Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MEDSD others(560): Show |
chr11 | 639233 | 700222 |
| a0002 | 0/0 | 565 | 6 | 0 | 0 | 6 | 0 | 0 | 5 | DEAF1_chr11_639233_700222 | DEAF1 | MEDSD others(560): Show |
chr11 | 639233 | 700222 |
| a0003 | 0/0 | 565 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | MEDSD others(560): Show |
chr11 | 639233 | 700222 |
| a0004 | 0/0 | 565 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | MEDSD others(560): Show |
chr11 | 639233 | 700222 |
| a0005 | 0/0 | 565 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | MEDSD others(560): Show |
chr11 | 639233 | 700222 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1695 | 169 | 28 | 41 | 71 | 5 | 23 | DEAF1_chr11_639233_700222 | DEAF1 | ATGGA others(1690): Show |
chr11 | 639233 | 700222 | ||
| a0001c0002 | 0/0 | 1695 | 91 | 47 | 11 | 22 | 1 | 10 | DEAF1_chr11_639233_700222 | DEAF1 | ATGGA others(1690): Show |
chr11 | 639233 | 700222 | ||
| a0001c0003 | 0/0 | 1695 | 53 | 7 | 11 | 30 | 1 | 4 | DEAF1_chr11_639233_700222 | DEAF1 | ATGGA others(1690): Show |
chr11 | 639233 | 700222 | ||
| a0001c0004 | 0/0 | 1695 | 10 | 0 | 3 | 2 | 0 | 5 | DEAF1_chr11_639233_700222 | DEAF1 | ATGGA others(1690): Show |
chr11 | 639233 | 700222 | ||
| a0001c0006 | 0/0 | 1695 | 5 | 5 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | ATGGA others(1690): Show |
chr11 | 639233 | 700222 | ||
| a0001c0008 | 0/0 | 1695 | 2 | 2 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | ATGGA others(1690): Show |
chr11 | 639233 | 700222 | ||
| a0001c0009 | 0/0 | 1695 | 2 | 0 | 0 | 2 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | ATGGA others(1690): Show |
chr11 | 639233 | 700222 | ||
| a0001c0011 | 0/0 | 1695 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | ATGGA others(1690): Show |
chr11 | 639233 | 700222 | ||
| a0001c0013 | 0/0 | 1695 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | ATGGA others(1690): Show |
chr11 | 639233 | 700222 | ||
| a0001c0014 | 0/0 | 1695 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | ATGGA others(1690): Show |
chr11 | 639233 | 700222 | ||
| a0002c0005 | 0/0 | 1695 | 6 | 0 | 0 | 6 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | ATGGA others(1690): Show |
chr11 | 639233 | 700222 | ||
| a0003c0007 | 0/0 | 1695 | 2 | 0 | 1 | 0 | 1 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | ATGGA others(1690): Show |
chr11 | 639233 | 700222 | ||
| a0004c0012 | 0/0 | 1695 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | ATGGA others(1690): Show |
chr11 | 639233 | 700222 | ||
| a0005c0010 | 0/0 | 1695 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | ATGGA others(1690): Show |
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 | GGACT others(2185): Show |
chr11 | 639233 | 700222 |
| a0001c0001t0002 | 0/0 | 2190 | 3 | 0 | 0 | 3 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | GGACT others(2185): Show |
chr11 | 639233 | 700222 |
| a0001c0001t0003 | 0/0 | 2190 | 2 | 0 | 1 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | GGACT others(2185): Show |
chr11 | 639233 | 700222 |
| a0001c0001t0004 | 0/0 | 2190 | 2 | 2 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | GGACT others(2185): Show |
chr11 | 639233 | 700222 |
| a0001c0001t0005 | 0/0 | 2190 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | GGACT others(2185): Show |
chr11 | 639233 | 700222 |
| a0001c0001t0006 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | GGACT others(2185): Show |
chr11 | 639233 | 700222 |
| a0001c0002t0001 | 0/0 | 2190 | 91 | 47 | 11 | 22 | 1 | 10 | DEAF1_chr11_639233_700222 | DEAF1 | GGACT others(2185): Show |
chr11 | 639233 | 700222 |
| a0001c0003t0001 | 0/0 | 2190 | 53 | 7 | 11 | 30 | 1 | 4 | DEAF1_chr11_639233_700222 | DEAF1 | GGACT others(2185): Show |
chr11 | 639233 | 700222 |
| a0001c0004t0001 | 0/0 | 2190 | 10 | 0 | 3 | 2 | 0 | 5 | DEAF1_chr11_639233_700222 | DEAF1 | GGACT others(2185): Show |
chr11 | 639233 | 700222 |
| a0001c0006t0001 | 0/0 | 2190 | 5 | 5 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | GGACT others(2185): Show |
chr11 | 639233 | 700222 |
| a0001c0008t0001 | 0/0 | 2190 | 2 | 2 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | GGACT others(2185): Show |
chr11 | 639233 | 700222 |
| a0001c0009t0001 | 0/0 | 2190 | 2 | 0 | 0 | 2 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | GGACT others(2185): Show |
chr11 | 639233 | 700222 |
| a0001c0011t0001 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | GGACT others(2185): Show |
chr11 | 639233 | 700222 |
| a0001c0013t0001 | 0/0 | 2190 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | GGACT others(2185): Show |
chr11 | 639233 | 700222 |
| a0001c0014t0001 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | GGACT others(2185): Show |
chr11 | 639233 | 700222 |
| a0002c0005t0001 | 0/0 | 2190 | 6 | 0 | 0 | 6 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | GGACT others(2185): Show |
chr11 | 639233 | 700222 |
| a0003c0007t0001 | 0/0 | 2190 | 2 | 0 | 1 | 0 | 1 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | GGACT others(2185): Show |
chr11 | 639233 | 700222 |
| a0004c0012t0001 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | GGACT others(2185): Show |
chr11 | 639233 | 700222 |
| a0005c0010t0001 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | GGACT others(2185): Show |
chr11 | 639233 | 700222 |
| actghapid | grch38/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 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0024 | 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 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0056 | 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 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0078 | 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 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0127 | 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 |
| a0001c0001t0001g0132 | 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 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0274 | 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 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 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 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0282 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0290 | 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 |
| a0001c0001t0001g0300 | 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 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0005g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0001t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 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 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0272 | 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 |
| a0001c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0328 | 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 |
| a0001c0002t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0003t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0003t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0004t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0004t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0004t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0006t0001g0020 | 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 |
| a0001c0006t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0006t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0006t0001g0118 | 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 |
| a0001c0009t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0009t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0011t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0013t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0001c0014t0001g0148 | 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 |
| a0002c0005t0001g0006 | 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 |
| a0002c0005t0001g0262 | 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 |
| a0002c0005t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0003c0007t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0003c0007t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0004c0012t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| a0005c0010t0001g0085 | 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 | g0150 | 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 | g0139 | EUR | FIN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0251 | EUR | FIN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0310 | EUR | FIN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | FIN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00423 | hp1 | a0001 | c0003 | t0001 | g0149 | EAS | CHS | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00438 | hp2 | a0001 | c0003 | t0001 | g0191 | EAS | CHS | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00558 | hp1 | a0001 | c0003 | t0001 | g0179 | EAS | CHS | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00597 | hp1 | a0002 | c0005 | t0001 | g0265 | EAS | CHS | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | CHS | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0210 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0208 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00673 | hp1 | a0001 | c0003 | t0001 | g0153 | EAS | CHS | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00673 | hp2 | a0001 | c0003 | t0001 | g0152 | EAS | CHS | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00735 | hp1 | a0001 | c0013 | t0001 | g0080 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0140 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01069 | hp2 | a0001 | c0003 | t0001 | g0311 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01070 | hp1 | a0001 | c0003 | t0001 | g0182 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01074 | hp1 | a0001 | c0003 | t0001 | g0164 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0119 | 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 | g0041 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01106 | hp2 | a0001 | c0004 | t0001 | g0023 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0204 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0301 | AMR | PUR | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01255 | hp1 | a0001 | c0003 | t0001 | g0165 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0221 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0213 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0300 | 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 | g0158 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0242 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01346 | hp2 | a0001 | c0003 | t0001 | g0146 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01358 | hp1 | a0001 | c0001 | t0005 | g0291 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0212 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0252 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0211 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01496 | hp2 | a0001 | c0004 | t0001 | g0021 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0054 | EUR | IBS | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01515 | hp2 | a0003 | c0007 | t0001 | g0040 | EUR | IBS | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0135 | 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 | g0057 | 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 | g0008 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0121 | 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 | g0036 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02004 | hp2 | a0001 | c0004 | t0001 | g0022 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02015 | hp1 | a0001 | c0003 | t0001 | g0174 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02040 | hp1 | a0001 | c0004 | t0001 | g0014 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0287 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0219 | 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 | g0009 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02071 | hp2 | a0001 | c0003 | t0001 | g0157 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0228 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02074 | hp2 | a0001 | c0003 | t0001 | g0180 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02083 | hp2 | a0001 | c0004 | t0001 | g0015 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02132 | hp2 | a0001 | c0014 | t0001 | g0148 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0218 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0246 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02155 | hp1 | a0001 | c0003 | t0001 | g0181 | EAS | CDX | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0224 | EAS | CDX | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02165 | hp1 | a0001 | c0011 | t0001 | g0086 | EAS | CDX | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CDX | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02258 | hp1 | a0001 | c0006 | t0001 | g0106 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02273 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02293 | hp2 | a0001 | c0003 | t0001 | g0156 | AMR | PEL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02451 | hp1 | a0001 | c0006 | t0001 | g0020 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0253 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0328 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0190 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0195 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02615 | hp2 | a0004 | c0012 | t0001 | g0271 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0280 | 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 | g0259 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0326 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0266 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0256 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0240 | 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 | g0200 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0338 | 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 | g0029 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0267 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0330 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0196 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0260 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0171 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0258 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0333 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0172 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0332 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0288 | AFR | ESN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0236 | AFR | ESN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0302 | AFR | ESN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0223 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03017 | hp2 | a0001 | c0004 | t0001 | g0025 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0243 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0249 | AFR | MSL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0334 | AFR | MSL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0244 | AFR | ESN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0245 | AFR | ESN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0199 | AFR | ESN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | ESN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0305 | AFR | ESN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03195 | hp2 | a0001 | c0006 | t0001 | g0118 | 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 | g0095 | AFR | MSL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03225 | hp2 | a0001 | c0006 | t0001 | g0107 | AFR | MSL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0235 | 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 | g0329 | AFR | MSL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0272 | 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 | g0309 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0312 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0237 | AFR | ESN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0255 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0241 | AFR | GWD | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0275 | AFR | MSL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0074 | 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 | g0222 | SAS | STU | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0141 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03710 | hp2 | a0001 | c0004 | t0001 | g0026 | SAS | PJL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | BEB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03831 | hp2 | a0001 | c0003 | t0001 | g0147 | SAS | BEB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0217 | SAS | BEB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | STU | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0250 | SAS | STU | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | STU | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0183 | SAS | STU | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | STU | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0220 | SAS | STU | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG04228 | hp1 | a0001 | c0004 | t0001 | g0028 | SAS | STU | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | STU | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0248 | AFR | YRI | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0202 | AFR | YRI | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | CHB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18747 | hp1 | a0001 | c0003 | t0001 | g0167 | EAS | CHB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0203 | EAS | CHB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | YRI | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0247 | AFR | YRI | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0113 | 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 | g0042 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18950 | hp2 | a0001 | c0003 | t0001 | g0145 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18952 | hp1 | a0001 | c0003 | t0001 | g0168 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18954 | hp1 | a0001 | c0003 | t0001 | g0178 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0137 | 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 | g0263 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18962 | hp1 | a0001 | c0009 | t0001 | g0064 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18962 | hp2 | a0001 | c0003 | t0001 | g0184 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18964 | hp1 | a0001 | c0003 | t0001 | g0143 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18971 | hp1 | a0001 | c0003 | t0001 | g0177 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18971 | hp2 | a0001 | c0003 | t0001 | g0033 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18978 | hp1 | a0002 | c0005 | t0001 | g0261 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18978 | hp2 | a0001 | c0003 | t0001 | g0144 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18981 | hp2 | a0001 | c0009 | t0001 | g0138 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18982 | hp2 | a0001 | c0003 | t0001 | g0154 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18983 | hp2 | a0005 | c0010 | t0001 | g0085 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0339 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18994 | hp2 | a0001 | c0003 | t0001 | g0142 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0233 | 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 | g0134 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0125 | 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 | g0194 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19005 | hp2 | a0001 | c0003 | t0001 | g0161 | 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 | g0122 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0207 | AFR | LWK | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0336 | AFR | LWK | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | LWK | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0239 | AFR | LWK | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0320 | 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 | g0016 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19055 | hp2 | a0002 | c0005 | t0001 | g0005 | 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 | g0131 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19064 | hp1 | a0002 | c0005 | t0001 | g0262 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19064 | hp2 | a0001 | c0003 | t0001 | g0166 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19065 | hp1 | a0001 | c0003 | t0001 | g0169 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19066 | hp2 | a0001 | c0003 | t0001 | g0155 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0051 | 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 | g0341 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19074 | hp2 | a0001 | c0003 | t0001 | g0185 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19079 | hp1 | a0002 | c0005 | t0001 | g0006 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19079 | hp2 | a0001 | c0003 | t0001 | g0176 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19081 | hp1 | a0001 | c0003 | t0001 | g0187 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19081 | hp2 | a0002 | c0005 | t0001 | g0264 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0340 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ASW | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0238 | AFR | ASW | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA20905 | hp1 | a0001 | c0003 | t0001 | g0175 | SAS | GIH | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA20905 | hp2 | a0001 | c0004 | t0001 | g0027 | SAS | GIH | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0214 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0151 | AMR | CLM | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0254 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0205 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0335 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02559 | hp1 | a0001 | c0006 | t0001 | g0108 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0270 | AFR | ACB | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0173 | AFR | MSL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0268 | AFR | MSL | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG06807 | hp1 | a0001 | c0003 | t0001 | g0160 | AFR | USA | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0331 | AFR | USA | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0269 | AFR | LWK | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0032 | AFR | LWK | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0282 | REF | REF | DEAF1_chr11_639233_700222 | DEAF1 | chr11 | 639233 | 700222 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:653968 | T | C | 4 | a0001c0002 a0001c0008 a0002c0005 others(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 | a0001c0003 a0001c0008 a0001c0014 |
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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:644748 | C | G | 49 | a0001c0001t0001g0122 a0001c0003t0001g0007 a0001c0003t0001g0033 others(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 | a0001c0002t0001g0252 | 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 | a0001c0001t0001g0125 a0001c0001t0001g0127 a0001c0001t0001g0131 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0069 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0047 | 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 | a0001c0002t0001g0235 a0001c0002t0001g0236 a0001c0002t0001g0237 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0119 a0001c0002t0001g0217 a0001c0002t0001g0223 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0308 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0003t0001g0181 | 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 | a0001c0001t0001g0103 | 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 | a0001c0001t0001g0325 | 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 | a0001c0002t0001g0256 | 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 | a0001c0014t0001g0148 | 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 | a0001c0002t0001g0196 | 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 | a0001c0003t0001g0156 | 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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | 13 | a0001c0001t0001g0004 a0001c0001t0001g0284 a0001c0001t0001g0285 others(10): 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 | a0001c0002t0001g0241 | 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 | a0001c0002t0001g0202 a0001c0002t0001g0268 |
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 | a0001c0003t0001g0181 | 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 | a0001c0003t0001g0165 | 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0002t0001g0245 a0001c0002t0001g0326 a0001c0002t0001g0334 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0094 others(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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0337 | 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 | a0001c0003t0001g0057 | 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 | a0001c0001t0006g0032 a0001c0008t0001g0003 |
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 | a0001c0003t0001g0183 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0050 a0001c0001t0001g0061 others(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 | a0001c0002t0001g0302 | 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 | a0001c0001t0001g0091 a0001c0001t0001g0308 a0001c0008t0001g0003 others(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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0048 a0001c0001t0001g0052 a0001c0001t0001g0062 others(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 | a0001c0001t0001g0039 a0001c0001t0001g0122 a0001c0001t0001g0276 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0036 a0001c0001t0001g0045 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0087 | 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 | a0001c0002t0001g0251 | 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 | a0001c0001t0001g0117 a0001c0003t0001g0162 a0001c0003t0001g0163 |
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 | a0001c0003t0001g0180 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0193 a0001c0002t0001g0266 |
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 | a0001c0001t0001g0052 a0001c0001t0001g0089 a0001c0001t0001g0113 others(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 | a0001c0001t0001g0319 | 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 | a0001c0001t0001g0039 a0001c0001t0001g0281 a0001c0001t0001g0313 others(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 | a0001c0001t0001g0117 | 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 | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(90): 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 | a0001c0001t0001g0049 a0001c0001t0001g0058 a0001c0001t0001g0059 others(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 | a0001c0002t0001g0219 a0001c0002t0001g0224 a0001c0004t0001g0014 others(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 | a0001c0001t0001g0036 a0001c0001t0001g0053 a0001c0001t0001g0120 others(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 | a0001c0002t0001g0267 a0001c0003t0001g0007 a0001c0003t0001g0033 others(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 | a0001c0002t0001g0202 a0001c0002t0001g0245 a0001c0002t0001g0268 others(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 | a0001c0003t0001g0174 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0104 a0001c0001t0001g0273 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0001t0001g0094 others(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 | a0001c0002t0001g0205 a0001c0002t0001g0208 a0001c0002t0001g0209 others(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 | a0001c0001t0003g0140 | 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 | a0001c0001t0001g0325 a0001c0001t0003g0140 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0325 a0001c0001t0003g0140 |
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 | a0001c0001t0001g0325 | 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 | a0001c0001t0003g0140 a0001c0003t0001g0155 |
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 | a0001c0001t0003g0140 | 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 | a0001c0002t0001g0231 a0001c0002t0001g0339 a0001c0002t0001g0341 |
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 | a0001c0001t0001g0094 a0001c0002t0001g0199 a0001c0002t0001g0202 others(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 | a0001c0001t0001g0105 | 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 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0198 |
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 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0067 others(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 | a0001c0003t0001g0143 a0001c0003t0001g0144 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0094 a0001c0001t0001g0299 others(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 | a0001c0001t0001g0094 a0001c0002t0001g0043 a0001c0002t0001g0199 others(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 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0198 |
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 | a0001c0001t0001g0094 a0001c0002t0001g0043 a0001c0002t0001g0199 others(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 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0198 |
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 | a0001c0001t0001g0012 a0001c0001t0001g0159 |
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 | a0001c0003t0001g0152 | 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 | a0001c0002t0001g0207 a0001c0002t0001g0254 a0001c0002t0001g0287 others(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 | a0001c0002t0001g0326 a0001c0002t0001g0334 a0001c0002t0001g0335 others(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 | a0001c0003t0001g0170 a0001c0003t0001g0171 a0001c0003t0001g0172 others(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 | a0002c0005t0001g0005 | 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 | a0001c0002t0001g0272 | 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 | a0001c0003t0001g0180 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0099 | 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 | a0001c0003t0001g0007 a0001c0003t0001g0033 a0001c0003t0001g0057 others(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 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0198 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0094 a0001c0002t0001g0043 a0001c0002t0001g0196 others(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 | a0001c0001t0002g0128 | 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 | a0001c0003t0001g0160 a0001c0003t0001g0188 a0001c0003t0001g0189 |
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 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0031 others(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 | a0001c0002t0001g0043 a0001c0002t0001g0203 a0001c0002t0001g0206 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0198 |
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 | a0001c0002t0001g0222 | 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 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0198 |
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 | a0001c0002t0001g0207 a0001c0002t0001g0254 a0001c0002t0001g0305 |
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 | a0001c0001t0001g0049 a0001c0001t0001g0068 a0001c0001t0001g0075 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0201 a0001c0001t0006g0032 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0031 a0001c0001t0001g0094 others(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 | a0001c0002t0001g0043 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0002t0001g0211 a0001c0002t0001g0212 a0001c0002t0001g0213 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0045 others(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 | a0001c0003t0001g0007 a0001c0003t0001g0033 a0001c0003t0001g0143 others(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 | a0001c0003t0001g0155 | 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 | a0001c0001t0001g0132 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0117 |
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 | a0001c0001t0001g0094 a0001c0002t0001g0043 a0001c0002t0001g0199 others(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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0050 a0001c0001t0001g0063 a0001c0001t0001g0074 others(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 | a0001c0003t0001g0007 a0001c0003t0001g0033 a0001c0003t0001g0057 others(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 | a0001c0001t0006g0032 | 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 | a0001c0002t0001g0043 a0001c0002t0001g0199 a0001c0002t0001g0203 others(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 | a0001c0002t0001g0269 a0001c0002t0001g0270 a0004c0012t0001g0271 |
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 | a0001c0002t0001g0216 | 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 | a0001c0002t0001g0272 | 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 | a0001c0003t0001g0007 a0001c0003t0001g0033 a0001c0003t0001g0057 others(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 | a0001c0001t0001g0116 | 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 | a0001c0003t0001g0057 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0310 others(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 | a0002c0005t0001g0005 | 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 | a0001c0002t0001g0043 a0001c0002t0001g0199 a0001c0002t0001g0202 others(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 | a0001c0001t0001g0337 | 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 | a0001c0001t0001g0127 | 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 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0198 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0002t0001g0043 a0001c0002t0001g0203 a0001c0002t0001g0206 others(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 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0198 |
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 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0198 |
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 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0198 |
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 | a0001c0002t0001g0210 | 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 | a0001c0002t0001g0272 | 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 | a0001c0002t0001g0272 | 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 | a0001c0002t0001g0272 | 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 | a0001c0002t0001g0272 | 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 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0198 |
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 | a0001c0002t0001g0246 a0001c0002t0001g0247 a0001c0002t0001g0253 others(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 | a0001c0002t0001g0227 | 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 | a0001c0002t0001g0246 a0001c0002t0001g0247 a0001c0002t0001g0253 others(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 | a0001c0002t0001g0288 | 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 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0071 others(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 | 191 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(188): 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 | a0001c0001t0001g0078 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0283 a0001c0001t0001g0289 a0001c0001t0001g0292 others(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 | a0001c0001t0001g0201 | 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 | a0001c0002t0001g0309 a0001c0002t0001g0312 |
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 | a0001c0001t0001g0285 a0001c0002t0001g0043 a0001c0002t0001g0199 others(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 | a0001c0002t0001g0245 | 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 | a0001c0001t0001g0285 a0001c0002t0001g0043 a0001c0002t0001g0196 others(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 | a0001c0003t0001g0150 | 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 | a0001c0001t0001g0127 | 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 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0198 others(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 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0198 others(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 | a0001c0003t0001g0142 a0001c0003t0001g0145 a0001c0003t0001g0161 |
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 |
6 | a0001c0001t0001g0004 a0001c0001t0001g0284 a0001c0001t0001g0316 others(3): 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 | a0001c0002t0001g0272 | 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 | a0001c0003t0001g0147 a0001c0003t0001g0169 |
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 | a0001c0001t0001g0076 | 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 | a0001c0001t0001g0109 | 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 | a0001c0003t0001g0147 a0001c0003t0001g0169 |
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 | a0001c0001t0001g0327 a0001c0003t0001g0183 |
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 | a0001c0003t0001g0142 a0001c0003t0001g0145 a0001c0003t0001g0147 others(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 | a0001c0003t0001g0142 a0001c0003t0001g0145 a0001c0003t0001g0147 others(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 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0198 |
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 | a0001c0003t0001g0007 a0001c0003t0001g0057 a0001c0003t0001g0143 others(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 | a0001c0003t0001g0033 | 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 | a0001c0002t0001g0205 | 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 | a0001c0004t0001g0021 a0001c0004t0001g0022 |
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 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0198 |
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 | a0001c0002t0001g0272 | 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 | a0001c0004t0001g0014 a0001c0004t0001g0015 a0001c0004t0001g0023 others(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 | a0001c0004t0001g0021 a0001c0004t0001g0022 |
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 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0198 others(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 | a0001c0001t0001g0323 | 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 | a0001c0001t0001g0089 | 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 | a0001c0003t0001g0007 a0001c0003t0001g0033 a0001c0003t0001g0057 others(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 | a0001c0001t0001g0318 | 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 | a0001c0001t0001g0318 | 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 | a0001c0001t0001g0318 | 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 | a0001c0003t0001g0176 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0002t0001g0043 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0001t0001g0010 | 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 | a0001c0002t0001g0252 | 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 | a0001c0002t0001g0043 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0002t0001g0043 a0001c0002t0001g0198 a0001c0002t0001g0208 others(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 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0199 others(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 | a0001c0002t0001g0202 a0001c0002t0001g0205 a0001c0002t0001g0227 others(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 | a0001c0002t0001g0259 a0001c0002t0001g0269 a0001c0002t0001g0270 others(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 | a0001c0002t0001g0043 a0001c0002t0001g0208 a0001c0002t0001g0210 others(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 | a0001c0003t0001g0170 a0001c0003t0001g0171 a0001c0003t0001g0172 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0002t0001g0043 a0001c0002t0001g0198 a0001c0002t0001g0199 others(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 | 13 | a0001c0001t0001g0004 a0001c0001t0001g0284 a0001c0001t0001g0285 others(10): 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 | a0001c0001t0001g0039 a0001c0001t0001g0193 a0001c0009t0001g0064 |
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 | a0001c0002t0001g0258 | 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 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0198 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0003t0001g0007 a0001c0003t0001g0033 a0001c0003t0001g0057 others(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 | a0001c0003t0001g0007 a0001c0003t0001g0033 a0001c0003t0001g0057 others(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 | a0001c0003t0001g0182 | 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 | a0001c0001t0001g0126 | 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 | a0001c0002t0001g0043 a0001c0002t0001g0199 a0001c0002t0001g0202 others(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 | a0001c0001t0001g0074 | 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 | a0001c0001t0001g0048 a0001c0001t0001g0116 a0001c0001t0001g0283 others(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 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0198 |
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 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0003t0001g0181 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0050 a0001c0001t0001g0061 others(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 | a0001c0001t0001g0281 a0001c0002t0001g0043 a0001c0002t0001g0202 others(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 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0198 others(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 | a0001c0002t0001g0272 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(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 | a0001c0001t0001g0327 a0001c0002t0001g0043 a0001c0002t0001g0196 others(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 | a0001c0002t0001g0301 a0001c0002t0001g0302 |
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 | a0001c0002t0001g0272 | 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 | a0001c0003t0001g0007 a0001c0003t0001g0033 a0001c0003t0001g0057 others(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 | a0001c0001t0001g0327 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0002t0001g0272 | 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 | a0001c0001t0001g0327 a0001c0002t0001g0043 a0001c0002t0001g0196 others(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 | a0001c0002t0001g0235 | 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 | a0001c0002t0001g0043 a0001c0002t0001g0202 a0001c0002t0001g0203 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0327 | 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 | a0001c0001t0001g0117 | 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 | a0001c0003t0001g0177 | 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 | a0001c0003t0001g0153 a0001c0003t0001g0166 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0002t0001g0219 | 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 | a0001c0003t0001g0170 a0001c0003t0001g0171 a0001c0003t0001g0172 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0069 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0062 | 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 | a0001c0003t0001g0146 a0001c0003t0001g0156 a0001c0003t0001g0182 |
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 | a0001c0002t0001g0231 a0001c0002t0001g0339 a0001c0002t0001g0341 |
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 | a0001c0003t0001g0007 a0001c0003t0001g0033 a0001c0003t0001g0057 others(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 | a0001c0001t0001g0073 | 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 | a0001c0001t0001g0327 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0002t0001g0203 | 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 | a0001c0003t0001g0182 | 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 | a0005c0010t0001g0085 | 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 | a0001c0001t0001g0290 a0001c0001t0001g0296 |
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 | a0001c0001t0001g0327 | 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 | a0001c0001t0001g0283 a0001c0001t0001g0289 a0001c0001t0001g0292 others(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 | a0001c0001t0001g0327 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0001t0001g0327 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0002t0001g0243 | 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 | a0001c0004t0001g0014 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0062 a0001c0001t0001g0082 a0001c0001t0001g0092 |
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 | a0001c0001t0001g0327 | 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 | a0001c0001t0001g0327 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0001t0001g0101 | 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 | a0001c0002t0001g0043 a0001c0002t0001g0203 a0001c0002t0001g0204 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0327 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0011t0001g0086 | 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 | a0001c0001t0001g0327 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0050 others(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 | a0001c0003t0001g0181 | 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 | a0001c0001t0001g0039 a0001c0001t0001g0079 a0001c0001t0001g0081 others(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 | a0001c0002t0001g0255 | 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 | a0001c0001t0001g0056 | 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 | a0001c0001t0001g0047 | 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 | a0001c0002t0001g0247 a0001c0002t0001g0253 a0001c0002t0001g0259 |
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 | a0001c0001t0001g0053 | 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 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0042 a0001c0001t0001g0081 a0001c0001t0001g0257 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0283 a0001c0001t0001g0289 a0001c0001t0001g0292 others(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 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0257 a0001c0001t0001g0327 a0001c0002t0001g0043 others(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 | a0001c0001t0001g0257 a0001c0002t0001g0043 a0001c0002t0001g0202 others(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 | a0001c0003t0001g0007 a0001c0003t0001g0033 a0001c0003t0001g0142 others(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 | a0001c0001t0001g0327 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0003t0001g0183 | 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 | a0001c0001t0001g0327 | 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 | a0001c0001t0001g0091 | 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 | a0001c0001t0001g0327 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0003t0001g0173 | 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 | a0001c0003t0001g0170 a0001c0003t0001g0171 a0001c0003t0001g0172 others(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 | a0001c0001t0001g0039 a0001c0001t0001g0079 a0001c0001t0001g0081 others(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 | a0001c0002t0001g0207 a0001c0002t0001g0254 a0001c0002t0001g0260 others(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 | a0001c0002t0001g0240 a0001c0002t0001g0241 a0001c0002t0001g0242 others(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 | a0001c0003t0001g0007 a0001c0003t0001g0033 a0001c0003t0001g0142 others(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 | a0001c0001t0001g0257 a0001c0001t0001g0327 a0001c0002t0001g0043 others(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 | a0001c0003t0001g0007 a0001c0003t0001g0033 a0001c0003t0001g0142 others(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 | a0001c0001t0001g0257 a0001c0002t0001g0043 a0001c0002t0001g0202 others(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 | a0001c0002t0001g0202 a0001c0002t0001g0207 a0001c0002t0001g0240 others(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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0257 a0001c0002t0001g0043 a0001c0002t0001g0202 others(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 | a0001c0001t0001g0323 | 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 | a0001c0001t0001g0327 | 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 | a0001c0002t0001g0210 | 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 | a0001c0001t0001g0327 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0001t0001g0039 | 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 | a0001c0001t0001g0257 a0001c0001t0001g0327 a0001c0002t0001g0043 others(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 | a0001c0001t0001g0137 a0001c0001t0001g0277 a0001c0002t0001g0196 others(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 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0198 others(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 | a0001c0001t0001g0313 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0257 a0001c0002t0001g0043 a0001c0002t0001g0203 others(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 | a0001c0002t0001g0211 a0001c0002t0001g0213 |
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 | a0001c0001t0001g0100 a0001c0001t0001g0112 |
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 | a0001c0002t0001g0272 | 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 | a0001c0001t0001g0257 a0001c0002t0001g0043 a0001c0002t0001g0202 others(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 | a0001c0001t0001g0327 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0001t0001g0327 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0001t0001g0257 a0001c0002t0001g0043 a0001c0002t0001g0203 others(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 | a0001c0003t0001g0007 a0001c0003t0001g0033 a0001c0003t0001g0142 others(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 | a0001c0001t0001g0257 a0001c0002t0001g0043 a0001c0002t0001g0202 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0279 a0001c0001t0001g0327 a0001c0002t0001g0196 others(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 | a0001c0001t0001g0024 | 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 | a0001c0001t0001g0308 | 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 | a0001c0002t0001g0328 a0001c0002t0001g0329 a0001c0002t0001g0330 others(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 | a0001c0002t0001g0231 a0001c0002t0001g0339 a0001c0002t0001g0341 |
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 | a0001c0001t0001g0257 a0001c0001t0001g0327 a0001c0002t0001g0043 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0004t0001g0014 a0001c0004t0001g0015 a0001c0004t0001g0021 others(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 | a0001c0003t0001g0160 a0001c0003t0001g0188 a0001c0003t0001g0189 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0257 a0001c0001t0001g0327 a0001c0002t0001g0043 others(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 | a0001c0002t0001g0244 a0001c0002t0001g0248 a0001c0002t0001g0249 |
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 | a0001c0001t0001g0257 a0001c0002t0001g0043 a0001c0002t0001g0202 others(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 | a0001c0002t0001g0234 | 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 | a0001c0002t0001g0209 a0001c0002t0001g0215 a0001c0002t0001g0226 others(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 | a0001c0001t0001g0019 | 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 | a0001c0001t0001g0324 a0001c0001t0001g0325 |
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 | a0001c0002t0001g0269 | 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 | a0001c0004t0001g0025 | 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 | a0001c0002t0001g0269 | 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 | a0001c0001t0001g0327 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0001t0001g0059 a0001c0001t0001g0283 a0001c0001t0002g0034 others(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 | a0001c0003t0001g0147 a0001c0003t0001g0169 |
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 |
23 | a0001c0001t0001g0004 a0001c0001t0001g0274 a0001c0001t0001g0276 others(20): 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 | a0001c0001t0001g0008 a0001c0001t0001g0273 a0001c0001t0001g0278 others(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 | a0001c0002t0001g0209 a0001c0002t0001g0215 a0001c0002t0001g0226 others(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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0073 |
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 | a0001c0002t0001g0196 a0001c0002t0001g0198 a0001c0002t0001g0199 |
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 | a0001c0001t0001g0056 a0001c0002t0001g0272 |
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 | a0001c0001t0001g0327 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0201 |
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 | a0001c0002t0001g0246 | 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 | a0001c0003t0001g0007 a0001c0003t0001g0033 a0001c0003t0001g0142 others(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 | a0001c0001t0001g0283 a0001c0001t0001g0289 a0001c0001t0001g0292 others(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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0075 | 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 | a0001c0002t0001g0338 | 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 | a0001c0003t0001g0158 | 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 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0083 | 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 | a0001c0001t0001g0071 | 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 | a0001c0002t0001g0266 a0001c0002t0001g0309 a0001c0002t0001g0312 |
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 | a0001c0001t0001g0011 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0016 others(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 | a0001c0002t0001g0043 a0001c0002t0001g0203 a0001c0002t0001g0206 others(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 | a0001c0002t0001g0235 | 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 | a0001c0002t0001g0224 a0001c0002t0001g0228 a0001c0002t0001g0232 others(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 | a0001c0002t0001g0231 a0001c0002t0001g0339 a0001c0002t0001g0341 |
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 | a0001c0002t0001g0231 a0001c0002t0001g0339 a0001c0002t0001g0341 |
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 | a0001c0002t0001g0260 | 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 | a0001c0002t0001g0240 a0001c0002t0001g0241 a0001c0002t0001g0242 others(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 | a0001c0002t0001g0326 a0001c0002t0001g0328 a0001c0002t0001g0329 others(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 | a0001c0002t0001g0207 a0001c0002t0001g0254 a0001c0002t0001g0305 |
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 | a0001c0002t0001g0269 | 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 | a0001c0002t0001g0211 a0001c0002t0001g0244 a0001c0002t0001g0247 others(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 | a0001c0001t0001g0257 a0001c0002t0001g0204 a0001c0002t0001g0205 others(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 | a0001c0002t0001g0202 a0001c0002t0001g0208 a0001c0002t0001g0210 others(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 | a0001c0002t0001g0246 | 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 | a0001c0002t0001g0255 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0159 |
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 | a0001c0001t0001g0104 | 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 | a0001c0002t0001g0225 a0001c0002t0001g0227 a0001c0002t0001g0340 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0071 |
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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0048 a0001c0001t0001g0100 a0001c0001t0001g0192 others(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 | a0001c0001t0001g0096 | 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 | a0001c0004t0001g0015 a0001c0004t0001g0028 |
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 | a0001c0004t0001g0014 a0001c0004t0001g0021 a0001c0004t0001g0022 others(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 | a0001c0001t0001g0130 a0001c0001t0001g0281 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0133 |
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 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0126 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0038 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0067 a0001c0001t0001g0091 |
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 | a0001c0001t0001g0049 | 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 | a0001c0001t0001g0280 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0056 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0257 a0001c0002t0001g0043 a0001c0002t0001g0202 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0201 |
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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0201 |
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 | a0001c0001t0001g0047 | 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 | a0001c0003t0001g0170 a0001c0003t0001g0171 a0001c0003t0001g0172 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0273 a0001c0001t0001g0290 others(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 | a0001c0003t0001g0142 | 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 | a0001c0003t0001g0007 a0001c0003t0001g0033 a0001c0003t0001g0142 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0257 a0001c0001t0001g0327 a0001c0002t0001g0043 others(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 | a0001c0001t0001g0257 a0001c0002t0001g0043 a0001c0002t0001g0202 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0047 others(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 | a0001c0001t0006g0032 | 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 | a0001c0002t0001g0246 | 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 | a0001c0003t0001g0007 a0001c0003t0001g0033 a0001c0003t0001g0142 others(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 | a0001c0001t0001g0327 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0001t0001g0103 | 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 | a0001c0001t0001g0281 | 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 | a0001c0001t0001g0308 | 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 | a0001c0001t0001g0257 a0001c0001t0001g0327 a0001c0002t0001g0043 others(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 | a0001c0001t0001g0257 a0001c0002t0001g0043 a0001c0002t0001g0202 others(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 | a0001c0001t0001g0257 a0001c0002t0001g0043 a0001c0002t0001g0202 others(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 | a0001c0001t0001g0257 a0001c0002t0001g0043 a0001c0002t0001g0202 others(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 | a0001c0001t0001g0257 a0001c0002t0001g0043 a0001c0002t0001g0202 others(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 | a0001c0001t0001g0257 a0001c0002t0001g0043 a0001c0002t0001g0202 others(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 | a0001c0001t0001g0257 a0001c0002t0001g0043 a0001c0002t0001g0202 others(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 | a0001c0001t0001g0257 a0001c0002t0001g0043 a0001c0002t0001g0202 others(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 | a0001c0001t0001g0257 a0001c0002t0001g0043 a0001c0002t0001g0202 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0201 |
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 | a0001c0001t0001g0257 a0001c0001t0001g0327 a0001c0002t0001g0043 others(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 | a0001c0001t0001g0076 | 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 | a0001c0002t0001g0244 a0001c0002t0001g0248 a0001c0002t0001g0249 |
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 | a0001c0001t0001g0257 a0001c0002t0001g0043 a0001c0002t0001g0202 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0257 a0001c0002t0001g0043 others(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 | a0001c0001t0001g0083 | 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 | a0001c0002t0001g0207 a0001c0002t0001g0254 |
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 | a0001c0001t0001g0286 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0058 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0003t0001g0007 a0001c0003t0001g0033 a0001c0003t0001g0142 others(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 | a0001c0001t0001g0042 a0001c0001t0001g0044 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | 13 | a0001c0001t0001g0004 a0001c0001t0001g0284 a0001c0001t0001g0285 others(10): 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 | a0001c0001t0001g0257 a0001c0001t0001g0308 a0001c0002t0001g0043 others(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 | a0001c0001t0001g0324 a0001c0002t0001g0218 a0001c0002t0001g0219 others(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 | 56 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0273 others(53): 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 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0004g0200 a0001c0001t0006g0032 a0001c0002t0001g0196 others(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 | a0001c0002t0001g0305 | 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 | a0001c0002t0001g0272 | 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 | a0001c0002t0001g0217 a0001c0002t0001g0223 a0001c0002t0001g0267 |
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 | a0001c0002t0001g0206 a0001c0002t0001g0231 a0001c0002t0001g0339 others(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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0050 a0001c0001t0001g0061 others(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 | a0004c0012t0001g0271 | 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 | a0001c0001t0001g0119 | 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 | a0001c0003t0001g0151 a0001c0003t0001g0177 |
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 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0061 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0076 a0001c0001t0001g0257 others(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 | a0001c0002t0001g0209 a0001c0002t0001g0215 a0001c0002t0001g0224 others(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 | a0001c0002t0001g0227 a0001c0002t0001g0340 |
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 | a0001c0002t0001g0247 a0001c0002t0001g0253 a0001c0002t0001g0259 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0006g0032 | 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 | a0001c0001t0001g0117 a0001c0001t0001g0308 a0001c0001t0001g0323 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0013t0001g0080 |
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 | a0001c0001t0005g0291 a0001c0002t0001g0272 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0257 a0001c0002t0001g0043 a0001c0002t0001g0203 others(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 | a0001c0001t0001g0327 a0001c0001t0004g0200 a0001c0002t0001g0196 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0074 a0001c0003t0001g0153 a0001c0004t0001g0014 others(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 | a0001c0001t0001g0306 a0001c0001t0001g0327 a0001c0001t0004g0200 others(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 | a0001c0001t0001g0257 a0001c0001t0001g0308 a0001c0002t0001g0043 others(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 | a0001c0004t0001g0015 | 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 | a0001c0001t0001g0074 a0001c0003t0001g0153 a0001c0004t0001g0014 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0002t0001g0272 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0050 others(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 | a0001c0001t0001g0257 a0001c0002t0001g0043 a0001c0002t0001g0196 others(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 | a0001c0002t0001g0204 a0001c0002t0001g0206 a0001c0002t0001g0211 others(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 | a0001c0002t0001g0237 | 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 | a0001c0001t0001g0104 | 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 | a0001c0002t0001g0252 | 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 | a0001c0002t0001g0251 | 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 | a0001c0002t0001g0272 | 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 | a0001c0001t0006g0032 | 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 | a0001c0001t0001g0049 | 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 | a0001c0003t0001g0154 | 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 | a0001c0001t0001g0327 a0001c0001t0004g0200 a0001c0002t0001g0196 others(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 | a0001c0002t0001g0272 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0327 | 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 | 41 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0273 others(38): 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 | a0001c0001t0001g0024 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0257 a0001c0001t0006g0032 others(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 | a0001c0001t0001g0308 a0001c0001t0004g0200 a0001c0002t0001g0198 others(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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0257 a0001c0001t0001g0308 a0001c0002t0001g0043 others(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 | a0001c0002t0001g0043 a0001c0002t0001g0203 a0001c0002t0001g0209 others(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 | a0001c0001t0001g0257 a0001c0001t0001g0308 a0001c0002t0001g0043 others(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 | a0001c0001t0001g0327 a0001c0001t0004g0200 a0001c0002t0001g0196 others(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 | a0001c0002t0001g0210 | 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 | a0001c0002t0001g0260 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0010 | 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 | a0001c0001t0001g0083 | 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 | a0001c0002t0001g0210 | 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 | a0001c0003t0001g0007 a0001c0003t0001g0033 a0001c0003t0001g0142 others(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 | a0001c0001t0001g0327 a0001c0001t0004g0200 a0001c0002t0001g0196 others(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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0087 a0001c0013t0001g0080 |
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 | a0001c0002t0001g0272 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0006g0032 | 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 | a0001c0001t0001g0130 | 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 | a0001c0002t0001g0206 a0001c0002t0001g0231 a0001c0002t0001g0339 others(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 | a0001c0001t0001g0105 | 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 | a0001c0003t0001g0033 | 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 | a0001c0014t0001g0148 | 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 | a0001c0002t0001g0301 a0001c0002t0001g0302 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0058 a0001c0001t0001g0059 |
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 | a0001c0001t0001g0257 a0001c0001t0001g0308 a0001c0002t0001g0043 others(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 | a0001c0001t0001g0327 | 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 | a0001c0002t0001g0305 | 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 | a0001c0002t0001g0212 a0001c0002t0001g0220 |
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 | a0001c0002t0001g0326 a0001c0002t0001g0334 a0001c0002t0001g0336 |
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 | a0001c0002t0001g0309 a0001c0002t0001g0312 |
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 | a0001c0002t0001g0212 a0001c0002t0001g0220 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0002t0001g0196 | 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 | a0001c0001t0006g0032 | 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 | a0002c0005t0001g0264 | 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 | a0001c0001t0001g0017 | 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 | a0001c0002t0001g0227 a0001c0002t0001g0340 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0003t0001g0007 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0004t0001g0014 a0001c0004t0001g0015 a0001c0004t0001g0021 others(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 | a0001c0002t0001g0202 a0001c0002t0001g0245 a0001c0002t0001g0268 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | |||||||
| chr11:675437 | G | A | 1 | a0001c0003t0001g0174 | 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 | a0001c0002t0001g0252 | 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 | a0001c0002t0001g0219 | 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 | a0001c0004t0001g0014 a0001c0004t0001g0015 a0001c0004t0001g0021 others(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 | a0001c0002t0001g0247 | 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 | a0001c0003t0001g0153 | 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 | a0001c0002t0001g0206 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0060 | 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 | a0001c0001t0001g0060 | 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 | a0001c0002t0001g0305 | 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 | a0001c0001t0001g0308 a0001c0002t0001g0202 a0001c0002t0001g0207 others(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 | a0001c0001t0001g0257 a0001c0001t0001g0308 a0001c0002t0001g0043 others(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 | a0001c0001t0001g0060 a0001c0002t0001g0305 |
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 | a0001c0002t0001g0218 | 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 | a0001c0002t0001g0255 | 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 | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(198): 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 | a0001c0002t0001g0240 a0001c0002t0001g0241 a0001c0002t0001g0242 others(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 | a0001c0004t0001g0023 | 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 | a0001c0001t0004g0275 | 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 | a0001c0001t0001g0327 a0001c0001t0004g0200 a0001c0002t0001g0196 others(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 | a0001c0002t0001g0328 | 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 | a0001c0002t0001g0287 a0001c0002t0001g0288 |
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 | a0001c0004t0001g0025 | 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 | a0001c0001t0001g0308 a0001c0002t0001g0207 a0001c0002t0001g0254 |
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 | a0001c0002t0001g0338 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0003t0001g0178 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0060 | 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 | a0001c0001t0001g0257 a0001c0001t0001g0308 a0001c0002t0001g0043 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0055 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0308 a0001c0002t0001g0207 a0001c0002t0001g0254 |
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 | a0001c0001t0001g0327 a0001c0001t0004g0200 a0001c0002t0001g0196 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0308 a0001c0001t0001g0327 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0201 |
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 | a0001c0003t0001g0180 | 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 | a0001c0001t0001g0284 a0001c0001t0001g0285 |
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 | 45 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0273 others(42): 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 | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(240): 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 | a0001c0001t0001g0017 | 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 | 45 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0273 others(42): 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 | a0001c0001t0001g0125 a0001c0001t0001g0127 a0001c0001t0001g0129 others(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 | a0001c0002t0001g0305 | 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 | a0001c0001t0001g0327 a0001c0001t0004g0200 a0001c0002t0001g0196 others(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 | 50 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0273 others(47): 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | 45 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0273 others(42): 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 | a0001c0002t0001g0272 | 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 | 45 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0273 others(42): 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 | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(241): 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 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0083 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0299 a0001c0001t0001g0300 others(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 | a0001c0001t0001g0072 | 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 | 45 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0273 others(42): 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0308 a0001c0002t0001g0207 a0001c0002t0001g0254 |
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 | a0001c0002t0001g0043 a0001c0002t0001g0203 a0001c0002t0001g0209 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0053 others(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 | 45 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0273 others(42): 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 | a0001c0002t0001g0272 | 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 | a0001c0001t0001g0257 a0001c0002t0001g0202 a0001c0002t0001g0203 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0110 others(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 | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(308): 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(320): 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0327 a0001c0001t0004g0200 a0001c0002t0001g0196 others(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 | a0001c0002t0001g0266 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0289 a0001c0001t0001g0292 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
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 | a0001c0002t0001g0272 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0159 a0001c0003t0001g0007 a0001c0003t0001g0033 others(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 | a0001c0002t0001g0250 | 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 | a0001c0002t0001g0251 | 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 | a0001c0004t0001g0014 a0001c0004t0001g0015 a0001c0004t0001g0021 others(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 | a0001c0001t0001g0327 a0001c0001t0004g0200 a0001c0002t0001g0196 others(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 | a0001c0001t0003g0140 | 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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0039 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0257 a0001c0002t0001g0202 a0001c0002t0001g0203 others(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 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0001g0277 others(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 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0001g0277 others(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 | a0001c0002t0001g0272 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0006g0032 | 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 | a0001c0002t0001g0336 | 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 | a0001c0004t0001g0021 a0001c0004t0001g0022 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0315 a0001c0001t0001g0337 a0001c0002t0001g0272 |
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 | a0001c0001t0001g0257 a0001c0002t0001g0202 a0001c0002t0001g0203 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0308 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0201 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0001g0277 others(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 | a0001c0001t0001g0071 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0323 |
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 | a0001c0002t0001g0202 | 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 | 53 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0273 others(50): 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 | a0001c0002t0001g0244 a0001c0002t0001g0246 a0001c0002t0001g0247 others(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 | a0001c0002t0001g0217 a0001c0002t0001g0223 a0001c0002t0001g0267 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0003t0001g0145 a0001c0003t0001g0149 a0001c0003t0001g0154 others(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 | a0001c0009t0001g0138 | 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 | a0001c0009t0001g0138 | 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 | a0001c0009t0001g0138 | 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 | a0001c0002t0001g0272 | 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 | a0001c0001t0001g0159 a0001c0003t0001g0007 a0001c0003t0001g0033 others(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 | a0001c0001t0001g0303 a0001c0001t0001g0306 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0065 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0066 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0066 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0066 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0066 others(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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0115 a0001c0001t0001g0116 |
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 | a0001c0001t0001g0117 | 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 | a0001c0001t0001g0037 | 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 | a0001c0002t0001g0203 | 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 | a0001c0003t0001g0174 | 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 | a0001c0009t0001g0138 | 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 | 179 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0159 others(176): 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0002t0001g0335 | 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 | a0001c0001t0001g0257 a0001c0002t0001g0202 a0001c0002t0001g0203 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0201 others(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 | a0001c0002t0001g0287 a0001c0002t0001g0288 |
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 | a0001c0001t0006g0032 | 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 | a0001c0003t0001g0175 | 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 | a0001c0001t0001g0111 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0001g0277 others(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 | a0001c0001t0001g0037 a0001c0001t0004g0200 a0001c0002t0001g0196 others(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 | a0001c0001t0001g0037 | 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 | a0001c0003t0001g0181 | 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 | a0001c0002t0001g0196 a0001c0002t0001g0199 |
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 | a0001c0003t0001g0152 a0001c0003t0001g0178 a0001c0003t0001g0179 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0137 a0001c0001t0001g0257 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0137 a0001c0001t0001g0257 others(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 | a0001c0001t0001g0318 | 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 | a0001c0002t0001g0202 a0001c0002t0001g0245 a0001c0002t0001g0268 |
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 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0066 others(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 | a0001c0002t0001g0272 | 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 | a0001c0002t0001g0202 a0001c0002t0001g0245 a0001c0002t0001g0268 |
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 | a0001c0002t0001g0272 | 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 | a0001c0001t0001g0319 a0001c0001t0001g0320 |
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 | a0001c0001t0001g0054 | 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 | a0001c0003t0001g0153 | 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 | a0001c0001t0001g0283 | 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 | 330 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(327): 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 | a0001c0001t0004g0200 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0006t0001g0118 | 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 | a0001c0002t0001g0222 | 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 | a0001c0001t0001g0194 | 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 | a0001c0001t0001g0257 a0001c0002t0001g0202 a0001c0002t0001g0203 others(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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0257 a0001c0002t0001g0202 a0001c0002t0001g0203 others(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 | a0001c0002t0001g0272 | 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 | a0001c0001t0001g0257 a0001c0002t0001g0202 a0001c0002t0001g0203 others(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 | a0001c0002t0001g0208 | 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 | a0001c0001t0001g0308 | 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 | 56 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0273 others(53): 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 | a0001c0001t0001g0019 | 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 | a0001c0001t0001g0125 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0119 a0001c0001t0001g0274 a0001c0001t0001g0276 others(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 | a0001c0001t0001g0024 | 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 | a0001c0001t0001g0024 | 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 | a0001c0001t0004g0200 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0201 |
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 | 60 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0052 others(57): 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 | a0001c0001t0001g0278 | 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 | a0001c0001t0001g0159 a0001c0003t0001g0007 a0001c0003t0001g0033 others(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 | a0001c0002t0001g0305 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0048 others(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 | a0001c0002t0001g0245 | 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 | a0001c0001t0001g0257 a0001c0002t0001g0204 a0001c0002t0001g0218 others(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 | a0001c0002t0001g0207 a0001c0002t0001g0254 |
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 | a0001c0001t0001g0024 | 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 | a0001c0002t0001g0272 | 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 | 55 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0273 others(52): 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 | a0001c0002t0001g0209 | 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 | a0001c0001t0001g0024 a0001c0004t0001g0014 a0001c0004t0001g0015 others(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 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0002t0001g0043 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
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 | a0001c0001t0001g0278 a0001c0001t0001g0279 |
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 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0324 others(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 | a0001c0002t0001g0287 | 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 | a0001c0001t0004g0200 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0001t0004g0200 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0002t0001g0205 a0001c0002t0001g0240 a0001c0002t0001g0241 others(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 | a0001c0003t0001g0186 a0001c0003t0001g0187 |
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 | a0001c0002t0001g0244 | 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 | a0001c0009t0001g0138 | 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 | a0001c0001t0004g0200 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0201 |
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 | a0001c0001t0001g0321 a0001c0003t0001g0143 |
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 | a0001c0002t0001g0255 a0001c0002t0001g0256 |
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 | a0001c0002t0001g0208 | 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 | a0001c0002t0001g0217 a0001c0002t0001g0218 |
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 | a0001c0002t0001g0219 a0001c0002t0001g0263 a0002c0005t0001g0262 others(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 | a0001c0002t0001g0202 a0001c0002t0001g0203 a0001c0002t0001g0204 others(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 | a0001c0001t0001g0257 a0001c0002t0001g0259 a0002c0005t0001g0005 others(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 | a0001c0002t0001g0338 | 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 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 |
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 | a0001c0002t0001g0210 | 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 | a0001c0003t0001g0188 a0001c0003t0001g0189 a0001c0003t0001g0190 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0137 a0001c0003t0001g0146 others(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 | a0001c0001t0001g0036 a0001c0001t0001g0049 a0001c0001t0001g0123 others(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 | a0001c0001t0006g0032 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0126 a0001c0001t0001g0130 others(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 | a0001c0001t0001g0273 a0001c0001t0001g0308 a0001c0001t0001g0310 others(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 | a0001c0001t0001g0306 a0001c0002t0001g0305 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0290 a0001c0001t0001g0292 others(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 | a0001c0001t0001g0274 | 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 | a0001c0001t0001g0289 | 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 | a0001c0001t0001g0327 | 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 | a0001c0003t0001g0183 | 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 | a0001c0001t0001g0307 | 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 | a0001c0001t0001g0050 | 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 | a0001c0002t0001g0209 | 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 | a0001c0001t0001g0051 | 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 | a0001c0001t0004g0200 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | 55 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(52): 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 | 129 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(126): 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 | a0001c0001t0001g0274 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0016 | 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 | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(181): 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 | 35 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0017 others(32): 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 |
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 | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(244): 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 | a0001c0002t0001g0266 | 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 | a0001c0002t0001g0216 | 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 | a0001c0002t0001g0239 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(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 | a0001c0002t0001g0223 a0001c0002t0001g0267 |
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 | a0002c0005t0001g0265 | 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 | a0001c0002t0001g0260 a0002c0005t0001g0006 |
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 | a0001c0002t0001g0221 a0001c0002t0001g0222 |
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 | a0001c0002t0001g0220 | 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 | a0001c0003t0001g0142 | 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 | a0001c0004t0001g0025 a0001c0004t0001g0026 a0001c0004t0001g0027 others(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 | a0001c0004t0001g0021 | 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 | a0001c0002t0001g0215 | 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 | a0001c0002t0001g0339 | 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 | a0001c0002t0001g0211 a0001c0002t0001g0212 a0001c0002t0001g0213 others(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 | a0001c0002t0001g0287 a0001c0002t0001g0288 |
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 | 324 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(321): 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 | a0001c0002t0001g0339 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0030 others(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 | a0001c0002t0001g0272 | 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 | 13 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0048 others(10): 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 | a0001c0001t0001g0307 | 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 | a0001c0003t0001g0145 | 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 | a0001c0001t0001g0321 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0003t0001g0188 others(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 | a0001c0003t0001g0143 | 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 | a0001c0001t0001g0313 a0001c0001t0001g0314 |
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 |
7 | a0001c0001t0001g0004 a0001c0001t0001g0315 a0001c0001t0001g0316 others(4): 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 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0002t0001g0043 |
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 | a0001c0001t0001g0016 a0001c0001t0006g0032 a0001c0002t0001g0211 others(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 | 14 | a0001c0001t0001g0004 a0001c0001t0001g0283 a0001c0001t0001g0313 others(11): 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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0126 others(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 | a0001c0001t0001g0137 | 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 | a0001c0001t0001g0159 a0001c0001t0001g0286 a0001c0003t0001g0007 others(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 | a0001c0002t0001g0235 | 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0273 a0001c0001t0001g0289 others(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 | a0001c0001t0001g0009 | 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 | a0001c0002t0001g0234 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0048 |
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 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
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 | a0001c0002t0001g0225 a0001c0002t0001g0226 a0001c0002t0001g0227 others(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 | a0001c0002t0001g0224 | 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 | a0001c0001t0001g0283 | 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 | a0001c0001t0004g0200 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0002t0001g0210 | 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 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0125 a0001c0001t0001g0127 a0001c0001t0001g0129 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(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 | a0003c0007t0001g0040 a0003c0007t0001g0041 |
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 | a0001c0001t0001g0039 | 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0037 | 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 | a0001c0002t0001g0210 a0001c0002t0001g0259 |
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 | a0001c0002t0001g0204 a0001c0002t0001g0216 a0001c0002t0001g0218 others(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 | a0001c0001t0004g0200 a0001c0002t0001g0197 a0001c0002t0001g0198 |
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 | a0001c0002t0001g0196 a0001c0002t0001g0199 |
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 | a0001c0001t0003g0141 | 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 | a0001c0002t0001g0220 a0001c0002t0001g0221 a0001c0002t0001g0222 others(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 | a0001c0001t0001g0257 a0001c0002t0001g0202 a0001c0002t0001g0203 others(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 | a0001c0002t0001g0211 a0001c0002t0001g0213 a0001c0002t0001g0214 |
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 | a0001c0002t0001g0212 | 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 | a0001c0003t0001g0144 | 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 | a0001c0002t0001g0215 | 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 | a0001c0003t0001g0143 | 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 | a0001c0009t0001g0138 | 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 | a0001c0002t0001g0209 | 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 | a0001c0003t0001g0142 | 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 | a0001c0001t0001g0036 | 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 | a0001c0001t0001g0036 | 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 | a0001c0001t0001g0337 | 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 | a0001c0001t0001g0035 | 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 | a0001c0002t0001g0258 | 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 | a0001c0002t0001g0207 a0001c0002t0001g0208 |
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 | a0001c0001t0001g0337 | 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 | a0001c0002t0001g0259 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0002t0001g0206 | 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 | a0001c0002t0001g0260 | 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 | a0001c0001t0001g0257 a0001c0002t0001g0202 a0001c0002t0001g0203 others(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 | a0001c0001t0001g0324 a0001c0001t0001g0325 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0002t0001g0205 | 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 | a0001c0001t0002g0034 | 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 | a0001c0001t0001g0257 a0001c0002t0001g0202 a0001c0002t0001g0203 others(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 | 57 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0273 others(54): 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 | a0001c0001t0001g0257 a0001c0002t0001g0202 a0001c0002t0001g0203 others(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 | a0001c0001t0004g0200 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0002t0001g0266 | 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 | 57 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0273 others(54): 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 | a0001c0001t0001g0257 a0001c0002t0001g0202 a0001c0002t0001g0203 others(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 | a0001c0002t0001g0204 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0002t0001g0260 | 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 | a0001c0002t0001g0263 a0002c0005t0001g0005 a0002c0005t0001g0006 others(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 | a0001c0001t0001g0273 | 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 | a0001c0001t0001g0139 | 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 | a0001c0006t0001g0020 | 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 | a0001c0002t0001g0266 | 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 | a0001c0002t0001g0335 | 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 | a0001c0001t0001g0257 a0001c0001t0004g0200 a0001c0002t0001g0202 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0159 a0001c0003t0001g0007 a0001c0003t0001g0142 others(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 | a0001c0001t0003g0140 a0001c0001t0003g0141 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0004t0001g0014 a0001c0004t0001g0015 |
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 | a0001c0002t0001g0203 | 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 | a0001c0001t0001g0159 a0001c0001t0001g0192 a0001c0003t0001g0007 others(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 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
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 | a0001c0002t0001g0326 | 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 | a0001c0001t0001g0257 a0001c0002t0001g0202 a0001c0002t0001g0203 others(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 | a0001c0001t0001g0013 | 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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(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 | a0001c0002t0001g0202 | 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 | a0001c0001t0001g0194 | 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 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0323 |
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 | a0001c0002t0001g0272 | 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 | a0001c0001t0001g0324 a0001c0001t0001g0325 |
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 | a0001c0003t0001g0195 | 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 | a0001c0001t0004g0200 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0001t0001g0327 a0001c0002t0001g0326 a0001c0002t0001g0328 others(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 | a0001c0001t0001g0201 | 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 | a0001c0003t0001g0007 | 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 | a0001c0001t0001g0257 a0001c0002t0001g0202 a0001c0002t0001g0203 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0337 | 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 | a0001c0002t0001g0338 | 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 | a0002c0005t0001g0005 a0002c0005t0001g0006 |
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 | a0001c0002t0001g0339 a0001c0002t0001g0340 a0001c0002t0001g0341 |
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 |