Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 81790 |
| ensemblid | ENSG00000120925.16 |
| hgncid | 25358 |
| symbol | RNF170 |
| name | ring finger protein 170 |
| refseq_nuc | NM_030954.4 |
| refseq_prot | NP_112216.3 |
| ensembl_nuc | ENST00000527424.6 |
| ensembl_prot | ENSP00000434797.1 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 42853301 |
| end | 42896605 |
| strand | - |
| ver | v1.2 |
| region | chr8:42853301-42896605 |
| region5000 | chr8:42848301-42901605 |
| regionname0 | RNF170_chr8_42853301_42896605 |
| regionname5000 | RNF170_chr8_42848301_42901605 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 258 | 207 | 76 | 54 | 53 | 2 | 20 | 24 | RNF170_chr8_42848301_42901605 | RNF170 | MAKYQ others(253): Show |
chr8 | 42848301 | 42901605 |
| a0002 | 0/0 | 258 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | MAKYQ others(253): Show |
chr8 | 42848301 | 42901605 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 774 | 192 | 62 | 53 | 53 | 2 | 20 | RNF170_chr8_42848301_42901605 | RNF170 | ATGGC others(769): Show |
chr8 | 42848301 | 42901605 | ||
| a0001c0002 | 0/0 | 774 | 15 | 14 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | ATGGC others(769): Show |
chr8 | 42848301 | 42901605 | ||
| a0002c0003 | 0/0 | 774 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | ATGGC others(769): Show |
chr8 | 42848301 | 42901605 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3764 | 157 | 40 | 49 | 50 | 2 | 14 | RNF170_chr8_42848301_42901605 | RNF170 | GCACT others(3759): Show |
chr8 | 42848301 | 42901605 |
| a0001c0001t0002 | 0/0 | 3764 | 4 | 4 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | GCACT others(3759): Show |
chr8 | 42848301 | 42901605 |
| a0001c0001t0003 | 0/0 | 3765 | 10 | 9 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | GCACT others(3760): Show |
chr8 | 42848301 | 42901605 |
| a0001c0001t0004 | 0/0 | 3765 | 8 | 0 | 2 | 2 | 0 | 4 | RNF170_chr8_42848301_42901605 | RNF170 | GCACT others(3760): Show |
chr8 | 42848301 | 42901605 |
| a0001c0001t0005 | 0/0 | 3764 | 4 | 4 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | GCACT others(3759): Show |
chr8 | 42848301 | 42901605 |
| a0001c0001t0006 | 0/0 | 3764 | 2 | 0 | 1 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | GCACT others(3759): Show |
chr8 | 42848301 | 42901605 |
| a0001c0001t0007 | 0/0 | 3764 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | GCACT others(3759): Show |
chr8 | 42848301 | 42901605 |
| a0001c0001t0008 | 0/0 | 3764 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | GCACT others(3759): Show |
chr8 | 42848301 | 42901605 |
| a0001c0001t0009 | 0/0 | 3766 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | GCACT others(3761): Show |
chr8 | 42848301 | 42901605 |
| a0001c0001t0010 | 0/0 | 3764 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | GCACT others(3759): Show |
chr8 | 42848301 | 42901605 |
| a0001c0001t0011 | 0/0 | 3764 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | GCACT others(3759): Show |
chr8 | 42848301 | 42901605 |
| a0001c0001t0012 | 0/0 | 3764 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | GCACT others(3759): Show |
chr8 | 42848301 | 42901605 |
| a0001c0001t0013 | 0/0 | 3764 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | GCACT others(3759): Show |
chr8 | 42848301 | 42901605 |
| a0001c0002t0002 | 0/0 | 3764 | 15 | 14 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | GCACT others(3759): Show |
chr8 | 42848301 | 42901605 |
| a0002c0003t0001 | 0/0 | 3764 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | GCACT others(3759): Show |
chr8 | 42848301 | 42901605 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 2 | 1 | 1 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0003 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0004 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0006 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0008 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0010 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0084 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0006g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0006g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0007g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0008g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0009g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0010g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0011g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0012g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0001t0013g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0002t0002g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0002t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0002t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0002t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0002t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0002t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0001c0002t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| a0002c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG00558 | hp2 | a0001 | c0001 | t0012 | g0106 | EAS | CHS | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0089 | EAS | CHS | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0026 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0027 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0138 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0124 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01261 | hp2 | a0001 | c0001 | t0006 | g0136 | AMR | CLM | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | ACB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02129 | hp2 | a0002 | c0003 | t0001 | g0049 | EAS | KHV | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CDX | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CDX | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0155 | AFR | ACB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0133 | AFR | ACB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0157 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0125 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0118 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0029 | SAS | PJL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02723 | hp2 | a0001 | c0001 | t0010 | g0024 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0123 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0174 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0132 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0160 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0134 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0119 | AFR | ESN | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03098 | hp1 | a0001 | c0001 | t0013 | g0188 | AFR | MSL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | MSL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0137 | AFR | ESN | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | ESN | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03139 | hp2 | a0001 | c0001 | t0009 | g0156 | AFR | ESN | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0159 | AFR | ESN | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | MSL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | MSL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0158 | AFR | MSL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0120 | AFR | MSL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03491 | hp1 | a0001 | c0001 | t0006 | g0135 | SAS | PJL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0173 | AFR | ESN | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0126 | AFR | ESN | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | MSL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03654 | hp1 | a0001 | c0001 | t0011 | g0095 | SAS | PJL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0028 | SAS | PJL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0025 | SAS | PJL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0172 | SAS | BEB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | STU | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | STU | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | STU | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | STU | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | YRI | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0186 | AFR | YRI | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0105 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | LWK | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | YRI | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | YRI | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ASW | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | ASW | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | GIH | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | GIH | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0127 | AFR | ACB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0061 | AFR | ACB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | USA | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0032 | AFR | USA | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | USA | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0084 | REF | REF | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0010 | REF | REF | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:42856374 | T | C | 1 | a0002 | 1 | HG02129.hp2 | missense_variant | MODERATE | c.562A>G | p.Met188Val | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 7/7 | 691/3764 | 562/777 | 188/258 | chr8 | 42856374 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:42870035 | C | T | 1 | a0001c0002 | 15 | HG01243.hp1 HG02109.hp1 HG02615.hp2 others(12): Show |
synonymous_variant | LOW | c.291G>A | p.Pro97Pro | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/7 | 420/3764 | 291/777 | 97/258 | chr8 | 42870035 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:42853437 | T | C | 1 | a0001c0001t0011 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2722A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 7/7 | 2722 | chr8 | 42853437 | ||||||
| chr8:42854296 | G | A | 1 | a0001c0001t0006 | 2 | HG01261.hp2 HG03491.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1863C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 7/7 | 1863 | chr8 | 42854296 | ||||||
| chr8:42854368 | T | C | 1 | a0001c0001t0005 | 4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1791A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 7/7 | 1791 | chr8 | 42854368 | ||||||
| chr8:42854500 | A | C | 1 | a0001c0001t0010 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1659T>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 7/7 | 1659 | chr8 | 42854500 | ||||||
| chr8:42854950 | A | C | 4 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(1): Show |
25 | HG01243.hp1 HG01261.hp2 HG02055.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1209T>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 7/7 | 1209 | chr8 | 42854950 | ||||||
| chr8:42855229 | C | CT | 2 | a0001c0001t0004 a0001c0001t0009 |
9 | HG00621.hp2 HG01069.hp1 HG01071.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*929dupA | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 7/7 | 929 | chr8 | 42855229 | ||||||
| chr8:42855251 | A | AG | 2 | a0001c0001t0003 a0001c0001t0009 |
11 | HG01192.hp1 HG02258.hp2 HG02615.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*907dupC | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 7/7 | 907 | chr8 | 42855251 | ||||||
| chr8:42855680 | A | C | 1 | a0001c0001t0008 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*479T>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 7/7 | 479 | chr8 | 42855680 | ||||||
| chr8:42855983 | A | C | 1 | a0001c0001t0007 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*176T>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 7/7 | 176 | chr8 | 42855983 | ||||||
| chr8:42856145 | T | A | 1 | a0001c0001t0012 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14A>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 7/7 | 14 | chr8 | 42856145 | ||||||
| chr8:42896566 | C | A | 1 | a0001c0001t0013 | 1 | HG03098.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-90G>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/7 | chr8 | 42896566 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:42856456 | A | G | 2 | a0001c0001t0006g0135 a0001c0001t0006g0136 |
2 | HG01261.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.508-28T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42856456 | |||||||
| chr8:42856463 | A | G | 39 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(36): Show |
43 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.508-35T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42856463 | |||||||
| chr8:42856632 | T | C | 1 | a0002c0003t0001g0049 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.508-204A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42856632 | |||||||
| chr8:42856739 | G | A | 1 | a0001c0001t0008g0186 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.508-311C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42856739 | |||||||
| chr8:42857269 | C | T | 6 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0145 others(3): Show |
6 | HG00423.hp1 HG00544.hp2 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.508-841G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42857269 | |||||||
| chr8:42857511 | C | G | 3 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0028 |
3 | HG01069.hp1 HG01071.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.508-1083G>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42857511 | |||||||
| chr8:42857814 | G | T | 2 | a0001c0001t0003g0174 a0001c0001t0003g0175 |
2 | HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.508-1386C>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42857814 | |||||||
| chr8:42857844 | G | C | 13 | a0001c0001t0001g0030 a0001c0001t0001g0035 a0001c0001t0001g0041 others(10): Show |
13 | HG00558.hp1 HG00597.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.508-1416C>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42857844 | |||||||
| chr8:42858009 | T | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0072 |
2 | HG00423.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.508-1581A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42858009 | |||||||
| chr8:42858021 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.508-1593G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42858021 | |||||||
| chr8:42858034 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.508-1606G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42858034 | |||||||
| chr8:42858212 | G | A | 10 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(7): Show |
10 | HG01261.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.508-1784C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42858212 | |||||||
| chr8:42858232 | GT | G | 22 | a0001c0001t0001g0150 a0001c0001t0002g0128 a0001c0001t0002g0129 others(19): Show |
26 | HG01243.hp1 HG01261.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.508-1805delA | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42858232 | |||||||
| chr8:42858357 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.508-1929C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42858357 | |||||||
| chr8:42858357 | G | T | 1 | a0001c0002t0002g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.508-1929C>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42858357 | |||||||
| chr8:42858367 | C | A | 2 | a0001c0001t0006g0135 a0001c0001t0006g0136 |
2 | HG01261.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.508-1939G>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42858367 | |||||||
| chr8:42858427 | T | C | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0076 |
3 | HG02896.hp1 HG02897.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.508-1999A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42858427 | |||||||
| chr8:42858573 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.508-2145C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42858573 | |||||||
| chr8:42858766 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0079 |
2 | HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.508-2338C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42858766 | |||||||
| chr8:42859027 | A | G | 19 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(16): Show |
20 | HG00438.hp1 HG00544.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.508-2599T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42859027 | |||||||
| chr8:42859325 | G | A | 3 | a0001c0001t0001g0052 a0001c0001t0001g0072 a0001c0001t0001g0087 |
3 | HG00423.hp2 NA18962.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.507+2420C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42859325 | |||||||
| chr8:42859364 | G | A | 5 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.507+2381C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42859364 | |||||||
| chr8:42859462 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.507+2283G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42859462 | |||||||
| chr8:42859575 | C | T | 1 | a0001c0002t0002g0124 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.507+2170G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42859575 | |||||||
| chr8:42859704 | A | G | 16 | a0001c0001t0003g0138 a0001c0001t0003g0155 a0001c0001t0003g0157 others(13): Show |
16 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.507+2041T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42859704 | |||||||
| chr8:42860503 | A | G | 5 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.507+1242T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42860503 | |||||||
| chr8:42860567 | C | A | 1 | a0001c0001t0001g0091 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.507+1178G>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42860567 | |||||||
| chr8:42860917 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.507+828G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42860917 | |||||||
| chr8:42860918 | G | A | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.507+827C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42860918 | |||||||
| chr8:42860964 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.507+781G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42860964 | |||||||
| chr8:42861320 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.507+425T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42861320 | |||||||
| chr8:42861655 | A | G | 1 | a0001c0001t0001g0059 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.507+90T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42861655 | |||||||
| chr8:42861994 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.397-139C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42861994 | |||||||
| chr8:42862086 | A | G | 1 | a0001c0001t0001g0150 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.397-231T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42862086 | |||||||
| chr8:42862100 | A | C | 1 | a0001c0001t0001g0146 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.397-245T>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42862100 | |||||||
| chr8:42862110 | A | G | 8 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0119 others(5): Show |
12 | HG01243.hp1 HG02615.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.397-255T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42862110 | |||||||
| chr8:42862133 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.397-278G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42862133 | |||||||
| chr8:42862298 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.397-443G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42862298 | |||||||
| chr8:42862306 | A | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0171 |
3 | HG01070.hp1 HG01071.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.397-451T>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42862306 | |||||||
| chr8:42862363 | T | G | 1 | a0001c0001t0003g0175 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.397-508A>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42862363 | |||||||
| chr8:42862693 | G | A | 1 | a0001c0002t0002g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.397-838C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42862693 | |||||||
| chr8:42862763 | T | C | 4 | a0001c0001t0005g0032 a0001c0001t0005g0132 a0001c0001t0005g0133 others(1): Show |
4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.397-908A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42862763 | |||||||
| chr8:42862800 | C | T | 11 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0118 others(8): Show |
15 | HG01243.hp1 HG02109.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.397-945G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42862800 | |||||||
| chr8:42862905 | C | T | 3 | a0001c0001t0001g0004 a0001c0001t0001g0065 a0001c0001t0001g0080 |
5 | HG00280.hp2 HG00735.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.397-1050G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42862905 | |||||||
| chr8:42863035 | G | T | 1 | a0001c0001t0001g0066 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.397-1180C>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863035 | |||||||
| chr8:42863083 | G | A | 10 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(7): Show |
10 | HG01261.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.397-1228C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863083 | |||||||
| chr8:42863301 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.397-1446A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863301 | |||||||
| chr8:42863419 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.397-1564T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863419 | |||||||
| chr8:42863423 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.397-1568G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863423 | |||||||
| chr8:42863454 | T | A | 3 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0028 |
3 | HG01069.hp1 HG01071.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.397-1599A>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863454 | |||||||
| chr8:42863473 | C | G | 21 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(18): Show |
25 | HG01243.hp1 HG01261.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.397-1618G>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863473 | |||||||
| chr8:42863473 | C | T | 1 | a0001c0001t0004g0089 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.397-1618G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863473 | |||||||
| chr8:42863498 | G | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG00738.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.397-1643C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863498 | |||||||
| chr8:42863590 | C | T | 10 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(7): Show |
10 | HG01261.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.397-1735G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863590 | |||||||
| chr8:42863678 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.396+1738C>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863678 | |||||||
| chr8:42863842 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.396+1574A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863842 | |||||||
| chr8:42863964 | G | GGA | 6 | a0001c0001t0001g0177 a0001c0001t0004g0025 a0001c0001t0004g0026 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.396+1450_396+1451d others(4): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863964 | |||||||
| chr8:42863964 | G | GGAGA | 3 | a0001c0002t0002g0012 a0001c0002t0002g0120 a0001c0002t0002g0124 |
4 | HG01243.hp1 HG02615.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.396+1448_396+1451d others(6): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863964 | |||||||
| chr8:42863978 | AGAGTGTG others(17): Show |
A | 1 | a0001c0001t0001g0085 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.396+1414_396+1437d others(26): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863978 | |||||||
| chr8:42863980 | A | AGAGT | 8 | a0001c0001t0001g0036 a0001c0002t0002g0002 a0001c0002t0002g0119 others(5): Show |
11 | HG02109.hp1 HG02622.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.396+1435_396+1436i others(6): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863980 | |||||||
| chr8:42863980 | A | AGT | 22 | a0001c0001t0001g0013 a0001c0001t0001g0057 a0001c0001t0001g0110 others(19): Show |
23 | HG00673.hp1 HG01070.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.396+1434_396+1435d others(4): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863980 | |||||||
| chr8:42863980 | A | AGTGT | 66 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(63): Show |
76 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.396+1432_396+1435d others(6): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863980 | |||||||
| chr8:42863980 | A | AGTGTGT | 14 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0031 others(11): Show |
14 | HG00597.hp2 HG01993.hp1 HG01993.hp2 others(11): Show |
intron_variant | MODIFIER | c.396+1430_396+1435d others(8): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863980 | |||||||
| chr8:42863980 | A | AGTGTGTG others(3): Show |
1 | a0001c0001t0001g0009 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.396+1426_396+1435d others(12): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863980 | |||||||
| chr8:42863980 | A | AGTGTGTG others(7): Show |
1 | a0001c0001t0001g0039 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.396+1422_396+1435d others(16): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863980 | |||||||
| chr8:42863980 | AGT | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0034 |
2 | HG01361.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.396+1434_396+1435d others(4): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863980 | |||||||
| chr8:42863980 | AGTGT | A | 2 | a0001c0001t0001g0041 a0001c0001t0007g0061 |
2 | HG01074.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.396+1432_396+1435d others(6): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863980 | |||||||
| chr8:42863980 | AGTGTGTG others(1): Show |
A | 11 | a0001c0001t0003g0138 a0001c0001t0003g0155 a0001c0001t0003g0157 others(8): Show |
11 | HG01192.hp1 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.396+1428_396+1435d others(10): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863980 | |||||||
| chr8:42863982 | T | A | 14 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0143 others(11): Show |
14 | HG00544.hp2 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.396+1434A>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863982 | |||||||
| chr8:42863982 | T | TGG | 8 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(5): Show |
8 | HG01261.hp2 HG02055.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.396+1433_396+1434i others(4): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863982 | |||||||
| chr8:42863984 | T | G | 2 | a0001c0001t0005g0032 a0001c0001t0005g0133 |
2 | HG02451.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.396+1432A>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863984 | |||||||
| chr8:42863990 | T | A | 11 | a0001c0001t0003g0138 a0001c0001t0003g0155 a0001c0001t0003g0157 others(8): Show |
11 | HG01192.hp1 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.396+1426A>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863990 | |||||||
| chr8:42863992 | T | A | 11 | a0001c0001t0003g0138 a0001c0001t0003g0155 a0001c0001t0003g0157 others(8): Show |
11 | HG01192.hp1 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.396+1424A>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863992 | |||||||
| chr8:42864045 | CT | C | 12 | a0001c0001t0001g0041 a0001c0001t0003g0138 a0001c0001t0003g0155 others(9): Show |
12 | HG01074.hp1 HG01192.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.396+1370delA | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42864045 | |||||||
| chr8:42864376 | C | T | 11 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0118 others(8): Show |
15 | HG01243.hp1 HG02109.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.396+1040G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42864376 | |||||||
| chr8:42864392 | C | T | 8 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(5): Show |
8 | HG02055.hp2 HG02451.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.396+1024G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42864392 | |||||||
| chr8:42864810 | A | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0081 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.396+606T>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42864810 | |||||||
| chr8:42864937 | C | T | 1 | a0001c0002t0002g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.396+479G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42864937 | |||||||
| chr8:42864955 | T | TA | 22 | a0001c0001t0001g0146 a0001c0001t0002g0128 a0001c0001t0002g0129 others(19): Show |
26 | HG01243.hp1 HG01261.hp2 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.396+460dupT | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42864955 | |||||||
| chr8:42865239 | CAAAAAAA others(3): Show |
C | 11 | a0001c0001t0003g0138 a0001c0001t0003g0155 a0001c0001t0003g0157 others(8): Show |
11 | HG01192.hp1 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.396+167_396+176del others(10): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42865239 | |||||||
| chr8:42865594 | C | T | 4 | a0001c0001t0005g0032 a0001c0001t0005g0132 a0001c0001t0005g0133 others(1): Show |
4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.323-105G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42865594 | |||||||
| chr8:42865847 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.323-358G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42865847 | |||||||
| chr8:42866155 | T | C | 8 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0119 others(5): Show |
12 | HG01243.hp1 HG02615.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.323-666A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42866155 | |||||||
| chr8:42866306 | C | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0073 |
2 | NA18939.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.323-817G>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42866306 | |||||||
| chr8:42866398 | G | A | 11 | a0001c0001t0003g0138 a0001c0001t0003g0155 a0001c0001t0003g0157 others(8): Show |
11 | HG01192.hp1 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.323-909C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42866398 | |||||||
| chr8:42866447 | A | G | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.323-958T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42866447 | |||||||
| chr8:42866478 | G | C | 51 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0016 others(48): Show |
53 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.323-989C>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42866478 | |||||||
| chr8:42866622 | A | G | 90 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0016 others(87): Show |
96 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.323-1133T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42866622 | |||||||
| chr8:42866869 | CT | C | 2 | a0001c0001t0006g0135 a0001c0001t0006g0136 |
2 | HG01261.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.323-1381delA | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42866869 | |||||||
| chr8:42867106 | A | T | 1 | a0001c0001t0001g0166 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.323-1617T>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42867106 | |||||||
| chr8:42867269 | C | T | 16 | a0001c0001t0003g0138 a0001c0001t0003g0155 a0001c0001t0003g0157 others(13): Show |
16 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.323-1780G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42867269 | |||||||
| chr8:42867398 | G | A | 51 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0016 others(48): Show |
53 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.323-1909C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42867398 | |||||||
| chr8:42867442 | G | A | 1 | a0001c0001t0010g0024 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.323-1953C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42867442 | |||||||
| chr8:42867471 | C | CA | 6 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0050 others(3): Show |
7 | HG00673.hp2 HG01069.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.323-1983dupT | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42867471 | |||||||
| chr8:42867471 | CA | C | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
111 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.323-1983delT | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42867471 | |||||||
| chr8:42867471 | CAA | C | 12 | a0001c0001t0003g0138 a0001c0001t0003g0155 a0001c0001t0003g0157 others(9): Show |
12 | HG01192.hp1 HG02258.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.323-1984_323-1983d others(4): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42867471 | |||||||
| chr8:42867498 | G | A | 5 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.323-2009C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42867498 | |||||||
| chr8:42867557 | C | T | 21 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(18): Show |
25 | HG01243.hp1 HG01261.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.323-2068G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42867557 | |||||||
| chr8:42867775 | C | CA | 27 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0054 others(24): Show |
31 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.322+2228dupT | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42867775 | |||||||
| chr8:42867775 | CA | C | 5 | a0001c0001t0001g0058 a0001c0001t0001g0062 a0001c0001t0004g0026 others(2): Show |
5 | HG00558.hp2 HG01069.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.322+2228delT | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42867775 | |||||||
| chr8:42867796 | A | G | 2 | a0001c0001t0003g0174 a0001c0001t0003g0175 |
2 | HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.322+2208T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42867796 | |||||||
| chr8:42867987 | T | C | 1 | a0001c0001t0004g0029 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.322+2017A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42867987 | |||||||
| chr8:42868309 | A | G | 2 | a0001c0001t0001g0057 a0001c0001t0001g0110 |
2 | HG02280.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.322+1695T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42868309 | |||||||
| chr8:42868651 | G | A | 5 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.322+1353C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42868651 | |||||||
| chr8:42868724 | C | T | 1 | a0001c0001t0004g0025 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.322+1280G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42868724 | |||||||
| chr8:42868806 | C | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0072 |
2 | HG00423.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.322+1198G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42868806 | |||||||
| chr8:42868848 | T | C | 1 | a0001c0002t0002g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.322+1156A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42868848 | |||||||
| chr8:42868851 | C | CA | 7 | a0001c0001t0001g0054 a0001c0001t0001g0144 a0001c0001t0001g0154 others(4): Show |
7 | HG01168.hp1 HG01192.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.322+1152dupT | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42868851 | |||||||
| chr8:42868851 | CA | C | 17 | a0001c0001t0001g0030 a0001c0001t0001g0053 a0001c0001t0001g0055 others(14): Show |
17 | HG01069.hp1 HG01070.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.322+1152delT | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42868851 | |||||||
| chr8:42869471 | C | T | 1 | a0001c0001t0010g0024 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.322+533G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42869471 | |||||||
| chr8:42869513 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.322+491G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42869513 | |||||||
| chr8:42869547 | A | T | 4 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(1): Show |
4 | HG02055.hp2 HG03209.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.322+457T>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42869547 | |||||||
| chr8:42869863 | T | C | 11 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0118 others(8): Show |
15 | HG01243.hp1 HG02109.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.322+141A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42869863 | |||||||
| chr8:42869991 | G | A | 11 | a0001c0001t0003g0138 a0001c0001t0003g0155 a0001c0001t0003g0157 others(8): Show |
11 | HG01192.hp1 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.322+13C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42869991 | |||||||
| chr8:42870291 | A | G | 1 | a0001c0001t0001g0046 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.214-179T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42870291 | |||||||
| chr8:42870420 | A | G | 8 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0119 others(5): Show |
12 | HG01243.hp1 HG02615.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.214-308T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42870420 | |||||||
| chr8:42870465 | G | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0065 a0001c0001t0001g0080 |
5 | HG00280.hp2 HG00735.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.214-353C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42870465 | |||||||
| chr8:42870552 | C | A | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0076 |
3 | HG02896.hp1 HG02897.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.214-440G>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42870552 | |||||||
| chr8:42870595 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.214-483A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42870595 | |||||||
| chr8:42870930 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.214-818G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42870930 | |||||||
| chr8:42871170 | G | A | 1 | a0001c0001t0010g0024 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.214-1058C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42871170 | |||||||
| chr8:42871750 | G | C | 11 | a0001c0001t0003g0138 a0001c0001t0003g0155 a0001c0001t0003g0157 others(8): Show |
11 | HG01192.hp1 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.214-1638C>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42871750 | |||||||
| chr8:42871850 | C | T | 1 | a0001c0001t0001g0035 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.214-1738G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42871850 | |||||||
| chr8:42872309 | G | A | 34 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(31): Show |
38 | HG01192.hp1 HG01243.hp1 HG01261.hp2 others(35): Show |
intron_variant | MODIFIER | c.213+1622C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42872309 | |||||||
| chr8:42872408 | A | G | 1 | a0001c0001t0010g0024 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.213+1523T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42872408 | |||||||
| chr8:42872658 | G | T | 51 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0016 others(48): Show |
53 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.213+1273C>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42872658 | |||||||
| chr8:42872723 | G | A | 5 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.213+1208C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42872723 | |||||||
| chr8:42872780 | T | G | 5 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.213+1151A>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42872780 | |||||||
| chr8:42873013 | G | C | 1 | a0001c0001t0001g0064 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.213+918C>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42873013 | |||||||
| chr8:42873164 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.213+767C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42873164 | |||||||
| chr8:42873218 | G | A | 4 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(1): Show |
4 | HG01106.hp2 HG02257.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+713C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42873218 | |||||||
| chr8:42873261 | G | T | 1 | a0001c0001t0001g0169 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.213+670C>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42873261 | |||||||
| chr8:42873277 | C | T | 11 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0118 others(8): Show |
15 | HG01243.hp1 HG02109.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.213+654G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42873277 | |||||||
| chr8:42873293 | C | CA | 38 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(35): Show |
42 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.213+637dupT | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42873293 | |||||||
| chr8:42873514 | G | A | 1 | a0001c0001t0004g0025 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.213+417C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42873514 | |||||||
| chr8:42873769 | T | C | 10 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(7): Show |
10 | HG01261.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.213+162A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42873769 | |||||||
| chr8:42874045 | T | C | 1 | a0001c0001t0003g0155 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.138-39A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42874045 | |||||||
| chr8:42874071 | G | C | 11 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0118 others(8): Show |
15 | HG01243.hp1 HG02109.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.138-65C>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42874071 | |||||||
| chr8:42874148 | C | T | 1 | a0001c0002t0002g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.138-142G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42874148 | |||||||
| chr8:42874709 | T | C | 1 | a0001c0001t0008g0186 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.138-703A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42874709 | |||||||
| chr8:42874739 | A | C | 4 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(1): Show |
4 | HG02055.hp2 HG03209.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-733T>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42874739 | |||||||
| chr8:42874819 | A | C | 2 | a0001c0001t0001g0108 a0001c0001t0012g0106 |
2 | HG00438.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.138-813T>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42874819 | |||||||
| chr8:42875127 | C | T | 12 | a0001c0001t0001g0013 a0001c0001t0001g0144 a0001c0001t0001g0146 others(9): Show |
13 | HG00673.hp1 HG01070.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.138-1121G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42875127 | |||||||
| chr8:42875163 | C | T | 1 | a0001c0001t0010g0024 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.138-1157G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42875163 | |||||||
| chr8:42875169 | T | TA | 19 | a0001c0001t0003g0138 a0001c0001t0003g0155 a0001c0001t0003g0157 others(16): Show |
19 | HG01071.hp2 HG01192.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.138-1164dupT | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42875169 | |||||||
| chr8:42875169 | T | TAA | 17 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(14): Show |
21 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.138-1165_138-1164d others(4): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42875169 | |||||||
| chr8:42875169 | TA | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0053 a0001c0001t0001g0054 others(3): Show |
6 | HG01070.hp2 HG01099.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.138-1164delT | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42875169 | |||||||
| chr8:42875408 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.138-1402C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42875408 | |||||||
| chr8:42875418 | T | C | 1 | a0001c0001t0003g0155 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.138-1412A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42875418 | |||||||
| chr8:42875631 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.138-1625G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42875631 | |||||||
| chr8:42876223 | T | A | 1 | a0001c0001t0010g0024 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.138-2217A>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42876223 | |||||||
| chr8:42876368 | G | T | 1 | a0001c0001t0004g0105 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.138-2362C>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42876368 | |||||||
| chr8:42876409 | G | C | 1 | a0001c0001t0001g0090 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.138-2403C>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42876409 | |||||||
| chr8:42876657 | G | GT | 63 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(60): Show |
67 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.138-2652dupA | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42876657 | |||||||
| chr8:42876657 | G | GTT | 8 | a0001c0001t0001g0019 a0001c0001t0001g0122 a0001c0001t0001g0139 others(5): Show |
8 | HG00544.hp1 HG00544.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.138-2653_138-2652d others(4): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42876657 | |||||||
| chr8:42876657 | GT | G | 18 | a0001c0001t0001g0066 a0001c0001t0002g0128 a0001c0001t0002g0129 others(15): Show |
22 | HG01243.hp1 HG01261.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.138-2652delA | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42876657 | |||||||
| chr8:42876950 | C | T | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.138-2944G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42876950 | |||||||
| chr8:42876954 | CTTT | C | 8 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(5): Show |
8 | HG02055.hp2 HG02451.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.138-2951_138-2949d others(5): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42876954 | |||||||
| chr8:42877005 | G | A | 1 | a0001c0001t0008g0186 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.138-2999C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42877005 | |||||||
| chr8:42877161 | C | T | 2 | a0001c0001t0006g0135 a0001c0001t0006g0136 |
2 | HG01261.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.138-3155G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42877161 | |||||||
| chr8:42877208 | G | A | 5 | a0001c0001t0003g0138 a0001c0001t0003g0158 a0001c0001t0003g0159 others(2): Show |
5 | HG01192.hp1 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-3202C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42877208 | |||||||
| chr8:42877740 | C | T | 1 | a0001c0001t0005g0133 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.138-3734G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42877740 | |||||||
| chr8:42877926 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.138-3920G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42877926 | |||||||
| chr8:42878023 | G | A | 1 | a0001c0001t0001g0013 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.138-4017C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42878023 | |||||||
| chr8:42878040 | G | GCAAT | 10 | a0001c0001t0001g0045 a0001c0001t0001g0149 a0001c0001t0001g0150 others(7): Show |
10 | HG00621.hp2 HG00673.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.138-4038_138-4035d others(6): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42878040 | |||||||
| chr8:42878040 | GCAAT | G | 34 | a0001c0001t0001g0078 a0001c0001t0001g0101 a0001c0001t0001g0116 others(31): Show |
34 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.138-4038_138-4035d others(6): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42878040 | |||||||
| chr8:42878305 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | HG02040.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.138-4299C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42878305 | |||||||
| chr8:42878694 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.138-4688A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42878694 | |||||||
| chr8:42878800 | A | G | 1 | a0001c0001t0008g0186 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.138-4794T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42878800 | |||||||
| chr8:42879084 | T | C | 8 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0119 others(5): Show |
12 | HG01243.hp1 HG02615.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.138-5078A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42879084 | |||||||
| chr8:42879212 | T | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0079 others(2): Show |
6 | HG02055.hp1 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.138-5206A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42879212 | |||||||
| chr8:42879494 | T | C | 1 | a0001c0001t0010g0024 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.138-5488A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42879494 | |||||||
| chr8:42879604 | T | A | 10 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(7): Show |
10 | HG01261.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.138-5598A>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42879604 | |||||||
| chr8:42879663 | T | G | 1 | a0001c0001t0001g0100 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.138-5657A>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42879663 | |||||||
| chr8:42879732 | T | C | 1 | a0001c0001t0001g0154 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.138-5726A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42879732 | |||||||
| chr8:42879920 | C | T | 8 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(5): Show |
8 | HG02055.hp2 HG02451.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.138-5914G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42879920 | |||||||
| chr8:42879923 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.138-5917G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42879923 | |||||||
| chr8:42879976 | A | G | 1 | a0001c0001t0001g0035 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.138-5970T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42879976 | |||||||
| chr8:42880067 | G | C | 5 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-6061C>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42880067 | |||||||
| chr8:42880139 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.138-6133C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42880139 | |||||||
| chr8:42880164 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.138-6158G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42880164 | |||||||
| chr8:42881480 | G | C | 1 | a0001c0001t0001g0013 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.137+6248C>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42881480 | |||||||
| chr8:42881483 | A | G | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 |
3 | HG01167.hp2 HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.137+6245T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42881483 | |||||||
| chr8:42881503 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.137+6225G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42881503 | |||||||
| chr8:42881687 | C | T | 2 | a0001c0001t0006g0135 a0001c0001t0006g0136 |
2 | HG01261.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.137+6041G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42881687 | |||||||
| chr8:42881752 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.137+5976A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42881752 | |||||||
| chr8:42881916 | C | CA | 11 | a0001c0001t0003g0138 a0001c0001t0003g0155 a0001c0001t0003g0157 others(8): Show |
11 | HG01192.hp1 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.137+5811dupT | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42881916 | |||||||
| chr8:42881968 | G | C | 1 | a0001c0001t0004g0025 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.137+5760C>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42881968 | |||||||
| chr8:42882750 | T | C | 11 | a0001c0001t0003g0138 a0001c0001t0003g0155 a0001c0001t0003g0157 others(8): Show |
11 | HG01192.hp1 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.137+4978A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42882750 | |||||||
| chr8:42883010 | A | C | 1 | a0001c0001t0010g0024 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.137+4718T>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42883010 | |||||||
| chr8:42883246 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(4): Show |
8 | HG01081.hp2 HG01099.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.137+4482G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42883246 | |||||||
| chr8:42883438 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.137+4290C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42883438 | |||||||
| chr8:42883501 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.137+4227C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42883501 | |||||||
| chr8:42883562 | C | G | 1 | a0001c0001t0008g0186 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.137+4166G>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42883562 | |||||||
| chr8:42883565 | T | A | 1 | a0001c0001t0001g0069 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.137+4163A>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42883565 | |||||||
| chr8:42883570 | GA | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
146 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.137+4157delT | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42883570 | |||||||
| chr8:42883589 | A | G | 1 | a0001c0001t0008g0186 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.137+4139T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42883589 | |||||||
| chr8:42883989 | T | C | 2 | a0001c0001t0001g0167 a0001c0001t0004g0172 |
2 | HG03831.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.137+3739A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42883989 | |||||||
| chr8:42884205 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.137+3523C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884205 | |||||||
| chr8:42884259 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.137+3469A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884259 | |||||||
| chr8:42884416 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.137+3312T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884416 | |||||||
| chr8:42884589 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.137+3139T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884589 | |||||||
| chr8:42884792 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.137+2936G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884792 | |||||||
| chr8:42884900 | T | TCATGTTG others(814): Show |
1 | a0001c0001t0001g0146 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.137+2827_137+2828i others(823): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | |||||||
| chr8:42884900 | T | TCATGTTG others(812): Show |
6 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0145 others(3): Show |
6 | HG00423.hp1 HG00544.hp2 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.137+2827_137+2828i others(821): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | |||||||
| chr8:42884900 | T | TCATGTTG others(814): Show |
2 | a0001c0002t0002g0120 a0001c0002t0002g0125 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.137+2827_137+2828i others(823): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | |||||||
| chr8:42884900 | T | TCATGTTG others(815): Show |
1 | a0001c0001t0002g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.137+2827_137+2828i others(824): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | |||||||
| chr8:42884900 | T | TCATGTTG others(813): Show |
9 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0118 others(6): Show |
13 | HG01243.hp1 HG02109.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.137+2827_137+2828i others(822): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | |||||||
| chr8:42884900 | T | TCATGTTG others(814): Show |
2 | a0001c0001t0006g0135 a0001c0001t0006g0136 |
2 | HG01261.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.137+2827_137+2828i others(823): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | |||||||
| chr8:42884900 | T | TCATGTTG others(813): Show |
3 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 |
3 | HG03209.hp2 NA20129.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.137+2827_137+2828i others(822): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | |||||||
| chr8:42884900 | T | TCATGTTG others(813): Show |
4 | a0001c0001t0005g0032 a0001c0001t0005g0132 a0001c0001t0005g0133 others(1): Show |
4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+2827_137+2828i others(822): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | |||||||
| chr8:42884900 | T | TCATGTTG others(813): Show |
2 | a0001c0001t0003g0174 a0001c0001t0003g0175 |
2 | HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.137+2827_137+2828i others(822): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | |||||||
| chr8:42884900 | T | TCATGTTG others(813): Show |
1 | a0001c0001t0001g0085 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.137+2827_137+2828i others(822): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | |||||||
| chr8:42884900 | T | TCATGTTG others(814): Show |
7 | a0001c0001t0001g0016 a0001c0001t0001g0094 a0001c0001t0001g0096 others(4): Show |
7 | HG00438.hp1 HG00438.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.137+2827_137+2828i others(823): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | |||||||
| chr8:42884900 | T | TCATGTTG others(813): Show |
1 | a0001c0001t0004g0025 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.137+2827_137+2828i others(822): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | |||||||
| chr8:42884900 | T | TCATGTTG others(810): Show |
1 | a0001c0001t0001g0086 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.137+2827_137+2828i others(819): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | |||||||
| chr8:42884900 | T | TCATGTTG others(813): Show |
1 | a0001c0001t0001g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.137+2827_137+2828i others(822): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | |||||||
| chr8:42884900 | T | TCATGTTG others(812): Show |
3 | a0001c0001t0001g0081 a0001c0001t0001g0104 a0001c0001t0008g0186 |
3 | HG01167.hp1 HG01169.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.137+2827_137+2828i others(821): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | |||||||
| chr8:42884900 | T | TCATGTTG others(813): Show |
1 | a0001c0001t0001g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.137+2827_137+2828i others(822): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | |||||||
| chr8:42884900 | T | TCATGTTG others(813): Show |
2 | a0001c0001t0001g0013 a0001c0001t0001g0171 |
3 | HG01070.hp1 HG01071.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.137+2827_137+2828i others(822): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | |||||||
| chr8:42884900 | T | TCATGTTG others(813): Show |
1 | a0001c0001t0001g0083 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.137+2827_137+2828i others(822): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | |||||||
| chr8:42884975 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.137+2753A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884975 | |||||||
| chr8:42885134 | C | T | 10 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(7): Show |
10 | HG01261.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.137+2594G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42885134 | |||||||
| chr8:42885667 | A | C | 1 | a0001c0001t0001g0041 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.137+2061T>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42885667 | |||||||
| chr8:42885843 | T | C | 1 | a0001c0001t0004g0105 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.137+1885A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42885843 | |||||||
| chr8:42886217 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.137+1511G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42886217 | |||||||
| chr8:42886232 | A | T | 10 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(7): Show |
10 | HG01261.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.137+1496T>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42886232 | |||||||
| chr8:42886235 | T | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0148 |
2 | HG01074.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.137+1493A>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42886235 | |||||||
| chr8:42886374 | C | G | 1 | a0001c0001t0001g0014 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.137+1354G>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42886374 | |||||||
| chr8:42886507 | C | A | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.137+1221G>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42886507 | |||||||
| chr8:42886508 | C | G | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.137+1220G>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42886508 | |||||||
| chr8:42886545 | C | T | 4 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(1): Show |
4 | HG02055.hp2 HG03209.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+1183G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42886545 | |||||||
| chr8:42886709 | G | A | 4 | a0001c0001t0001g0090 a0001c0001t0001g0115 a0001c0001t0004g0089 others(1): Show |
4 | HG00621.hp2 HG02015.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+1019C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42886709 | |||||||
| chr8:42886725 | C | A | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0102 |
3 | HG01993.hp2 HG02293.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.137+1003G>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42886725 | |||||||
| chr8:42886919 | T | G | 5 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(2): Show |
5 | HG01993.hp2 HG02293.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.137+809A>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42886919 | |||||||
| chr8:42887021 | A | G | 1 | a0001c0001t0001g0017 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.137+707T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42887021 | |||||||
| chr8:42887062 | G | A | 5 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.137+666C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42887062 | |||||||
| chr8:42887294 | AAAAT | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0040 a0001c0001t0001g0096 others(6): Show |
10 | HG00438.hp2 HG00558.hp2 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.137+430_137+433del others(4): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42887294 | |||||||
| chr8:42887308 | A | C | 1 | a0001c0001t0008g0186 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.137+420T>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42887308 | |||||||
| chr8:42887356 | T | C | 5 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.137+372A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42887356 | |||||||
| chr8:42887490 | G | A | 10 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(7): Show |
10 | HG01261.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.137+238C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42887490 | |||||||
| chr8:42887660 | CATT | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0098 others(1): Show |
5 | HG02055.hp1 HG02622.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.137+65_137+67delAA others(1): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42887660 | |||||||
| chr8:42888123 | G | C | 1 | a0001c0001t0001g0114 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-7-252C>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42888123 | |||||||
| chr8:42888128 | G | A | 10 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(7): Show |
10 | HG01261.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7-257C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42888128 | |||||||
| chr8:42888136 | G | C | 1 | a0001c0001t0001g0100 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-7-265C>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42888136 | |||||||
| chr8:42888510 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-7-639G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42888510 | |||||||
| chr8:42888543 | A | C | 1 | a0001c0002t0002g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-7-672T>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42888543 | |||||||
| chr8:42888626 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0040 |
3 | HG00738.hp1 HG03710.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-7-755G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42888626 | |||||||
| chr8:42888685 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-7-814C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42888685 | |||||||
| chr8:42888687 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-7-816C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42888687 | |||||||
| chr8:42888742 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-7-871C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42888742 | |||||||
| chr8:42888880 | T | C | 21 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(18): Show |
25 | HG01243.hp1 HG01261.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.-7-1009A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42888880 | |||||||
| chr8:42889000 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-7-1129C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42889000 | |||||||
| chr8:42889370 | A | AT | 11 | a0001c0001t0003g0138 a0001c0001t0003g0155 a0001c0001t0003g0157 others(8): Show |
11 | HG01192.hp1 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.-7-1500dupA | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42889370 | |||||||
| chr8:42889407 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-7-1536A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42889407 | |||||||
| chr8:42889673 | T | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-7-1802A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42889673 | |||||||
| chr8:42889716 | T | G | 1 | a0001c0001t0001g0154 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-7-1845A>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42889716 | |||||||
| chr8:42890048 | G | A | 21 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(18): Show |
25 | HG01243.hp1 HG01261.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.-7-2177C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42890048 | |||||||
| chr8:42890187 | G | C | 1 | a0001c0001t0003g0173 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-7-2316C>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42890187 | |||||||
| chr8:42890277 | CT | C | 8 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(5): Show |
8 | HG02055.hp2 HG02451.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-7-2407delA | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42890277 | |||||||
| chr8:42890438 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-7-2567G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42890438 | |||||||
| chr8:42890445 | T | C | 21 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(18): Show |
25 | HG01243.hp1 HG01261.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.-7-2574A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42890445 | |||||||
| chr8:42890541 | T | G | 1 | a0001c0001t0004g0105 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-7-2670A>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42890541 | |||||||
| chr8:42890817 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-7-2946C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42890817 | |||||||
| chr8:42890878 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-7-3007A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42890878 | |||||||
| chr8:42891154 | G | A | 4 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
4 | HG00438.hp2 HG00558.hp2 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-3283C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42891154 | |||||||
| chr8:42891380 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-7-3509C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42891380 | |||||||
| chr8:42891456 | C | A | 1 | a0001c0002t0002g0126 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-7-3585G>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42891456 | |||||||
| chr8:42891542 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-7-3671T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42891542 | |||||||
| chr8:42891624 | T | C | 3 | a0001c0001t0003g0174 a0001c0001t0003g0175 a0001c0001t0010g0024 |
3 | HG02723.hp2 HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-7-3753A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42891624 | |||||||
| chr8:42891901 | GAC | G | 6 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(3): Show |
6 | HG00673.hp1 HG02523.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-4032_-7-4031del others(2): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42891901 | |||||||
| chr8:42891998 | T | G | 1 | a0001c0002t0002g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-7-4127A>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42891998 | |||||||
| chr8:42892059 | C | T | 8 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(5): Show |
8 | HG02055.hp2 HG02451.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-7-4188G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42892059 | |||||||
| chr8:42892179 | T | C | 10 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(7): Show |
10 | HG01261.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8+4305A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42892179 | |||||||
| chr8:42892227 | A | T | 1 | a0001c0001t0001g0038 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-8+4257T>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42892227 | |||||||
| chr8:42892445 | G | A | 2 | a0001c0001t0006g0135 a0001c0001t0006g0136 |
2 | HG01261.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.-8+4039C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42892445 | |||||||
| chr8:42892593 | G | A | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | HG00597.hp1 NA18946.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.-8+3891C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42892593 | |||||||
| chr8:42892627 | T | C | 1 | a0001c0002t0002g0137 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-8+3857A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42892627 | |||||||
| chr8:42892673 | C | T | 21 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(18): Show |
25 | HG01243.hp1 HG01261.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8+3811G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42892673 | |||||||
| chr8:42892674 | G | GT | 43 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0017 others(40): Show |
48 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.-8+3809dupA | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42892674 | |||||||
| chr8:42892674 | G | GTT | 6 | a0001c0001t0001g0016 a0001c0001t0001g0121 a0001c0001t0001g0122 others(3): Show |
6 | HG01361.hp1 HG02132.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+3808_-8+3809dup others(2): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42892674 | |||||||
| chr8:42892883 | A | G | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG02015.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.-8+3601T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42892883 | |||||||
| chr8:42893553 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-8+2931A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42893553 | |||||||
| chr8:42893698 | C | A | 4 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(1): Show |
4 | HG01106.hp2 HG02257.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+2786G>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42893698 | |||||||
| chr8:42894243 | A | T | 1 | a0001c0001t0001g0033 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-8+2241T>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42894243 | |||||||
| chr8:42894467 | T | G | 1 | a0001c0001t0001g0115 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-8+2017A>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42894467 | |||||||
| chr8:42894545 | C | A | 90 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0016 others(87): Show |
96 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.-8+1939G>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42894545 | |||||||
| chr8:42894735 | T | G | 5 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(2): Show |
5 | HG02647.hp1 HG02809.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+1749A>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42894735 | |||||||
| chr8:42894805 | C | G | 1 | a0001c0001t0005g0032 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-8+1679G>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42894805 | |||||||
| chr8:42894836 | G | T | 1 | a0001c0001t0001g0031 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-8+1648C>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42894836 | |||||||
| chr8:42895145 | T | C | 1 | a0001c0001t0001g0185 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-8+1339A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42895145 | |||||||
| chr8:42895238 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-8+1246G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42895238 | |||||||
| chr8:42895931 | G | GT | 5 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+552dupA | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42895931 | |||||||
| chr8:42896244 | C | T | 1 | a0001c0001t0010g0024 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-8+240G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42896244 | |||||||
| chr8:42896261 | C | A | 1 | a0001c0001t0008g0186 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-8+223G>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42896261 | |||||||
| chr8:42896442 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-8+42C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42896442 | |||||||
| chr8:42896467 | C | T | 11 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0015 others(8): Show |
12 | HG01081.hp2 HG01099.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.-8+17G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42896467 |