Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 153830 |
| ensemblid | ENSG00000145860.13 |
| hgncid | 20853 |
| symbol | RNF145 |
| name | ring finger protein 145 |
| refseq_nuc | NM_001199383.2 |
| refseq_prot | NP_001186312.1 |
| ensembl_nuc | ENST00000424310.7 |
| ensembl_prot | ENSP00000409064.2 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 159157409 |
| end | 159209553 |
| strand | - |
| ver | v1.2 |
| region | chr5:159157409-159209553 |
| region5000 | chr5:159152409-159214553 |
| regionname0 | RNF145_chr5_159157409_159209553 |
| regionname5000 | RNF145_chr5_159152409_159214553 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 663 | 393 | 77 | 74 | 184 | 16 | 40 | 142 | RNF145_chr5_159152409_159214553 | RNF145 | MAAKE others(658): Show |
chr5 | 159152409 | 159214553 |
| a0002 | 0/0 | 663 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | MAAKE others(658): Show |
chr5 | 159152409 | 159214553 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1989 | 385 | 72 | 73 | 183 | 15 | 40 | RNF145_chr5_159152409_159214553 | RNF145 | ATGGC others(1984): Show |
chr5 | 159152409 | 159214553 | ||
| a0001c0002 | 0/0 | 1989 | 4 | 4 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | ATGGC others(1984): Show |
chr5 | 159152409 | 159214553 | ||
| a0001c0003 | 0/0 | 1989 | 2 | 0 | 1 | 0 | 1 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | ATGGC others(1984): Show |
chr5 | 159152409 | 159214553 | ||
| a0001c0004 | 0/0 | 1989 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | ATGGC others(1984): Show |
chr5 | 159152409 | 159214553 | ||
| a0001c0006 | 0/0 | 1989 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | ATGGC others(1984): Show |
chr5 | 159152409 | 159214553 | ||
| a0002c0005 | 0/0 | 1989 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | ATGGC others(1984): Show |
chr5 | 159152409 | 159214553 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3615 | 312 | 59 | 57 | 159 | 7 | 30 | RNF145_chr5_159152409_159214553 | RNF145 | GCAGA others(3610): Show |
chr5 | 159152409 | 159214553 |
| a0001c0001t0002 | 0/0 | 3607 | 26 | 1 | 9 | 8 | 3 | 5 | RNF145_chr5_159152409_159214553 | RNF145 | GCAGA others(3602): Show |
chr5 | 159152409 | 159214553 |
| a0001c0001t0003 | 1/0 | 3615 | 28 | 1 | 5 | 13 | 4 | 4 | RNF145_chr5_159152409_159214553 | RNF145 | GCAGA others(3610): Show |
chr5 | 159152409 | 159214553 |
| a0001c0001t0004 | 0/0 | 3615 | 3 | 3 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | GCAGA others(3610): Show |
chr5 | 159152409 | 159214553 |
| a0001c0001t0005 | 0/0 | 3609 | 3 | 1 | 0 | 1 | 1 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | GCAGA others(3604): Show |
chr5 | 159152409 | 159214553 |
| a0001c0001t0006 | 0/0 | 3615 | 2 | 1 | 0 | 0 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | GCAGA others(3610): Show |
chr5 | 159152409 | 159214553 |
| a0001c0001t0007 | 0/0 | 3615 | 2 | 0 | 2 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | GCAGA others(3610): Show |
chr5 | 159152409 | 159214553 |
| a0001c0001t0008 | 0/0 | 3615 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | GCAGA others(3610): Show |
chr5 | 159152409 | 159214553 |
| a0001c0001t0009 | 0/0 | 3615 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | GCAGA others(3610): Show |
chr5 | 159152409 | 159214553 |
| a0001c0001t0010 | 0/0 | 3615 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | GCAGA others(3610): Show |
chr5 | 159152409 | 159214553 |
| a0001c0001t0011 | 0/0 | 3615 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | GCAGA others(3610): Show |
chr5 | 159152409 | 159214553 |
| a0001c0001t0012 | 0/0 | 3615 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | GCAGA others(3610): Show |
chr5 | 159152409 | 159214553 |
| a0001c0001t0013 | 0/0 | 3615 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | GCAGA others(3610): Show |
chr5 | 159152409 | 159214553 |
| a0001c0001t0014 | 0/1 | 3630 | 1 | 0 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | GCAGA others(3625): Show |
chr5 | 159152409 | 159214553 |
| a0001c0001t0015 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | GCAGA others(3625): Show |
chr5 | 159152409 | 159214553 |
| a0001c0001t0016 | 0/0 | 3615 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | GCAGA others(3610): Show |
chr5 | 159152409 | 159214553 |
| a0001c0002t0002 | 0/0 | 3607 | 4 | 4 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | GCAGA others(3602): Show |
chr5 | 159152409 | 159214553 |
| a0001c0003t0003 | 0/0 | 3615 | 2 | 0 | 1 | 0 | 1 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | GCAGA others(3610): Show |
chr5 | 159152409 | 159214553 |
| a0001c0004t0001 | 0/0 | 3615 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | GCAGA others(3610): Show |
chr5 | 159152409 | 159214553 |
| a0001c0006t0002 | 0/0 | 3607 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | GCAGA others(3602): Show |
chr5 | 159152409 | 159214553 |
| a0002c0005t0001 | 0/0 | 3615 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | GCAGA others(3610): Show |
chr5 | 159152409 | 159214553 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 17 | 2 | 4 | 9 | 0 | 2 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0002 | 0/0 | 9 | 0 | 2 | 6 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0006 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0002g0048 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0002g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0002g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0002g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0002g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0003g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0003g0013 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0003g0234 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0004g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0005g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0006g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0006g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0007g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0009g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0010g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0011g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0012g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0013g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0014g0294 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0015g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0001t0016g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0002t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0002t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0002t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0002t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0003t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0003t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0004t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0001c0006t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| a0002c0005t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0189 | EUR | GBR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | GBR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG00140 | hp1 | a0001 | c0001 | t0005 | g0293 | EUR | GBR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0173 | EUR | GBR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0047 | EUR | FIN | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0013 | EUR | FIN | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0237 | EUR | FIN | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0047 | EUR | FIN | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0235 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0275 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0233 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01069 | hp1 | a0001 | c0003 | t0003 | g0191 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0188 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0236 | AMR | CLM | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01256 | hp2 | a0001 | c0001 | t0007 | g0046 | AMR | CLM | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01258 | hp1 | a0001 | c0001 | t0007 | g0046 | AMR | CLM | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0277 | AMR | CLM | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | IBS | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01517 | hp1 | a0001 | c0003 | t0003 | g0193 | EUR | IBS | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | IBS | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PEL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0256 | EAS | KHV | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0291 | AFR | ACB | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02074 | hp2 | a0001 | c0006 | t0002 | g0288 | EAS | KHV | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | KHV | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CDX | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0274 | AFR | ACB | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0280 | AMR | PEL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02572 | hp1 | a0002 | c0005 | t0001 | g0135 | AFR | GWD | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0285 | SAS | PJL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02622 | hp1 | a0001 | c0001 | t0010 | g0258 | AFR | GWD | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02717 | hp2 | a0001 | c0004 | t0001 | g0165 | AFR | GWD | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | GWD | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0290 | AFR | GWD | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02922 | hp2 | a0001 | c0001 | t0009 | g0110 | AFR | ESN | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0077 | AFR | ESN | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02970 | hp2 | a0001 | c0001 | t0011 | g0123 | AFR | ESN | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | MSL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0278 | SAS | PJL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0289 | AFR | MSL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0292 | AFR | MSL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0013 | SAS | PJL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0013 | SAS | PJL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03516 | hp1 | a0001 | c0001 | t0016 | g0296 | AFR | ESN | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | MSL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | STU | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | STU | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0230 | SAS | PJL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0257 | SAS | BEB | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG04184 | hp2 | a0001 | c0001 | t0006 | g0273 | SAS | BEB | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | STU | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | STU | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | STU | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0276 | SAS | STU | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | YRI | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHB | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CHB | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0287 | AFR | YRI | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | YRI | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18939 | hp2 | a0001 | c0001 | t0012 | g0199 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18952 | hp1 | a0001 | c0001 | t0005 | g0281 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18997 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | LWK | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | LWK | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19059 | hp1 | a0001 | c0001 | t0013 | g0152 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ASW | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ASW | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | TSI | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0020 | EUR | TSI | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0048 | EUR | TSI | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0219 | EUR | TSI | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | GIH | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | GIH | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0231 | AFR | ACB | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0286 | AFR | MSL | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG06807 | hp1 | a0001 | c0001 | t0008 | g0053 | AFR | USA | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | USA | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | USA | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | LWK | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| NA21309 | hp2 | a0001 | c0001 | t0015 | g0295 | AFR | LWK | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0014 | g0294 | REF | REF | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0234 | REF | REF | RNF145_chr5_159152409_159214553 | RNF145 | chr5 | 159152409 | 159214553 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:159161285 | A | C | 1 | a0002 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.1607T>G | p.Ile536Ser | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 10/11 | 1969/3615 | 1607/1992 | 536/663 | chr5 | 159161285 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:159158679 | T | C | 1 | a0001c0006 | 1 | HG02074.hp2 | synonymous_variant | LOW | c.1983A>G | p.Glu661Glu | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 11/11 | 2345/3615 | 1983/1992 | 661/663 | chr5 | 159158679 | |||
| chr5:159169024 | G | A | 1 | a0001c0002 | 4 | HG02818.hp1 HG03453.hp2 HG03471.hp2 others(1): Show |
synonymous_variant | LOW | c.970C>T | p.Leu324Leu | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/11 | 1332/3615 | 970/1992 | 324/663 | chr5 | 159169024 | |||
| chr5:159169768 | C | T | 1 | a0001c0004 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.849G>A | p.Thr283Thr | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 7/11 | 1211/3615 | 849/1992 | 283/663 | chr5 | 159169768 | |||
| chr5:159174087 | G | A | 1 | a0001c0003 | 2 | HG01069.hp1 HG01517.hp1 |
synonymous_variant | LOW | c.693C>T | p.Phe231Phe | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/11 | 1055/3615 | 693/1992 | 231/663 | chr5 | 159174087 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:159157600 | TAC | T | 3 | a0001c0001t0002 a0001c0002t0002 a0001c0006t0002 |
31 | HG00280.hp1 HG00323.hp2 HG00738.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1068_*1069delGT | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 11/11 | 1068 | chr5 | 159157600 | ||||||
| chr5:159157883 | C | T | 1 | a0001c0001t0012 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*787G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 11/11 | 787 | chr5 | 159157883 | ||||||
| chr5:159157983 | C | T | 18 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(15): Show |
363 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(360): Show |
3_prime_UTR_variant | MODIFIER | c.*687G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 11/11 | 687 | chr5 | 159157983 | ||||||
| chr5:159158172 | G | C | 1 | a0001c0001t0004 | 3 | HG02723.hp2 HG02965.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*498C>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 11/11 | 498 | chr5 | 159158172 | ||||||
| chr5:159158180 | A | G | 1 | a0001c0001t0011 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*490T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 11/11 | 490 | chr5 | 159158180 | ||||||
| chr5:159158304 | C | A | 1 | a0001c0001t0010 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*366G>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 11/11 | 366 | chr5 | 159158304 | ||||||
| chr5:159158443 | G | T | 1 | a0001c0001t0010 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*227C>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 11/11 | 227 | chr5 | 159158443 | ||||||
| chr5:159158641 | A | G | 1 | a0001c0001t0009 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*29T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 11/11 | 29 | chr5 | 159158641 | ||||||
| chr5:159203649 | G | A | 1 | a0001c0001t0013 | 1 | NA19059.hp1 | 5_prime_UTR_variant | MODIFIER | c.-32C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/11 | 32 | chr5 | 159203649 | ||||||
| chr5:159209273 | G | A | 1 | a0001c0001t0006 | 2 | HG02257.hp1 HG04184.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-82C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/11 | chr5 | 159209273 | |||||||
| chr5:159209373 | G | T | 1 | a0001c0001t0008 | 1 | HG06807.hp1 | 5_prime_UTR_variant | MODIFIER | c.-182C>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/11 | 5756 | chr5 | 159209373 | ||||||
| chr5:159209404 | G | A | 1 | a0001c0001t0007 | 2 | HG01256.hp2 HG01258.hp1 |
5_prime_UTR_variant | MODIFIER | c.-213C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/11 | 5787 | chr5 | 159209404 | ||||||
| chr5:159209408 | AGGCAGC | A | 4 | a0001c0001t0002 a0001c0001t0005 a0001c0002t0002 others(1): Show |
34 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(31): Show |
5_prime_UTR_variant | MODIFIER | c.-223_-218delGCTGCC | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/11 | 5792 | chr5 | 159209408 | ||||||
| chr5:159209498 | C | CCGGCGGC others(8): Show |
1 | a0001c0001t0015 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-308_-307insCCGCCG others(9): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/11 | 5882 | chr5 | 159209498 | ||||||
| chr5:159209504 | T | G | 1 | a0001c0001t0015 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-313A>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/11 | 5887 | chr5 | 159209504 | ||||||
| chr5:159209504 | T | TCGGCGGC others(8): Show |
18 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(15): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(362): Show |
5_prime_UTR_variant | MODIFIER | c.-314_-313insCCGCCG others(9): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/11 | 5888 | chr5 | 159209504 | ||||||
| chr5:159209504 | T | TCGGCGGC others(11): Show |
1 | a0001c0001t0001 | 4 | HG00642.hp1 NA18999.hp2 NA20805.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-314_-313insCCGCCG others(12): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/11 | 5888 | chr5 | 159209504 | ||||||
| chr5:159209504 | T | TCGGCGGC others(14): Show |
1 | a0001c0001t0001 | 6 | HG01243.hp2 HG01891.hp1 HG02886.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-314_-313insCCGCCG others(15): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/11 | 5888 | chr5 | 159209504 | ||||||
| chr5:159209504 | T | TCGGCGTC others(8): Show |
1 | a0001c0001t0004 | 3 | HG02723.hp2 HG02965.hp2 HG03579.hp1 |
5_prime_UTR_variant | MODIFIER | c.-314_-313insCCGCCG others(9): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/11 | 5888 | chr5 | 159209504 | ||||||
| chr5:159209525 | G | C | 1 | a0001c0001t0016 | 1 | HG03516.hp1 | 5_prime_UTR_variant | MODIFIER | c.-334C>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/11 | 5908 | chr5 | 159209525 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:159159038 | A | G | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | splice_region_variant&intron_variant | LOW | c.1627-3T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 10/10 | chr5 | 159159038 | |||||||
| chr5:159159215 | A | T | 1 | a0001c0001t0005g0289 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1627-180T>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 10/10 | chr5 | 159159215 | |||||||
| chr5:159159423 | T | C | 3 | a0001c0001t0001g0026 a0001c0001t0001g0109 a0001c0001t0009g0110 |
4 | HG01069.hp2 HG01071.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1627-388A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 10/10 | chr5 | 159159423 | |||||||
| chr5:159159601 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1627-566T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 10/10 | chr5 | 159159601 | |||||||
| chr5:159159709 | T | A | 1 | a0001c0001t0002g0279 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1627-674A>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 10/10 | chr5 | 159159709 | |||||||
| chr5:159159839 | G | A | 2 | a0001c0001t0004g0023 a0001c0001t0004g0077 |
3 | HG02723.hp2 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1627-804C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 10/10 | chr5 | 159159839 | |||||||
| chr5:159159974 | G | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0073 a0001c0001t0001g0074 others(2): Show |
7 | HG00741.hp2 HG01168.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1627-939C>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 10/10 | chr5 | 159159974 | |||||||
| chr5:159160035 | C | G | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1627-1000G>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 10/10 | chr5 | 159160035 | |||||||
| chr5:159160085 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1627-1050G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 10/10 | chr5 | 159160085 | |||||||
| chr5:159160110 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1627-1075C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 10/10 | chr5 | 159160110 | |||||||
| chr5:159160267 | G | C | 1 | a0001c0001t0005g0289 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1626+999C>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 10/10 | chr5 | 159160267 | |||||||
| chr5:159160510 | T | G | 2 | a0001c0001t0001g0133 a0001c0001t0007g0046 |
3 | HG01256.hp2 HG01258.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1626+756A>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 10/10 | chr5 | 159160510 | |||||||
| chr5:159160514 | T | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0120 |
3 | HG01515.hp1 HG01517.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1626+752A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 10/10 | chr5 | 159160514 | |||||||
| chr5:159160654 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1626+612C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 10/10 | chr5 | 159160654 | |||||||
| chr5:159160955 | C | A | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1626+311G>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 10/10 | chr5 | 159160955 | |||||||
| chr5:159161238 | C | G | 1 | a0001c0001t0001g0009 | 3 | HG01070.hp2 HG01071.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.1626+28G>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 10/10 | chr5 | 159161238 | |||||||
| chr5:159161625 | GA | G | 10 | a0001c0001t0001g0007 a0001c0001t0001g0190 a0001c0001t0001g0225 others(7): Show |
13 | HG00423.hp2 HG02056.hp1 HG02155.hp2 others(10): Show |
splice_region_variant&intron_variant | LOW | c.1270-4delT | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 9/10 | chr5 | 159161625 | |||||||
| chr5:159161625 | GAAAAA | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
257 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(254): Show |
splice_region_variant&intron_variant | LOW | c.1270-8_1270-4delTT others(3): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 9/10 | chr5 | 159161625 | |||||||
| chr5:159161741 | G | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(74): Show |
102 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1270-119C>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 9/10 | chr5 | 159161741 | |||||||
| chr5:159161915 | C | A | 4 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0223 others(1): Show |
4 | HG01952.hp2 HG01978.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.1270-293G>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 9/10 | chr5 | 159161915 | |||||||
| chr5:159162064 | C | T | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1270-442G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 9/10 | chr5 | 159162064 | |||||||
| chr5:159162070 | C | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(190): Show |
258 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.1270-448G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 9/10 | chr5 | 159162070 | |||||||
| chr5:159162129 | T | C | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1270-507A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 9/10 | chr5 | 159162129 | |||||||
| chr5:159162184 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1270-562T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 9/10 | chr5 | 159162184 | |||||||
| chr5:159162213 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1270-591G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 9/10 | chr5 | 159162213 | |||||||
| chr5:159162363 | C | T | 8 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0056 others(5): Show |
9 | HG01109.hp1 HG01261.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.1269+569G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 9/10 | chr5 | 159162363 | |||||||
| chr5:159162392 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1269+540A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 9/10 | chr5 | 159162392 | |||||||
| chr5:159162425 | C | CT | 32 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0014 others(29): Show |
38 | HG00323.hp1 HG01109.hp1 HG01255.hp2 others(35): Show |
intron_variant | MODIFIER | c.1269+506dupA | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 9/10 | chr5 | 159162425 | |||||||
| chr5:159162425 | C | CTTTTTT | 19 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(16): Show |
23 | HG00642.hp1 HG01081.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.1269+501_1269+506d others(8): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 9/10 | chr5 | 159162425 | |||||||
| chr5:159162425 | CT | C | 5 | a0001c0001t0001g0022 a0001c0001t0001g0040 a0001c0001t0001g0072 others(2): Show |
6 | HG01257.hp2 HG02717.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1269+506delA | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 9/10 | chr5 | 159162425 | |||||||
| chr5:159162425 | CTTTTTTT others(1): Show |
C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
146 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.1269+499_1269+506d others(10): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 9/10 | chr5 | 159162425 | |||||||
| chr5:159162458 | C | T | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1269+474G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 9/10 | chr5 | 159162458 | |||||||
| chr5:159162466 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0148 |
3 | NA18956.hp2 NA18981.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1269+466G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 9/10 | chr5 | 159162466 | |||||||
| chr5:159162467 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1269+465C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 9/10 | chr5 | 159162467 | |||||||
| chr5:159162495 | C | T | 1 | a0001c0001t0003g0256 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1269+437G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 9/10 | chr5 | 159162495 | |||||||
| chr5:159162559 | C | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
148 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.1269+373G>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 9/10 | chr5 | 159162559 | |||||||
| chr5:159162576 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1269+356T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 9/10 | chr5 | 159162576 | |||||||
| chr5:159162617 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0093 |
2 | HG01123.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1269+315C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 9/10 | chr5 | 159162617 | |||||||
| chr5:159162726 | G | C | 1 | a0001c0001t0003g0197 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1269+206C>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 9/10 | chr5 | 159162726 | |||||||
| chr5:159162850 | T | C | 20 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(17): Show |
25 | HG00544.hp2 HG00642.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.1269+82A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 9/10 | chr5 | 159162850 | |||||||
| chr5:159162890 | C | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
206 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1269+42G>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 9/10 | chr5 | 159162890 | |||||||
| chr5:159163176 | T | C | 1 | a0001c0001t0005g0289 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1122-97A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159163176 | |||||||
| chr5:159163446 | C | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(74): Show |
102 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1122-367G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159163446 | |||||||
| chr5:159163462 | C | G | 1 | a0001c0001t0001g0210 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1122-383G>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159163462 | |||||||
| chr5:159163534 | C | A | 1 | a0001c0001t0001g0272 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1122-455G>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159163534 | |||||||
| chr5:159163856 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1122-777G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159163856 | |||||||
| chr5:159163926 | A | T | 1 | a0001c0001t0008g0053 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1122-847T>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159163926 | |||||||
| chr5:159163940 | T | C | 1 | a0001c0001t0003g0237 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1122-861A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159163940 | |||||||
| chr5:159164026 | G | T | 1 | a0001c0001t0001g0009 | 3 | HG01070.hp2 HG01071.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.1122-947C>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159164026 | |||||||
| chr5:159164102 | C | A | 4 | a0001c0001t0001g0080 a0001c0001t0001g0083 a0001c0001t0001g0089 others(1): Show |
4 | HG02280.hp1 HG03942.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1122-1023G>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159164102 | |||||||
| chr5:159164109 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1122-1030G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159164109 | |||||||
| chr5:159164121 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1122-1042G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159164121 | |||||||
| chr5:159164140 | T | C | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1122-1061A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159164140 | |||||||
| chr5:159164158 | G | A | 58 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(55): Show |
77 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.1122-1079C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159164158 | |||||||
| chr5:159164176 | T | C | 1 | a0001c0001t0004g0023 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1122-1097A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159164176 | |||||||
| chr5:159164234 | C | CTAA | 8 | a0001c0001t0001g0109 a0001c0001t0001g0119 a0001c0001t0001g0130 others(5): Show |
8 | HG00609.hp2 HG02083.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.1122-1158_1122-115 others(7): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159164234 | |||||||
| chr5:159164238 | T | C | 10 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
14 | HG00140.hp2 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.1122-1159A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159164238 | |||||||
| chr5:159164240 | A | G | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1122-1161T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159164240 | |||||||
| chr5:159164324 | TA | T | 2 | a0001c0001t0004g0023 a0001c0001t0004g0077 |
3 | HG02723.hp2 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1122-1246delT | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159164324 | |||||||
| chr5:159164337 | T | C | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1122-1258A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159164337 | |||||||
| chr5:159164367 | G | T | 2 | a0001c0001t0001g0176 a0001c0001t0016g0296 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1122-1288C>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159164367 | |||||||
| chr5:159164502 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1122-1423G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159164502 | |||||||
| chr5:159164565 | A | G | 18 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(15): Show |
22 | HG00544.hp2 HG00642.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1122-1486T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159164565 | |||||||
| chr5:159164683 | G | C | 78 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(75): Show |
103 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.1122-1604C>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159164683 | |||||||
| chr5:159164700 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1122-1621T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159164700 | |||||||
| chr5:159164952 | G | A | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1122-1873C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159164952 | |||||||
| chr5:159165007 | G | C | 23 | a0001c0001t0002g0017 a0001c0001t0002g0047 a0001c0001t0002g0048 others(20): Show |
31 | HG00280.hp1 HG00323.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1122-1928C>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165007 | |||||||
| chr5:159165010 | C | T | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1122-1931G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165010 | |||||||
| chr5:159165078 | GTACTGTC others(3): Show |
G | 8 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0056 others(5): Show |
9 | HG01109.hp1 HG01261.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.1122-2009_1122-200 others(14): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165078 | |||||||
| chr5:159165143 | T | C | 23 | a0001c0001t0002g0017 a0001c0001t0002g0047 a0001c0001t0002g0048 others(20): Show |
31 | HG00280.hp1 HG00323.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1122-2064A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165143 | |||||||
| chr5:159165200 | G | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(193): Show |
261 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1122-2121C>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165200 | |||||||
| chr5:159165263 | C | T | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1122-2184G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165263 | |||||||
| chr5:159165386 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1122-2307A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165386 | |||||||
| chr5:159165389 | AAATAATA others(338): Show |
A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(190): Show |
258 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.1122-2655_1122-231 others(4): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165389 | |||||||
| chr5:159165555 | C | T | 1 | a0001c0001t0001g0002 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1122-2476G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165555 | |||||||
| chr5:159165682 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0003g0020 | 2 | HG00639.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1122-2613_1122-260 others(14): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165682 | |||||||
| chr5:159165682 | CAAAAAAA others(3): Show |
C | 4 | a0001c0001t0001g0270 a0001c0001t0003g0003 a0001c0001t0003g0189 others(1): Show |
5 | HG00099.hp1 HG02622.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.1122-2613_1122-260 others(14): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165682 | |||||||
| chr5:159165682 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0272 a0001c0001t0003g0188 |
2 | HG01106.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1122-2614_1122-260 others(15): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165682 | |||||||
| chr5:159165682 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0003g0013 | 3 | HG00280.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1122-2617_1122-260 others(18): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165682 | |||||||
| chr5:159165682 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0003g0233 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1122-2618_1122-260 others(19): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165682 | |||||||
| chr5:159165682 | CAAAAAAA others(11): Show |
C | 1 | a0001c0001t0001g0181 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1122-2621_1122-260 others(22): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165682 | |||||||
| chr5:159165682 | CAAAAAAA others(12): Show |
C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0254 |
2 | NA18747.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1122-2622_1122-260 others(23): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165682 | |||||||
| chr5:159165682 | CAAAAAAA others(14): Show |
C | 1 | a0001c0001t0003g0235 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1122-2624_1122-260 others(25): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165682 | |||||||
| chr5:159165682 | CAAAAAAA others(18): Show |
C | 2 | a0001c0001t0003g0236 a0001c0001t0003g0237 |
2 | HG00323.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.1122-2628_1122-260 others(29): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165682 | |||||||
| chr5:159165698 | AAAAAAAA others(29): Show |
A | 1 | a0001c0001t0001g0184 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1122-2655_1122-262 others(40): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165698 | |||||||
| chr5:159165703 | AAAAAAAA others(24): Show |
A | 1 | a0001c0001t0001g0251 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1122-2655_1122-262 others(35): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165703 | |||||||
| chr5:159165709 | AAAAAAAA others(18): Show |
A | 1 | a0001c0003t0003g0191 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1122-2655_1122-263 others(29): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165709 | |||||||
| chr5:159165711 | AAAAAAAA others(16): Show |
A | 2 | a0001c0001t0003g0196 a0001c0001t0003g0249 |
2 | NA18978.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1122-2655_1122-263 others(27): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165711 | |||||||
| chr5:159165712 | AAAAAAAA others(15): Show |
A | 1 | a0001c0001t0003g0197 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1122-2655_1122-263 others(26): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165712 | |||||||
| chr5:159165714 | AAAAAAAA others(13): Show |
A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0190 |
3 | HG00738.hp2 NA18946.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1122-2655_1122-263 others(24): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165714 | |||||||
| chr5:159165715 | AAAAAAAA others(12): Show |
A | 35 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(32): Show |
42 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.1122-2655_1122-263 others(23): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165715 | |||||||
| chr5:159165716 | AAAAAAAA others(11): Show |
A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(31): Show |
39 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.1122-2655_1122-263 others(22): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165716 | |||||||
| chr5:159165717 | AAAAAAAA others(10): Show |
A | 8 | a0001c0001t0001g0016 a0001c0001t0001g0038 a0001c0001t0001g0043 others(5): Show |
8 | NA18941.hp1 NA18948.hp2 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.1122-2655_1122-263 others(21): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165717 | |||||||
| chr5:159165718 | AAAAAAAA others(9): Show |
A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | NA18947.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.1122-2655_1122-264 others(20): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165718 | |||||||
| chr5:159165719 | AAAAAAAA others(8): Show |
A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | NA18961.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1122-2655_1122-264 others(19): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165719 | |||||||
| chr5:159165720 | AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0001g0229 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1122-2655_1122-264 others(18): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165720 | |||||||
| chr5:159165725 | A | T | 2 | a0001c0001t0001g0270 a0001c0001t0001g0272 |
2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1122-2646T>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165725 | |||||||
| chr5:159165728 | A | T | 3 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 |
3 | HG02622.hp2 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1122-2649T>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165728 | |||||||
| chr5:159165731 | A | AAAAAAAA others(3): Show |
1 | a0001c0001t0003g0231 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1122-2653_1122-265 others(14): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165731 | |||||||
| chr5:159165731 | A | T | 5 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(2): Show |
6 | HG00099.hp1 HG02622.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1122-2652T>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165731 | |||||||
| chr5:159165734 | T | A | 1 | a0001c0003t0003g0193 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1122-2655A>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165734 | |||||||
| chr5:159165781 | G | A | 1 | a0001c0001t0003g0230 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1122-2702C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165781 | |||||||
| chr5:159165829 | T | C | 1 | a0001c0001t0001g0031 | 2 | NA18973.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1122-2750A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165829 | |||||||
| chr5:159165958 | G | T | 3 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0202 |
3 | HG02165.hp2 NA18988.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1122-2879C>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159165958 | |||||||
| chr5:159166040 | A | AGTACCAT others(27): Show |
1 | a0001c0001t0003g0197 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1121+2799_1121+283 others(38): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159166040 | |||||||
| chr5:159166084 | G | C | 1 | a0001c0001t0001g0153 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1121+2789C>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159166084 | |||||||
| chr5:159166117 | C | G | 1 | a0001c0001t0001g0195 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1121+2756G>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159166117 | |||||||
| chr5:159166365 | T | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
173 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1121+2508A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159166365 | |||||||
| chr5:159166528 | G | A | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1121+2345C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159166528 | |||||||
| chr5:159166566 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1121+2307A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159166566 | |||||||
| chr5:159166586 | T | G | 4 | a0001c0001t0002g0051 a0001c0001t0002g0052 a0001c0001t0002g0282 others(1): Show |
6 | HG02132.hp1 NA18939.hp1 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.1121+2287A>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159166586 | |||||||
| chr5:159166662 | G | A | 77 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(74): Show |
102 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1121+2211C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159166662 | |||||||
| chr5:159166941 | T | C | 1 | a0001c0001t0001g0041 | 2 | NA19009.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.1121+1932A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159166941 | |||||||
| chr5:159166960 | A | AAAAT | 15 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0056 others(12): Show |
18 | HG01109.hp1 HG01261.hp1 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.1121+1909_1121+191 others(8): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159166960 | |||||||
| chr5:159167077 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1121+1796G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159167077 | |||||||
| chr5:159167100 | T | C | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1121+1773A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159167100 | |||||||
| chr5:159167913 | A | G | 18 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(15): Show |
22 | HG00544.hp2 HG00642.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1121+960T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159167913 | |||||||
| chr5:159168839 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0095 |
3 | HG03139.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1121+34C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 8/10 | chr5 | 159168839 | |||||||
| chr5:159169209 | T | C | 1 | a0001c0001t0001g0212 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.939-154A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 7/10 | chr5 | 159169209 | |||||||
| chr5:159169365 | C | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(74): Show |
102 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.939-310G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 7/10 | chr5 | 159169365 | |||||||
| chr5:159169416 | C | T | 2 | a0001c0001t0004g0023 a0001c0001t0004g0077 |
3 | HG02723.hp2 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.938+263G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 7/10 | chr5 | 159169416 | |||||||
| chr5:159169447 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0102 |
3 | HG02109.hp2 HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.938+232C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 7/10 | chr5 | 159169447 | |||||||
| chr5:159169831 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.798-12C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159169831 | |||||||
| chr5:159169875 | C | A | 1 | a0001c0001t0002g0284 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.798-56G>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159169875 | |||||||
| chr5:159169981 | T | C | 19 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0078 others(16): Show |
23 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.798-162A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159169981 | |||||||
| chr5:159170184 | T | C | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.798-365A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159170184 | |||||||
| chr5:159170210 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.798-391C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159170210 | |||||||
| chr5:159170484 | A | G | 1 | a0001c0001t0002g0048 | 2 | HG01981.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.798-665T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159170484 | |||||||
| chr5:159170501 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.798-682A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159170501 | |||||||
| chr5:159170515 | T | TATTA | 3 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0202 |
3 | HG02165.hp2 NA18988.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.798-700_798-697dup others(4): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159170515 | |||||||
| chr5:159170516 | A | T | 2 | a0001c0001t0001g0176 a0001c0001t0016g0296 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.798-697T>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159170516 | |||||||
| chr5:159170597 | T | A | 1 | a0001c0001t0007g0046 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.798-778A>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159170597 | |||||||
| chr5:159170828 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.798-1009G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159170828 | |||||||
| chr5:159170845 | C | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0225 |
5 | NA18947.hp2 NA18961.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.798-1026G>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159170845 | |||||||
| chr5:159170854 | G | T | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0225 |
5 | NA18947.hp2 NA18961.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.798-1035C>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159170854 | |||||||
| chr5:159170908 | T | C | 2 | a0001c0001t0001g0124 a0001c0001t0001g0134 |
2 | HG01891.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.798-1089A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159170908 | |||||||
| chr5:159170928 | A | G | 18 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(15): Show |
22 | HG00544.hp2 HG00642.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.798-1109T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159170928 | |||||||
| chr5:159170973 | A | G | 18 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(15): Show |
22 | HG00544.hp2 HG00642.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.798-1154T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159170973 | |||||||
| chr5:159170997 | C | G | 2 | a0001c0001t0004g0023 a0001c0001t0004g0077 |
3 | HG02723.hp2 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.798-1178G>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159170997 | |||||||
| chr5:159171373 | C | T | 19 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0078 others(16): Show |
23 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.798-1554G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159171373 | |||||||
| chr5:159171416 | A | G | 3 | a0001c0001t0001g0081 a0001c0001t0001g0086 a0001c0001t0001g0087 |
3 | NA18968.hp2 NA18995.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.798-1597T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159171416 | |||||||
| chr5:159171450 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.798-1631A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159171450 | |||||||
| chr5:159171535 | T | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.798-1716A>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159171535 | |||||||
| chr5:159171537 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.798-1718C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159171537 | |||||||
| chr5:159171539 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.798-1720C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159171539 | |||||||
| chr5:159171540 | A | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.798-1721T>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159171540 | |||||||
| chr5:159171544 | G | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.798-1725C>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159171544 | |||||||
| chr5:159171545 | A | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.798-1726T>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159171545 | |||||||
| chr5:159171546 | A | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.798-1727T>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159171546 | |||||||
| chr5:159171547 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.798-1728T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159171547 | |||||||
| chr5:159171548 | G | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.798-1729C>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159171548 | |||||||
| chr5:159171549 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.798-1730T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159171549 | |||||||
| chr5:159171553 | T | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.798-1734A>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159171553 | |||||||
| chr5:159171553 | T | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0072 |
3 | HG02717.hp1 HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.798-1734A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159171553 | |||||||
| chr5:159171557 | A | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.798-1738T>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159171557 | |||||||
| chr5:159171560 | TTTATAAA others(544): Show |
T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1872_798-1742d others(2): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159171560 | |||||||
| chr5:159171636 | C | CA | 7 | a0001c0001t0001g0012 a0001c0001t0001g0074 a0001c0001t0001g0091 others(4): Show |
7 | HG01168.hp1 HG01978.hp2 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.798-1818dupT | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159171636 | |||||||
| chr5:159171889 | C | A | 2 | a0001c0001t0001g0176 a0001c0001t0016g0296 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.798-2070G>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159171889 | |||||||
| chr5:159171955 | A | G | 19 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0078 others(16): Show |
23 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.797+2028T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159171955 | |||||||
| chr5:159172112 | C | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1871G>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172112 | |||||||
| chr5:159172115 | T | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1868A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172115 | |||||||
| chr5:159172120 | T | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1863A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172120 | |||||||
| chr5:159172121 | C | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1862G>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172121 | |||||||
| chr5:159172123 | C | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1860G>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172123 | |||||||
| chr5:159172125 | C | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1858G>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172125 | |||||||
| chr5:159172126 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1857C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172126 | |||||||
| chr5:159172131 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1852C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172131 | |||||||
| chr5:159172134 | T | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1849A>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172134 | |||||||
| chr5:159172135 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1848T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172135 | |||||||
| chr5:159172137 | T | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1846A>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172137 | |||||||
| chr5:159172138 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1845T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172138 | |||||||
| chr5:159172140 | C | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1843G>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172140 | |||||||
| chr5:159172151 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1832T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172151 | |||||||
| chr5:159172153 | C | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1830G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172153 | |||||||
| chr5:159172157 | C | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1826G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172157 | |||||||
| chr5:159172158 | T | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1825A>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172158 | |||||||
| chr5:159172160 | T | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1823A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172160 | |||||||
| chr5:159172162 | T | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1821A>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172162 | |||||||
| chr5:159172163 | T | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1820A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172163 | |||||||
| chr5:159172168 | T | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1815A>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172168 | |||||||
| chr5:159172170 | T | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1813A>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172170 | |||||||
| chr5:159172172 | T | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1811A>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172172 | |||||||
| chr5:159172173 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1810T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172173 | |||||||
| chr5:159172174 | T | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1809A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172174 | |||||||
| chr5:159172175 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1808C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172175 | |||||||
| chr5:159172180 | T | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1803A>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172180 | |||||||
| chr5:159172185 | T | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1798A>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172185 | |||||||
| chr5:159172186 | T | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.797+1797A>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172186 | |||||||
| chr5:159172248 | TGA | T | 2 | a0001c0001t0004g0023 a0001c0001t0004g0077 |
3 | HG02723.hp2 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.797+1733_797+1734d others(4): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172248 | |||||||
| chr5:159172297 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.797+1686G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172297 | |||||||
| chr5:159172350 | G | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
173 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.797+1633C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172350 | |||||||
| chr5:159172389 | G | A | 2 | a0001c0001t0004g0023 a0001c0001t0004g0077 |
3 | HG02723.hp2 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.797+1594C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172389 | |||||||
| chr5:159172645 | T | C | 2 | a0001c0001t0001g0121 a0001c0001t0001g0142 |
2 | HG02071.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.797+1338A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172645 | |||||||
| chr5:159172929 | A | G | 18 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(15): Show |
22 | HG00544.hp2 HG00642.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.797+1054T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172929 | |||||||
| chr5:159172986 | T | A | 1 | a0001c0001t0001g0202 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.797+997A>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159172986 | |||||||
| chr5:159173292 | T | C | 18 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(15): Show |
22 | HG00544.hp2 HG00642.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.797+691A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159173292 | |||||||
| chr5:159173338 | G | A | 196 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(193): Show |
261 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.797+645C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159173338 | |||||||
| chr5:159173393 | C | G | 1 | a0001c0001t0001g0099 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.797+590G>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159173393 | |||||||
| chr5:159173449 | G | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(193): Show |
261 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.797+534C>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159173449 | |||||||
| chr5:159173577 | G | C | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.797+406C>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159173577 | |||||||
| chr5:159173768 | C | T | 18 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(15): Show |
22 | HG00544.hp2 HG00642.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.797+215G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159173768 | |||||||
| chr5:159173874 | G | A | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.797+109C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159173874 | |||||||
| chr5:159173913 | C | G | 18 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(15): Show |
22 | HG00544.hp2 HG00642.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.797+70G>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 6/10 | chr5 | 159173913 | |||||||
| chr5:159174263 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.622-105A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 5/10 | chr5 | 159174263 | |||||||
| chr5:159174559 | A | G | 4 | a0001c0001t0001g0004 a0001c0001t0001g0115 a0001c0001t0001g0158 others(1): Show |
8 | HG02572.hp2 HG02922.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.622-401T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 5/10 | chr5 | 159174559 | |||||||
| chr5:159174601 | A | G | 2 | a0001c0001t0004g0023 a0001c0001t0004g0077 |
3 | HG02723.hp2 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.622-443T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 5/10 | chr5 | 159174601 | |||||||
| chr5:159174648 | T | C | 2 | a0001c0001t0001g0176 a0001c0001t0016g0296 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.622-490A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 5/10 | chr5 | 159174648 | |||||||
| chr5:159174784 | T | TA | 9 | a0001c0001t0001g0063 a0001c0001t0001g0069 a0001c0001t0001g0154 others(6): Show |
9 | HG00544.hp1 HG00642.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.622-627dupT | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 5/10 | chr5 | 159174784 | |||||||
| chr5:159175323 | C | T | 3 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 |
3 | HG01168.hp1 HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.622-1165G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 5/10 | chr5 | 159175323 | |||||||
| chr5:159175344 | T | C | 2 | a0001c0001t0001g0176 a0001c0001t0016g0296 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.622-1186A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 5/10 | chr5 | 159175344 | |||||||
| chr5:159175451 | G | T | 1 | a0001c0001t0001g0174 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.621+1181C>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 5/10 | chr5 | 159175451 | |||||||
| chr5:159175580 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.621+1052A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 5/10 | chr5 | 159175580 | |||||||
| chr5:159175638 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.621+994C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 5/10 | chr5 | 159175638 | |||||||
| chr5:159175686 | A | G | 18 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(15): Show |
22 | HG00544.hp2 HG00642.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.621+946T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 5/10 | chr5 | 159175686 | |||||||
| chr5:159175805 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.621+827A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 5/10 | chr5 | 159175805 | |||||||
| chr5:159175999 | A | C | 18 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(15): Show |
22 | HG00544.hp2 HG00642.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.621+633T>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 5/10 | chr5 | 159175999 | |||||||
| chr5:159176177 | C | A | 1 | a0001c0001t0001g0166 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.621+455G>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 5/10 | chr5 | 159176177 | |||||||
| chr5:159176263 | T | C | 24 | a0001c0001t0001g0176 a0001c0001t0002g0017 a0001c0001t0002g0047 others(21): Show |
32 | HG00280.hp1 HG00323.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.621+369A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 5/10 | chr5 | 159176263 | |||||||
| chr5:159176303 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.621+329A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 5/10 | chr5 | 159176303 | |||||||
| chr5:159176338 | G | A | 2 | a0001c0001t0001g0176 a0001c0001t0016g0296 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.621+294C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 5/10 | chr5 | 159176338 | |||||||
| chr5:159176563 | T | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
173 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.621+69A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 5/10 | chr5 | 159176563 | |||||||
| chr5:159177117 | G | A | 4 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0086 others(1): Show |
4 | NA18612.hp1 NA18968.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-250C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159177117 | |||||||
| chr5:159177252 | T | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0072 |
3 | HG02717.hp1 HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.386-385A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159177252 | |||||||
| chr5:159177376 | A | G | 19 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0078 others(16): Show |
23 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.386-509T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159177376 | |||||||
| chr5:159177482 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.386-615A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159177482 | |||||||
| chr5:159177503 | G | A | 7 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0049 others(4): Show |
11 | HG00280.hp1 HG00323.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.386-636C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159177503 | |||||||
| chr5:159177622 | C | T | 1 | a0001c0001t0002g0278 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.386-755G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159177622 | |||||||
| chr5:159177632 | T | C | 27 | a0001c0001t0001g0176 a0001c0001t0002g0017 a0001c0001t0002g0047 others(24): Show |
36 | HG00280.hp1 HG00323.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.386-765A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159177632 | |||||||
| chr5:159177847 | A | G | 1 | a0001c0001t0002g0282 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.386-980T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159177847 | |||||||
| chr5:159177934 | C | T | 5 | a0001c0001t0001g0119 a0001c0001t0001g0129 a0001c0001t0001g0130 others(2): Show |
5 | HG00609.hp2 HG02129.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.386-1067G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159177934 | |||||||
| chr5:159177955 | G | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
173 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.386-1088C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159177955 | |||||||
| chr5:159177973 | G | A | 2 | a0001c0001t0001g0176 a0001c0001t0016g0296 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.386-1106C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159177973 | |||||||
| chr5:159178048 | C | A | 8 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0095 others(5): Show |
12 | HG01943.hp2 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.386-1181G>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159178048 | |||||||
| chr5:159178073 | T | C | 5 | a0001c0001t0001g0028 a0001c0001t0001g0064 a0001c0001t0001g0104 others(2): Show |
6 | HG01891.hp1 HG02109.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.386-1206A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159178073 | |||||||
| chr5:159178217 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.386-1350G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159178217 | |||||||
| chr5:159178252 | G | A | 1 | a0001c0001t0001g0267 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.386-1385C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159178252 | |||||||
| chr5:159178579 | T | C | 19 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0078 others(16): Show |
23 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.386-1712A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159178579 | |||||||
| chr5:159178619 | T | G | 23 | a0001c0001t0002g0017 a0001c0001t0002g0047 a0001c0001t0002g0048 others(20): Show |
31 | HG00280.hp1 HG00323.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.386-1752A>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159178619 | |||||||
| chr5:159178650 | C | T | 8 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0056 others(5): Show |
9 | HG01109.hp1 HG01261.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.386-1783G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159178650 | |||||||
| chr5:159178712 | T | G | 1 | a0001c0001t0001g0217 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.386-1845A>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159178712 | |||||||
| chr5:159179144 | T | G | 1 | a0001c0001t0001g0056 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.386-2277A>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159179144 | |||||||
| chr5:159179331 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.386-2464T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159179331 | |||||||
| chr5:159179411 | T | C | 1 | a0001c0001t0002g0279 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.386-2544A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159179411 | |||||||
| chr5:159179487 | A | G | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.385+2473T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159179487 | |||||||
| chr5:159179700 | T | C | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.385+2260A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159179700 | |||||||
| chr5:159180087 | T | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0102 a0001c0001t0001g0103 |
4 | HG02109.hp2 HG03041.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+1873A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159180087 | |||||||
| chr5:159180289 | G | A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0027 others(8): Show |
16 | HG01943.hp2 HG02109.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.385+1671C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159180289 | |||||||
| chr5:159180472 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.385+1488G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159180472 | |||||||
| chr5:159180473 | T | C | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.385+1487A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159180473 | |||||||
| chr5:159180474 | A | C | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.385+1486T>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159180474 | |||||||
| chr5:159180544 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.385+1416G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159180544 | |||||||
| chr5:159180958 | A | T | 1 | a0001c0001t0001g0148 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.385+1002T>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159180958 | |||||||
| chr5:159180983 | C | T | 292 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(289): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.385+977G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159180983 | |||||||
| chr5:159181039 | T | G | 1 | a0001c0001t0001g0156 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.385+921A>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159181039 | |||||||
| chr5:159181078 | T | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(193): Show |
261 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.385+882A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159181078 | |||||||
| chr5:159181118 | G | C | 4 | a0001c0001t0001g0006 a0001c0001t0001g0112 a0001c0001t0001g0157 others(1): Show |
7 | HG01943.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.385+842C>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159181118 | |||||||
| chr5:159181128 | C | CA | 93 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(90): Show |
122 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.385+831dupT | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159181128 | |||||||
| chr5:159181242 | C | T | 1 | a0001c0001t0002g0278 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.385+718G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159181242 | |||||||
| chr5:159181724 | A | G | 4 | a0001c0001t0001g0015 a0001c0001t0001g0200 a0001c0001t0001g0212 others(1): Show |
6 | NA18944.hp1 NA18972.hp2 NA19012.hp1 others(3): Show |
intron_variant | MODIFIER | c.385+236T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159181724 | |||||||
| chr5:159181730 | AC | A | 19 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0078 others(16): Show |
23 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.385+229delG | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159181730 | |||||||
| chr5:159181750 | T | G | 1 | a0001c0001t0001g0272 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.385+210A>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159181750 | |||||||
| chr5:159181800 | T | TA | 10 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0056 others(7): Show |
11 | HG00423.hp2 HG01109.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.385+159dupT | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159181800 | |||||||
| chr5:159181817 | C | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(193): Show |
261 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.385+143G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159181817 | |||||||
| chr5:159181830 | T | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0070 |
2 | HG01081.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.385+130A>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159181830 | |||||||
| chr5:159181872 | T | C | 24 | a0001c0001t0001g0063 a0001c0001t0002g0017 a0001c0001t0002g0047 others(21): Show |
32 | HG00280.hp1 HG00323.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.385+88A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159181872 | |||||||
| chr5:159181890 | T | A | 1 | a0001c0001t0001g0217 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.385+70A>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 4/10 | chr5 | 159181890 | |||||||
| chr5:159182168 | T | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0072 |
3 | HG02717.hp1 HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.294-117A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159182168 | |||||||
| chr5:159182360 | T | A | 17 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(14): Show |
21 | HG00544.hp2 HG00642.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.294-309A>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159182360 | |||||||
| chr5:159182445 | C | G | 1 | a0001c0001t0001g0063 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.294-394G>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159182445 | |||||||
| chr5:159182472 | G | A | 1 | a0001c0001t0005g0289 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.294-421C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159182472 | |||||||
| chr5:159182608 | T | C | 19 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0078 others(16): Show |
23 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.294-557A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159182608 | |||||||
| chr5:159182843 | G | T | 2 | a0001c0001t0004g0023 a0001c0001t0004g0077 |
3 | HG02723.hp2 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.294-792C>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159182843 | |||||||
| chr5:159183010 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.294-959A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159183010 | |||||||
| chr5:159183032 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0072 |
3 | HG02717.hp1 HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.294-981G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159183032 | |||||||
| chr5:159183057 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.294-1006C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159183057 | |||||||
| chr5:159183186 | T | C | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.294-1135A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159183186 | |||||||
| chr5:159183250 | A | C | 2 | a0001c0001t0004g0023 a0001c0001t0004g0077 |
3 | HG02723.hp2 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.294-1199T>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159183250 | |||||||
| chr5:159183401 | G | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(193): Show |
261 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.294-1350C>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159183401 | |||||||
| chr5:159183568 | A | C | 1 | a0001c0001t0001g0109 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.294-1517T>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159183568 | |||||||
| chr5:159183587 | A | T | 1 | a0001c0001t0001g0112 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.294-1536T>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159183587 | |||||||
| chr5:159183613 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.294-1562A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159183613 | |||||||
| chr5:159183737 | C | T | 7 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0056 others(4): Show |
8 | HG01109.hp1 HG01261.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.294-1686G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159183737 | |||||||
| chr5:159183847 | C | T | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(270): Show |
363 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(360): Show |
intron_variant | MODIFIER | c.294-1796G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159183847 | |||||||
| chr5:159183907 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.294-1856C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159183907 | |||||||
| chr5:159183987 | A | T | 1 | a0001c0001t0001g0073 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.294-1936T>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159183987 | |||||||
| chr5:159184453 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.294-2402G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159184453 | |||||||
| chr5:159184507 | T | G | 1 | a0001c0001t0001g0177 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.294-2456A>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159184507 | |||||||
| chr5:159184511 | A | C | 1 | a0001c0002t0002g0290 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.294-2460T>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159184511 | |||||||
| chr5:159184986 | G | A | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.294-2935C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159184986 | |||||||
| chr5:159185034 | T | C | 2 | a0001c0001t0001g0122 a0001c0001t0001g0149 |
2 | HG02027.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.294-2983A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159185034 | |||||||
| chr5:159185101 | T | C | 1 | a0001c0001t0001g0126 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.294-3050A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159185101 | |||||||
| chr5:159185139 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.294-3088G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159185139 | |||||||
| chr5:159185504 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.294-3453A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159185504 | |||||||
| chr5:159185565 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.294-3514A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159185565 | |||||||
| chr5:159185948 | C | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(193): Show |
261 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.294-3897G>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159185948 | |||||||
| chr5:159186130 | C | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(193): Show |
261 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.294-4079G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159186130 | |||||||
| chr5:159186142 | GT | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0065 a0001c0001t0001g0066 |
4 | HG01243.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.294-4092delA | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159186142 | |||||||
| chr5:159186229 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.294-4178T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159186229 | |||||||
| chr5:159186531 | T | G | 1 | a0001c0001t0001g0139 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.294-4480A>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159186531 | |||||||
| chr5:159186755 | G | GTATT | 2 | a0001c0001t0001g0022 a0001c0001t0001g0072 |
3 | HG02717.hp1 HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.294-4708_294-4705d others(6): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159186755 | |||||||
| chr5:159186781 | C | A | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(269): Show |
362 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(359): Show |
intron_variant | MODIFIER | c.294-4730G>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159186781 | |||||||
| chr5:159186944 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.294-4893A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159186944 | |||||||
| chr5:159187037 | T | C | 41 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(38): Show |
53 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.294-4986A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159187037 | |||||||
| chr5:159187079 | A | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(129): Show |
180 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.294-5028T>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159187079 | |||||||
| chr5:159187098 | T | G | 1 | a0001c0001t0001g0168 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.294-5047A>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159187098 | |||||||
| chr5:159187148 | G | C | 1 | a0001c0001t0001g0128 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.294-5097C>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159187148 | |||||||
| chr5:159187239 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.294-5188C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159187239 | |||||||
| chr5:159187316 | T | G | 5 | a0001c0001t0001g0119 a0001c0001t0001g0129 a0001c0001t0001g0130 others(2): Show |
5 | HG00609.hp2 HG02129.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.294-5265A>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159187316 | |||||||
| chr5:159187327 | A | T | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.294-5276T>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159187327 | |||||||
| chr5:159187339 | T | A | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.294-5288A>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159187339 | |||||||
| chr5:159187349 | A | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(133): Show |
186 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.294-5298T>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159187349 | |||||||
| chr5:159187404 | T | C | 2 | a0001c0001t0001g0082 a0001c0001t0001g0093 |
2 | HG01123.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.294-5353A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159187404 | |||||||
| chr5:159187460 | T | C | 19 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0062 others(16): Show |
23 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.294-5409A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159187460 | |||||||
| chr5:159187472 | T | C | 4 | a0001c0001t0001g0066 a0001c0001t0001g0103 a0001c0001t0001g0153 others(1): Show |
4 | HG01169.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.294-5421A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159187472 | |||||||
| chr5:159187476 | T | C | 4 | a0001c0001t0001g0066 a0001c0001t0001g0103 a0001c0001t0001g0153 others(1): Show |
4 | HG01169.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.294-5425A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159187476 | |||||||
| chr5:159187515 | T | C | 5 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0002t0002g0286 others(2): Show |
5 | HG03098.hp2 HG03453.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.294-5464A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159187515 | |||||||
| chr5:159187538 | A | G | 32 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0037 others(29): Show |
44 | HG00438.hp1 HG00544.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.294-5487T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159187538 | |||||||
| chr5:159187599 | C | T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(244): Show |
333 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.294-5548G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159187599 | |||||||
| chr5:159187610 | T | A | 1 | a0001c0001t0003g0235 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.294-5559A>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159187610 | |||||||
| chr5:159187617 | A | G | 113 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0015 others(110): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.294-5566T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159187617 | |||||||
| chr5:159187622 | C | T | 1 | a0001c0001t0001g0042 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.294-5571G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159187622 | |||||||
| chr5:159187633 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.294-5582A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159187633 | |||||||
| chr5:159188033 | C | A | 12 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0041 others(9): Show |
17 | HG00597.hp1 HG02015.hp2 HG02129.hp2 others(14): Show |
intron_variant | MODIFIER | c.294-5982G>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159188033 | |||||||
| chr5:159188210 | A | G | 10 | a0001c0001t0001g0018 a0001c0001t0001g0035 a0001c0001t0001g0055 others(7): Show |
12 | HG01099.hp2 HG01109.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.294-6159T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159188210 | |||||||
| chr5:159188218 | TA | T | 25 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(22): Show |
33 | HG00280.hp1 HG00323.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.294-6168delT | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159188218 | |||||||
| chr5:159188304 | G | A | 19 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0078 others(16): Show |
23 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.294-6253C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159188304 | |||||||
| chr5:159188319 | G | A | 66 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(63): Show |
86 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.294-6268C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159188319 | |||||||
| chr5:159188349 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.294-6298C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159188349 | |||||||
| chr5:159188393 | C | CA | 11 | a0001c0001t0001g0022 a0001c0001t0001g0062 a0001c0001t0001g0072 others(8): Show |
14 | HG00597.hp1 HG02132.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.293+6322dupT | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159188393 | |||||||
| chr5:159188399 | A | C | 1 | a0001c0001t0003g0189 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.293+6317T>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159188399 | |||||||
| chr5:159188485 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.293+6231G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159188485 | |||||||
| chr5:159188559 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.293+6157G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159188559 | |||||||
| chr5:159188891 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.293+5825T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159188891 | |||||||
| chr5:159188929 | T | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
260 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.293+5787A>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159188929 | |||||||
| chr5:159189017 | T | C | 2 | a0001c0001t0003g0236 a0001c0001t0003g0237 |
2 | HG00323.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.293+5699A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159189017 | |||||||
| chr5:159189091 | T | TATAGATC others(30): Show |
1 | a0001c0001t0001g0085 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.293+5588_293+5624d others(39): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159189091 | |||||||
| chr5:159189091 | TATAGATC others(30): Show |
T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0063 a0001c0001t0001g0072 |
4 | HG01081.hp2 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.293+5588_293+5624d others(39): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159189091 | |||||||
| chr5:159189175 | A | G | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.293+5541T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159189175 | |||||||
| chr5:159189232 | A | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0095 others(5): Show |
12 | HG01943.hp2 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.293+5484T>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159189232 | |||||||
| chr5:159189238 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.293+5478T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159189238 | |||||||
| chr5:159189282 | T | C | 6 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(3): Show |
7 | HG02622.hp2 HG02723.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.293+5434A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159189282 | |||||||
| chr5:159189395 | C | A | 19 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0078 others(16): Show |
23 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.293+5321G>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159189395 | |||||||
| chr5:159189407 | C | A | 1 | a0002c0005t0001g0135 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.293+5309G>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159189407 | |||||||
| chr5:159189745 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.293+4971G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159189745 | |||||||
| chr5:159189776 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0010g0258 |
2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.293+4940G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159189776 | |||||||
| chr5:159190087 | G | C | 1 | a0001c0001t0001g0136 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.293+4629C>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159190087 | |||||||
| chr5:159190109 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0072 |
3 | HG02717.hp1 HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.293+4607G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159190109 | |||||||
| chr5:159190413 | C | T | 1 | a0001c0001t0001g0012 | 3 | NA18967.hp1 NA19072.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.293+4303G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159190413 | |||||||
| chr5:159190517 | T | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(112): Show |
161 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.293+4199A>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159190517 | |||||||
| chr5:159190681 | CA | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(154): Show |
215 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.293+4034delT | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159190681 | |||||||
| chr5:159190681 | CAA | C | 32 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0018 others(29): Show |
40 | HG00099.hp2 HG01070.hp2 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.293+4033_293+4034d others(4): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159190681 | |||||||
| chr5:159190767 | C | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0072 |
3 | HG02717.hp1 HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.293+3949G>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159190767 | |||||||
| chr5:159190801 | T | C | 1 | a0001c0001t0007g0046 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.293+3915A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159190801 | |||||||
| chr5:159190885 | T | C | 5 | a0001c0001t0001g0024 a0001c0001t0001g0098 a0001c0001t0001g0099 others(2): Show |
6 | NA18949.hp2 NA18969.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.293+3831A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159190885 | |||||||
| chr5:159190911 | T | G | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.293+3805A>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159190911 | |||||||
| chr5:159191079 | C | CA | 6 | a0001c0001t0001g0244 a0001c0001t0001g0247 a0001c0001t0001g0248 others(3): Show |
6 | HG00423.hp2 HG03516.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.293+3636dupT | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159191079 | |||||||
| chr5:159191192 | G | C | 13 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0041 others(10): Show |
18 | HG00597.hp1 HG02015.hp2 HG02129.hp2 others(15): Show |
intron_variant | MODIFIER | c.293+3524C>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159191192 | |||||||
| chr5:159191257 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(112): Show |
161 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.293+3459A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159191257 | |||||||
| chr5:159191298 | A | G | 1 | a0001c0001t0001g0116 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.293+3418T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159191298 | |||||||
| chr5:159191485 | A | C | 1 | a0001c0001t0001g0209 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.293+3231T>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159191485 | |||||||
| chr5:159191561 | G | A | 8 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0056 others(5): Show |
9 | HG01109.hp1 HG01261.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.293+3155C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159191561 | |||||||
| chr5:159191601 | G | A | 2 | a0001c0001t0001g0153 a0001c0004t0001g0165 |
2 | HG01169.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.293+3115C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159191601 | |||||||
| chr5:159191654 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.293+3062A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159191654 | |||||||
| chr5:159191664 | T | C | 1 | a0001c0001t0001g0272 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.293+3052A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159191664 | |||||||
| chr5:159191741 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.293+2975C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159191741 | |||||||
| chr5:159191849 | T | G | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.293+2867A>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159191849 | |||||||
| chr5:159191925 | C | T | 17 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(14): Show |
22 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.293+2791G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159191925 | |||||||
| chr5:159192051 | G | GA | 19 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(16): Show |
25 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.293+2664dupT | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159192051 | |||||||
| chr5:159192060 | A | G | 1 | a0001c0001t0016g0296 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.293+2656T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159192060 | |||||||
| chr5:159192064 | A | C | 1 | a0001c0001t0002g0047 | 2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.293+2652T>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159192064 | |||||||
| chr5:159192083 | T | C | 1 | a0001c0001t0003g0189 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.293+2633A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159192083 | |||||||
| chr5:159192108 | C | G | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.293+2608G>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159192108 | |||||||
| chr5:159192181 | G | T | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.293+2535C>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159192181 | |||||||
| chr5:159192500 | CA | C | 6 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(3): Show |
7 | HG02622.hp2 HG02723.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.293+2215delT | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159192500 | |||||||
| chr5:159192529 | C | T | 1 | a0001c0001t0008g0053 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.293+2187G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159192529 | |||||||
| chr5:159192666 | A | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0109 a0001c0001t0009g0110 |
4 | HG01069.hp2 HG01071.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.293+2050T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159192666 | |||||||
| chr5:159192725 | G | C | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.293+1991C>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159192725 | |||||||
| chr5:159192827 | G | A | 25 | a0001c0001t0002g0017 a0001c0001t0002g0047 a0001c0001t0002g0048 others(22): Show |
33 | HG00280.hp1 HG00323.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.293+1889C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159192827 | |||||||
| chr5:159192951 | G | T | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | NA18977.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.293+1765C>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159192951 | |||||||
| chr5:159193040 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.293+1676C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159193040 | |||||||
| chr5:159193071 | T | G | 26 | a0001c0001t0001g0063 a0001c0001t0002g0017 a0001c0001t0002g0047 others(23): Show |
34 | HG00280.hp1 HG00323.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.293+1645A>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159193071 | |||||||
| chr5:159193164 | A | G | 2 | a0001c0001t0001g0105 a0001c0001t0001g0159 |
2 | NA18993.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.293+1552T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159193164 | |||||||
| chr5:159193322 | G | A | 1 | a0001c0001t0002g0284 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.293+1394C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159193322 | |||||||
| chr5:159193434 | C | T | 1 | a0001c0001t0002g0277 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.293+1282G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159193434 | |||||||
| chr5:159193513 | C | T | 19 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0078 others(16): Show |
23 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.293+1203G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159193513 | |||||||
| chr5:159193688 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.293+1028A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159193688 | |||||||
| chr5:159194010 | T | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0140 a0001c0001t0001g0163 |
5 | HG02040.hp1 NA18967.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.293+706A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159194010 | |||||||
| chr5:159194073 | A | G | 1 | a0001c0001t0001g0190 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.293+643T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159194073 | |||||||
| chr5:159194102 | T | C | 2 | a0001c0001t0004g0023 a0001c0001t0004g0077 |
3 | HG02723.hp2 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.293+614A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159194102 | |||||||
| chr5:159194174 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.293+542A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159194174 | |||||||
| chr5:159194325 | C | A | 8 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0056 others(5): Show |
9 | HG01109.hp1 HG01261.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.293+391G>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159194325 | |||||||
| chr5:159194360 | C | T | 65 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(62): Show |
85 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.293+356G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159194360 | |||||||
| chr5:159194482 | T | C | 4 | a0001c0001t0001g0036 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
5 | HG00140.hp2 HG00735.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.293+234A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 3/10 | chr5 | 159194482 | |||||||
| chr5:159194972 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.185-148A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159194972 | |||||||
| chr5:159194986 | T | C | 1 | a0001c0004t0001g0165 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.185-162A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159194986 | |||||||
| chr5:159195026 | CT | C | 16 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(13): Show |
21 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.185-203delA | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159195026 | |||||||
| chr5:159195077 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.185-253G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159195077 | |||||||
| chr5:159195092 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.185-268G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159195092 | |||||||
| chr5:159195108 | A | C | 1 | a0001c0001t0001g0251 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.185-284T>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159195108 | |||||||
| chr5:159195403 | G | C | 1 | a0001c0001t0001g0266 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.185-579C>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159195403 | |||||||
| chr5:159195415 | AC | A | 3 | a0001c0001t0003g0196 a0001c0001t0003g0197 a0001c0001t0003g0249 |
3 | NA18978.hp1 NA18997.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.185-592delG | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159195415 | |||||||
| chr5:159195524 | C | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(87): Show |
125 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.185-700G>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159195524 | |||||||
| chr5:159195583 | C | A | 1 | a0001c0001t0001g0090 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.185-759G>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159195583 | |||||||
| chr5:159196140 | C | A | 1 | a0001c0001t0001g0142 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.185-1316G>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159196140 | |||||||
| chr5:159196167 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.185-1343C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159196167 | |||||||
| chr5:159196229 | G | GT | 24 | a0001c0001t0001g0018 a0001c0001t0001g0037 a0001c0001t0001g0038 others(21): Show |
28 | HG00438.hp1 HG00597.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.185-1406dupA | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159196229 | |||||||
| chr5:159196229 | GT | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(168): Show |
233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.185-1406delA | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159196229 | |||||||
| chr5:159196232 | T | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0072 |
3 | HG02717.hp1 HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.185-1408A>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159196232 | |||||||
| chr5:159196275 | G | A | 5 | a0001c0001t0001g0024 a0001c0001t0001g0098 a0001c0001t0001g0099 others(2): Show |
6 | NA18949.hp2 NA18969.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.185-1451C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159196275 | |||||||
| chr5:159196278 | T | G | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.185-1454A>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159196278 | |||||||
| chr5:159196308 | T | C | 1 | a0001c0001t0001g0255 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.185-1484A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159196308 | |||||||
| chr5:159196592 | C | A | 3 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 |
3 | HG02622.hp2 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.185-1768G>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159196592 | |||||||
| chr5:159196873 | T | C | 19 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0190 others(16): Show |
24 | HG00423.hp2 HG00597.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.185-2049A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159196873 | |||||||
| chr5:159196881 | C | T | 12 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0067 others(9): Show |
16 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.185-2057G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159196881 | |||||||
| chr5:159196925 | C | T | 2 | a0001c0001t0004g0023 a0001c0001t0004g0077 |
3 | HG02723.hp2 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.185-2101G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159196925 | |||||||
| chr5:159196940 | G | C | 2 | a0001c0001t0001g0062 a0001c0001t0010g0258 |
2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.185-2116C>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159196940 | |||||||
| chr5:159196973 | T | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0072 |
3 | HG02717.hp1 HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.185-2149A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159196973 | |||||||
| chr5:159197042 | T | A | 1 | a0001c0001t0001g0267 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.185-2218A>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159197042 | |||||||
| chr5:159197335 | T | C | 4 | a0001c0002t0002g0286 a0001c0002t0002g0287 a0001c0002t0002g0290 others(1): Show |
4 | HG02818.hp1 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.185-2511A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159197335 | |||||||
| chr5:159197449 | C | T | 1 | a0001c0001t0001g0272 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.185-2625G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159197449 | |||||||
| chr5:159197506 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.185-2682C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159197506 | |||||||
| chr5:159197561 | A | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
260 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.185-2737T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159197561 | |||||||
| chr5:159197567 | TACTA | T | 3 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 |
3 | HG02622.hp2 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.185-2747_185-2744d others(6): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159197567 | |||||||
| chr5:159197576 | T | C | 1 | a0001c0001t0001g0272 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.185-2752A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159197576 | |||||||
| chr5:159197743 | T | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(112): Show |
161 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.185-2919A>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159197743 | |||||||
| chr5:159197960 | G | A | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.185-3136C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159197960 | |||||||
| chr5:159198160 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.185-3336G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159198160 | |||||||
| chr5:159198196 | T | C | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(256): Show |
345 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(342): Show |
intron_variant | MODIFIER | c.185-3372A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159198196 | |||||||
| chr5:159198239 | CTAAA | C | 105 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(102): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.185-3419_185-3416d others(6): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159198239 | |||||||
| chr5:159198239 | CTAAATAA others(1): Show |
C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(122): Show |
173 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.185-3423_185-3416d others(10): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159198239 | |||||||
| chr5:159198239 | CTAAATAA others(5): Show |
C | 32 | a0001c0001t0001g0062 a0001c0001t0001g0091 a0001c0001t0002g0017 others(29): Show |
45 | HG00280.hp1 HG00323.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.185-3427_185-3416d others(14): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159198239 | |||||||
| chr5:159198449 | T | C | 1 | a0001c0001t0016g0296 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.185-3625A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159198449 | |||||||
| chr5:159198780 | T | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.185-3956A>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159198780 | |||||||
| chr5:159198975 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.185-4151G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159198975 | |||||||
| chr5:159199011 | T | C | 1 | a0001c0001t0001g0243 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.185-4187A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159199011 | |||||||
| chr5:159199054 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.185-4230G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159199054 | |||||||
| chr5:159199103 | T | C | 22 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0078 others(19): Show |
26 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.185-4279A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159199103 | |||||||
| chr5:159199199 | C | G | 16 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(13): Show |
21 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.184+4235G>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159199199 | |||||||
| chr5:159199266 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.184+4168G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159199266 | |||||||
| chr5:159199329 | C | A | 3 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 |
3 | HG02622.hp2 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.184+4105G>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159199329 | |||||||
| chr5:159199339 | C | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.184+4095G>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159199339 | |||||||
| chr5:159199389 | GA | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(185): Show |
254 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.184+4044delT | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159199389 | |||||||
| chr5:159199889 | C | A | 1 | a0001c0001t0002g0285 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.184+3545G>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159199889 | |||||||
| chr5:159199962 | T | A | 2 | a0001c0001t0004g0023 a0001c0001t0004g0077 |
3 | HG02723.hp2 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.184+3472A>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159199962 | |||||||
| chr5:159200005 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0102 a0001c0001t0001g0103 |
4 | HG02109.hp2 HG03041.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.184+3429G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159200005 | |||||||
| chr5:159200012 | A | T | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.184+3422T>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159200012 | |||||||
| chr5:159200125 | C | T | 3 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 |
3 | HG02622.hp2 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.184+3309G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159200125 | |||||||
| chr5:159200130 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0065 a0001c0001t0001g0066 |
4 | HG01243.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.184+3304G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159200130 | |||||||
| chr5:159200241 | T | C | 1 | a0001c0001t0001g0163 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.184+3193A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159200241 | |||||||
| chr5:159200294 | G | C | 1 | a0001c0001t0001g0147 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.184+3140C>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159200294 | |||||||
| chr5:159200373 | C | T | 3 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 |
3 | HG02622.hp2 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.184+3061G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159200373 | |||||||
| chr5:159200461 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0148 |
3 | NA18956.hp2 NA18981.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.184+2973C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159200461 | |||||||
| chr5:159200810 | T | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0072 |
3 | HG02717.hp1 HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.184+2624A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159200810 | |||||||
| chr5:159200903 | T | C | 1 | a0001c0001t0010g0258 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.184+2531A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159200903 | |||||||
| chr5:159200999 | C | A | 1 | a0001c0001t0001g0089 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.184+2435G>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159200999 | |||||||
| chr5:159201179 | C | T | 17 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(14): Show |
22 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.184+2255G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159201179 | |||||||
| chr5:159201185 | C | A | 19 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0078 others(16): Show |
23 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.184+2249G>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159201185 | |||||||
| chr5:159201305 | T | G | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG01261.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.184+2129A>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159201305 | |||||||
| chr5:159201434 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.184+2000T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159201434 | |||||||
| chr5:159201584 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.184+1850A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159201584 | |||||||
| chr5:159201613 | T | C | 3 | a0001c0001t0001g0062 a0001c0001t0004g0023 a0001c0001t0004g0077 |
4 | HG02559.hp2 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.184+1821A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159201613 | |||||||
| chr5:159201695 | A | G | 27 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0018 others(24): Show |
32 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.184+1739T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159201695 | |||||||
| chr5:159201901 | T | A | 1 | a0001c0001t0001g0269 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.184+1533A>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159201901 | |||||||
| chr5:159201908 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.184+1526C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159201908 | |||||||
| chr5:159201968 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.184+1466C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159201968 | |||||||
| chr5:159202134 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.184+1300C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159202134 | |||||||
| chr5:159202554 | AGTTTTAG | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0072 |
3 | HG02717.hp1 HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.184+873_184+879del others(7): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159202554 | |||||||
| chr5:159202602 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.184+832G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159202602 | |||||||
| chr5:159202870 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.184+564G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159202870 | |||||||
| chr5:159202920 | C | CA | 8 | a0001c0001t0001g0079 a0001c0001t0001g0150 a0001c0001t0001g0164 others(5): Show |
8 | HG03453.hp2 HG03471.hp2 NA18906.hp1 others(5): Show |
intron_variant | MODIFIER | c.184+513dupT | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159202920 | |||||||
| chr5:159202979 | T | C | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 |
3 | HG00597.hp2 NA18953.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.184+455A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159202979 | |||||||
| chr5:159203033 | G | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.184+401C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159203033 | |||||||
| chr5:159203038 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(111): Show |
160 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.184+396G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159203038 | |||||||
| chr5:159203131 | G | A | 1 | a0001c0001t0001g0042 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.184+303C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159203131 | |||||||
| chr5:159203162 | T | A | 1 | a0001c0001t0001g0269 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.184+272A>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159203162 | |||||||
| chr5:159203275 | T | C | 1 | a0001c0001t0007g0046 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.184+159A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 2/10 | chr5 | 159203275 | |||||||
| chr5:159203901 | A | G | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | NA18983.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-39-245T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159203901 | |||||||
| chr5:159204170 | C | A | 3 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 |
3 | HG02622.hp2 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-39-514G>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159204170 | |||||||
| chr5:159204207 | G | A | 1 | a0001c0006t0002g0288 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-39-551C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159204207 | |||||||
| chr5:159204386 | TG | T | 38 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0018 others(35): Show |
45 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.-39-731delC | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159204386 | |||||||
| chr5:159204395 | G | T | 1 | a0001c0001t0001g0154 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-39-739C>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159204395 | |||||||
| chr5:159204396 | C | G | 1 | a0001c0001t0001g0100 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-39-740G>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159204396 | |||||||
| chr5:159204485 | T | C | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-39-829A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159204485 | |||||||
| chr5:159204528 | G | A | 2 | a0001c0001t0001g0153 a0001c0004t0001g0165 |
2 | HG01169.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-39-872C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159204528 | |||||||
| chr5:159204596 | G | A | 1 | a0001c0001t0016g0296 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-39-940C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159204596 | |||||||
| chr5:159204803 | C | CA | 17 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0246 others(14): Show |
19 | HG00423.hp2 HG01123.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.-39-1148dupT | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159204803 | |||||||
| chr5:159204803 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0016g0296 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-39-1158_-39-1148d others(13): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159204803 | |||||||
| chr5:159204827 | A | AAG | 29 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0061 others(26): Show |
34 | HG00741.hp2 HG01106.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.-39-1172_-39-1171i others(4): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159204827 | |||||||
| chr5:159204827 | A | AG | 147 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(144): Show |
203 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.-39-1172dupC | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159204827 | |||||||
| chr5:159204827 | A | G | 15 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0034 others(12): Show |
20 | HG00140.hp2 HG00639.hp1 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.-39-1171T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159204827 | |||||||
| chr5:159204971 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-39-1315G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159204971 | |||||||
| chr5:159205020 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-39-1364A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159205020 | |||||||
| chr5:159205099 | G | A | 1 | a0001c0001t0006g0274 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-39-1443C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159205099 | |||||||
| chr5:159205154 | AT | A | 16 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(13): Show |
21 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-39-1499delA | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159205154 | |||||||
| chr5:159205199 | T | C | 3 | a0001c0001t0001g0062 a0001c0001t0004g0023 a0001c0001t0004g0077 |
4 | HG02559.hp2 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39-1543A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159205199 | |||||||
| chr5:159205292 | T | G | 1 | a0001c0001t0001g0170 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-39-1636A>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159205292 | |||||||
| chr5:159205372 | T | A | 4 | a0001c0001t0001g0062 a0001c0001t0004g0023 a0001c0001t0004g0077 others(1): Show |
5 | HG02559.hp2 HG02622.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-39-1716A>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159205372 | |||||||
| chr5:159205393 | G | A | 31 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0018 others(28): Show |
36 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.-39-1737C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159205393 | |||||||
| chr5:159205559 | G | A | 19 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0078 others(16): Show |
23 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.-39-1903C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159205559 | |||||||
| chr5:159205602 | T | C | 16 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(13): Show |
21 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-39-1946A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159205602 | |||||||
| chr5:159205978 | C | G | 17 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(14): Show |
22 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.-39-2322G>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159205978 | |||||||
| chr5:159206130 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-39-2474T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159206130 | |||||||
| chr5:159206133 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-39-2477C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159206133 | |||||||
| chr5:159206581 | G | A | 9 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(6): Show |
13 | HG00140.hp2 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.-40+2650C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159206581 | |||||||
| chr5:159206635 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0073 a0001c0001t0001g0074 others(2): Show |
7 | HG00741.hp2 HG01168.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.-40+2596C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159206635 | |||||||
| chr5:159206961 | C | CA | 31 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0018 others(28): Show |
37 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.-40+2269dupT | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159206961 | |||||||
| chr5:159206961 | CA | C | 27 | a0001c0001t0001g0095 a0001c0001t0002g0017 a0001c0001t0002g0047 others(24): Show |
35 | HG00280.hp1 HG00323.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.-40+2269delT | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159206961 | |||||||
| chr5:159207218 | C | G | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-40+2013G>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159207218 | |||||||
| chr5:159207319 | T | A | 1 | a0001c0001t0001g0259 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-40+1912A>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159207319 | |||||||
| chr5:159207362 | T | C | 8 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0056 others(5): Show |
9 | HG01109.hp1 HG01261.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.-40+1869A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159207362 | |||||||
| chr5:159207366 | T | A | 1 | a0001c0001t0001g0272 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-40+1865A>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159207366 | |||||||
| chr5:159207434 | C | G | 1 | a0001c0001t0016g0296 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-40+1797G>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159207434 | |||||||
| chr5:159207500 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-40+1731G>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159207500 | |||||||
| chr5:159207504 | TAAAAA | T | 8 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0056 others(5): Show |
9 | HG01109.hp1 HG01261.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.-40+1722_-40+1726d others(7): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159207504 | |||||||
| chr5:159207701 | A | C | 1 | a0001c0001t0002g0275 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-40+1530T>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159207701 | |||||||
| chr5:159207706 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-40+1525A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159207706 | |||||||
| chr5:159207781 | T | C | 1 | a0001c0001t0003g0260 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-40+1450A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159207781 | |||||||
| chr5:159207866 | A | G | 1 | a0001c0001t0001g0055 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-40+1365T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159207866 | |||||||
| chr5:159207918 | G | A | 4 | a0001c0001t0001g0036 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
5 | HG00140.hp2 HG00735.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-40+1313C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159207918 | |||||||
| chr5:159208063 | G | C | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-40+1168C>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159208063 | |||||||
| chr5:159208064 | G | C | 1 | a0001c0001t0001g0178 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-40+1167C>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159208064 | |||||||
| chr5:159208094 | T | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(111): Show |
160 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.-40+1137A>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159208094 | |||||||
| chr5:159208204 | G | A | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 |
3 | HG00597.hp2 NA18953.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.-40+1027C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159208204 | |||||||
| chr5:159208415 | A | AG | 8 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0056 others(5): Show |
9 | HG01109.hp1 HG01261.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.-40+815_-40+816ins others(1): Show |
RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159208415 | |||||||
| chr5:159208416 | A | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(190): Show |
259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.-40+815T>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159208416 | |||||||
| chr5:159208556 | G | A | 5 | a0001c0001t0001g0045 a0001c0001t0001g0264 a0001c0001t0001g0265 others(2): Show |
6 | NA18943.hp2 NA18951.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.-40+675C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159208556 | |||||||
| chr5:159208560 | G | T | 1 | a0001c0001t0001g0054 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-40+671C>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159208560 | |||||||
| chr5:159208625 | C | G | 3 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 |
3 | HG02622.hp2 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-40+606G>C | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159208625 | |||||||
| chr5:159208661 | G | T | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-40+570C>A | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159208661 | |||||||
| chr5:159208669 | G | C | 1 | a0001c0001t0001g0268 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-40+562C>G | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159208669 | |||||||
| chr5:159208963 | G | A | 1 | a0001c0001t0001g0269 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-40+268C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159208963 | |||||||
| chr5:159209188 | G | A | 3 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 |
3 | HG02622.hp2 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-40+43C>T | RNF145 | ENSG00000145860.13 | transcript | ENST00000424310.7 | protein_coding | 1/10 | chr5 | 159209188 |