0001g0337 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.870+1388C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 683510 | ||||||
| chr11:683557
|
A | ATTTCAAA others(18): Show |
2 | a0001c0004t0001g0020a0001c0004t0001g0021 | 2 | HG01496.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.870+1316_870+1340d others(27): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 683557 | ||||||
| chr11:683761
|
G | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(198): Show | 203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.870+1137C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 683761 | ||||||
| chr11:683975
|
C | T | 3 | a0001c0001t0001g0314a0001c0001t0001g0338a0001c0002t0001g0271 | 3 | HG00597.hp2 HG03486.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.870+923G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 683975 | ||||||
| chr11:684056
|
A | G | 76 | a0001c0001t0001g0253a0001c0002t0001g0201a0001c0002t0001g0202others(73): Show | 76 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.870+842T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 684056 | ||||||
| chr11:684123
|
C | CT | 266 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(263): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.870+774dupA | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 684123 | ||||||
| chr11:684123
|
C | CTT | 6 | a0001c0001t0001g0023a0001c0001t0001g0036a0001c0001t0001g0066others(3): Show | 6 | HG00438.hp2 HG01192.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.870+773_870+774dup others(2): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 684123 | ||||||
| chr11:684155
|
C | G | 1 | a0001c0001t0001g0307 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.870+743G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 684155 | ||||||
| chr11:684263
|
C | T | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0200 | 3 | HG02622.hp1 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.870+635G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 684263 | ||||||
| chr11:684274
|
T | C | 285 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(282): Show | 287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.870+624A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 684274 | ||||||
| chr11:684419
|
G | GA | 16 | a0001c0001t0001g0273a0001c0001t0001g0275a0001c0001t0001g0276others(13): Show | 16 | HG01109.hp2 HG01192.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.870+478dupT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 684419 | ||||||
| chr11:684459
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.870+439T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 684459 | ||||||
| chr11:684489
|
C | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(131): Show | 136 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.870+409G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 684489 | ||||||
| chr11:684514
|
C | T | 3 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324 | 3 | HG01175.hp1 HG01981.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.870+384G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 684514 | ||||||
| chr11:684636
|
C | T | 1 | a0001c0002t0001g0201 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.870+262G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 684636 | ||||||
| chr11:684697
|
C | T | 54 | a0001c0001t0001g0007a0001c0001t0001g0272a0001c0001t0001g0282others(51): Show | 54 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.870+201G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 684697 | ||||||
| chr11:684798
|
G | C | 8 | a0001c0002t0001g0240a0001c0002t0001g0242a0001c0002t0001g0243others(5): Show | 8 | HG01433.hp1 HG02145.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.870+100C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 684798 | ||||||
| chr11:684849
|
G | A | 3 | a0001c0002t0001g0210a0001c0002t0001g0219a0001c0002t0001g0266 | 3 | HG02738.hp2 HG03017.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.870+49C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 6/11 | chr11 | 684849 | ||||||
| chr11:685082
|
C | CT | 38 | a0001c0001t0001g0007a0001c0001t0001g0023a0001c0001t0001g0030others(35): Show | 38 | HG00639.hp2 HG01106.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.805-120dupA | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 685082 | ||||||
| chr11:685082
|
C | CTT | 155 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(152): Show | 156 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.805-121_805-120dup others(2): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 685082 | ||||||
| chr11:685082
|
C | CTTT | 92 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(89): Show | 93 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.805-122_805-120dup others(3): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 685082 | ||||||
| chr11:685082
|
C | CTTTT | 9 | a0001c0003t0001g0144a0001c0003t0001g0148a0001c0003t0001g0153others(6): Show | 9 | HG00423.hp1 HG01261.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.805-123_805-120dup others(4): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 685082 | ||||||
| chr11:685137
|
T | G | 1 | a0001c0009t0001g0137 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.805-174A>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 685137 | ||||||
| chr11:685138
|
G | T | 1 | a0001c0009t0001g0137 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.805-175C>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 685138 | ||||||
| chr11:685139
|
C | G | 1 | a0001c0009t0001g0137 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.805-176G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 685139 | ||||||
| chr11:685259
|
A | C | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.805-296T>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 685259 | ||||||
| chr11:685619
|
C | T | 47 | a0001c0001t0001g0158a0001c0003t0001g0006a0001c0003t0001g0032others(44): Show | 47 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.805-656G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 685619 | ||||||
| chr11:685641
|
G | C | 2 | a0001c0001t0001g0302a0001c0001t0001g0305 | 2 | HG01192.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.805-678C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 685641 | ||||||
| chr11:685695
|
C | CA | 17 | a0001c0001t0001g0036a0001c0001t0001g0064a0001c0001t0001g0108others(14): Show | 17 | HG01109.hp2 HG02109.hp2 HG02129.hp1 others(14): Show |
intron_variant | MODIFIER | c.805-733dupT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 685695 | ||||||
| chr11:685790
|
T | C | 6 | a0001c0001t0001g0016a0001c0001t0001g0036a0001c0001t0001g0065others(3): Show | 6 | HG00423.hp2 HG00621.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.805-827A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 685790 | ||||||
| chr11:685793
|
C | A | 6 | a0001c0001t0001g0016a0001c0001t0001g0036a0001c0001t0001g0065others(3): Show | 6 | HG00423.hp2 HG00621.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.805-830G>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 685793 | ||||||
| chr11:685797
|
CTT | C | 6 | a0001c0001t0001g0016a0001c0001t0001g0036a0001c0001t0001g0065others(3): Show | 6 | HG00423.hp2 HG00621.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.805-836_805-835del others(2): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 685797 | ||||||
| chr11:685800
|
A | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0036a0001c0001t0001g0065others(3): Show | 6 | HG00423.hp2 HG00621.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.805-837T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 685800 | ||||||
| chr11:685805
|
C | CAGGAGAT others(235): Show |
1 | a0001c0001t0001g0065 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.805-843_805-842ins others(242): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 685805 | ||||||
| chr11:685805
|
C | CAGGAGAT others(236): Show |
3 | a0001c0001t0001g0016a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | HG00423.hp2 HG00621.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.805-843_805-842ins others(243): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 685805 | ||||||
| chr11:685805
|
C | CAGGAGAT others(237): Show |
1 | a0001c0001t0001g0116 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.805-843_805-842ins others(244): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 685805 | ||||||
| chr11:685805
|
C | CAGGAGAT others(238): Show |
1 | a0001c0001t0001g0036 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.805-843_805-842ins others(245): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 685805 | ||||||
| chr11:685880
|
C | T | 1 | a0001c0002t0001g0202 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.805-917G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 685880 | ||||||
| chr11:685883
|
G | A | 1 | a0001c0003t0001g0173 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.805-920C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 685883 | ||||||
| chr11:686125
|
A | T | 1 | a0001c0009t0001g0137 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.804+733T>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 686125 | ||||||
| chr11:686127
|
TA | T | 180 | a0001c0001t0001g0007a0001c0001t0001g0158a0001c0001t0001g0253others(177): Show | 181 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.804+730delT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 686127 | ||||||
| chr11:686127
|
TAA | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(133): Show | 138 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.804+729_804+730del others(2): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 686127 | ||||||
| chr11:686128
|
A | T | 1 | a0001c0002t0001g0336 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.804+730T>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 686128 | ||||||
| chr11:686129
|
A | T | 75 | a0001c0001t0001g0253a0001c0002t0001g0201a0001c0002t0001g0202others(72): Show | 75 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.804+729T>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 686129 | ||||||
| chr11:686130
|
A | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0200others(1): Show | 4 | HG02109.hp2 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.804+728T>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 686130 | ||||||
| chr11:686161
|
G | A | 2 | a0001c0002t0001g0286a0001c0002t0001g0287 | 2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.804+697C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 686161 | ||||||
| chr11:686187
|
G | A | 1 | a0001c0001t0006g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.804+671C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 686187 | ||||||
| chr11:686229
|
T | C | 1 | a0001c0003t0001g0174 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.804+629A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 686229 | ||||||
| chr11:686277
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.804+581C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 686277 | ||||||
| chr11:686291
|
C | CA | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(169): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.804+566dupT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 686291 | ||||||
| chr11:686291
|
C | CAA | 27 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0018others(24): Show | 27 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.804+565_804+566dup others(2): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 686291 | ||||||
| chr11:686306
|
A | AAC | 9 | a0001c0001t0001g0273a0001c0001t0001g0275a0001c0001t0001g0276others(6): Show | 9 | HG01192.hp2 HG01884.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.804+551_804+552ins others(2): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 686306 | ||||||
| chr11:686310
|
C | A | 6 | a0001c0001t0001g0036a0001c0001t0004g0199a0001c0002t0001g0195others(3): Show | 6 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.804+548G>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 686310 | ||||||
| chr11:686311
|
C | A | 1 | a0001c0001t0001g0036 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.804+547G>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 686311 | ||||||
| chr11:686517
|
C | T | 1 | a0001c0003t0001g0180 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.804+341G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 686517 | ||||||
| chr11:686559
|
A | G | 2 | a0001c0002t0001g0195a0001c0002t0001g0196 | 2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.804+299T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 686559 | ||||||
| chr11:686597
|
T | C | 3 | a0001c0003t0001g0151a0001c0003t0001g0177a0001c0003t0001g0178 | 3 | HG00558.hp1 HG00673.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.804+261A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 686597 | ||||||
| chr11:686714
|
G | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(117): Show | 122 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.804+144C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 686714 | ||||||
| chr11:686798
|
G | A | 78 | a0001c0001t0001g0051a0001c0001t0001g0136a0001c0001t0001g0253others(75): Show | 78 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.804+60C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 686798 | ||||||
| chr11:686839
|
G | A | 73 | a0001c0001t0001g0051a0001c0001t0001g0136a0001c0001t0001g0253others(70): Show | 73 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.804+19C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 5/11 | chr11 | 686839 | ||||||
| chr11:687079
|
C | A | 1 | a0001c0001t0001g0319 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.665-82G>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 4/11 | chr11 | 687079 | ||||||
| chr11:687156
|
C | T | 3 | a0001c0002t0001g0201a0001c0002t0001g0241a0001c0002t0001g0267 | 3 | HG03130.hp2 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.665-159G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 4/11 | chr11 | 687156 | ||||||
| chr11:687157
|
G | A | 6 | a0001c0001t0001g0016a0001c0001t0001g0036a0001c0001t0001g0065others(3): Show | 6 | HG00423.hp2 HG00621.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.665-160C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 4/11 | chr11 | 687157 | ||||||
| chr11:687204
|
C | T | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.665-207G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 4/11 | chr11 | 687204 | ||||||
| chr11:687266
|
A | AC | 3 | a0001c0002t0001g0201a0001c0002t0001g0241a0001c0002t0001g0267 | 3 | HG03130.hp2 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.665-270dupG | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 4/11 | chr11 | 687266 | ||||||
| chr11:687368
|
C | A | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.665-371G>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 4/11 | chr11 | 687368 | ||||||
| chr11:687369
|
G | A | 2 | a0001c0001t0001g0320a0001c0001t0001g0321 | 2 | NA19054.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.665-372C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 4/11 | chr11 | 687369 | ||||||
| chr11:687512
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.664+399G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 4/11 | chr11 | 687512 | ||||||
| chr11:687533
|
A | G | 1 | a0001c0003t0001g0152 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.664+378T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 4/11 | chr11 | 687533 | ||||||
| chr11:687550
|
C | CGTGATCT others(9): Show |
1 | a0001c0001t0001g0282 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.664+345_664+360dup others(16): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 4/11 | chr11 | 687550 | ||||||
| chr11:687699
|
G | A | 331 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(328): Show | 334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.664+212C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 4/11 | chr11 | 687699 | ||||||
| chr11:687830
|
T | C | 5 | a0001c0001t0004g0199a0001c0002t0001g0195a0001c0002t0001g0196others(2): Show | 5 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.664+81A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 4/11 | chr11 | 687830 | ||||||
| chr11:688091
|
C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(135): Show | 140 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.518-34G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 3/11 | chr11 | 688091 | ||||||
| chr11:688145
|
G | A | 1 | a0001c0006t0001g0117 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.518-88C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 3/11 | chr11 | 688145 | ||||||
| chr11:688155
|
T | G | 1 | a0001c0002t0001g0218 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.518-98A>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 3/11 | chr11 | 688155 | ||||||
| chr11:688177
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.518-120C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 3/11 | chr11 | 688177 | ||||||
| chr11:688217
|
A | G | 77 | a0001c0001t0001g0253a0001c0002t0001g0201a0001c0002t0001g0202others(74): Show | 77 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.517+114T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 3/11 | chr11 | 688217 | ||||||
| chr11:688253
|
T | TAAATAAA others(7): Show |
1 | a0001c0001t0001g0015 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.517+64_517+77dupTC others(12): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 3/11 | chr11 | 688253 | ||||||
| chr11:688312
|
G | A | 78 | a0001c0001t0001g0253a0001c0002t0001g0201a0001c0002t0001g0202others(75): Show | 78 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.517+19C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 3/11 | chr11 | 688312 | ||||||
| chr11:688770
|
A | G | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.388-310T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 688770 | ||||||
| chr11:688804
|
C | T | 78 | a0001c0001t0001g0253a0001c0002t0001g0201a0001c0002t0001g0202others(75): Show | 78 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.388-344G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 688804 | ||||||
| chr11:689059
|
C | T | 1 | a0001c0002t0001g0207 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.388-599G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 689059 | ||||||
| chr11:689092
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.388-632G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 689092 | ||||||
| chr11:689116
|
G | A | 57 | a0001c0001t0001g0007a0001c0001t0001g0272a0001c0001t0001g0282others(54): Show | 58 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.388-656C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 689116 | ||||||
| chr11:689121
|
T | A | 1 | a0001c0001t0001g0018 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.388-661A>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 689121 | ||||||
| chr11:689179
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.388-719G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 689179 | ||||||
| chr11:689202
|
C | CT | 10 | a0001c0001t0001g0007a0001c0001t0001g0036a0001c0001t0001g0052others(7): Show | 10 | HG00597.hp2 HG00735.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.388-743dupA | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 689202 | ||||||
| chr11:689202
|
CT | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(162): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.388-743delA | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 689202 | ||||||
| chr11:689202
|
CTT | C | 78 | a0001c0001t0001g0118a0001c0001t0001g0273a0001c0001t0001g0275others(75): Show | 78 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.388-744_388-743del others(2): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 689202 | ||||||
| chr11:689204
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.388-744A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 689204 | ||||||
| chr11:689259
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.388-799C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 689259 | ||||||
| chr11:689275
|
G | A | 5 | a0001c0001t0004g0199a0001c0002t0001g0195a0001c0002t0001g0196others(2): Show | 5 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.388-815C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 689275 | ||||||
| chr11:689310
|
A | G | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0200 | 3 | HG02622.hp1 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.388-850T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 689310 | ||||||
| chr11:689381
|
A | AT | 61 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0124others(58): Show | 61 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.388-922dupA | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 689381 | ||||||
| chr11:689412
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.388-952G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 689412 | ||||||
| chr11:689469
|
C | T | 53 | a0001c0001t0001g0158a0001c0003t0001g0006a0001c0003t0001g0032others(50): Show | 53 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.388-1009G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 689469 | ||||||
| chr11:689496
|
C | T | 1 | a0001c0002t0001g0304 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.388-1036G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 689496 | ||||||
| chr11:689583
|
G | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0035a0001c0001t0001g0047others(4): Show | 7 | HG01934.hp1 HG01975.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.388-1123C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 689583 | ||||||
| chr11:689709
|
C | T | 1 | a0001c0002t0001g0241 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.388-1249G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 689709 | ||||||
| chr11:689867
|
C | T | 4 | a0001c0001t0001g0253a0001c0002t0001g0203a0001c0002t0001g0255others(1): Show | 4 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-1407G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 689867 | ||||||
| chr11:689954
|
G | A | 2 | a0001c0002t0001g0206a0001c0002t0001g0250 | 2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.388-1494C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 689954 | ||||||
| chr11:690158
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.387+1343C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690158 | ||||||
| chr11:690163
|
T | C | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.387+1338A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690163 | ||||||
| chr11:690168
|
GTGAGT | G | 56 | a0001c0001t0001g0007a0001c0001t0001g0272a0001c0001t0001g0282others(53): Show | 56 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.387+1328_387+1332d others(7): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690168 | ||||||
| chr11:690242
|
A | G | 1 | a0001c0002t0001g0208 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.387+1259T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690242 | ||||||
| chr11:690249
|
A | AGGAGGGG others(48): Show |
5 | a0001c0001t0001g0023a0001c0004t0001g0013a0001c0004t0001g0014others(2): Show | 5 | HG01106.hp2 HG02004.hp2 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.387+1251_387+1252i others(57): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690249 | ||||||
| chr11:690249
|
A | AGGAGGGG others(78): Show |
3 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0002t0001g0042 | 3 | HG02132.hp1 NA18950.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.387+1251_387+1252i others(87): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690249 | ||||||
| chr11:690249
|
A | AGGAGGGG others(128): Show |
2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.387+1251_387+1252i others(137): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690249 | ||||||
| chr11:690249
|
A | AGGAGGGG others(133): Show |
2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | HG01192.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.387+1251_387+1252i others(142): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690249 | ||||||
| chr11:690249
|
A | AGGAGGGG others(108): Show |
6 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0325others(3): Show | 6 | HG01884.hp2 HG02896.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.387+1251_387+1252i others(117): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690249 | ||||||
| chr11:690249
|
A | AGGAGGGG others(109): Show |
1 | a0001c0002t0001g0286 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.387+1251_387+1252i others(118): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690249 | ||||||
| chr11:690249
|
A | G | 5 | a0001c0001t0004g0199a0001c0002t0001g0195a0001c0002t0001g0196others(2): Show | 5 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+1252T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690249 | ||||||
| chr11:690251
|
G | GAGGGGAG others(38): Show |
5 | a0001c0001t0004g0199a0001c0002t0001g0195a0001c0002t0001g0196others(2): Show | 5 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+1249_387+1250i others(47): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690251 | ||||||
| chr11:690256
|
G | GAGGGGAG others(88): Show |
6 | a0001c0002t0001g0204a0001c0002t0001g0236a0001c0002t0001g0237others(3): Show | 6 | HG01346.hp1 HG02109.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.387+1244_387+1245i others(97): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690256 | ||||||
| chr11:690256
|
G | GAGGGGAG others(28): Show |
2 | a0001c0003t0001g0185a0001c0003t0001g0186 | 2 | NA19009.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.387+1244_387+1245i others(37): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690256 | ||||||
| chr11:690256
|
G | GAGGGGGA others(100): Show |
1 | a0001c0002t0001g0240 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.387+1244_387+1245i others(109): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690256 | ||||||
| chr11:690258
|
G | GGGGAGGG others(81): Show |
1 | a0001c0009t0001g0137 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.387+1242_387+1243i others(90): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690258 | ||||||
| chr11:690261
|
G | C | 5 | a0001c0001t0004g0199a0001c0002t0001g0195a0001c0002t0001g0196others(2): Show | 5 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+1240C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690261 | ||||||
| chr11:690266
|
C | CAGGAG | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0200 | 3 | HG02622.hp1 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.387+1234_387+1235i others(7): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690266 | ||||||
| chr11:690266
|
C | CAGGAGAG others(3): Show |
2 | a0001c0001t0001g0322a0001c0003t0001g0142 | 2 | HG01175.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.387+1234_387+1235i others(12): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690266 | ||||||
| chr11:690266
|
C | CAGGAGAG others(88): Show |
2 | a0001c0002t0001g0251a0001c0002t0001g0252 | 2 | HG02698.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.387+1234_387+1235i others(97): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690266 | ||||||
| chr11:690266
|
C | CAGGAGAG others(78): Show |
1 | a0001c0002t0001g0207 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.387+1234_387+1235i others(87): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690266 | ||||||
| chr11:690266
|
C | CAGGAGAG others(93): Show |
2 | a0001c0002t0001g0210a0001c0002t0001g0255 | 2 | HG02145.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.387+1234_387+1235i others(102): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690266 | ||||||
| chr11:690266
|
C | CAGGAGAG others(103): Show |
4 | a0001c0002t0001g0256a0001c0002t0001g0262a0002c0005t0001g0261others(1): Show | 4 | HG02056.hp1 NA18961.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.387+1234_387+1235i others(112): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690266 | ||||||
| chr11:690266
|
C | CAGGAGAG others(98): Show |
21 | a0001c0002t0001g0201a0001c0002t0001g0202a0001c0002t0001g0203others(18): Show | 21 | HG00280.hp2 HG01243.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.387+1234_387+1235i others(107): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690266 | ||||||
| chr11:690266
|
C | CAGGAGAG others(108): Show |
4 | a0001c0001t0001g0253a0001c0002t0001g0258a0002c0005t0001g0004others(1): Show | 4 | HG02257.hp2 HG02630.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.387+1234_387+1235i others(117): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690266 | ||||||
| chr11:690266
|
C | CAGGAGAG others(123): Show |
1 | a0001c0002t0001g0339 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.387+1234_387+1235i others(132): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690266 | ||||||
| chr11:690266
|
C | CAGGAGAG others(128): Show |
3 | a0001c0002t0001g0232a0001c0002t0001g0233a0001c0002t0001g0234 | 3 | HG02970.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.387+1234_387+1235i others(137): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690266 | ||||||
| chr11:690266
|
C | CAGGAGAG others(110): Show |
1 | a0001c0002t0001g0211 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.387+1234_387+1235i others(119): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690266 | ||||||
| chr11:690266
|
C | CAGGAGAG others(23): Show |
3 | a0001c0003t0001g0187a0001c0003t0001g0188a0001c0003t0001g0189 | 3 | HG01258.hp2 HG02572.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.387+1234_387+1235i others(32): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690266 | ||||||
| chr11:690266
|
C | CAGGAGAG others(33): Show |
5 | a0001c0001t0001g0008a0001c0001t0001g0136a0001c0003t0001g0145others(2): Show | 5 | HG01346.hp2 HG02071.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.387+1234_387+1235i others(42): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690266 | ||||||
| chr11:690266
|
C | CAGGAGAG others(38): Show |
45 | a0001c0001t0001g0035a0001c0001t0001g0048a0001c0001t0001g0122others(42): Show | 45 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.387+1234_387+1235i others(47): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690266 | ||||||
| chr11:690266
|
C | CAGGAGAG others(88): Show |
1 | a0001c0001t0006g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.387+1234_387+1235i others(97): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690266 | ||||||
| chr11:690266
|
C | CAGGAGAG others(43): Show |
99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(96): Show | 101 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.387+1234_387+1235i others(52): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690266 | ||||||
| chr11:690266
|
C | CAGGAGAG others(68): Show |
9 | a0001c0001t0001g0121a0001c0001t0001g0125a0001c0001t0001g0129others(6): Show | 9 | HG01934.hp1 HG04204.hp1 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.387+1234_387+1235i others(77): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690266 | ||||||
| chr11:690266
|
C | CAGGAGAG others(63): Show |
6 | a0001c0001t0001g0272a0001c0001t0001g0307a0001c0001t0001g0309others(3): Show | 6 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.387+1234_387+1235i others(72): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690266 | ||||||
| chr11:690266
|
C | CAGGAGAG others(68): Show |
2 | a0001c0001t0001g0305a0001c0002t0001g0304 | 2 | HG02602.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.387+1234_387+1235i others(77): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690266 | ||||||
| chr11:690266
|
C | CAGGAGAG others(73): Show |
29 | a0001c0001t0001g0007a0001c0001t0001g0289a0001c0001t0001g0291others(26): Show | 30 | HG00735.hp2 HG01099.hp2 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.387+1234_387+1235i others(82): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690266 | ||||||
| chr11:690266
|
C | CAGGAGAG others(143): Show |
1 | a0001c0001t0001g0273 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.387+1234_387+1235i others(152): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690266 | ||||||
| chr11:690266
|
C | CAGGAGAG others(74): Show |
1 | a0001c0001t0001g0288 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.387+1234_387+1235i others(83): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690266 | ||||||
| chr11:690266
|
C | CAGGAGAG others(78): Show |
1 | a0001c0001t0001g0328 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.387+1234_387+1235i others(87): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690266 | ||||||
| chr11:690266
|
C | CAGGAGAG others(28): Show |
1 | a0001c0003t0001g0182 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.387+1234_387+1235i others(37): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690266 | ||||||
| chr11:690266
|
C | CAGGAGAG others(105): Show |
1 | a0001c0001t0001g0306 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.387+1234_387+1235i others(114): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690266 | ||||||
| chr11:690266
|
C | CAGGAGAG others(44): Show |
1 | a0001c0001t0001g0049 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.387+1234_387+1235i others(53): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690266 | ||||||
| chr11:690266
|
C | CAGGAGAG others(121): Show |
1 | a0001c0002t0001g0208 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.387+1234_387+1235i others(130): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690266 | ||||||
| chr11:690266
|
C | CAGGAGAG others(44): Show |
1 | a0001c0001t0001g0050 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.387+1234_387+1235i others(53): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690266 | ||||||
| chr11:690266
|
C | G | 6 | a0001c0001t0004g0199a0001c0002t0001g0195a0001c0002t0001g0196others(3): Show | 6 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.387+1235G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690266 | ||||||
| chr11:690270
|
G | A | 56 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0047others(53): Show | 56 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.387+1231C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690270 | ||||||
| chr11:690271
|
C | G | 130 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0015others(127): Show | 131 | HG00323.hp1 HG00423.hp2 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.387+1230G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690271 | ||||||
| chr11:690275
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.387+1226C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690275 | ||||||
| chr11:690276
|
G | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(159): Show | 164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.387+1225C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690276 | ||||||
| chr11:690276
|
G | GAGGGGAG others(4): Show |
1 | a0001c0001t0001g0015 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.387+1224_387+1225i others(13): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690276 | ||||||
| chr11:690281
|
C | G | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(182): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.387+1220G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690281 | ||||||
| chr11:690286
|
G | C | 36 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0029others(33): Show | 36 | HG00423.hp2 HG00597.hp2 HG01258.hp2 others(33): Show |
intron_variant | MODIFIER | c.387+1215C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690286 | ||||||
| chr11:690291
|
C | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(200): Show | 206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.387+1210G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690291 | ||||||
| chr11:690296
|
G | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0200others(2): Show | 5 | HG02622.hp1 HG02970.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+1205C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690296 | ||||||
| chr11:690296
|
G | GAGGGCAG others(103): Show |
3 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285 | 3 | HG02523.hp2 NA18966.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.387+1204_387+1205i others(112): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690296 | ||||||
| chr11:690301
|
G | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(245): Show | 251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.387+1200C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690301 | ||||||
| chr11:690301
|
G | GAGGGGAA others(103): Show |
1 | a0001c0002t0001g0265 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.387+1199_387+1200i others(112): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690301 | ||||||
| chr11:690301
|
G | GAGGGGAA others(83): Show |
1 | a0001c0002t0001g0254 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.387+1199_387+1200i others(92): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690301 | ||||||
| chr11:690301
|
G | GAGGGGAA others(73): Show |
1 | a0001c0002t0001g0235 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.387+1199_387+1200i others(82): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690301 | ||||||
| chr11:690306
|
G | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(203): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.387+1195C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690306 | ||||||
| chr11:690306
|
G | GAAGGCAG others(68): Show |
2 | a0001c0002t0001g0219a0001c0002t0001g0266 | 2 | HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.387+1194_387+1195i others(77): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690306 | ||||||
| chr11:690306
|
G | GAAGGCAG others(98): Show |
1 | a0002c0005t0001g0264 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.387+1194_387+1195i others(107): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690306 | ||||||
| chr11:690306
|
G | GAAGGCAG others(118): Show |
2 | a0001c0002t0001g0259a0002c0005t0001g0005 | 2 | HG02886.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.387+1194_387+1195i others(127): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690306 | ||||||
| chr11:690306
|
G | GAAGGCAG others(78): Show |
2 | a0001c0002t0001g0215a0001c0002t0001g0218 | 2 | HG01255.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.387+1194_387+1195i others(87): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690306 | ||||||
| chr11:690306
|
G | GAAGGCAG others(83): Show |
1 | a0001c0002t0001g0212 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.387+1194_387+1195i others(92): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690306 | ||||||
| chr11:690306
|
G | GAGGGGAG others(40): Show |
1 | a0001c0003t0001g0141 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.387+1194_387+1195i others(49): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690306 | ||||||
| chr11:690306
|
G | GAGGGGAG others(53): Show |
5 | a0001c0004t0001g0024a0001c0004t0001g0025a0001c0004t0001g0026others(2): Show | 5 | HG02735.hp2 HG03017.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+1194_387+1195i others(62): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690306 | ||||||
| chr11:690306
|
G | GAGGGGAG others(49): Show |
1 | a0001c0004t0001g0020 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.387+1194_387+1195i others(58): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690306 | ||||||
| chr11:690307
|
A | AAGGCAGG others(74): Show |
1 | a0001c0002t0001g0209 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.387+1193_387+1194i others(83): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690307 | ||||||
| chr11:690307
|
A | AAGGCAGG others(119): Show |
1 | a0001c0002t0001g0340 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.387+1193_387+1194i others(128): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690307 | ||||||
| chr11:690308
|
G | A | 16 | a0001c0002t0001g0213a0001c0002t0001g0214a0001c0002t0001g0216others(13): Show | 16 | HG01123.hp1 HG01257.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.387+1193C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690308 | ||||||
| chr11:690310
|
A | AGAGGGCA others(3): Show |
2 | a0001c0002t0001g0286a0001c0002t0001g0287 | 2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.387+1181_387+1190d others(12): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690310 | ||||||
| chr11:690310
|
A | G | 325 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(322): Show | 328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.387+1191T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690310 | ||||||
| chr11:690310
|
A | T | 1 | a0001c0002t0001g0340 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.387+1191T>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690310 | ||||||
| chr11:690311
|
G | C | 36 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0029others(33): Show | 36 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.387+1190C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690311 | ||||||
| chr11:690311
|
G | GAAGGCAG others(83): Show |
1 | a0001c0002t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.387+1189_387+1190i others(92): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690311 | ||||||
| chr11:690316
|
C | G | 14 | a0001c0001t0001g0016a0001c0001t0001g0047a0001c0001t0001g0282others(11): Show | 14 | HG00423.hp2 HG00597.hp2 HG02148.hp1 others(11): Show |
intron_variant | MODIFIER | c.387+1185G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690316 | ||||||
| chr11:690316
|
CAGGGGAG others(8): Show |
C | 1 | a0001c0001t0001g0306 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.387+1170_387+1184d others(17): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690316 | ||||||
| chr11:690317
|
A | AGGGCAGG others(39): Show |
1 | a0001c0003t0001g0144 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.387+1183_387+1184i others(48): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690317 | ||||||
| chr11:690317
|
A | AGGGCAGG others(64): Show |
1 | a0001c0001t0001g0322 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.387+1183_387+1184i others(73): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690317 | ||||||
| chr11:690321
|
G | C | 5 | a0001c0001t0001g0016a0001c0001t0001g0047a0001c0003t0001g0187others(2): Show | 5 | HG00423.hp2 HG01258.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.387+1180C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690321 | ||||||
| chr11:690322
|
A | AGGGGGAG others(37): Show |
1 | a0001c0003t0001g0142 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.387+1178_387+1179i others(46): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690322 | ||||||
| chr11:690326
|
C | CAGGGCAG others(68): Show |
2 | a0001c0001t0001g0312a0001c0001t0001g0313 | 2 | NA18951.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.387+1174_387+1175i others(77): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690326 | ||||||
| chr11:690326
|
C | CAGGGCAG others(88): Show |
8 | a0001c0001t0001g0314a0001c0001t0001g0315a0001c0001t0001g0316others(5): Show | 8 | NA18612.hp2 NA18963.hp1 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.387+1174_387+1175i others(97): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690326 | ||||||
| chr11:690326
|
C | CAGGGG | 3 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0002t0001g0042 | 3 | HG02132.hp1 NA18950.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.387+1170_387+1174d others(7): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690326 | ||||||
| chr11:690326
|
C | G | 21 | a0001c0001t0001g0015a0001c0001t0006g0031a0001c0002t0001g0213others(18): Show | 21 | HG01123.hp1 HG01257.hp2 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.387+1175G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690326 | ||||||
| chr11:690331
|
G | C | 15 | a0001c0001t0001g0282a0001c0001t0001g0312a0001c0001t0001g0313others(12): Show | 15 | HG00597.hp2 HG01258.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.387+1170C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690331 | ||||||
| chr11:690331
|
G | GAGGGC | 59 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0125others(56): Show | 59 | HG00280.hp2 HG00597.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.387+1169_387+1170i others(7): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690331 | ||||||
| chr11:690331
|
G | GAGGGCAG others(40): Show |
1 | a0001c0001t0001g0136 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.387+1169_387+1170i others(49): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690331 | ||||||
| chr11:690331
|
G | GAGGGGAG others(3): Show |
46 | a0001c0001t0001g0158a0001c0001t0001g0285a0001c0003t0001g0006others(43): Show | 46 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.387+1160_387+1169d others(12): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690331 | ||||||
| chr11:690331
|
G | GAGGGGAG others(83): Show |
1 | a0001c0002t0001g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.387+1169_387+1170i others(92): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690331 | ||||||
| chr11:690331
|
G | GAGGGGAG others(54): Show |
1 | a0001c0001t0001g0015 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.387+1169_387+1170i others(63): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690331 | ||||||
| chr11:690331
|
G | GAGGGGAG others(13): Show |
42 | a0001c0001t0001g0007a0001c0001t0001g0272a0001c0001t0001g0288others(39): Show | 43 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.387+1169_387+1170i others(22): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690331 | ||||||
| chr11:690331
|
G | GAGGGGAG others(98): Show |
1 | a0001c0001t0001g0008 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.387+1169_387+1170i others(107): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690331 | ||||||
| chr11:690331
|
G | GAGGGGAG others(88): Show |
1 | a0001c0002t0001g0230 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.387+1169_387+1170i others(97): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690331 | ||||||
| chr11:690331
|
G | GAGGGGAG others(64): Show |
2 | a0001c0001t0001g0016a0001c0001t0001g0047 | 2 | HG00423.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.387+1169_387+1170i others(73): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690331 | ||||||
| chr11:690331
|
G | GAGGGGAG others(23): Show |
2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG01943.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.387+1169_387+1170i others(32): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690331 | ||||||
| chr11:690331
|
G | GAGGGGAG others(93): Show |
9 | a0001c0002t0001g0221a0001c0002t0001g0222a0001c0002t0001g0223others(6): Show | 9 | HG02040.hp2 HG02074.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.387+1169_387+1170i others(102): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690331 | ||||||
| chr11:690331
|
G | GAGGGGGA others(94): Show |
1 | a0001c0002t0001g0220 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.387+1169_387+1170i others(103): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690331 | ||||||
| chr11:690332
|
A | AGGGGAGG others(95): Show |
1 | a0001c0001t0001g0282 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.387+1168_387+1169i others(104): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690332 | ||||||
| chr11:690336
|
G | C | 5 | a0001c0001t0004g0199a0001c0002t0001g0195a0001c0002t0001g0196others(2): Show | 5 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+1165C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690336 | ||||||
| chr11:690337
|
A | G | 1 | a0001c0002t0001g0211 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.387+1164T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690337 | ||||||
| chr11:690341
|
C | CAGGGGAG others(18): Show |
1 | a0001c0001t0001g0191 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.387+1159_387+1160i others(27): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690341 | ||||||
| chr11:690341
|
C | CAGGGGAG others(33): Show |
5 | a0001c0001t0001g0124a0001c0001t0001g0126a0001c0001t0001g0128others(2): Show | 5 | HG02004.hp1 NA18970.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.387+1159_387+1160i others(42): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690341 | ||||||
| chr11:690341
|
C | CAGGGGAG others(23): Show |
101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(98): Show | 103 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.387+1159_387+1160i others(32): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690341 | ||||||
| chr11:690341
|
C | CAGGGGAG others(28): Show |
2 | a0003c0007t0001g0039a0003c0007t0001g0040 | 2 | HG01106.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.387+1159_387+1160i others(37): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690341 | ||||||
| chr11:690341
|
C | CAGGGGAG others(33): Show |
1 | a0001c0001t0001g0038 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.387+1159_387+1160i others(42): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690341 | ||||||
| chr11:690341
|
C | CAGGGGAG others(13): Show |
1 | a0001c0001t0001g0046 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.387+1159_387+1160i others(22): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690341 | ||||||
| chr11:690341
|
C | CAGGGGAG others(3): Show |
17 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0029others(14): Show | 17 | HG00423.hp2 HG01934.hp1 HG02132.hp1 others(14): Show |
intron_variant | MODIFIER | c.387+1150_387+1159d others(12): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690341 | ||||||
| chr11:690341
|
C | G | 12 | a0001c0001t0001g0008a0001c0001t0001g0044a0001c0001t0001g0045others(9): Show | 12 | HG00597.hp2 HG00642.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.387+1160G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690341 | ||||||
| chr11:690342
|
A | AGGGGAGG others(24): Show |
1 | a0001c0001t0001g0037 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.387+1158_387+1159i others(33): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690342 | ||||||
| chr11:690342
|
A | AGGGGAGG others(25): Show |
1 | a0001c0001t0001g0036 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.387+1158_387+1159i others(34): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690342 | ||||||
| chr11:690346
|
G | C | 2 | a0001c0002t0001g0211a0001c0002t0001g0258 | 2 | HG00642.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.387+1155C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690346 | ||||||
| chr11:690346
|
G | GAGGGC | 4 | a0001c0002t0001g0203a0001c0002t0001g0254a0001c0002t0001g0255others(1): Show | 4 | HG01243.hp1 HG02015.hp2 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.387+1154_387+1155i others(7): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690346 | ||||||
| chr11:690346
|
G | GAGGGCAG others(53): Show |
3 | a0001c0001t0004g0199a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02630.hp1 HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.387+1154_387+1155i others(62): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690346 | ||||||
| chr11:690346
|
G | GAGGGCAG others(63): Show |
2 | a0001c0002t0001g0195a0001c0002t0001g0196 | 2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.387+1154_387+1155i others(72): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690346 | ||||||
| chr11:690346
|
G | GAGGGCAG others(23): Show |
1 | a0001c0001t0003g0140 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.387+1154_387+1155i others(32): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690346 | ||||||
| chr11:690346
|
G | GAGGGCAG others(13): Show |
5 | a0001c0002t0001g0212a0001c0002t0001g0215a0001c0002t0001g0218others(2): Show | 5 | HG01255.hp2 HG02738.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.387+1154_387+1155i others(22): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690346 | ||||||
| chr11:690346
|
G | GAGGGGAG others(3): Show |
56 | a0001c0001t0001g0253a0001c0002t0001g0201a0001c0002t0001g0202others(53): Show | 56 | HG00280.hp2 HG00597.hp1 HG01258.hp2 others(53): Show |
intron_variant | MODIFIER | c.387+1145_387+1154d others(12): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690346 | ||||||
| chr11:690346
|
G | GAGGGGAG others(98): Show |
3 | a0001c0002t0001g0214a0001c0002t0001g0216a0001c0002t0001g0217 | 3 | HG01123.hp1 HG01257.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.387+1154_387+1155i others(107): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690346 | ||||||
| chr11:690346
|
G | GAGGGGAG others(103): Show |
1 | a0001c0002t0001g0213 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.387+1154_387+1155i others(112): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690346 | ||||||
| chr11:690347
|
A | AGGGCAGG others(4): Show |
1 | a0001c0003t0001g0143 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.387+1153_387+1154i others(13): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690347 | ||||||
| chr11:690347
|
A | AGGGCAGG others(25): Show |
1 | a0001c0002t0001g0209 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.387+1153_387+1154i others(34): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690347 | ||||||
| chr11:690347
|
A | AGGGCAGG others(5): Show |
1 | a0001c0003t0001g0142 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.387+1153_387+1154i others(14): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690347 | ||||||
| chr11:690348
|
G | A | 1 | a0001c0009t0001g0137 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.387+1153C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690348 | ||||||
| chr11:690348
|
G | T | 1 | a0001c0002t0001g0208 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.387+1153C>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690348 | ||||||
| chr11:690350
|
G | GCAGGGGA others(4): Show |
1 | a0001c0003t0001g0141 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.387+1150_387+1151i others(13): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690350 | ||||||
| chr11:690351
|
G | C | 1 | a0001c0001t0001g0035 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.387+1150C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690351 | ||||||
| chr11:690352
|
A | AGGGGAGG others(24): Show |
1 | a0001c0001t0001g0035 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.387+1148_387+1149i others(33): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690352 | ||||||
| chr11:690352
|
A | AGGGGAGG others(75): Show |
1 | a0001c0001t0001g0338 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.387+1148_387+1149i others(84): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690352 | ||||||
| chr11:690356
|
C | G | 1 | a0001c0001t0001g0034 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.387+1145G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690356 | ||||||
| chr11:690361
|
G | GAGGGCAG others(8): Show |
1 | a0001c0002t0001g0257 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.387+1139_387+1140i others(17): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690361 | ||||||
| chr11:690362
|
A | AGGGCAGG others(4): Show |
2 | a0001c0002t0001g0206a0001c0002t0001g0207 | 2 | HG00642.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.387+1138_387+1139i others(13): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690362 | ||||||
| chr11:690372
|
A | AGGGGAGG others(9): Show |
1 | a0001c0001t0001g0338 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.387+1128_387+1129i others(18): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690372 | ||||||
| chr11:690373
|
G | A | 1 | a0001c0002t0001g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.387+1128C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690373 | ||||||
| chr11:690462
|
A | C | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(269): Show | 274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.387+1039T>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690462 | ||||||
| chr11:690472
|
T | C | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(270): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.387+1029A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690472 | ||||||
| chr11:690508
|
C | G | 1 | a0001c0002t0001g0205 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.387+993G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690508 | ||||||
| chr11:690555
|
C | A | 1 | a0001c0002t0001g0259 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.387+946G>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690555 | ||||||
| chr11:690602
|
C | T | 77 | a0001c0001t0001g0253a0001c0002t0001g0201a0001c0002t0001g0202others(74): Show | 77 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.387+899G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690602 | ||||||
| chr11:690660
|
G | A | 2 | a0001c0001t0001g0325a0001c0001t0001g0326 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.387+841C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690660 | ||||||
| chr11:690741
|
G | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(193): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.387+760C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690741 | ||||||
| chr11:690846
|
A | G | 1 | a0001c0002t0001g0204 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.387+655T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690846 | ||||||
| chr11:690972
|
A | T | 1 | a0001c0001t0002g0033 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.387+529T>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 690972 | ||||||
| chr11:691018
|
A | T | 77 | a0001c0001t0001g0253a0001c0002t0001g0201a0001c0002t0001g0202others(74): Show | 77 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.387+483T>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 691018 | ||||||
| chr11:691029
|
T | C | 58 | a0001c0001t0001g0007a0001c0001t0001g0272a0001c0001t0001g0282others(55): Show | 59 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.387+472A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 691029 | ||||||
| chr11:691090
|
C | T | 77 | a0001c0001t0001g0253a0001c0002t0001g0201a0001c0002t0001g0202others(74): Show | 77 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.387+411G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 691090 | ||||||
| chr11:691099
|
T | C | 5 | a0001c0001t0004g0199a0001c0002t0001g0195a0001c0002t0001g0196others(2): Show | 5 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+402A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 691099 | ||||||
| chr11:691186
|
C | T | 1 | a0001c0002t0001g0265 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.387+315G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 691186 | ||||||
| chr11:691194
|
G | A | 58 | a0001c0001t0001g0007a0001c0001t0001g0272a0001c0001t0001g0282others(55): Show | 59 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.387+307C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 691194 | ||||||
| chr11:691240
|
T | C | 77 | a0001c0001t0001g0253a0001c0002t0001g0201a0001c0002t0001g0202others(74): Show | 77 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.387+261A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 691240 | ||||||
| chr11:691443
|
C | T | 1 | a0001c0002t0001g0203 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.387+58G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 2/11 | chr11 | 691443 | ||||||
| chr11:691636
|
G | A | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(120): Show | 125 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.290-38C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 691636 | ||||||
| chr11:691718
|
G | A | 1 | a0001c0002t0001g0259 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.290-120C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 691718 | ||||||
| chr11:691723
|
T | G | 7 | a0001c0002t0001g0262a0002c0005t0001g0004a0002c0005t0001g0005others(4): Show | 7 | HG00597.hp1 NA18961.hp1 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.290-125A>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 691723 | ||||||
| chr11:691743
|
C | T | 1 | a0001c0001t0001g0272 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.290-145G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 691743 | ||||||
| chr11:691888
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.290-290A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 691888 | ||||||
| chr11:691923
|
G | T | 1 | a0001c0006t0001g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.290-325C>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 691923 | ||||||
| chr11:691978
|
G | A | 1 | a0001c0002t0001g0265 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.290-380C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 691978 | ||||||
| chr11:692040
|
T | C | 1 | a0001c0002t0001g0336 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.290-442A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 692040 | ||||||
| chr11:692221
|
T | C | 78 | a0001c0001t0001g0253a0001c0001t0004g0199a0001c0002t0001g0201others(75): Show | 78 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.290-623A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 692221 | ||||||
| chr11:692384
|
C | G | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(188): Show | 193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.290-786G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 692384 | ||||||
| chr11:692585
|
G | T | 52 | a0001c0001t0001g0158a0001c0003t0001g0006a0001c0003t0001g0141others(49): Show | 52 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.290-987C>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 692585 | ||||||
| chr11:692629
|
G | A | 2 | a0001c0001t0003g0139a0001c0001t0003g0140 | 2 | HG00738.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.290-1031C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 692629 | ||||||
| chr11:692853
|
C | CA | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(140): Show | 145 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.290-1256dupT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 692853 | ||||||
| chr11:692908
|
T | C | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(270): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.290-1310A>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 692908 | ||||||
| chr11:692963
|
C | T | 2 | a0001c0004t0001g0013a0001c0004t0001g0014 | 2 | HG02040.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.290-1365G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 692963 | ||||||
| chr11:692993
|
A | G | 1 | a0001c0002t0001g0202 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.290-1395T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 692993 | ||||||
| chr11:693041
|
G | C | 53 | a0001c0001t0001g0158a0001c0001t0001g0191a0001c0003t0001g0006others(50): Show | 53 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.290-1443C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 693041 | ||||||
| chr11:693078
|
G | A | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG02083.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.290-1480C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 693078 | ||||||
| chr11:693163
|
C | T | 1 | a0001c0002t0001g0327 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.290-1565G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 693163 | ||||||
| chr11:693168
|
G | A | 77 | a0001c0001t0001g0253a0001c0002t0001g0201a0001c0002t0001g0202others(74): Show | 77 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.290-1570C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 693168 | ||||||
| chr11:693356
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.289+1403T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 693356 | ||||||
| chr11:693557
|
C | G | 1 | a0001c0001t0001g0011 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.289+1202G>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 693557 | ||||||
| chr11:693567
|
A | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010 | 3 | HG02071.hp1 HG04184.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.289+1192T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 693567 | ||||||
| chr11:693787
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(193): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.289+972T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 693787 | ||||||
| chr11:693831
|
G | A | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(270): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.289+928C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 693831 | ||||||
| chr11:693846
|
A | T | 1 | a0001c0002t0001g0201 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.289+913T>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 693846 | ||||||
| chr11:693902
|
T | G | 1 | a0001c0001t0001g0193 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.289+857A>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 693902 | ||||||
| chr11:693970
|
CT | C | 3 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324 | 3 | HG01175.hp1 HG01981.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.289+788delA | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 693970 | ||||||
| chr11:693975
|
C | A | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.289+784G>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 693975 | ||||||
| chr11:694065
|
G | A | 2 | a0001c0001t0001g0325a0001c0001t0001g0326 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.289+694C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 694065 | ||||||
| chr11:694138
|
G | A | 1 | a0001c0003t0001g0194 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.289+621C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 694138 | ||||||
| chr11:694159
|
C | CA | 5 | a0001c0001t0004g0199a0001c0002t0001g0195a0001c0002t0001g0196others(2): Show | 5 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.289+599dupT | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 694159 | ||||||
| chr11:694220
|
G | GGGGGGCA | 11 | a0001c0001t0001g0328a0001c0002t0001g0327a0001c0002t0001g0329others(8): Show | 11 | HG01109.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.289+532_289+538dup others(7): Show |
DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 694220 | ||||||
| chr11:694221
|
G | C | 1 | a0001c0001t0001g0200 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.289+538C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 694221 | ||||||
| chr11:694252
|
G | T | 1 | a0001c0003t0001g0006 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.289+507C>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 694252 | ||||||
| chr11:694257
|
G | A | 77 | a0001c0001t0001g0253a0001c0002t0001g0201a0001c0002t0001g0202others(74): Show | 77 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.289+502C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 694257 | ||||||
| chr11:694270
|
A | G | 274 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(271): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.289+489T>C | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 694270 | ||||||
| chr11:694530
|
G | C | 1 | a0001c0001t0001g0338 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.289+229C>G | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 694530 | ||||||
| chr11:694697
|
G | A | 1 | a0001c0002t0001g0339 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.289+62C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 694697 | ||||||
| chr11:694698
|
C | T | 2 | a0002c0005t0001g0004a0002c0005t0001g0005 | 2 | NA19055.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.289+61G>A | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 694698 | ||||||
| chr11:694731
|
G | A | 3 | a0001c0002t0001g0340a0001c0002t0001g0341a0001c0002t0001g0342 | 3 | NA18993.hp1 NA19070.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.289+28C>T | DEAF1 | ENSG00000177030.19 | transcript | ENST00000382409.4 | protein_coding | 1/11 | chr11 | 694731 |