Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 221687 |
| ensemblid | ENSG00000180537.13 |
| hgncid | 28522 |
| symbol | RNF182 |
| name | ring finger protein 182 |
| refseq_nuc | NM_152737.4 |
| refseq_prot | NP_689950.1 |
| ensembl_nuc | ENST00000488300.6 |
| ensembl_prot | ENSP00000420465.1 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 13924952 |
| end | 13980310 |
| strand | + |
| ver | v1.2 |
| region | chr6:13924952-13980310 |
| region5000 | chr6:13919952-13985310 |
| regionname0 | RNF182_chr6_13924952_13980310 |
| regionname5000 | RNF182_chr6_13919952_13985310 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 247 | 355 | 92 | 58 | 158 | 8 | 37 | 122 | RNF182_chr6_13919952_13985310 | RNF182 | MASQP others(242): Show |
chr6 | 13919952 | 13985310 |
| a0002 | 0/0 | 247 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | MASQP others(242): Show |
chr6 | 13919952 | 13985310 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 741 | 340 | 86 | 55 | 154 | 8 | 35 | RNF182_chr6_13919952_13985310 | RNF182 | ATGGC others(736): Show |
chr6 | 13919952 | 13985310 | ||
| a0001c0002 | 0/0 | 741 | 7 | 6 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | ATGGC others(736): Show |
chr6 | 13919952 | 13985310 | ||
| a0001c0003 | 0/0 | 741 | 4 | 0 | 2 | 0 | 0 | 2 | RNF182_chr6_13919952_13985310 | RNF182 | ATGGC others(736): Show |
chr6 | 13919952 | 13985310 | ||
| a0001c0004 | 0/0 | 741 | 3 | 0 | 0 | 3 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | ATGGC others(736): Show |
chr6 | 13919952 | 13985310 | ||
| a0001c0006 | 0/0 | 741 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | ATGGC others(736): Show |
chr6 | 13919952 | 13985310 | ||
| a0002c0005 | 0/0 | 741 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | ATGGC others(736): Show |
chr6 | 13919952 | 13985310 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3631 | 104 | 16 | 19 | 57 | 3 | 8 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3626): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0002 | 1/0 | 3629 | 87 | 32 | 15 | 26 | 1 | 12 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3624): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0003 | 0/0 | 3634 | 47 | 9 | 1 | 33 | 0 | 4 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3629): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0004 | 0/0 | 3639 | 33 | 5 | 12 | 6 | 4 | 6 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3634): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0005 | 0/0 | 3618 | 10 | 0 | 0 | 10 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3613): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0007 | 0/0 | 3636 | 7 | 0 | 2 | 4 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3631): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0008 | 0/0 | 3634 | 5 | 0 | 0 | 5 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3629): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0009 | 0/0 | 3634 | 4 | 2 | 1 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3629): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0010 | 0/0 | 3644 | 4 | 0 | 1 | 3 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3639): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0011 | 0/0 | 3619 | 4 | 4 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3614): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0012 | 0/0 | 3631 | 4 | 0 | 0 | 4 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3626): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0013 | 0/0 | 3629 | 3 | 2 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3624): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0014 | 0/0 | 3626 | 3 | 2 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3621): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0015 | 0/0 | 3629 | 2 | 2 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3624): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0016 | 0/0 | 3629 | 2 | 0 | 0 | 1 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3624): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0017 | 0/0 | 3615 | 2 | 2 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3610): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0018 | 0/0 | 3636 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3631): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0019 | 0/0 | 3614 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3609): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0020 | 0/0 | 3629 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3624): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0021 | 0/0 | 3634 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3629): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0022 | 0/0 | 3629 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3624): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0023 | 0/0 | 3614 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3609): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0024 | 0/0 | 3629 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3624): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0025 | 0/0 | 3629 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3624): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0026 | 0/0 | 3619 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3614): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0027 | 0/0 | 3629 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3624): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0028 | 0/0 | 3629 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3624): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0029 | 0/0 | 3619 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3614): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0030 | 0/0 | 3619 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3614): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0031 | 0/0 | 3631 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3626): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0032 | 0/0 | 3631 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3626): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0033 | 0/0 | 3636 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3631): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0034 | 0/0 | 3631 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3626): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0036 | 0/0 | 3629 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3624): Show |
chr6 | 13919952 | 13985310 |
| a0001c0001t0037 | 0/0 | 3631 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3626): Show |
chr6 | 13919952 | 13985310 |
| a0001c0002t0006 | 0/0 | 3619 | 7 | 6 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3614): Show |
chr6 | 13919952 | 13985310 |
| a0001c0003t0001 | 0/0 | 3631 | 4 | 0 | 2 | 0 | 0 | 2 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3626): Show |
chr6 | 13919952 | 13985310 |
| a0001c0004t0003 | 0/0 | 3634 | 3 | 0 | 0 | 3 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3629): Show |
chr6 | 13919952 | 13985310 |
| a0001c0006t0035 | 0/0 | 3636 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3631): Show |
chr6 | 13919952 | 13985310 |
| a0002c0005t0004 | 0/0 | 3639 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | GGGAA others(3634): Show |
chr6 | 13919952 | 13985310 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0165 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0009 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0091 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0005g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0005g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0005g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0007g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0007g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0007g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0007g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0007g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0007g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0007g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0008g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0008g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0008g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0008g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0009g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0009g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0009g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0009g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0010g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0010g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0010g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0011g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0011g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0011g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0011g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0012g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0012g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0012g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0013g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0013g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0014g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0014g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0014g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0015g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0015g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0016g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0016g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0017g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0018g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0019g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0020g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0021g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0022g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0023g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0024g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0025g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0026g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0027g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0028g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0029g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0030g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0031g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0032g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0033g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0034g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0036g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0001t0037g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0002t0006g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0002t0006g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0002t0006g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0002t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0002t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0002t0006g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0003t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0003t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0004t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0004t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0004t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0001c0006t0035g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| a0002c0005t0004g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0054 | EUR | FIN | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0209 | EUR | FIN | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0204 | EAS | CHS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG00408 | hp2 | a0001 | c0001 | t0008 | g0170 | EAS | CHS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | CHS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | CHS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0207 | EAS | CHS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | CHS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | CHS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0206 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | CHS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG00673 | hp2 | a0001 | c0001 | t0008 | g0018 | EAS | CHS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG00733 | hp2 | a0001 | c0001 | t0010 | g0021 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0112 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0213 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0264 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01106 | hp2 | a0001 | c0003 | t0001 | g0275 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0259 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01243 | hp1 | a0001 | c0002 | t0006 | g0151 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01243 | hp2 | a0001 | c0001 | t0013 | g0183 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0055 | AMR | CLM | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0043 | AMR | CLM | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0097 | AMR | CLM | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | CLM | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01361 | hp2 | a0001 | c0001 | t0025 | g0117 | AMR | CLM | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01496 | hp2 | a0001 | c0001 | t0009 | g0133 | AMR | CLM | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0056 | EUR | IBS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0200 | EUR | IBS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01884 | hp2 | a0001 | c0001 | t0011 | g0220 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01928 | hp1 | a0001 | c0001 | t0007 | g0085 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0100 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01943 | hp1 | a0001 | c0003 | t0001 | g0099 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01952 | hp1 | a0001 | c0001 | t0007 | g0075 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0284 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0096 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0281 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0262 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02027 | hp1 | a0001 | c0001 | t0010 | g0228 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02055 | hp1 | a0001 | c0001 | t0011 | g0159 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02055 | hp2 | a0001 | c0001 | t0028 | g0160 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02056 | hp1 | a0001 | c0001 | t0008 | g0158 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02074 | hp1 | a0001 | c0001 | t0008 | g0153 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02129 | hp2 | a0001 | c0001 | t0008 | g0018 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0105 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02145 | hp2 | a0001 | c0001 | t0030 | g0144 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | CDX | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02155 | hp2 | a0001 | c0001 | t0012 | g0166 | EAS | CDX | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02258 | hp2 | a0001 | c0002 | t0006 | g0162 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0098 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02273 | hp2 | a0001 | c0001 | t0027 | g0046 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02293 | hp1 | a0001 | c0001 | t0037 | g0273 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02451 | hp1 | a0001 | c0001 | t0013 | g0020 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02451 | hp2 | a0001 | c0001 | t0020 | g0113 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02523 | hp2 | a0001 | c0001 | t0012 | g0019 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02572 | hp1 | a0001 | c0001 | t0009 | g0128 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02602 | hp1 | a0001 | c0001 | t0009 | g0245 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0260 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02615 | hp2 | a0001 | c0001 | t0017 | g0032 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0196 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02647 | hp1 | a0001 | c0001 | t0014 | g0299 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0149 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02683 | hp2 | a0001 | c0003 | t0001 | g0291 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0236 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02698 | hp2 | a0001 | c0001 | t0016 | g0060 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0146 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0251 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02735 | hp2 | a0001 | c0001 | t0007 | g0246 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0169 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0231 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02809 | hp2 | a0001 | c0001 | t0019 | g0229 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02886 | hp1 | a0001 | c0002 | t0006 | g0222 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02886 | hp2 | a0001 | c0001 | t0015 | g0172 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02895 | hp1 | a0001 | c0001 | t0013 | g0020 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | ESN | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02970 | hp2 | a0001 | c0001 | t0023 | g0115 | AFR | ESN | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0145 | AFR | ESN | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | ESN | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03041 | hp1 | a0001 | c0001 | t0017 | g0032 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | MSL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | MSL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | ESN | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | ESN | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03139 | hp1 | a0001 | c0001 | t0009 | g0135 | AFR | ESN | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | ESN | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0212 | AFR | MSL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | MSL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0244 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03239 | hp2 | a0002 | c0005 | t0004 | g0257 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | MSL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | MSL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03486 | hp1 | a0001 | c0001 | t0032 | g0107 | AFR | MSL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03486 | hp2 | a0001 | c0002 | t0006 | g0016 | AFR | MSL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0197 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0300 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0221 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0150 | AFR | ESN | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03516 | hp2 | a0001 | c0002 | t0006 | g0016 | AFR | ESN | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03540 | hp2 | a0001 | c0002 | t0006 | g0163 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | MSL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | MSL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0287 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0089 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0199 | SAS | BEB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0120 | SAS | BEB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | STU | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG04115 | hp2 | a0001 | c0001 | t0026 | g0218 | SAS | STU | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0241 | SAS | BEB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | BEB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0157 | SAS | STU | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | STU | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG04204 | hp1 | a0001 | c0001 | t0024 | g0263 | SAS | STU | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0235 | SAS | STU | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | YRI | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | YRI | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | CHB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | CHB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | YRI | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | YRI | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18941 | hp2 | a0001 | c0001 | t0010 | g0025 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18942 | hp2 | a0001 | c0001 | t0005 | g0214 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18945 | hp2 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18946 | hp2 | a0001 | c0004 | t0003 | g0178 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18948 | hp2 | a0001 | c0001 | t0012 | g0168 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18949 | hp2 | a0001 | c0001 | t0005 | g0187 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18951 | hp2 | a0001 | c0001 | t0007 | g0049 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18959 | hp2 | a0001 | c0001 | t0010 | g0025 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0154 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18968 | hp2 | a0001 | c0004 | t0003 | g0177 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18975 | hp2 | a0001 | c0001 | t0034 | g0002 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18979 | hp1 | a0001 | c0001 | t0018 | g0005 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18981 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18984 | hp2 | a0001 | c0006 | t0035 | g0047 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18990 | hp1 | a0001 | c0001 | t0005 | g0188 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18993 | hp1 | a0001 | c0001 | t0012 | g0019 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18994 | hp2 | a0001 | c0001 | t0007 | g0051 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18995 | hp1 | a0001 | c0004 | t0003 | g0176 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA18995 | hp2 | a0001 | c0001 | t0007 | g0087 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19009 | hp1 | a0001 | c0001 | t0033 | g0005 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19030 | hp1 | a0001 | c0001 | t0021 | g0104 | AFR | LWK | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | LWK | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | LWK | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | LWK | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19058 | hp1 | a0001 | c0001 | t0005 | g0185 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19060 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19068 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19072 | hp1 | a0001 | c0001 | t0016 | g0205 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19080 | hp1 | a0001 | c0001 | t0005 | g0186 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19087 | hp1 | a0001 | c0001 | t0022 | g0118 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19091 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19091 | hp2 | a0001 | c0001 | t0014 | g0240 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19240 | hp1 | a0001 | c0001 | t0011 | g0310 | AFR | YRI | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | YRI | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | ASW | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA20129 | hp2 | a0001 | c0001 | t0029 | g0143 | AFR | ASW | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0058 | EUR | TSI | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0258 | EUR | TSI | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0279 | EUR | TSI | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0034 | EUR | TSI | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | GIH | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0121 | SAS | GIH | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02109 | hp2 | a0001 | c0001 | t0036 | g0161 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02559 | hp1 | a0001 | c0002 | t0006 | g0173 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG02559 | hp2 | a0001 | c0001 | t0031 | g0308 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03471 | hp1 | a0001 | c0001 | t0015 | g0171 | AFR | MSL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | MSL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | USA | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0108 | AFR | USA | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA20300 | hp1 | a0001 | c0001 | t0011 | g0174 | AFR | USA | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | USA | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0116 | AFR | LWK | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| NA21309 | hp2 | a0001 | c0001 | t0014 | g0276 | AFR | LWK | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0165 | REF | REF | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0091 | REF | REF | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:13977774 | G | T | 1 | a0002 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.655G>T | p.Val219Phe | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 1093/3629 | 655/744 | 219/247 | chr6 | 13977774 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:13977171 | C | T | 1 | a0001c0006 | 1 | NA18984.hp2 | synonymous_variant | LOW | c.52C>T | p.Leu18Leu | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 490/3629 | 52/744 | 18/247 | chr6 | 13977171 | |||
| chr6:13977392 | G | A | 1 | a0001c0004 | 3 | NA18946.hp2 NA18968.hp2 NA18995.hp1 |
synonymous_variant | LOW | c.273G>A | p.Leu91Leu | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 711/3629 | 273/744 | 91/247 | chr6 | 13977392 | |||
| chr6:13977467 | C | T | 1 | a0001c0003 | 4 | HG01106.hp2 HG01943.hp1 HG02683.hp2 others(1): Show |
synonymous_variant | LOW | c.348C>T | p.Ala116Ala | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 786/3629 | 348/744 | 116/247 | chr6 | 13977467 | |||
| chr6:13977641 | G | A | 1 | a0001c0002 | 7 | HG01243.hp1 HG02258.hp2 HG02559.hp1 others(4): Show |
synonymous_variant | LOW | c.522G>A | p.Thr174Thr | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 960/3629 | 522/744 | 174/247 | chr6 | 13977641 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:13924993 | G | C | 1 | a0001c0001t0018 | 1 | NA18979.hp1 | 5_prime_UTR_variant | MODIFIER | c.-397G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/3 | 52127 | chr6 | 13924993 | ||||||
| chr6:13976916 | A | G | 1 | a0001c0001t0008 | 5 | HG00408.hp2 HG00673.hp2 HG02056.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-204A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 204 | chr6 | 13976916 | ||||||
| chr6:13976957 | C | T | 1 | a0001c0001t0037 | 1 | HG02293.hp1 | 5_prime_UTR_variant | MODIFIER | c.-163C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 163 | chr6 | 13976957 | ||||||
| chr6:13976963 | T | G | 1 | a0001c0001t0019 | 1 | HG02809.hp2 | 5_prime_UTR_variant | MODIFIER | c.-157T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 157 | chr6 | 13976963 | ||||||
| chr6:13977088 | C | G | 1 | a0001c0001t0036 | 1 | HG02109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-32C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 32 | chr6 | 13977088 | ||||||
| chr6:13977101 | A | G | 1 | a0001c0001t0019 | 1 | HG02809.hp2 | 5_prime_UTR_variant | MODIFIER | c.-19A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 19 | chr6 | 13977101 | ||||||
| chr6:13977976 | CA | C | 1 | a0001c0001t0005 | 10 | NA18942.hp2 NA18949.hp2 NA18950.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*117delA | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 117 | INFO_REALIGN_3_PRIME | chr6 | 13977976 | |||||
| chr6:13978044 | A | C | 13 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0012 others(10): Show |
130 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*181A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 181 | chr6 | 13978044 | ||||||
| chr6:13978056 | G | C | 1 | a0001c0001t0005 | 10 | NA18942.hp2 NA18949.hp2 NA18950.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*193G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 193 | chr6 | 13978056 | ||||||
| chr6:13978188 | G | C | 1 | a0001c0001t0036 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*325G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 325 | chr6 | 13978188 | ||||||
| chr6:13978284 | C | G | 1 | a0001c0001t0030 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*421C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 421 | chr6 | 13978284 | ||||||
| chr6:13978358 | G | A | 1 | a0001c0001t0036 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*495G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 495 | chr6 | 13978358 | ||||||
| chr6:13978387 | C | A | 2 | a0001c0001t0020 a0001c0001t0021 |
2 | HG02451.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*524C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 524 | chr6 | 13978387 | ||||||
| chr6:13978387 | C | G | 18 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0011 others(15): Show |
138 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*524C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 524 | chr6 | 13978387 | ||||||
| chr6:13978571 | TCTC | T | 13 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0012 others(10): Show |
130 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*712_*714delCTC | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 712 | INFO_REALIGN_3_PRIME | chr6 | 13978571 | |||||
| chr6:13978606 | G | T | 16 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0012 others(13): Show |
133 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*743G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 743 | chr6 | 13978606 | ||||||
| chr6:13978623 | G | T | 9 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(6): Show |
97 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*760G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 760 | chr6 | 13978623 | ||||||
| chr6:13978667 | A | G | 1 | a0001c0001t0025 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*804A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 804 | chr6 | 13978667 | ||||||
| chr6:13978679 | G | T | 1 | a0001c0001t0005 | 10 | NA18942.hp2 NA18949.hp2 NA18950.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*816G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 816 | chr6 | 13978679 | ||||||
| chr6:13978778 | T | C | 1 | a0001c0001t0015 | 2 | HG02886.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*915T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 915 | chr6 | 13978778 | ||||||
| chr6:13978836 | A | G | 1 | a0001c0001t0024 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*973A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 973 | chr6 | 13978836 | ||||||
| chr6:13978920 | C | A | 1 | a0001c0001t0022 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1057C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 1057 | chr6 | 13978920 | ||||||
| chr6:13978945 | A | T | 1 | a0001c0006t0035 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1082A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 1082 | chr6 | 13978945 | ||||||
| chr6:13979006 | C | T | 1 | a0001c0001t0029 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1143C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 1143 | chr6 | 13979006 | ||||||
| chr6:13979138 | T | C | 1 | a0001c0001t0012 | 4 | HG02155.hp2 HG02523.hp2 NA18948.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1275T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 1275 | chr6 | 13979138 | ||||||
| chr6:13979295 | A | G | 9 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(6): Show |
97 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*1432A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 1432 | chr6 | 13979295 | ||||||
| chr6:13979456 | T | G | 1 | a0001c0001t0031 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1593T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 1593 | chr6 | 13979456 | ||||||
| chr6:13979721 | GAAATGTA others(9): Show |
G | 1 | a0001c0001t0017 | 2 | HG02615.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1863_*1878delGTAA others(12): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 1863 | INFO_REALIGN_3_PRIME | chr6 | 13979721 | |||||
| chr6:13979743 | G | A | 1 | a0001c0001t0032 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1880G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 1880 | chr6 | 13979743 | ||||||
| chr6:13979827 | A | C | 1 | a0001c0001t0034 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1964A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 1964 | chr6 | 13979827 | ||||||
| chr6:13979839 | C | T | 1 | a0001c0001t0013 | 3 | HG01243.hp2 HG02451.hp1 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1976C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 1976 | chr6 | 13979839 | ||||||
| chr6:13979926 | A | T | 1 | a0001c0001t0005 | 10 | NA18942.hp2 NA18949.hp2 NA18950.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2063A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2063 | chr6 | 13979926 | ||||||
| chr6:13980056 | G | T | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2193G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2193 | chr6 | 13980056 | ||||||
| chr6:13980066 | T | A | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2203T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2203 | chr6 | 13980066 | ||||||
| chr6:13980076 | T | G | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2213T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2213 | chr6 | 13980076 | ||||||
| chr6:13980085 | A | T | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2222A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2222 | chr6 | 13980085 | ||||||
| chr6:13980098 | G | T | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2235G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2235 | chr6 | 13980098 | ||||||
| chr6:13980103 | G | T | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2240G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2240 | chr6 | 13980103 | ||||||
| chr6:13980118 | G | A | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2255G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2255 | chr6 | 13980118 | ||||||
| chr6:13980142 | T | A | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2279T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2279 | chr6 | 13980142 | ||||||
| chr6:13980143 | C | A | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2280C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2280 | chr6 | 13980143 | ||||||
| chr6:13980145 | G | C | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2282G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2282 | chr6 | 13980145 | ||||||
| chr6:13980148 | C | A | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2285C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2285 | chr6 | 13980148 | ||||||
| chr6:13980149 | T | A | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2286T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2286 | chr6 | 13980149 | ||||||
| chr6:13980151 | T | A | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2288T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2288 | chr6 | 13980151 | ||||||
| chr6:13980152 | C | G | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2289C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2289 | chr6 | 13980152 | ||||||
| chr6:13980153 | C | T | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2290C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2290 | chr6 | 13980153 | ||||||
| chr6:13980155 | A | T | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2292A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2292 | chr6 | 13980155 | ||||||
| chr6:13980158 | A | C | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2295A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2295 | chr6 | 13980158 | ||||||
| chr6:13980161 | G | T | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2298G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2298 | chr6 | 13980161 | ||||||
| chr6:13980163 | G | A | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2300G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2300 | chr6 | 13980163 | ||||||
| chr6:13980166 | C | T | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2303C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2303 | chr6 | 13980166 | ||||||
| chr6:13980170 | C | A | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2307C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2307 | chr6 | 13980170 | ||||||
| chr6:13980171 | C | G | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2308C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2308 | chr6 | 13980171 | ||||||
| chr6:13980175 | C | T | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2312C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2312 | chr6 | 13980175 | ||||||
| chr6:13980177 | C | T | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2314C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2314 | chr6 | 13980177 | ||||||
| chr6:13980178 | A | C | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2315A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2315 | chr6 | 13980178 | ||||||
| chr6:13980179 | C | T | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2316C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2316 | chr6 | 13980179 | ||||||
| chr6:13980187 | A | T | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2324A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2324 | chr6 | 13980187 | ||||||
| chr6:13980188 | G | A | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2325G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2325 | chr6 | 13980188 | ||||||
| chr6:13980191 | C | A | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2328C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2328 | chr6 | 13980191 | ||||||
| chr6:13980193 | T | G | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2330T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2330 | chr6 | 13980193 | ||||||
| chr6:13980194 | C | A | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2331C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2331 | chr6 | 13980194 | ||||||
| chr6:13980196 | T | G | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2333T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2333 | chr6 | 13980196 | ||||||
| chr6:13980201 | T | TTTTTA | 13 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(10): Show |
177 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*2377_*2381dupTATT others(1): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2382 | INFO_REALIGN_3_PRIME | chr6 | 13980201 | |||||
| chr6:13980201 | T | TTTTTATT others(3): Show |
6 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0018 others(3): Show |
44 | HG00280.hp2 HG00408.hp1 HG00642.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*2372_*2381dupTATT others(6): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2382 | INFO_REALIGN_3_PRIME | chr6 | 13980201 | |||||
| chr6:13980201 | T | TTTTTATT others(8): Show |
1 | a0001c0001t0010 | 4 | HG00733.hp2 HG02027.hp1 NA18941.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2367_*2381dupTATT others(11): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2382 | INFO_REALIGN_3_PRIME | chr6 | 13980201 | |||||
| chr6:13980201 | TTTTTATT others(3): Show |
T | 6 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0026 others(3): Show |
24 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2372_*2381delTATT others(6): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2372 | INFO_REALIGN_3_PRIME | chr6 | 13980201 | |||||
| chr6:13980201 | TTTTTATT others(8): Show |
T | 2 | a0001c0001t0019 a0001c0001t0023 |
2 | HG02809.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2367_*2381delTATT others(11): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2367 | INFO_REALIGN_3_PRIME | chr6 | 13980201 | |||||
| chr6:13980296 | G | A | 7 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(4): Show |
95 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*2433G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2433 | chr6 | 13980296 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:13925040 | C | A | 1 | a0001c0001t0002g0034 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-367+17C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925040 | |||||||
| chr6:13925069 | G | GAGCGGGG others(193): Show |
1 | a0001c0001t0002g0034 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-367+46_-367+47ins others(200): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925069 | |||||||
| chr6:13925069 | G | GGGCGGGG others(194): Show |
1 | a0001c0001t0003g0103 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-367+49_-367+50ins others(201): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | ||||||
| chr6:13925069 | G | GGGCGGGG others(168): Show |
21 | a0001c0001t0001g0109 a0001c0001t0001g0114 a0001c0001t0001g0122 others(18): Show |
23 | HG00735.hp2 HG00741.hp1 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.-367+49_-367+50ins others(175): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | ||||||
| chr6:13925069 | G | GGGCGGGG others(177): Show |
2 | a0001c0001t0002g0105 a0001c0001t0002g0106 |
2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-367+49_-367+50ins others(184): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | ||||||
| chr6:13925069 | G | GGGCGGGG others(186): Show |
1 | a0001c0001t0021g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-367+49_-367+50ins others(193): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | ||||||
| chr6:13925069 | G | GGGCGGGG others(179): Show |
6 | a0001c0001t0002g0015 a0001c0001t0002g0127 a0001c0001t0002g0129 others(3): Show |
7 | HG01884.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-367+49_-367+50ins others(186): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | ||||||
| chr6:13925069 | G | GGGCGGGG others(178): Show |
11 | a0001c0001t0002g0132 a0001c0001t0002g0134 a0001c0001t0002g0136 others(8): Show |
12 | HG01496.hp2 HG01891.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-367+49_-367+50ins others(185): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | ||||||
| chr6:13925069 | G | GGGCGGGG others(177): Show |
1 | a0001c0001t0002g0142 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-367+49_-367+50ins others(184): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | ||||||
| chr6:13925069 | G | GGGCGGGG others(173): Show |
16 | a0001c0001t0001g0156 a0001c0001t0002g0152 a0001c0001t0002g0155 others(13): Show |
18 | HG00673.hp2 HG01243.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.-367+49_-367+50ins others(180): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | ||||||
| chr6:13925069 | G | GGGCGGGG others(182): Show |
2 | a0001c0001t0029g0143 a0001c0001t0030g0144 |
2 | HG02145.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-367+49_-367+50ins others(189): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | ||||||
| chr6:13925069 | G | GGGCGGGG others(173): Show |
1 | a0001c0001t0011g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-367+49_-367+50ins others(180): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | ||||||
| chr6:13925069 | G | GGGCGGGG others(187): Show |
3 | a0001c0001t0036g0161 a0001c0002t0006g0162 a0001c0002t0006g0163 |
3 | HG02109.hp2 HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-367+49_-367+50ins others(194): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | ||||||
| chr6:13925069 | G | GGGCGGGG others(196): Show |
1 | a0001c0001t0028g0160 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-367+49_-367+50ins others(203): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | ||||||
| chr6:13925069 | G | GGGCGGGG others(192): Show |
1 | a0001c0001t0002g0164 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-367+49_-367+50ins others(199): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | ||||||
| chr6:13925069 | G | GGGCGGGG others(201): Show |
4 | a0001c0001t0002g0167 a0001c0001t0012g0019 a0001c0001t0012g0166 others(1): Show |
5 | HG02155.hp2 HG02523.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.-367+49_-367+50ins others(208): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | ||||||
| chr6:13925069 | G | GGGCGGGG others(185): Show |
1 | a0001c0001t0004g0169 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-367+49_-367+50ins others(192): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | ||||||
| chr6:13925069 | G | GGGCGGGG others(187): Show |
1 | a0001c0001t0008g0170 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-367+49_-367+50ins others(194): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | ||||||
| chr6:13925069 | G | GGGCGGGG others(188): Show |
73 | a0001c0001t0001g0024 a0001c0001t0001g0175 a0001c0001t0001g0180 others(70): Show |
87 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.-367+49_-367+50ins others(195): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | ||||||
| chr6:13925069 | G | GGGCGGGG others(197): Show |
4 | a0001c0001t0011g0174 a0001c0001t0015g0171 a0001c0001t0015g0172 others(1): Show |
4 | HG02559.hp1 HG02886.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-367+49_-367+50ins others(204): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | ||||||
| chr6:13925069 | G | GGGCGGGG others(193): Show |
31 | a0001c0001t0001g0261 a0001c0001t0002g0009 a0001c0001t0002g0026 others(28): Show |
36 | HG01070.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.-367+49_-367+50ins others(200): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | ||||||
| chr6:13925069 | G | GGGCGGGG others(198): Show |
3 | a0001c0001t0002g0262 a0001c0001t0004g0264 a0001c0001t0024g0263 |
3 | HG00741.hp2 HG02004.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-367+49_-367+50ins others(205): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | ||||||
| chr6:13925069 | G | GGGCGGGG others(193): Show |
3 | a0001c0001t0002g0265 a0001c0001t0002g0266 a0001c0001t0002g0267 |
3 | NA18949.hp1 NA18957.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-367+49_-367+50ins others(200): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | ||||||
| chr6:13925069 | G | GGGTGGGG others(186): Show |
40 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(37): Show |
44 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.-367+48_-367+49ins others(193): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | ||||||
| chr6:13925069 | G | GGGTGGGG others(195): Show |
4 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | HG01257.hp2 HG01978.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.-367+48_-367+49ins others(202): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | ||||||
| chr6:13925069 | G | GGGTGGGG others(198): Show |
3 | a0001c0001t0001g0033 a0001c0001t0001g0309 a0001c0001t0011g0310 |
4 | HG02280.hp2 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-367+48_-367+49ins others(205): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | ||||||
| chr6:13925069 | G | GGGTGGGG others(207): Show |
1 | a0001c0001t0031g0308 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-367+48_-367+49ins others(214): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | ||||||
| chr6:13925084 | T | C | 52 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(49): Show |
58 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-367+61T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925084 | |||||||
| chr6:13925091 | G | A | 1 | a0001c0001t0001g0272 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-367+68G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925091 | |||||||
| chr6:13925142 | G | T | 1 | a0001c0001t0001g0307 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-367+119G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925142 | |||||||
| chr6:13925282 | C | T | 1 | a0001c0001t0002g0014 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-367+259C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925282 | |||||||
| chr6:13925308 | CTGT | C | 37 | a0001c0001t0001g0175 a0001c0001t0002g0009 a0001c0001t0002g0026 others(34): Show |
42 | HG01070.hp1 HG01071.hp2 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.-367+296_-367+298d others(5): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925308 | ||||||
| chr6:13925495 | C | T | 52 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(49): Show |
58 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-367+472C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925495 | |||||||
| chr6:13925555 | C | A | 1 | a0001c0001t0001g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-367+532C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925555 | |||||||
| chr6:13925590 | C | G | 1 | a0001c0001t0002g0036 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-367+567C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925590 | |||||||
| chr6:13925661 | C | T | 113 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0156 others(110): Show |
128 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.-367+638C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925661 | |||||||
| chr6:13925786 | G | A | 1 | a0001c0001t0032g0107 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-367+763G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925786 | |||||||
| chr6:13925788 | A | G | 1 | a0001c0001t0002g0131 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-367+765A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925788 | |||||||
| chr6:13925821 | G | C | 2 | a0001c0001t0029g0143 a0001c0001t0030g0144 |
2 | HG02145.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-367+798G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925821 | |||||||
| chr6:13925871 | G | C | 124 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0102 others(121): Show |
139 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-367+848G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925871 | |||||||
| chr6:13925959 | C | T | 1 | a0001c0001t0024g0263 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-367+936C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925959 | |||||||
| chr6:13926332 | C | T | 11 | a0001c0001t0001g0093 a0001c0001t0002g0013 a0001c0001t0002g0094 others(8): Show |
12 | HG01071.hp1 HG01175.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.-367+1309C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13926332 | |||||||
| chr6:13926515 | A | T | 124 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0102 others(121): Show |
139 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-367+1492A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13926515 | |||||||
| chr6:13926621 | A | G | 3 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 |
3 | HG02896.hp2 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-367+1598A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13926621 | |||||||
| chr6:13926656 | G | A | 1 | a0001c0001t0003g0189 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-367+1633G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13926656 | |||||||
| chr6:13926705 | G | T | 2 | a0001c0002t0006g0162 a0001c0002t0006g0163 |
2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-367+1682G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13926705 | |||||||
| chr6:13926712 | C | T | 1 | a0001c0001t0004g0108 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-367+1689C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13926712 | |||||||
| chr6:13926791 | G | GT | 56 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(53): Show |
62 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.-367+1781dupT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13926791 | ||||||
| chr6:13926791 | G | T | 6 | a0001c0001t0002g0015 a0001c0001t0002g0130 a0001c0001t0002g0138 others(3): Show |
7 | HG01891.hp1 HG02280.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-367+1768G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13926791 | |||||||
| chr6:13926791 | GT | G | 26 | a0001c0001t0001g0109 a0001c0001t0001g0114 a0001c0001t0002g0006 others(23): Show |
29 | HG00735.hp2 HG00741.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-367+1781delT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13926791 | ||||||
| chr6:13926793 | T | G | 75 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(72): Show |
84 | HG00280.hp1 HG00558.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.-367+1770T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13926793 | |||||||
| chr6:13926794 | T | G | 25 | a0001c0001t0001g0109 a0001c0001t0001g0114 a0001c0001t0002g0006 others(22): Show |
28 | HG00735.hp2 HG00741.hp1 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.-367+1771T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13926794 | |||||||
| chr6:13926795 | T | G | 6 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0093 others(3): Show |
6 | HG02027.hp2 HG02148.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.-367+1772T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13926795 | |||||||
| chr6:13926871 | A | T | 6 | a0001c0001t0001g0092 a0001c0001t0001g0302 a0001c0001t0001g0303 others(3): Show |
6 | HG02056.hp2 NA18612.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.-367+1848A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13926871 | |||||||
| chr6:13927105 | A | G | 1 | a0001c0002t0006g0151 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-367+2082A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13927105 | |||||||
| chr6:13927116 | T | A | 1 | a0001c0001t0001g0175 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-367+2093T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13927116 | |||||||
| chr6:13927116 | T | C | 1 | a0001c0001t0011g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-367+2093T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13927116 | |||||||
| chr6:13927187 | C | T | 122 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0156 others(119): Show |
137 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.-367+2164C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13927187 | |||||||
| chr6:13927278 | T | C | 1 | a0001c0001t0036g0161 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-367+2255T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13927278 | |||||||
| chr6:13927279 | A | G | 55 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(52): Show |
61 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.-367+2256A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13927279 | |||||||
| chr6:13927348 | T | C | 1 | a0001c0001t0002g0235 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-367+2325T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13927348 | |||||||
| chr6:13927480 | T | C | 149 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0102 others(146): Show |
167 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.-367+2457T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13927480 | |||||||
| chr6:13927498 | G | A | 70 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(67): Show |
79 | HG00280.hp1 HG00558.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.-367+2475G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13927498 | |||||||
| chr6:13927535 | T | C | 11 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0164 others(8): Show |
11 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-367+2512T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13927535 | |||||||
| chr6:13927865 | AC | A | 1 | a0001c0001t0002g0009 | 3 | HG01070.hp1 HG01071.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-367+2844delC | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13927865 | ||||||
| chr6:13927995 | T | C | 5 | a0001c0001t0001g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(2): Show |
5 | HG00735.hp2 HG01891.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-367+2972T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13927995 | |||||||
| chr6:13928034 | A | G | 1 | a0001c0001t0011g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-367+3011A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13928034 | |||||||
| chr6:13928128 | A | G | 1 | a0001c0001t0028g0160 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-367+3105A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13928128 | |||||||
| chr6:13928246 | A | G | 1 | a0001c0001t0021g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-367+3223A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13928246 | |||||||
| chr6:13928269 | A | G | 3 | a0001c0001t0015g0171 a0001c0001t0015g0172 a0001c0002t0006g0173 |
3 | HG02559.hp1 HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-367+3246A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13928269 | |||||||
| chr6:13928738 | T | C | 1 | a0001c0001t0002g0236 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-367+3715T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13928738 | |||||||
| chr6:13928796 | G | C | 3 | a0001c0004t0003g0176 a0001c0004t0003g0177 a0001c0004t0003g0178 |
3 | NA18946.hp2 NA18968.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.-367+3773G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13928796 | |||||||
| chr6:13928969 | C | G | 1 | a0001c0001t0036g0161 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-367+3946C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13928969 | |||||||
| chr6:13928972 | A | C | 1 | a0001c0001t0008g0158 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-367+3949A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13928972 | |||||||
| chr6:13929271 | A | G | 69 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(66): Show |
78 | HG00280.hp1 HG00558.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.-367+4248A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13929271 | |||||||
| chr6:13929330 | A | T | 2 | a0001c0001t0002g0105 a0001c0001t0002g0106 |
2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-367+4307A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13929330 | |||||||
| chr6:13929331 | G | C | 2 | a0001c0001t0002g0105 a0001c0001t0002g0106 |
2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-367+4308G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13929331 | |||||||
| chr6:13929896 | C | A | 1 | a0001c0001t0002g0132 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-367+4873C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13929896 | |||||||
| chr6:13929929 | G | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0274 |
3 | HG00735.hp1 HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-367+4906G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13929929 | |||||||
| chr6:13930111 | T | A | 132 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0156 others(129): Show |
152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.-367+5088T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13930111 | |||||||
| chr6:13930120 | T | A | 132 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0156 others(129): Show |
152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.-367+5097T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13930120 | |||||||
| chr6:13930122 | T | A | 132 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0156 others(129): Show |
152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.-367+5099T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13930122 | |||||||
| chr6:13930123 | T | A | 129 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0156 others(126): Show |
146 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.-367+5100T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13930123 | |||||||
| chr6:13930123 | TTG | T | 3 | a0001c0001t0003g0003 a0001c0001t0003g0233 a0001c0001t0003g0234 |
6 | HG00609.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.-367+5101_-367+510 others(6): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13930123 | |||||||
| chr6:13930124 | TG | T | 129 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0156 others(126): Show |
146 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.-367+5103delG | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13930124 | ||||||
| chr6:13930127 | A | C | 132 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0156 others(129): Show |
152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.-367+5104A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13930127 | |||||||
| chr6:13930130 | A | C | 132 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0156 others(129): Show |
152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.-367+5107A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13930130 | |||||||
| chr6:13930131 | T | G | 132 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0156 others(129): Show |
152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.-367+5108T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13930131 | |||||||
| chr6:13930133 | TTCC | T | 132 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0156 others(129): Show |
152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.-367+5111_-367+511 others(7): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13930133 | |||||||
| chr6:13930364 | A | G | 1 | a0001c0001t0011g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-367+5341A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13930364 | |||||||
| chr6:13930465 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-367+5442C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13930465 | |||||||
| chr6:13930470 | T | C | 4 | a0001c0001t0002g0237 a0001c0001t0002g0265 a0001c0001t0002g0266 others(1): Show |
4 | NA18949.hp1 NA18957.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.-367+5447T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13930470 | |||||||
| chr6:13930528 | C | A | 3 | a0001c0001t0011g0159 a0001c0001t0029g0143 a0001c0001t0030g0144 |
3 | HG02055.hp1 HG02145.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-367+5505C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13930528 | |||||||
| chr6:13931039 | A | C | 133 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0102 others(130): Show |
153 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.-367+6016A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13931039 | |||||||
| chr6:13931425 | C | T | 5 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0015g0171 others(2): Show |
5 | HG02145.hp1 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-367+6402C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13931425 | |||||||
| chr6:13931560 | A | G | 1 | a0001c0002t0006g0151 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-367+6537A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13931560 | |||||||
| chr6:13931592 | A | T | 218 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0030 others(215): Show |
247 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.-367+6569A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13931592 | |||||||
| chr6:13931610 | A | G | 1 | a0001c0002t0006g0173 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-367+6587A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13931610 | |||||||
| chr6:13931620 | A | G | 124 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0102 others(121): Show |
139 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-367+6597A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13931620 | |||||||
| chr6:13931626 | A | G | 55 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(52): Show |
61 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.-367+6603A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13931626 | |||||||
| chr6:13931651 | C | CT | 84 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(81): Show |
93 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.-367+6638dupT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13931651 | ||||||
| chr6:13931689 | G | A | 1 | a0001c0001t0002g0164 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-367+6666G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13931689 | |||||||
| chr6:13931719 | A | G | 3 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0121 |
3 | HG03491.hp2 HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-367+6696A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13931719 | |||||||
| chr6:13931839 | A | C | 1 | a0001c0001t0002g0235 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-367+6816A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13931839 | |||||||
| chr6:13931999 | A | G | 133 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0102 others(130): Show |
153 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.-367+6976A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13931999 | |||||||
| chr6:13932005 | G | A | 1 | a0001c0002t0006g0151 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-367+6982G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13932005 | |||||||
| chr6:13932426 | G | C | 1 | a0001c0001t0029g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-367+7403G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13932426 | |||||||
| chr6:13932492 | G | A | 55 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(52): Show |
61 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.-367+7469G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13932492 | |||||||
| chr6:13932550 | A | C | 1 | a0001c0001t0003g0089 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-367+7527A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13932550 | |||||||
| chr6:13932636 | A | G | 2 | a0001c0001t0002g0253 a0001c0001t0002g0254 |
2 | NA18971.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.-367+7613A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13932636 | |||||||
| chr6:13932832 | A | G | 1 | a0001c0001t0003g0089 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-367+7809A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13932832 | |||||||
| chr6:13932838 | C | G | 1 | a0001c0001t0004g0300 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-367+7815C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13932838 | |||||||
| chr6:13932884 | G | A | 133 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0102 others(130): Show |
153 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.-367+7861G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13932884 | |||||||
| chr6:13933179 | A | G | 213 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0030 others(210): Show |
242 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(239): Show |
intron_variant | MODIFIER | c.-367+8156A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13933179 | |||||||
| chr6:13933212 | T | A | 2 | a0001c0001t0012g0019 a0001c0001t0012g0166 |
3 | HG02155.hp2 HG02523.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.-367+8189T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13933212 | |||||||
| chr6:13933226 | A | G | 1 | a0001c0001t0002g0252 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-367+8203A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13933226 | |||||||
| chr6:13933392 | T | C | 1 | a0001c0001t0002g0164 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-367+8369T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13933392 | |||||||
| chr6:13933438 | A | AT | 133 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0102 others(130): Show |
153 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.-367+8416dupT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13933438 | ||||||
| chr6:13933495 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0020g0113 |
2 | HG00741.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-367+8472G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13933495 | |||||||
| chr6:13933609 | T | A | 12 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0164 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-367+8586T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13933609 | |||||||
| chr6:13933665 | C | T | 1 | a0001c0001t0011g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-367+8642C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13933665 | |||||||
| chr6:13933891 | G | A | 1 | a0001c0001t0011g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-367+8868G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13933891 | |||||||
| chr6:13933940 | C | A | 12 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0164 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-367+8917C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13933940 | |||||||
| chr6:13934142 | A | T | 1 | a0001c0001t0002g0121 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-367+9119A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13934142 | |||||||
| chr6:13934257 | C | G | 68 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(65): Show |
77 | HG00280.hp1 HG00558.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.-367+9234C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13934257 | |||||||
| chr6:13934296 | A | G | 124 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0102 others(121): Show |
139 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-367+9273A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13934296 | |||||||
| chr6:13934366 | T | C | 133 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0102 others(130): Show |
153 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.-367+9343T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13934366 | |||||||
| chr6:13934400 | C | T | 1 | a0001c0001t0021g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-367+9377C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13934400 | |||||||
| chr6:13934787 | T | TTAAAA | 133 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0102 others(130): Show |
153 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.-367+9767_-367+976 others(9): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13934787 | ||||||
| chr6:13934835 | A | G | 54 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(51): Show |
60 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.-367+9812A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13934835 | |||||||
| chr6:13934949 | C | A | 25 | a0001c0001t0001g0109 a0001c0001t0001g0114 a0001c0001t0002g0006 others(22): Show |
28 | HG00741.hp1 HG01243.hp1 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.-367+9926C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13934949 | |||||||
| chr6:13934949 | C | G | 2 | a0001c0001t0002g0105 a0001c0001t0002g0106 |
2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-367+9926C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13934949 | |||||||
| chr6:13934949 | C | T | 1 | a0001c0001t0003g0232 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-367+9926C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13934949 | |||||||
| chr6:13935194 | T | C | 133 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0102 others(130): Show |
153 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.-367+10171T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13935194 | |||||||
| chr6:13935265 | G | A | 3 | a0001c0001t0001g0190 a0001c0001t0013g0020 a0001c0001t0013g0183 |
4 | HG01243.hp2 HG02451.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-367+10242G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13935265 | |||||||
| chr6:13935304 | C | CT | 135 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0102 others(132): Show |
155 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.-367+10291dupT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13935304 | ||||||
| chr6:13935417 | G | C | 3 | a0001c0001t0028g0160 a0001c0002t0006g0162 a0001c0002t0006g0163 |
3 | HG02055.hp2 HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-367+10394G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13935417 | |||||||
| chr6:13935421 | T | C | 6 | a0001c0001t0003g0191 a0001c0001t0003g0192 a0001c0001t0003g0193 others(3): Show |
6 | HG00558.hp1 HG02083.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.-367+10398T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13935421 | |||||||
| chr6:13935559 | C | T | 81 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(78): Show |
90 | HG00280.hp1 HG00558.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.-367+10536C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13935559 | |||||||
| chr6:13935570 | T | G | 1 | a0001c0003t0001g0275 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-367+10547T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13935570 | |||||||
| chr6:13935816 | G | A | 1 | a0001c0001t0004g0112 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-367+10793G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13935816 | |||||||
| chr6:13935916 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-367+10893A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13935916 | |||||||
| chr6:13936113 | C | T | 1 | a0001c0001t0004g0300 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-367+11090C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13936113 | |||||||
| chr6:13936126 | T | C | 1 | a0001c0001t0013g0020 | 2 | HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-367+11103T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13936126 | |||||||
| chr6:13936186 | C | T | 1 | a0001c0001t0001g0306 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-367+11163C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13936186 | |||||||
| chr6:13937103 | T | C | 295 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(292): Show |
333 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(330): Show |
intron_variant | MODIFIER | c.-367+12080T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13937103 | |||||||
| chr6:13937110 | G | C | 1 | a0001c0001t0003g0195 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-367+12087G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13937110 | |||||||
| chr6:13937140 | A | G | 1 | a0001c0001t0004g0251 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-367+12117A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13937140 | |||||||
| chr6:13937184 | A | G | 71 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(68): Show |
80 | HG00280.hp1 HG00558.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.-367+12161A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13937184 | |||||||
| chr6:13937192 | A | T | 3 | a0001c0004t0003g0176 a0001c0004t0003g0177 a0001c0004t0003g0178 |
3 | NA18946.hp2 NA18968.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.-367+12169A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13937192 | |||||||
| chr6:13937514 | C | T | 1 | a0001c0001t0024g0263 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-367+12491C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13937514 | |||||||
| chr6:13937559 | A | G | 3 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 |
3 | HG02896.hp2 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-367+12536A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13937559 | |||||||
| chr6:13937763 | C | T | 5 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0015g0171 others(2): Show |
5 | HG02145.hp1 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-367+12740C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13937763 | |||||||
| chr6:13937771 | T | C | 1 | a0001c0001t0011g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-367+12748T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13937771 | |||||||
| chr6:13937773 | C | G | 1 | a0001c0001t0011g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-367+12750C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13937773 | |||||||
| chr6:13937849 | T | C | 131 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0156 others(128): Show |
151 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.-367+12826T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13937849 | |||||||
| chr6:13937948 | A | G | 1 | a0001c0001t0011g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-367+12925A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13937948 | |||||||
| chr6:13938004 | G | GT | 192 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(189): Show |
224 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.-367+13004dupT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13938004 | ||||||
| chr6:13938004 | G | GTT | 34 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(31): Show |
34 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.-367+13003_-367+13 others(8): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13938004 | ||||||
| chr6:13938004 | GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0021g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-367+12995_-367+13 others(16): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13938004 | ||||||
| chr6:13938101 | C | T | 2 | a0001c0001t0002g0152 a0001c0001t0009g0128 |
2 | HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-367+13078C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13938101 | |||||||
| chr6:13938102 | G | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0274 |
3 | HG00735.hp1 HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-367+13079G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13938102 | |||||||
| chr6:13938175 | A | AT | 96 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(93): Show |
107 | HG00280.hp1 HG00558.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.-367+13175dupT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13938175 | ||||||
| chr6:13938175 | A | ATT | 9 | a0001c0001t0001g0081 a0001c0001t0002g0053 a0001c0001t0003g0017 others(6): Show |
10 | HG00735.hp2 HG01496.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.-367+13174_-367+13 others(8): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13938175 | ||||||
| chr6:13938175 | A | ATTT | 8 | a0001c0001t0003g0103 a0001c0001t0003g0149 a0001c0001t0003g0150 others(5): Show |
13 | HG02451.hp1 HG02647.hp2 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.-367+13173_-367+13 others(9): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13938175 | ||||||
| chr6:13938175 | AT | A | 7 | a0001c0001t0001g0123 a0001c0001t0001g0302 a0001c0001t0002g0238 others(4): Show |
7 | HG01167.hp1 HG01496.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-367+13175delT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13938175 | ||||||
| chr6:13938375 | A | G | 240 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(237): Show |
272 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.-367+13352A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13938375 | |||||||
| chr6:13938375 | A | T | 55 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(52): Show |
61 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.-367+13352A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13938375 | |||||||
| chr6:13938552 | T | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(73): Show |
86 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.-367+13529T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13938552 | |||||||
| chr6:13938743 | A | G | 2 | a0001c0001t0004g0197 a0001c0001t0004g0221 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-367+13720A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13938743 | |||||||
| chr6:13938797 | G | A | 25 | a0001c0001t0001g0109 a0001c0001t0001g0114 a0001c0001t0002g0006 others(22): Show |
28 | HG00741.hp1 HG01243.hp1 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.-367+13774G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13938797 | |||||||
| chr6:13938909 | C | T | 1 | a0001c0001t0001g0012 | 2 | HG00738.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.-367+13886C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13938909 | |||||||
| chr6:13938955 | C | T | 122 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0156 others(119): Show |
137 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.-367+13932C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13938955 | |||||||
| chr6:13939005 | C | A | 122 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0156 others(119): Show |
137 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.-367+13982C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13939005 | |||||||
| chr6:13939108 | T | A | 1 | a0001c0001t0023g0115 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-367+14085T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13939108 | |||||||
| chr6:13939220 | A | T | 3 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 |
3 | HG02896.hp2 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-367+14197A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13939220 | |||||||
| chr6:13939336 | A | G | 1 | a0001c0001t0001g0080 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-367+14313A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13939336 | |||||||
| chr6:13939388 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-367+14365G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13939388 | |||||||
| chr6:13939478 | T | G | 1 | a0001c0001t0002g0236 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-367+14455T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13939478 | |||||||
| chr6:13939483 | G | A | 1 | a0001c0001t0002g0155 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-367+14460G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13939483 | |||||||
| chr6:13939594 | A | G | 1 | a0001c0001t0032g0107 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-367+14571A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13939594 | |||||||
| chr6:13939672 | T | A | 1 | a0001c0001t0002g0134 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-367+14649T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13939672 | |||||||
| chr6:13939701 | G | A | 1 | a0001c0001t0011g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-367+14678G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13939701 | |||||||
| chr6:13939800 | T | C | 295 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(292): Show |
333 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(330): Show |
intron_variant | MODIFIER | c.-367+14777T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13939800 | |||||||
| chr6:13939839 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-367+14816G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13939839 | |||||||
| chr6:13940303 | A | G | 2 | a0001c0001t0001g0294 a0001c0001t0001g0298 |
2 | NA18965.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.-367+15280A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940303 | |||||||
| chr6:13940321 | A | G | 1 | a0001c0001t0002g0248 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-367+15298A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940321 | |||||||
| chr6:13940357 | T | C | 1 | a0001c0001t0002g0035 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-367+15334T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940357 | |||||||
| chr6:13940420 | A | G | 3 | a0001c0001t0015g0171 a0001c0001t0015g0172 a0001c0002t0006g0173 |
3 | HG02559.hp1 HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-367+15397A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940420 | |||||||
| chr6:13940426 | A | G | 1 | a0001c0001t0002g0008 | 3 | HG03209.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-367+15403A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940426 | |||||||
| chr6:13940565 | A | C | 38 | a0001c0001t0001g0031 a0001c0001t0001g0079 a0001c0001t0001g0092 others(35): Show |
40 | HG00438.hp2 HG00621.hp1 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.-367+15542A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940565 | |||||||
| chr6:13940577 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-367+15554T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940577 | |||||||
| chr6:13940758 | G | T | 1 | a0001c0001t0003g0194 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-367+15735G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940758 | |||||||
| chr6:13940762 | G | C | 274 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(271): Show |
307 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(304): Show |
intron_variant | MODIFIER | c.-367+15739G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940762 | |||||||
| chr6:13940864 | A | G | 2 | a0001c0001t0015g0171 a0001c0001t0015g0172 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-367+15841A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940864 | |||||||
| chr6:13940865 | C | T | 1 | a0001c0001t0004g0264 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-367+15842C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940865 | |||||||
| chr6:13940866 | G | A | 1 | a0001c0001t0002g0127 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-367+15843G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940866 | |||||||
| chr6:13940896 | G | A | 7 | a0001c0001t0005g0001 a0001c0001t0005g0185 a0001c0001t0005g0186 others(4): Show |
12 | HG01243.hp2 HG02451.hp1 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.-367+15873G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940896 | |||||||
| chr6:13940946 | A | G | 2 | a0001c0001t0003g0103 a0001c0001t0003g0219 |
2 | NA18979.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.-367+15923A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940946 | |||||||
| chr6:13940988 | A | G | 1 | a0001c0001t0001g0293 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-367+15965A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940988 | |||||||
| chr6:13941069 | A | C | 1 | a0001c0001t0012g0166 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-367+16046A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13941069 | |||||||
| chr6:13941079 | G | C | 1 | a0001c0001t0020g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-367+16056G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13941079 | |||||||
| chr6:13941115 | T | C | 7 | a0001c0001t0001g0031 a0001c0001t0001g0272 a0001c0001t0001g0283 others(4): Show |
8 | HG01952.hp2 HG02293.hp1 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.-367+16092T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13941115 | |||||||
| chr6:13941150 | C | T | 1 | a0001c0001t0020g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-367+16127C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13941150 | |||||||
| chr6:13941252 | T | C | 1 | a0002c0005t0004g0257 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-367+16229T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13941252 | |||||||
| chr6:13941458 | G | A | 1 | a0001c0001t0002g0137 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-367+16435G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13941458 | |||||||
| chr6:13941525 | A | T | 3 | a0001c0001t0001g0084 a0001c0001t0007g0075 a0001c0001t0007g0085 |
3 | HG00597.hp1 HG01928.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.-367+16502A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13941525 | |||||||
| chr6:13941586 | C | T | 1 | a0001c0002t0006g0151 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-367+16563C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13941586 | |||||||
| chr6:13941780 | G | C | 1 | a0001c0001t0004g0055 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-367+16757G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13941780 | |||||||
| chr6:13941840 | C | G | 1 | a0001c0001t0020g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-367+16817C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13941840 | |||||||
| chr6:13941918 | A | G | 2 | a0001c0001t0015g0171 a0001c0001t0015g0172 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-367+16895A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13941918 | |||||||
| chr6:13941967 | G | T | 2 | a0001c0001t0010g0025 a0001c0001t0010g0228 |
3 | HG02027.hp1 NA18941.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.-367+16944G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13941967 | |||||||
| chr6:13942100 | A | G | 1 | a0001c0001t0026g0218 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-367+17077A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13942100 | |||||||
| chr6:13942352 | T | A | 1 | a0001c0001t0002g0239 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-367+17329T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13942352 | |||||||
| chr6:13942364 | C | T | 13 | a0001c0001t0003g0189 a0001c0001t0003g0191 a0001c0001t0003g0192 others(10): Show |
13 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.-367+17341C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13942364 | |||||||
| chr6:13942368 | A | G | 1 | a0001c0001t0002g0247 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-367+17345A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13942368 | |||||||
| chr6:13942392 | A | G | 1 | a0001c0001t0004g0098 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-367+17369A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13942392 | |||||||
| chr6:13942600 | C | G | 129 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(126): Show |
146 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.-367+17577C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13942600 | |||||||
| chr6:13942630 | C | A | 1 | a0001c0001t0030g0144 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-367+17607C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13942630 | |||||||
| chr6:13942819 | C | T | 1 | a0001c0001t0020g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-367+17796C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13942819 | |||||||
| chr6:13942841 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-367+17818A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13942841 | |||||||
| chr6:13942868 | C | A | 1 | a0001c0001t0020g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-367+17845C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13942868 | |||||||
| chr6:13942920 | C | T | 3 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0182 |
3 | HG00642.hp2 HG01106.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-367+17897C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13942920 | |||||||
| chr6:13943035 | T | C | 1 | a0001c0001t0002g0252 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-367+18012T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13943035 | |||||||
| chr6:13943282 | C | CT | 16 | a0001c0001t0001g0024 a0001c0001t0001g0184 a0001c0001t0002g0155 others(13): Show |
22 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.-367+18272dupT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13943282 | ||||||
| chr6:13943308 | A | G | 1 | a0001c0001t0002g0041 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-367+18285A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13943308 | |||||||
| chr6:13943550 | C | T | 228 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(225): Show |
253 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.-367+18527C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13943550 | |||||||
| chr6:13943722 | G | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0274 |
3 | HG00735.hp1 HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-367+18699G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13943722 | |||||||
| chr6:13943724 | C | T | 82 | a0001c0001t0001g0033 a0001c0001t0001g0102 a0001c0001t0001g0123 others(79): Show |
91 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.-367+18701C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13943724 | |||||||
| chr6:13943793 | G | A | 1 | a0001c0001t0004g0043 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-367+18770G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13943793 | |||||||
| chr6:13943916 | T | G | 1 | a0001c0001t0020g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-367+18893T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13943916 | |||||||
| chr6:13944022 | A | G | 1 | a0001c0001t0028g0160 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-367+18999A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13944022 | |||||||
| chr6:13944064 | C | T | 5 | a0001c0001t0003g0022 a0001c0001t0003g0103 a0001c0001t0003g0195 others(2): Show |
6 | NA18979.hp2 NA18980.hp2 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.-367+19041C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13944064 | |||||||
| chr6:13944199 | T | C | 7 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0134 others(4): Show |
7 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-367+19176T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13944199 | |||||||
| chr6:13944275 | G | A | 2 | a0001c0001t0015g0171 a0001c0001t0015g0172 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-367+19252G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13944275 | |||||||
| chr6:13944836 | G | T | 229 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(226): Show |
255 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-367+19813G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13944836 | |||||||
| chr6:13944956 | GTGCC | G | 5 | a0001c0001t0001g0012 a0001c0001t0001g0056 a0001c0001t0001g0268 others(2): Show |
6 | HG00738.hp1 HG01167.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.-367+19936_-367+19 others(10): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13944956 | ||||||
| chr6:13944966 | C | G | 1 | a0001c0001t0002g0210 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-367+19943C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13944966 | |||||||
| chr6:13945589 | CT | C | 3 | a0001c0001t0001g0054 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG00280.hp1 HG00733.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-367+20568delT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13945589 | ||||||
| chr6:13945881 | T | C | 227 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(224): Show |
253 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.-367+20858T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13945881 | |||||||
| chr6:13945985 | G | C | 48 | a0001c0001t0001g0175 a0001c0001t0002g0009 a0001c0001t0002g0013 others(45): Show |
55 | HG01070.hp1 HG01071.hp1 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.-367+20962G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13945985 | |||||||
| chr6:13946083 | A | G | 1 | a0001c0001t0003g0157 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-367+21060A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13946083 | |||||||
| chr6:13946124 | T | C | 2 | a0001c0001t0002g0110 a0001c0001t0002g0111 |
2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-367+21101T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13946124 | |||||||
| chr6:13946140 | C | CATT | 47 | a0001c0001t0001g0109 a0001c0001t0001g0175 a0001c0001t0001g0298 others(44): Show |
56 | HG00280.hp2 HG00741.hp2 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.-367+21157_-367+21 others(9): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13946140 | ||||||
| chr6:13946140 | C | CATTATT | 86 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0030 others(83): Show |
92 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.-367+21154_-367+21 others(12): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13946140 | ||||||
| chr6:13946140 | C | CATTATTA others(2): Show |
101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
113 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.-367+21151_-367+21 others(15): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13946140 | ||||||
| chr6:13946140 | C | CATTATTA others(5): Show |
26 | a0001c0001t0001g0076 a0001c0001t0001g0283 a0001c0001t0001g0288 others(23): Show |
26 | HG00438.hp1 HG00558.hp2 HG01516.hp2 others(23): Show |
intron_variant | MODIFIER | c.-367+21148_-367+21 others(18): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13946140 | ||||||
| chr6:13946140 | CATT | C | 22 | a0001c0001t0001g0072 a0001c0001t0001g0230 a0001c0001t0002g0105 others(19): Show |
25 | HG00673.hp2 HG02040.hp1 HG02056.hp1 others(22): Show |
intron_variant | MODIFIER | c.-367+21157_-367+21 others(9): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13946140 | ||||||
| chr6:13946140 | CATTATT | C | 8 | a0001c0001t0005g0001 a0001c0001t0005g0186 a0001c0001t0005g0187 others(5): Show |
13 | HG01243.hp2 HG02451.hp1 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.-367+21154_-367+21 others(12): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13946140 | ||||||
| chr6:13946182 | T | TATTATTA others(3): Show |
1 | a0001c0001t0001g0071 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-367+21159_-367+21 others(16): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13946182 | |||||||
| chr6:13946184 | T | A | 1 | a0001c0004t0003g0177 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-367+21161T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13946184 | |||||||
| chr6:13946596 | C | G | 1 | a0001c0001t0010g0025 | 2 | NA18941.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.-367+21573C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13946596 | |||||||
| chr6:13946898 | G | A | 3 | a0001c0001t0001g0184 a0001c0001t0001g0294 a0001c0001t0001g0298 |
3 | NA18965.hp2 NA18981.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.-367+21875G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13946898 | |||||||
| chr6:13947059 | AT | A | 93 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0102 others(90): Show |
102 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.-367+22038delT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13947059 | ||||||
| chr6:13947060 | T | TAAAC | 134 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(131): Show |
151 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(148): Show |
intron_variant | MODIFIER | c.-367+22037_-367+22 others(10): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13947060 | |||||||
| chr6:13947117 | G | A | 1 | a0001c0001t0021g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-367+22094G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13947117 | |||||||
| chr6:13947168 | A | T | 1 | a0001c0001t0010g0228 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-367+22145A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13947168 | |||||||
| chr6:13947212 | C | T | 3 | a0001c0001t0003g0191 a0001c0001t0003g0193 a0001c0001t0003g0194 |
3 | HG00558.hp1 HG02083.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-367+22189C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13947212 | |||||||
| chr6:13947368 | T | C | 1 | a0001c0001t0021g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-367+22345T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13947368 | |||||||
| chr6:13947440 | T | C | 1 | a0001c0001t0020g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-367+22417T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13947440 | |||||||
| chr6:13947502 | A | G | 1 | a0001c0001t0001g0288 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-367+22479A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13947502 | |||||||
| chr6:13947717 | C | T | 1 | a0001c0001t0021g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-367+22694C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13947717 | |||||||
| chr6:13947913 | A | G | 1 | a0001c0001t0011g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-367+22890A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13947913 | |||||||
| chr6:13947954 | A | AAATCAGG others(5): Show |
1 | a0001c0001t0001g0184 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+22933_-367+22 others(18): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13947954 | ||||||
| chr6:13948041 | A | C | 1 | a0001c0001t0001g0184 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+23018A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948041 | |||||||
| chr6:13948045 | A | C | 1 | a0001c0001t0001g0184 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+23022A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948045 | |||||||
| chr6:13948052 | T | A | 1 | a0001c0001t0001g0184 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+23029T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948052 | |||||||
| chr6:13948059 | T | G | 1 | a0001c0001t0001g0184 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+23036T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948059 | |||||||
| chr6:13948066 | A | C | 1 | a0001c0001t0001g0184 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+23043A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948066 | |||||||
| chr6:13948107 | C | T | 1 | a0001c0001t0004g0281 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-367+23084C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948107 | |||||||
| chr6:13948150 | A | T | 1 | a0001c0001t0001g0184 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+23127A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948150 | |||||||
| chr6:13948157 | C | T | 3 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0134 |
3 | HG02145.hp1 HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-367+23134C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948157 | |||||||
| chr6:13948158 | A | G | 227 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(224): Show |
253 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.-367+23135A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948158 | |||||||
| chr6:13948192 | G | A | 1 | a0001c0001t0030g0144 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-367+23169G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948192 | |||||||
| chr6:13948214 | A | C | 1 | a0001c0001t0001g0184 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+23191A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948214 | |||||||
| chr6:13948312 | G | T | 1 | a0001c0001t0001g0184 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+23289G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948312 | |||||||
| chr6:13948453 | T | A | 1 | a0001c0001t0001g0184 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+23430T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948453 | |||||||
| chr6:13948489 | T | A | 1 | a0001c0001t0020g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-367+23466T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948489 | |||||||
| chr6:13948513 | T | A | 1 | a0001c0001t0001g0184 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+23490T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948513 | |||||||
| chr6:13948586 | C | T | 1 | a0001c0001t0002g0045 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-367+23563C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948586 | |||||||
| chr6:13948603 | T | G | 5 | a0001c0001t0036g0161 a0001c0002t0006g0162 a0001c0002t0006g0163 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-367+23580T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948603 | |||||||
| chr6:13948628 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-367+23605A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948628 | |||||||
| chr6:13948643 | T | G | 1 | a0001c0001t0001g0184 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+23620T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948643 | |||||||
| chr6:13948653 | C | A | 1 | a0001c0001t0020g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-367+23630C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948653 | |||||||
| chr6:13948663 | A | C | 1 | a0001c0001t0001g0184 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+23640A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948663 | |||||||
| chr6:13948794 | C | T | 1 | a0001c0001t0002g0116 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-367+23771C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948794 | |||||||
| chr6:13948828 | C | A | 1 | a0001c0001t0001g0184 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+23805C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948828 | |||||||
| chr6:13948830 | A | C | 1 | a0001c0001t0001g0184 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+23807A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948830 | |||||||
| chr6:13948881 | GACAA | G | 4 | a0001c0001t0002g0152 a0001c0001t0009g0133 a0001c0001t0009g0135 others(1): Show |
4 | HG01496.hp2 HG03139.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-367+23864_-367+23 others(10): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13948881 | ||||||
| chr6:13948972 | A | T | 1 | a0001c0001t0029g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-367+23949A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948972 | |||||||
| chr6:13949037 | A | G | 1 | a0001c0001t0020g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-367+24014A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13949037 | |||||||
| chr6:13949064 | A | G | 75 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0102 others(72): Show |
84 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.-367+24041A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13949064 | |||||||
| chr6:13949083 | G | A | 1 | a0001c0001t0020g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-367+24060G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13949083 | |||||||
| chr6:13949239 | A | G | 3 | a0001c0002t0006g0162 a0001c0002t0006g0163 a0001c0002t0006g0222 |
3 | HG02258.hp2 HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-367+24216A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13949239 | |||||||
| chr6:13949442 | T | C | 227 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(224): Show |
253 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.-367+24419T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13949442 | |||||||
| chr6:13949444 | A | G | 2 | a0001c0001t0011g0159 a0001c0001t0028g0160 |
2 | HG02055.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-367+24421A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13949444 | |||||||
| chr6:13949467 | C | T | 1 | a0001c0003t0001g0291 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-367+24444C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13949467 | |||||||
| chr6:13949492 | A | G | 1 | a0001c0001t0009g0245 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-367+24469A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13949492 | |||||||
| chr6:13949804 | T | C | 2 | a0001c0001t0002g0253 a0001c0001t0002g0254 |
2 | NA18971.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.-366-24406T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13949804 | |||||||
| chr6:13949935 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-366-24275G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13949935 | |||||||
| chr6:13950106 | T | G | 1 | a0001c0001t0001g0123 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-366-24104T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13950106 | |||||||
| chr6:13950167 | G | T | 1 | a0001c0001t0003g0207 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-366-24043G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13950167 | |||||||
| chr6:13950249 | C | G | 3 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 |
3 | HG02896.hp2 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-366-23961C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13950249 | |||||||
| chr6:13950498 | C | CT | 13 | a0001c0001t0001g0048 a0001c0001t0001g0059 a0001c0001t0001g0065 others(10): Show |
13 | HG01981.hp2 HG02109.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-366-23693dupT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13950498 | ||||||
| chr6:13950498 | C | CTT | 181 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(178): Show |
200 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.-366-23694_-366-23 others(8): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13950498 | ||||||
| chr6:13950498 | C | CTTT | 27 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0271 others(24): Show |
34 | HG00280.hp2 HG00642.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.-366-23695_-366-23 others(9): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13950498 | ||||||
| chr6:13950498 | C | T | 1 | a0001c0001t0001g0294 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-366-23712C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13950498 | |||||||
| chr6:13950498 | CT | C | 9 | a0001c0001t0002g0006 a0001c0001t0002g0034 a0001c0001t0002g0110 others(6): Show |
11 | HG01167.hp1 HG01891.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.-366-23693delT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13950498 | ||||||
| chr6:13950543 | G | A | 7 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0134 others(4): Show |
7 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-366-23667G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13950543 | |||||||
| chr6:13950719 | A | G | 2 | a0001c0001t0002g0152 a0001c0001t0009g0128 |
2 | HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-366-23491A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13950719 | |||||||
| chr6:13950731 | A | G | 2 | a0001c0001t0002g0028 a0001c0001t0002g0238 |
3 | HG01167.hp1 HG01169.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-366-23479A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13950731 | |||||||
| chr6:13950819 | T | TA | 2 | a0001c0001t0001g0295 a0001c0001t0017g0032 |
3 | HG01255.hp2 HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-366-23390dupA | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13950819 | ||||||
| chr6:13950941 | C | T | 1 | a0001c0001t0020g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-366-23269C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13950941 | |||||||
| chr6:13950997 | A | G | 1 | a0001c0001t0001g0071 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-366-23213A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13950997 | |||||||
| chr6:13951032 | G | A | 1 | a0001c0001t0024g0263 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-366-23178G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13951032 | |||||||
| chr6:13951279 | C | T | 113 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(110): Show |
123 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(120): Show |
intron_variant | MODIFIER | c.-366-22931C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13951279 | |||||||
| chr6:13951450 | G | A | 1 | a0001c0001t0020g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-366-22760G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13951450 | |||||||
| chr6:13951468 | A | G | 6 | a0001c0001t0002g0152 a0001c0001t0009g0128 a0001c0001t0009g0133 others(3): Show |
6 | HG01496.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-366-22742A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13951468 | |||||||
| chr6:13951512 | C | G | 4 | a0001c0002t0006g0162 a0001c0002t0006g0163 a0001c0002t0006g0173 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-366-22698C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13951512 | |||||||
| chr6:13951537 | C | G | 1 | a0001c0001t0002g0137 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-366-22673C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13951537 | |||||||
| chr6:13951852 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0077 |
3 | NA18940.hp2 NA18942.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.-366-22358G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13951852 | |||||||
| chr6:13951860 | A | G | 1 | a0001c0001t0002g0038 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-366-22350A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13951860 | |||||||
| chr6:13951920 | C | T | 2 | a0001c0001t0008g0018 a0001c0001t0008g0158 |
3 | HG00673.hp2 HG02056.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.-366-22290C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13951920 | |||||||
| chr6:13951976 | T | A | 1 | a0001c0001t0002g0038 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-366-22234T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13951976 | |||||||
| chr6:13952132 | C | T | 81 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0102 others(78): Show |
91 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.-366-22078C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952132 | |||||||
| chr6:13952138 | G | A | 1 | a0001c0001t0020g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-366-22072G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952138 | |||||||
| chr6:13952179 | G | A | 1 | a0001c0001t0003g0157 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-366-22031G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952179 | |||||||
| chr6:13952198 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-366-22012C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952198 | |||||||
| chr6:13952251 | A | G | 94 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0037 others(91): Show |
109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.-366-21959A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952251 | |||||||
| chr6:13952270 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-366-21940G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952270 | |||||||
| chr6:13952363 | C | T | 1 | a0001c0001t0020g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-366-21847C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952363 | |||||||
| chr6:13952389 | C | A | 21 | a0001c0001t0002g0152 a0001c0001t0005g0001 a0001c0001t0005g0185 others(18): Show |
26 | HG01243.hp2 HG01496.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.-366-21821C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952389 | |||||||
| chr6:13952399 | C | T | 3 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0134 |
3 | HG02145.hp1 HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-366-21811C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952399 | |||||||
| chr6:13952555 | G | A | 115 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(112): Show |
126 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.-366-21655G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952555 | |||||||
| chr6:13952561 | C | G | 115 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(112): Show |
126 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.-366-21649C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952561 | |||||||
| chr6:13952570 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-366-21640G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952570 | |||||||
| chr6:13952622 | G | A | 96 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0037 others(93): Show |
106 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.-366-21588G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952622 | |||||||
| chr6:13952665 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0109 |
3 | HG02896.hp1 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-366-21545A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952665 | |||||||
| chr6:13952990 | T | C | 1 | a0001c0001t0001g0066 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-366-21220T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952990 | |||||||
| chr6:13952996 | T | C | 199 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(196): Show |
220 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.-366-21214T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952996 | |||||||
| chr6:13953078 | G | T | 1 | a0001c0001t0020g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-366-21132G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13953078 | |||||||
| chr6:13953226 | C | G | 3 | a0001c0001t0002g0152 a0001c0001t0009g0133 a0001c0001t0009g0135 |
3 | HG01496.hp2 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-366-20984C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13953226 | |||||||
| chr6:13953386 | G | C | 10 | a0001c0001t0005g0001 a0001c0001t0005g0185 a0001c0001t0005g0186 others(7): Show |
15 | HG01243.hp2 HG02451.hp1 HG02895.hp1 others(12): Show |
intron_variant | MODIFIER | c.-366-20824G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13953386 | |||||||
| chr6:13953579 | C | G | 9 | a0001c0001t0001g0083 a0001c0001t0001g0190 a0001c0001t0001g0280 others(6): Show |
9 | HG00738.hp2 HG01070.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.-366-20631C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13953579 | |||||||
| chr6:13953718 | T | C | 1 | a0001c0001t0001g0230 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-366-20492T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13953718 | |||||||
| chr6:13953725 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-366-20485G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13953725 | |||||||
| chr6:13953767 | C | T | 1 | a0001c0001t0002g0237 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-366-20443C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13953767 | |||||||
| chr6:13953807 | T | C | 298 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(295): Show |
336 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(333): Show |
intron_variant | MODIFIER | c.-366-20403T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13953807 | |||||||
| chr6:13953808 | G | A | 1 | a0001c0001t0003g0223 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-366-20402G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13953808 | |||||||
| chr6:13953860 | C | T | 9 | a0001c0001t0002g0106 a0001c0001t0002g0134 a0001c0001t0002g0152 others(6): Show |
9 | HG01496.hp2 HG02055.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-366-20350C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13953860 | |||||||
| chr6:13953996 | A | G | 2 | a0001c0001t0015g0171 a0001c0001t0015g0172 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-366-20214A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13953996 | |||||||
| chr6:13954063 | T | A | 49 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0156 others(46): Show |
56 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.-366-20147T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13954063 | |||||||
| chr6:13954261 | C | T | 1 | a0001c0001t0002g0039 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-366-19949C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13954261 | |||||||
| chr6:13954401 | G | A | 107 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(104): Show |
119 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.-366-19809G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13954401 | |||||||
| chr6:13954499 | T | G | 1 | a0001c0001t0030g0144 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-366-19711T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13954499 | |||||||
| chr6:13954861 | T | C | 18 | a0001c0001t0005g0001 a0001c0001t0005g0185 a0001c0001t0005g0186 others(15): Show |
23 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.-366-19349T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13954861 | |||||||
| chr6:13954949 | C | T | 1 | a0001c0001t0003g0227 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-366-19261C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13954949 | |||||||
| chr6:13955017 | G | A | 46 | a0001c0001t0002g0009 a0001c0001t0002g0013 a0001c0001t0002g0014 others(43): Show |
53 | HG01070.hp1 HG01071.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.-366-19193G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13955017 | |||||||
| chr6:13955069 | G | T | 1 | a0001c0001t0001g0123 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-366-19141G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13955069 | |||||||
| chr6:13955179 | C | T | 10 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0134 others(7): Show |
11 | HG01243.hp1 HG02145.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-366-19031C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13955179 | |||||||
| chr6:13955180 | G | A | 1 | a0001c0001t0015g0171 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-366-19030G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13955180 | |||||||
| chr6:13955181 | G | A | 1 | a0001c0001t0003g0089 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-366-19029G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13955181 | |||||||
| chr6:13955196 | G | C | 1 | a0001c0001t0004g0281 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-366-19014G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13955196 | |||||||
| chr6:13955263 | C | T | 5 | a0001c0001t0002g0237 a0001c0001t0002g0252 a0001c0001t0002g0265 others(2): Show |
5 | NA18949.hp1 NA18957.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.-366-18947C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13955263 | |||||||
| chr6:13955316 | C | T | 6 | a0001c0001t0005g0001 a0001c0001t0005g0185 a0001c0001t0005g0186 others(3): Show |
10 | NA18942.hp2 NA18949.hp2 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-366-18894C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13955316 | |||||||
| chr6:13955333 | C | G | 228 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(225): Show |
255 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-366-18877C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13955333 | |||||||
| chr6:13955464 | G | T | 1 | a0001c0001t0002g0155 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-366-18746G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13955464 | |||||||
| chr6:13955663 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-366-18547C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13955663 | |||||||
| chr6:13955741 | A | G | 1 | a0001c0001t0001g0058 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-366-18469A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13955741 | |||||||
| chr6:13955888 | A | G | 6 | a0001c0001t0001g0030 a0001c0001t0001g0109 a0001c0001t0001g0190 others(3): Show |
7 | HG02451.hp2 HG02717.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-366-18322A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13955888 | |||||||
| chr6:13956077 | A | G | 229 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(226): Show |
256 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.-366-18133A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13956077 | |||||||
| chr6:13956152 | A | G | 117 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(114): Show |
131 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.-366-18058A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13956152 | |||||||
| chr6:13956312 | C | CT | 7 | a0001c0001t0002g0250 a0001c0001t0004g0204 a0001c0001t0008g0018 others(4): Show |
8 | HG00408.hp1 HG00408.hp2 HG00673.hp2 others(5): Show |
intron_variant | MODIFIER | c.-366-17885dupT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13956312 | ||||||
| chr6:13956312 | CT | C | 6 | a0001c0001t0005g0001 a0001c0001t0005g0185 a0001c0001t0005g0186 others(3): Show |
10 | NA18942.hp2 NA18949.hp2 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-366-17885delT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13956312 | ||||||
| chr6:13956413 | C | G | 117 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(114): Show |
131 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.-366-17797C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13956413 | |||||||
| chr6:13956443 | GCCTCCCT others(7): Show |
G | 1 | a0001c0001t0001g0024 | 2 | HG03834.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-366-17766_-366-17 others(20): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13956443 | |||||||
| chr6:13956459 | G | A | 1 | a0001c0001t0001g0024 | 2 | HG03834.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-366-17751G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13956459 | |||||||
| chr6:13956597 | T | G | 4 | a0001c0001t0011g0174 a0001c0001t0011g0220 a0001c0001t0011g0310 others(1): Show |
4 | HG01884.hp2 HG02145.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-366-17613T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13956597 | |||||||
| chr6:13956635 | G | A | 2 | a0001c0001t0013g0020 a0001c0001t0013g0183 |
3 | HG01243.hp2 HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-366-17575G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13956635 | |||||||
| chr6:13956660 | C | G | 3 | a0001c0001t0013g0020 a0001c0001t0013g0183 a0001c0001t0020g0113 |
4 | HG01243.hp2 HG02451.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-366-17550C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13956660 | |||||||
| chr6:13956674 | T | C | 7 | a0001c0001t0011g0174 a0001c0001t0011g0220 a0001c0001t0011g0310 others(4): Show |
8 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-366-17536T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13956674 | |||||||
| chr6:13956825 | C | T | 1 | a0001c0001t0025g0117 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-366-17385C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13956825 | |||||||
| chr6:13957000 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-366-17210C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957000 | |||||||
| chr6:13957095 | A | G | 6 | a0001c0001t0005g0001 a0001c0001t0005g0185 a0001c0001t0005g0186 others(3): Show |
10 | NA18942.hp2 NA18949.hp2 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-366-17115A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957095 | |||||||
| chr6:13957121 | C | T | 3 | a0001c0004t0003g0176 a0001c0004t0003g0177 a0001c0004t0003g0178 |
3 | NA18946.hp2 NA18968.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.-366-17089C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957121 | |||||||
| chr6:13957205 | T | TA | 4 | a0001c0001t0011g0159 a0001c0001t0015g0171 a0001c0001t0015g0172 others(1): Show |
4 | HG02055.hp1 HG02055.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-366-16999dupA | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13957205 | ||||||
| chr6:13957225 | T | C | 1 | a0001c0001t0002g0014 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-366-16985T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957225 | |||||||
| chr6:13957339 | A | G | 1 | a0001c0001t0020g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-366-16871A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957339 | |||||||
| chr6:13957413 | T | G | 242 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(239): Show |
270 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.-366-16797T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957413 | |||||||
| chr6:13957461 | A | G | 116 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(113): Show |
130 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.-366-16749A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957461 | |||||||
| chr6:13957531 | G | A | 1 | a0001c0001t0004g0279 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-366-16679G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957531 | |||||||
| chr6:13957534 | C | T | 3 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0134 |
3 | HG02145.hp1 HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-366-16676C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957534 | |||||||
| chr6:13957589 | T | A | 1 | a0001c0001t0001g0277 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-366-16621T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957589 | |||||||
| chr6:13957620 | T | A | 6 | a0001c0001t0002g0152 a0001c0001t0009g0128 a0001c0001t0009g0133 others(3): Show |
6 | HG01496.hp2 HG02572.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-366-16590T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957620 | |||||||
| chr6:13957759 | T | C | 6 | a0001c0001t0002g0152 a0001c0001t0009g0128 a0001c0001t0009g0133 others(3): Show |
6 | HG01496.hp2 HG02572.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-366-16451T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957759 | |||||||
| chr6:13957787 | A | G | 2 | a0001c0001t0013g0020 a0001c0001t0013g0183 |
3 | HG01243.hp2 HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-366-16423A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957787 | |||||||
| chr6:13957795 | T | G | 1 | a0001c0002t0006g0163 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-366-16415T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957795 | |||||||
| chr6:13957884 | T | C | 6 | a0001c0001t0002g0152 a0001c0001t0009g0128 a0001c0001t0009g0133 others(3): Show |
6 | HG01496.hp2 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-366-16326T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957884 | |||||||
| chr6:13958074 | T | TA | 3 | a0001c0001t0011g0159 a0001c0001t0015g0171 a0001c0001t0015g0172 |
3 | HG02055.hp1 HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-366-16135dupA | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13958074 | ||||||
| chr6:13958154 | G | A | 93 | a0001c0001t0001g0037 a0001c0001t0003g0003 a0001c0001t0003g0007 others(90): Show |
101 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.-366-16056G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13958154 | |||||||
| chr6:13958259 | G | A | 115 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(112): Show |
129 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.-366-15951G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13958259 | |||||||
| chr6:13958300 | C | T | 9 | a0001c0001t0002g0152 a0001c0001t0009g0133 a0001c0001t0009g0135 others(6): Show |
10 | HG01243.hp1 HG01496.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-366-15910C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13958300 | |||||||
| chr6:13958326 | C | T | 8 | a0001c0001t0001g0064 a0001c0001t0001g0102 a0001c0001t0001g0175 others(5): Show |
8 | HG00438.hp2 HG00621.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.-366-15884C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13958326 | |||||||
| chr6:13958423 | G | A | 227 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(224): Show |
254 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.-366-15787G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13958423 | |||||||
| chr6:13958597 | T | G | 6 | a0001c0001t0002g0152 a0001c0001t0009g0133 a0001c0001t0009g0135 others(3): Show |
6 | HG01496.hp2 HG02451.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-366-15613T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13958597 | |||||||
| chr6:13958647 | T | C | 1 | a0001c0001t0011g0220 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-366-15563T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13958647 | |||||||
| chr6:13958717 | G | A | 1 | a0001c0001t0004g0169 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-366-15493G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13958717 | |||||||
| chr6:13958796 | C | T | 1 | a0001c0001t0002g0137 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-366-15414C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13958796 | |||||||
| chr6:13958927 | T | C | 13 | a0001c0001t0005g0001 a0001c0001t0005g0185 a0001c0001t0005g0186 others(10): Show |
18 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-366-15283T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13958927 | |||||||
| chr6:13959023 | G | A | 1 | a0001c0001t0002g0198 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-366-15187G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13959023 | |||||||
| chr6:13959074 | T | G | 228 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(225): Show |
255 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-366-15136T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13959074 | |||||||
| chr6:13959177 | A | G | 89 | a0001c0001t0001g0037 a0001c0001t0003g0003 a0001c0001t0003g0007 others(86): Show |
97 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.-366-15033A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13959177 | |||||||
| chr6:13959319 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-366-14891G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13959319 | |||||||
| chr6:13959429 | G | A | 1 | a0001c0001t0029g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-366-14781G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13959429 | |||||||
| chr6:13959429 | G | C | 1 | a0001c0001t0001g0056 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-366-14781G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13959429 | |||||||
| chr6:13959652 | C | T | 3 | a0001c0001t0002g0152 a0001c0001t0009g0133 a0001c0001t0009g0135 |
3 | HG01496.hp2 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-366-14558C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13959652 | |||||||
| chr6:13959653 | A | G | 5 | a0001c0001t0002g0152 a0001c0001t0009g0133 a0001c0001t0009g0135 others(2): Show |
5 | HG01496.hp2 HG03139.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.-366-14557A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13959653 | |||||||
| chr6:13959811 | G | T | 6 | a0001c0001t0005g0001 a0001c0001t0005g0185 a0001c0001t0005g0186 others(3): Show |
10 | NA18942.hp2 NA18949.hp2 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-366-14399G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13959811 | |||||||
| chr6:13959911 | A | T | 13 | a0001c0001t0005g0001 a0001c0001t0005g0185 a0001c0001t0005g0186 others(10): Show |
18 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-366-14299A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13959911 | |||||||
| chr6:13959971 | C | T | 1 | a0001c0001t0029g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-366-14239C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13959971 | |||||||
| chr6:13960035 | G | T | 2 | a0001c0001t0008g0018 a0001c0001t0008g0158 |
3 | HG00673.hp2 HG02056.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.-366-14175G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960035 | |||||||
| chr6:13960513 | C | T | 3 | a0001c0001t0007g0005 a0001c0001t0018g0005 a0001c0001t0033g0005 |
3 | NA18945.hp2 NA18979.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-366-13697C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960513 | |||||||
| chr6:13960588 | G | A | 116 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(113): Show |
130 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.-366-13622G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960588 | |||||||
| chr6:13960642 | G | GGA | 7 | a0001c0001t0008g0018 a0001c0001t0008g0158 a0001c0001t0008g0170 others(4): Show |
8 | HG00408.hp2 HG00673.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.-366-13566_-366-13 others(8): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960642 | ||||||
| chr6:13960642 | G | GGAGAGAG others(5): Show |
1 | a0001c0001t0013g0020 | 2 | HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-366-13565_-366-13 others(18): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960642 | ||||||
| chr6:13960646 | G | A | 227 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(224): Show |
254 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.-366-13564G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960646 | |||||||
| chr6:13960656 | A | AGAGAGAG others(13): Show |
1 | a0001c0001t0013g0183 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-366-13553_-366-13 others(26): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960656 | ||||||
| chr6:13960656 | A | AGAGAGAG others(3): Show |
1 | a0001c0001t0020g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-366-13553_-366-13 others(16): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960656 | ||||||
| chr6:13960656 | A | AGAGAGT | 6 | a0001c0001t0005g0001 a0001c0001t0005g0185 a0001c0001t0005g0186 others(3): Show |
10 | NA18942.hp2 NA18949.hp2 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-366-13553_-366-13 others(12): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960656 | ||||||
| chr6:13960656 | A | AGT | 5 | a0001c0001t0002g0053 a0001c0001t0002g0110 a0001c0001t0002g0111 others(2): Show |
5 | HG01891.hp2 HG03098.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-366-13518_-366-13 others(8): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960656 | ||||||
| chr6:13960656 | A | AGTGT | 4 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0179 others(1): Show |
5 | HG01169.hp1 HG01361.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.-366-13520_-366-13 others(10): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960656 | ||||||
| chr6:13960656 | A | T | 9 | a0001c0001t0001g0064 a0001c0001t0001g0102 a0001c0001t0001g0282 others(6): Show |
9 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.-366-13554A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960656 | |||||||
| chr6:13960656 | AGT | A | 11 | a0001c0001t0002g0041 a0001c0001t0002g0095 a0001c0001t0002g0119 others(8): Show |
11 | HG01943.hp2 HG02572.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.-366-13518_-366-13 others(8): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960656 | ||||||
| chr6:13960656 | AGTGT | A | 13 | a0001c0001t0002g0013 a0001c0001t0002g0038 a0001c0001t0002g0040 others(10): Show |
15 | HG01071.hp1 HG01175.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.-366-13520_-366-13 others(10): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960656 | ||||||
| chr6:13960656 | AGTGTGTG others(1): Show |
A | 8 | a0001c0001t0002g0094 a0001c0001t0002g0152 a0001c0001t0009g0133 others(5): Show |
8 | HG01361.hp2 HG01496.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-366-13524_-366-13 others(14): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960656 | ||||||
| chr6:13960656 | AGTGTGTG others(3): Show |
A | 1 | a0001c0001t0029g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-366-13526_-366-13 others(16): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960656 | ||||||
| chr6:13960656 | AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0028g0160 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-366-13528_-366-13 others(18): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960656 | ||||||
| chr6:13960658 | T | A | 8 | a0001c0001t0001g0083 a0001c0001t0004g0108 a0001c0001t0008g0153 others(5): Show |
8 | HG01070.hp2 HG01884.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.-366-13552T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960658 | |||||||
| chr6:13960660 | T | A | 4 | a0001c0001t0011g0174 a0001c0001t0011g0220 a0001c0001t0011g0310 others(1): Show |
4 | HG01884.hp2 HG02145.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-366-13550T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960660 | |||||||
| chr6:13960664 | T | A | 1 | a0001c0001t0021g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-366-13546T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960664 | |||||||
| chr6:13960666 | T | A | 4 | a0001c0001t0002g0152 a0001c0001t0009g0133 a0001c0001t0009g0135 others(1): Show |
4 | HG01361.hp2 HG01496.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-366-13544T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960666 | |||||||
| chr6:13960668 | T | A | 1 | a0001c0001t0029g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-366-13542T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960668 | |||||||
| chr6:13960686 | T | C | 7 | a0001c0001t0002g0164 a0001c0001t0003g0213 a0001c0001t0011g0159 others(4): Show |
7 | HG00738.hp2 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-366-13524T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960686 | |||||||
| chr6:13960688 | T | C | 54 | a0001c0001t0001g0230 a0001c0001t0002g0152 a0001c0001t0002g0164 others(51): Show |
57 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.-366-13522T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960688 | |||||||
| chr6:13960688 | T | TGC | 40 | a0001c0001t0001g0037 a0001c0001t0003g0003 a0001c0001t0003g0007 others(37): Show |
45 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.-366-13521_-366-13 others(8): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960688 | ||||||
| chr6:13960690 | T | C | 117 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0064 others(114): Show |
130 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-366-13520T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960690 | |||||||
| chr6:13960691 | G | A | 5 | a0001c0001t0004g0055 a0001c0001t0004g0097 a0001c0001t0004g0098 others(2): Show |
5 | HG01257.hp1 HG01346.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.-366-13519G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960691 | |||||||
| chr6:13960692 | T | C | 170 | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0001g0030 others(167): Show |
190 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.-366-13518T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960692 | |||||||
| chr6:13960692 | T | TGTGCGCG others(3): Show |
14 | a0001c0001t0001g0011 a0001c0001t0001g0048 a0001c0001t0001g0059 others(11): Show |
15 | HG00597.hp1 HG02080.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.-366-13517_-366-13 others(16): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960692 | ||||||
| chr6:13960692 | T | TGTGTGCG others(5): Show |
4 | a0001c0001t0001g0074 a0001c0001t0001g0123 a0001c0002t0006g0151 others(1): Show |
4 | HG00642.hp2 HG01243.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.-366-13517_-366-13 others(18): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960692 | ||||||
| chr6:13960692 | T | TGTGTGTG others(5): Show |
2 | a0001c0002t0006g0162 a0001c0002t0006g0163 |
2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-366-13517_-366-13 others(18): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960692 | ||||||
| chr6:13960692 | T | TGTGTGTG others(7): Show |
2 | a0001c0001t0001g0181 a0001c0002t0006g0016 |
3 | HG03486.hp2 HG03516.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-366-13517_-366-13 others(20): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960692 | ||||||
| chr6:13960692 | T | TGTGTGTG others(9): Show |
3 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0002t0006g0222 |
3 | HG02145.hp1 HG02486.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-366-13517_-366-13 others(22): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960692 | ||||||
| chr6:13960692 | T | TGTGTGTG others(11): Show |
2 | a0001c0001t0001g0063 a0001c0001t0002g0134 |
2 | HG02976.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-366-13517_-366-13 others(24): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960692 | ||||||
| chr6:13960692 | T | TGTGTGTG others(11): Show |
1 | a0001c0001t0007g0246 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-366-13517_-366-13 others(24): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960692 | ||||||
| chr6:13960697 | G | A | 21 | a0001c0001t0001g0011 a0001c0001t0001g0048 a0001c0001t0001g0059 others(18): Show |
22 | HG00597.hp1 HG00642.hp2 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.-366-13513G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960697 | |||||||
| chr6:13960697 | G | GCGCA | 10 | a0001c0001t0001g0033 a0001c0001t0001g0064 a0001c0001t0001g0102 others(7): Show |
11 | HG00621.hp1 HG02040.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-366-13511_-366-13 others(10): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960697 | ||||||
| chr6:13960697 | G | GCGCGCA | 46 | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0001g0030 others(43): Show |
52 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.-366-13511_-366-13 others(12): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960697 | ||||||
| chr6:13960697 | G | GCGCGCGC others(1): Show |
37 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(34): Show |
43 | HG00609.hp1 HG00733.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.-366-13511_-366-13 others(14): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960697 | ||||||
| chr6:13960697 | G | GCGCGCGC others(3): Show |
1 | a0001c0001t0001g0261 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-366-13511_-366-13 others(16): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960697 | ||||||
| chr6:13961052 | A | G | 7 | a0001c0001t0005g0001 a0001c0001t0005g0185 a0001c0001t0005g0186 others(4): Show |
11 | HG04115.hp2 NA18942.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-366-13158A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13961052 | |||||||
| chr6:13961181 | A | G | 14 | a0001c0001t0005g0001 a0001c0001t0005g0185 a0001c0001t0005g0186 others(11): Show |
19 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-366-13029A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13961181 | |||||||
| chr6:13961214 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-366-12996C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13961214 | |||||||
| chr6:13961216 | T | C | 1 | a0001c0001t0003g0157 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-366-12994T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13961216 | |||||||
| chr6:13961314 | C | T | 88 | a0001c0001t0001g0037 a0001c0001t0003g0003 a0001c0001t0003g0007 others(85): Show |
96 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.-366-12896C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13961314 | |||||||
| chr6:13961559 | T | C | 7 | a0001c0001t0011g0174 a0001c0001t0011g0220 a0001c0001t0011g0310 others(4): Show |
8 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-366-12651T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13961559 | |||||||
| chr6:13961763 | A | T | 228 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(225): Show |
255 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-366-12447A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13961763 | |||||||
| chr6:13961821 | T | C | 1 | a0001c0001t0021g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-366-12389T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13961821 | |||||||
| chr6:13961824 | C | T | 14 | a0001c0001t0005g0001 a0001c0001t0005g0185 a0001c0001t0005g0186 others(11): Show |
19 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-366-12386C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13961824 | |||||||
| chr6:13961959 | G | A | 1 | a0001c0001t0021g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-366-12251G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13961959 | |||||||
| chr6:13962028 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-366-12182G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13962028 | |||||||
| chr6:13962030 | A | G | 1 | a0001c0002t0006g0222 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-366-12180A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13962030 | |||||||
| chr6:13962075 | A | G | 2 | a0001c0001t0003g0232 a0001c0001t0003g0260 |
2 | HG02602.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.-366-12135A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13962075 | |||||||
| chr6:13962173 | C | T | 2 | a0001c0001t0010g0025 a0001c0001t0010g0228 |
3 | HG02027.hp1 NA18941.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.-366-12037C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13962173 | |||||||
| chr6:13962226 | A | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(58): Show |
69 | HG00280.hp1 HG00558.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.-366-11984A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13962226 | |||||||
| chr6:13962345 | T | C | 1 | a0001c0001t0004g0199 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-366-11865T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13962345 | |||||||
| chr6:13962349 | C | T | 1 | a0001c0001t0029g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-366-11861C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13962349 | |||||||
| chr6:13962421 | C | T | 3 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0134 |
3 | HG02145.hp1 HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-366-11789C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13962421 | |||||||
| chr6:13962632 | T | C | 1 | a0001c0001t0003g0207 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-366-11578T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13962632 | |||||||
| chr6:13962728 | G | A | 3 | a0001c0001t0004g0206 a0001c0001t0004g0251 a0002c0005t0004g0257 |
3 | HG00642.hp1 HG02735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-366-11482G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13962728 | |||||||
| chr6:13962730 | G | T | 1 | a0001c0001t0029g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-366-11480G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13962730 | |||||||
| chr6:13962792 | G | A | 1 | a0001c0001t0028g0160 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-366-11418G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13962792 | |||||||
| chr6:13962867 | C | T | 117 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(114): Show |
131 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.-366-11343C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13962867 | |||||||
| chr6:13962991 | T | G | 7 | a0001c0001t0005g0001 a0001c0001t0005g0185 a0001c0001t0005g0186 others(4): Show |
11 | HG04115.hp2 NA18942.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-366-11219T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13962991 | |||||||
| chr6:13963025 | T | C | 1 | a0001c0001t0002g0132 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-366-11185T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13963025 | |||||||
| chr6:13963052 | T | C | 117 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(114): Show |
131 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.-366-11158T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13963052 | |||||||
| chr6:13963307 | A | G | 6 | a0001c0001t0005g0001 a0001c0001t0005g0185 a0001c0001t0005g0186 others(3): Show |
10 | NA18942.hp2 NA18949.hp2 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-366-10903A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13963307 | |||||||
| chr6:13963329 | T | C | 1 | a0001c0001t0020g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-366-10881T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13963329 | |||||||
| chr6:13963407 | C | T | 5 | a0001c0001t0002g0152 a0001c0001t0009g0133 a0001c0001t0009g0135 others(2): Show |
5 | HG01496.hp2 HG03139.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.-366-10803C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13963407 | |||||||
| chr6:13963646 | G | T | 3 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0134 |
3 | HG02145.hp1 HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-366-10564G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13963646 | |||||||
| chr6:13963755 | A | C | 5 | a0001c0001t0002g0152 a0001c0001t0009g0133 a0001c0001t0009g0135 others(2): Show |
5 | HG01496.hp2 HG03139.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.-366-10455A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13963755 | |||||||
| chr6:13963881 | A | G | 2 | a0001c0001t0013g0020 a0001c0001t0013g0183 |
3 | HG01243.hp2 HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-366-10329A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13963881 | |||||||
| chr6:13964367 | C | A | 3 | a0001c0001t0002g0235 a0001c0001t0002g0236 a0001c0001t0002g0241 |
3 | HG02698.hp1 HG04184.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-366-9843C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13964367 | |||||||
| chr6:13964400 | C | T | 116 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(113): Show |
130 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.-366-9810C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13964400 | |||||||
| chr6:13964553 | C | T | 3 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0134 |
3 | HG02145.hp1 HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-366-9657C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13964553 | |||||||
| chr6:13964663 | G | C | 7 | a0001c0001t0011g0174 a0001c0001t0011g0220 a0001c0001t0011g0310 others(4): Show |
8 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-366-9547G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13964663 | |||||||
| chr6:13964695 | T | G | 240 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(237): Show |
268 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.-366-9515T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13964695 | |||||||
| chr6:13964795 | C | T | 1 | a0001c0001t0002g0132 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-366-9415C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13964795 | |||||||
| chr6:13964848 | T | G | 138 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(135): Show |
157 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.-366-9362T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13964848 | |||||||
| chr6:13964876 | A | G | 8 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0134 others(5): Show |
8 | HG01496.hp2 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-366-9334A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13964876 | |||||||
| chr6:13965196 | A | G | 7 | a0001c0001t0003g0017 a0001c0001t0003g0145 a0001c0001t0003g0146 others(4): Show |
8 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-366-9014A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13965196 | |||||||
| chr6:13965287 | C | G | 1 | a0001c0001t0002g0164 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-366-8923C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13965287 | |||||||
| chr6:13965445 | A | C | 3 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0182 |
3 | HG00642.hp2 HG01106.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-366-8765A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13965445 | |||||||
| chr6:13965833 | A | G | 1 | a0001c0001t0004g0108 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-366-8377A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13965833 | |||||||
| chr6:13965885 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-366-8325A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13965885 | |||||||
| chr6:13965894 | A | G | 10 | a0001c0001t0002g0013 a0001c0001t0002g0038 a0001c0001t0002g0040 others(7): Show |
11 | HG01071.hp1 HG01175.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.-366-8316A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13965894 | |||||||
| chr6:13965926 | G | A | 227 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(224): Show |
254 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.-366-8284G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13965926 | |||||||
| chr6:13965949 | G | C | 13 | a0001c0001t0005g0001 a0001c0001t0005g0185 a0001c0001t0005g0186 others(10): Show |
18 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-366-8261G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13965949 | |||||||
| chr6:13965998 | A | G | 2 | a0001c0001t0001g0295 a0001c0001t0017g0032 |
3 | HG01255.hp2 HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-366-8212A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13965998 | |||||||
| chr6:13966007 | A | C | 14 | a0001c0001t0005g0001 a0001c0001t0005g0185 a0001c0001t0005g0186 others(11): Show |
19 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-366-8203A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966007 | |||||||
| chr6:13966019 | A | T | 3 | a0001c0001t0011g0159 a0001c0001t0015g0171 a0001c0001t0015g0172 |
3 | HG02055.hp1 HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-366-8191A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966019 | |||||||
| chr6:13966151 | C | T | 115 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(112): Show |
129 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.-366-8059C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966151 | |||||||
| chr6:13966292 | A | G | 116 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(113): Show |
130 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.-366-7918A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966292 | |||||||
| chr6:13966543 | G | A | 115 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(112): Show |
129 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.-366-7667G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966543 | |||||||
| chr6:13966592 | G | A | 2 | a0001c0001t0003g0213 a0001c0001t0016g0060 |
2 | HG00738.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.-366-7618G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966592 | |||||||
| chr6:13966624 | G | A | 6 | a0001c0001t0005g0001 a0001c0001t0005g0185 a0001c0001t0005g0186 others(3): Show |
10 | NA18942.hp2 NA18949.hp2 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-366-7586G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966624 | |||||||
| chr6:13966669 | G | A | 88 | a0001c0001t0001g0037 a0001c0001t0003g0003 a0001c0001t0003g0007 others(85): Show |
96 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.-366-7541G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966669 | |||||||
| chr6:13966693 | G | T | 4 | a0001c0001t0011g0174 a0001c0001t0011g0220 a0001c0001t0011g0310 others(1): Show |
4 | HG01884.hp2 HG02145.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-366-7517G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966693 | |||||||
| chr6:13966826 | G | A | 2 | a0001c0002t0006g0151 a0001c0002t0006g0173 |
2 | HG01243.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-366-7384G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966826 | |||||||
| chr6:13966828 | G | A | 1 | a0001c0001t0014g0299 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-366-7382G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966828 | |||||||
| chr6:13966832 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-366-7378G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966832 | |||||||
| chr6:13966832 | G | GTA | 94 | a0001c0001t0001g0037 a0001c0001t0003g0003 a0001c0001t0003g0007 others(91): Show |
106 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.-366-7377_-366-737 others(6): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13966832 | ||||||
| chr6:13966834 | G | A | 128 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(125): Show |
143 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.-366-7376G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966834 | |||||||
| chr6:13966835 | T | C | 1 | a0001c0001t0002g0164 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-366-7375T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966835 | |||||||
| chr6:13966836 | G | A | 5 | a0001c0001t0002g0152 a0001c0001t0009g0133 a0001c0001t0009g0135 others(2): Show |
5 | HG01496.hp2 HG03139.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.-366-7374G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966836 | |||||||
| chr6:13966840 | G | GTGCGCGT others(11): Show |
4 | a0001c0001t0011g0159 a0001c0001t0015g0171 a0001c0001t0015g0172 others(1): Show |
4 | HG02055.hp1 HG02055.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-366-7368_-366-736 others(22): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13966840 | ||||||
| chr6:13966889 | T | C | 89 | a0001c0001t0001g0037 a0001c0001t0003g0003 a0001c0001t0003g0007 others(86): Show |
97 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.-366-7321T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966889 | |||||||
| chr6:13967215 | G | A | 1 | a0001c0001t0012g0168 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-366-6995G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13967215 | |||||||
| chr6:13967281 | A | G | 1 | a0001c0001t0020g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-366-6929A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13967281 | |||||||
| chr6:13967318 | A | C | 1 | a0001c0001t0004g0101 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-366-6892A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13967318 | |||||||
| chr6:13967623 | T | C | 1 | a0001c0001t0002g0094 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-366-6587T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13967623 | |||||||
| chr6:13967626 | A | T | 2 | a0001c0001t0013g0020 a0001c0001t0013g0183 |
3 | HG01243.hp2 HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-366-6584A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13967626 | |||||||
| chr6:13967745 | T | A | 3 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0134 |
3 | HG02145.hp1 HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-366-6465T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13967745 | |||||||
| chr6:13967746 | A | T | 1 | a0001c0001t0012g0168 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-366-6464A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13967746 | |||||||
| chr6:13967849 | C | A | 1 | a0001c0001t0001g0123 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-366-6361C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13967849 | |||||||
| chr6:13967849 | C | G | 114 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(111): Show |
128 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.-366-6361C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13967849 | |||||||
| chr6:13968038 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-366-6172T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13968038 | |||||||
| chr6:13968058 | A | G | 114 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(111): Show |
128 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.-366-6152A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13968058 | |||||||
| chr6:13968080 | T | TA | 115 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(112): Show |
129 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.-366-6129dupA | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13968080 | ||||||
| chr6:13968191 | GTAAT | G | 4 | a0001c0001t0011g0159 a0001c0001t0015g0171 a0001c0001t0015g0172 others(1): Show |
4 | HG02055.hp1 HG02055.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-366-6014_-366-601 others(8): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13968191 | ||||||
| chr6:13968225 | A | G | 2 | a0001c0001t0015g0171 a0001c0001t0015g0172 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-366-5985A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13968225 | |||||||
| chr6:13968540 | C | T | 1 | a0001c0001t0002g0242 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-366-5670C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13968540 | |||||||
| chr6:13968541 | G | A | 3 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0134 |
3 | HG02145.hp1 HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-366-5669G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13968541 | |||||||
| chr6:13968658 | G | A | 6 | a0001c0001t0011g0174 a0001c0001t0011g0220 a0001c0001t0011g0310 others(3): Show |
7 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-366-5552G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13968658 | |||||||
| chr6:13968761 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-366-5449T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13968761 | |||||||
| chr6:13968936 | C | T | 2 | a0001c0001t0002g0129 a0001c0001t0002g0139 |
2 | HG01884.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.-366-5274C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13968936 | |||||||
| chr6:13969048 | T | C | 4 | a0001c0001t0011g0159 a0001c0001t0015g0171 a0001c0001t0015g0172 others(1): Show |
4 | HG02055.hp1 HG02055.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-366-5162T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13969048 | |||||||
| chr6:13969105 | T | TTTG | 79 | a0001c0001t0001g0037 a0001c0001t0002g0126 a0001c0001t0002g0155 others(76): Show |
83 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.-366-5078_-366-507 others(7): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13969105 | ||||||
| chr6:13969105 | T | TTTGTTG | 16 | a0001c0001t0003g0003 a0001c0001t0003g0022 a0001c0001t0003g0103 others(13): Show |
20 | HG00408.hp1 HG00609.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.-366-5081_-366-507 others(10): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13969105 | ||||||
| chr6:13969105 | TTTGTTGT others(5): Show |
T | 1 | a0001c0001t0002g0036 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-366-5087_-366-507 others(16): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13969105 | ||||||
| chr6:13969108 | G | T | 8 | a0001c0001t0002g0094 a0001c0001t0002g0152 a0001c0001t0009g0133 others(5): Show |
8 | HG01496.hp2 HG01884.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-366-5102G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13969108 | |||||||
| chr6:13969111 | G | T | 3 | a0001c0001t0011g0174 a0001c0001t0011g0310 a0001c0001t0030g0144 |
3 | HG02145.hp2 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-366-5099G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13969111 | |||||||
| chr6:13969192 | C | A | 115 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(112): Show |
129 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.-366-5018C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13969192 | |||||||
| chr6:13969219 | T | C | 238 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(235): Show |
266 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.-366-4991T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13969219 | |||||||
| chr6:13969267 | C | T | 4 | a0001c0001t0011g0174 a0001c0001t0011g0220 a0001c0001t0011g0310 others(1): Show |
4 | HG01884.hp2 HG02145.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-366-4943C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13969267 | |||||||
| chr6:13969317 | T | G | 1 | a0001c0001t0001g0065 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-366-4893T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13969317 | |||||||
| chr6:13969494 | C | T | 3 | a0001c0004t0003g0176 a0001c0004t0003g0177 a0001c0004t0003g0178 |
3 | NA18946.hp2 NA18968.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.-366-4716C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13969494 | |||||||
| chr6:13969497 | G | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(117): Show |
138 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.-366-4713G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13969497 | |||||||
| chr6:13969581 | A | G | 2 | a0001c0001t0009g0133 a0001c0001t0009g0135 |
2 | HG01496.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-366-4629A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13969581 | |||||||
| chr6:13969659 | G | T | 115 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(112): Show |
129 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.-366-4551G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13969659 | |||||||
| chr6:13969719 | A | G | 3 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0134 |
3 | HG02145.hp1 HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-366-4491A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13969719 | |||||||
| chr6:13969763 | ATTAT | A | 3 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0134 |
3 | HG02145.hp1 HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-366-4440_-366-443 others(8): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13969763 | ||||||
| chr6:13969832 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-366-4378A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13969832 | |||||||
| chr6:13969841 | A | AG | 91 | a0001c0001t0001g0037 a0001c0001t0003g0003 a0001c0001t0003g0007 others(88): Show |
99 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.-366-4368dupG | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13969841 | ||||||
| chr6:13969971 | T | G | 10 | a0001c0001t0002g0152 a0001c0001t0009g0133 a0001c0001t0009g0135 others(7): Show |
10 | HG01496.hp2 HG01884.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-366-4239T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13969971 | |||||||
| chr6:13970032 | A | G | 86 | a0001c0001t0001g0037 a0001c0001t0003g0003 a0001c0001t0003g0007 others(83): Show |
94 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.-366-4178A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13970032 | |||||||
| chr6:13970101 | A | G | 2 | a0001c0001t0013g0020 a0001c0001t0013g0183 |
3 | HG01243.hp2 HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-366-4109A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13970101 | |||||||
| chr6:13970161 | G | A | 3 | a0001c0001t0003g0232 a0001c0001t0003g0260 a0001c0001t0004g0203 |
3 | HG02602.hp2 NA18993.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.-366-4049G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13970161 | |||||||
| chr6:13970287 | C | T | 1 | a0001c0001t0003g0147 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-366-3923C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13970287 | |||||||
| chr6:13970336 | A | G | 7 | a0001c0001t0011g0159 a0001c0001t0011g0174 a0001c0001t0011g0220 others(4): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-366-3874A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13970336 | |||||||
| chr6:13970467 | A | G | 1 | a0001c0001t0003g0232 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-366-3743A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13970467 | |||||||
| chr6:13970578 | A | T | 2 | a0001c0001t0020g0113 a0001c0001t0021g0104 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-366-3632A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13970578 | |||||||
| chr6:13970610 | A | G | 229 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(226): Show |
256 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.-366-3600A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13970610 | |||||||
| chr6:13970737 | A | G | 1 | a0001c0001t0036g0161 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-366-3473A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13970737 | |||||||
| chr6:13970767 | G | C | 2 | a0001c0001t0020g0113 a0001c0001t0021g0104 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-366-3443G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13970767 | |||||||
| chr6:13970790 | A | G | 7 | a0001c0001t0005g0001 a0001c0001t0005g0185 a0001c0001t0005g0186 others(4): Show |
11 | HG02109.hp2 NA18942.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-366-3420A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13970790 | |||||||
| chr6:13970828 | C | T | 1 | a0001c0001t0003g0211 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-366-3382C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13970828 | |||||||
| chr6:13971110 | G | A | 4 | a0001c0001t0001g0302 a0001c0001t0001g0304 a0001c0001t0001g0305 others(1): Show |
4 | NA18612.hp1 NA18939.hp2 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.-366-3100G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13971110 | |||||||
| chr6:13971113 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-366-3097G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13971113 | |||||||
| chr6:13971130 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0052 |
4 | NA18963.hp1 NA18987.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.-366-3080G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13971130 | |||||||
| chr6:13971437 | C | T | 1 | a0001c0001t0004g0300 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-366-2773C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13971437 | |||||||
| chr6:13971464 | G | A | 3 | a0001c0001t0005g0185 a0001c0001t0005g0186 a0001c0001t0005g0187 |
3 | NA18949.hp2 NA19058.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.-366-2746G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13971464 | |||||||
| chr6:13971505 | G | A | 131 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(128): Show |
149 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(146): Show |
intron_variant | MODIFIER | c.-366-2705G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13971505 | |||||||
| chr6:13971521 | A | G | 2 | a0001c0001t0002g0119 a0001c0001t0002g0120 |
2 | HG03491.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-366-2689A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13971521 | |||||||
| chr6:13971558 | A | C | 1 | a0001c0001t0001g0081 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-366-2652A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13971558 | |||||||
| chr6:13971635 | T | C | 1 | a0001c0001t0036g0161 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-366-2575T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13971635 | |||||||
| chr6:13971658 | T | C | 90 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0017 others(87): Show |
98 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.-366-2552T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13971658 | |||||||
| chr6:13972018 | C | T | 1 | a0001c0001t0008g0170 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-366-2192C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13972018 | |||||||
| chr6:13972270 | A | C | 1 | a0001c0001t0010g0228 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-366-1940A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13972270 | |||||||
| chr6:13972294 | G | A | 1 | a0001c0003t0001g0099 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-366-1916G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13972294 | |||||||
| chr6:13972304 | C | CA | 14 | a0001c0001t0001g0309 a0001c0001t0002g0152 a0001c0001t0002g0265 others(11): Show |
17 | HG00609.hp2 HG01496.hp2 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.-366-1889dupA | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13972304 | ||||||
| chr6:13972332 | A | G | 1 | a0001c0001t0003g0157 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-366-1878A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13972332 | |||||||
| chr6:13972349 | C | T | 2 | a0001c0001t0020g0113 a0001c0001t0021g0104 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-366-1861C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13972349 | |||||||
| chr6:13972716 | G | A | 1 | a0001c0001t0036g0161 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-366-1494G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13972716 | |||||||
| chr6:13973018 | G | A | 131 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(128): Show |
149 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(146): Show |
intron_variant | MODIFIER | c.-366-1192G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13973018 | |||||||
| chr6:13973059 | A | G | 2 | a0001c0001t0020g0113 a0001c0001t0021g0104 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-366-1151A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13973059 | |||||||
| chr6:13973155 | G | A | 1 | a0001c0001t0013g0020 | 2 | HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-366-1055G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13973155 | |||||||
| chr6:13973242 | G | T | 1 | a0001c0001t0001g0292 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-366-968G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13973242 | |||||||
| chr6:13973254 | C | G | 1 | a0001c0001t0001g0292 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-366-956C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13973254 | |||||||
| chr6:13973788 | A | G | 3 | a0001c0001t0003g0202 a0001c0001t0003g0226 a0001c0001t0016g0205 |
3 | NA18977.hp1 NA19072.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-366-422A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13973788 | |||||||
| chr6:13973852 | C | T | 1 | a0001c0001t0002g0111 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-366-358C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13973852 | |||||||
| chr6:13974084 | T | C | 1 | a0001c0001t0002g0155 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-366-126T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13974084 | |||||||
| chr6:13974431 | T | C | 5 | a0001c0001t0011g0174 a0001c0001t0011g0220 a0001c0001t0011g0310 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.-212+67T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13974431 | |||||||
| chr6:13974472 | C | T | 2 | a0001c0001t0020g0113 a0001c0001t0021g0104 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-212+108C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13974472 | |||||||
| chr6:13974714 | C | T | 2 | a0001c0001t0013g0020 a0001c0001t0013g0183 |
3 | HG01243.hp2 HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-212+350C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13974714 | |||||||
| chr6:13974875 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-212+511C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13974875 | |||||||
| chr6:13974879 | A | T | 1 | a0001c0001t0001g0086 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-212+515A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13974879 | |||||||
| chr6:13974961 | G | T | 2 | a0001c0001t0013g0020 a0001c0001t0013g0183 |
3 | HG01243.hp2 HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-212+597G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13974961 | |||||||
| chr6:13975025 | A | T | 88 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0017 others(85): Show |
96 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.-212+661A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13975025 | |||||||
| chr6:13975059 | A | G | 1 | a0001c0001t0011g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-212+695A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13975059 | |||||||
| chr6:13975143 | A | G | 1 | a0001c0001t0002g0155 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-212+779A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13975143 | |||||||
| chr6:13975327 | G | A | 2 | a0001c0001t0020g0113 a0001c0001t0021g0104 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-212+963G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13975327 | |||||||
| chr6:13975369 | G | T | 1 | a0001c0001t0036g0161 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-212+1005G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13975369 | |||||||
| chr6:13975400 | G | T | 12 | a0001c0001t0005g0001 a0001c0001t0005g0185 a0001c0001t0005g0186 others(9): Show |
16 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-212+1036G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13975400 | |||||||
| chr6:13975431 | C | T | 1 | a0001c0001t0029g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-212+1067C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13975431 | |||||||
| chr6:13975439 | C | T | 116 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(113): Show |
130 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.-212+1075C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13975439 | |||||||
| chr6:13975704 | A | G | 1 | a0001c0001t0013g0183 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-211-1205A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13975704 | |||||||
| chr6:13975910 | G | C | 12 | a0001c0001t0005g0001 a0001c0001t0005g0185 a0001c0001t0005g0186 others(9): Show |
16 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-211-999G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13975910 | |||||||
| chr6:13975970 | T | C | 2 | a0001c0001t0015g0171 a0001c0001t0015g0172 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-211-939T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13975970 | |||||||
| chr6:13976121 | A | G | 1 | a0001c0001t0036g0161 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-211-788A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13976121 | |||||||
| chr6:13976200 | G | A | 1 | a0001c0001t0003g0231 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-211-709G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13976200 | |||||||
| chr6:13976234 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-211-675G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13976234 | |||||||
| chr6:13976328 | A | G | 1 | a0001c0001t0036g0161 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-211-581A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13976328 | |||||||
| chr6:13976334 | C | T | 3 | a0001c0001t0002g0152 a0001c0001t0009g0133 a0001c0001t0009g0135 |
3 | HG01496.hp2 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-211-575C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13976334 | |||||||
| chr6:13976344 | A | G | 3 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 |
3 | HG02896.hp2 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-211-565A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13976344 | |||||||
| chr6:13976378 | A | T | 1 | a0001c0001t0001g0114 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-211-531A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13976378 | |||||||
| chr6:13976399 | A | G | 1 | a0001c0001t0001g0306 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-211-510A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13976399 | |||||||
| chr6:13976706 | A | G | 1 | a0001c0001t0036g0161 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-211-203A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13976706 | |||||||
| chr6:13976738 | A | T | 116 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(113): Show |
130 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.-211-171A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13976738 | |||||||
| chr6:13976751 | G | A | 2 | a0001c0001t0002g0248 a0001c0001t0002g0285 |
2 | NA18966.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.-211-158G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13976751 | |||||||
| chr6:13976755 | C | T | 222 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(219): Show |
249 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.-211-154C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13976755 |