Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 25897 |
| ensemblid | ENSG00000034677.13 |
| hgncid | 13432 |
| symbol | RNF19A |
| name | ring finger protein 19A, RBR E3 ubiquitin protein ligase |
| refseq_nuc | NM_183419.4 |
| refseq_prot | NP_904355.1 |
| ensembl_nuc | ENST00000341084.7 |
| ensembl_prot | ENSP00000342667.2 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 100257067 |
| end | 100309953 |
| strand | - |
| ver | v1.2 |
| region | chr8:100257067-100309953 |
| region5000 | chr8:100252067-100314953 |
| regionname0 | RNF19A_chr8_100257067_100309953 |
| regionname5000 | RNF19A_chr8_100252067_100314953 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2514 | 343 | 80 | 62 | 149 | 12 | 38 | RNF19A_chr8_100252067_100314953 | RNF19A | ATGCA others(2509): Show |
chr8 | 100252067 | 100314953 | ||
| a0001c0002 | 0/0 | 2514 | 3 | 3 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | ATGCA others(2509): Show |
chr8 | 100252067 | 100314953 | ||
| a0001c0003 | 0/0 | 2514 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | ATGCA others(2509): Show |
chr8 | 100252067 | 100314953 | ||
| a0001c0004 | 0/0 | 2514 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | ATGCA others(2509): Show |
chr8 | 100252067 | 100314953 | ||
| a0001c0005 | 0/0 | 2514 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | ATGCA others(2509): Show |
chr8 | 100252067 | 100314953 | ||
| a0001c0006 | 0/0 | 2514 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | ATGCA others(2509): Show |
chr8 | 100252067 | 100314953 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4186 | 269 | 46 | 55 | 123 | 10 | 33 | RNF19A_chr8_100252067_100314953 | RNF19A | GCGCT others(4181): Show |
chr8 | 100252067 | 100314953 |
| a0001c0001t0002 | 0/0 | 4182 | 42 | 17 | 2 | 18 | 0 | 5 | RNF19A_chr8_100252067_100314953 | RNF19A | GCGCT others(4177): Show |
chr8 | 100252067 | 100314953 |
| a0001c0001t0003 | 0/0 | 4186 | 10 | 8 | 2 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | GCGCT others(4181): Show |
chr8 | 100252067 | 100314953 |
| a0001c0001t0004 | 0/0 | 4183 | 6 | 5 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | GCGCT others(4178): Show |
chr8 | 100252067 | 100314953 |
| a0001c0001t0005 | 0/0 | 4186 | 3 | 0 | 1 | 0 | 2 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | GCGCT others(4181): Show |
chr8 | 100252067 | 100314953 |
| a0001c0001t0006 | 0/0 | 4186 | 3 | 3 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | GCGCT others(4181): Show |
chr8 | 100252067 | 100314953 |
| a0001c0001t0007 | 0/0 | 4186 | 2 | 0 | 0 | 2 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | GCGCT others(4181): Show |
chr8 | 100252067 | 100314953 |
| a0001c0001t0008 | 0/0 | 4186 | 2 | 0 | 0 | 2 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | GCGCT others(4181): Show |
chr8 | 100252067 | 100314953 |
| a0001c0001t0009 | 0/0 | 4186 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | GCGCT others(4181): Show |
chr8 | 100252067 | 100314953 |
| a0001c0001t0010 | 0/0 | 4186 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | GCGCT others(4181): Show |
chr8 | 100252067 | 100314953 |
| a0001c0001t0011 | 0/0 | 4186 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | GCGCT others(4181): Show |
chr8 | 100252067 | 100314953 |
| a0001c0001t0012 | 0/0 | 4186 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | GCGCT others(4181): Show |
chr8 | 100252067 | 100314953 |
| a0001c0001t0013 | 0/0 | 4186 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | GCGCT others(4181): Show |
chr8 | 100252067 | 100314953 |
| a0001c0001t0014 | 0/0 | 4186 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | GCGCT others(4181): Show |
chr8 | 100252067 | 100314953 |
| a0001c0002t0001 | 0/0 | 4186 | 3 | 3 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | GCGCT others(4181): Show |
chr8 | 100252067 | 100314953 |
| a0001c0003t0001 | 0/0 | 4186 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | GCGCT others(4181): Show |
chr8 | 100252067 | 100314953 |
| a0001c0004t0001 | 0/0 | 4186 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | GCGCT others(4181): Show |
chr8 | 100252067 | 100314953 |
| a0001c0005t0001 | 0/0 | 4186 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | GCGCT others(4181): Show |
chr8 | 100252067 | 100314953 |
| a0001c0006t0001 | 0/0 | 4186 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | GCGCT others(4181): Show |
chr8 | 100252067 | 100314953 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 14 | 0 | 1 | 11 | 1 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0002 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0007 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0189 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0227 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0003g0022 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0003g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0003g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0005g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0005g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0007g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0007g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0008g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0009g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0010g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0011g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0012g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0013g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0001t0014g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0004t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0005t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| a0001c0006t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | GBR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0216 | EUR | GBR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | GBR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | GBR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG00323 | hp1 | a0001 | c0001 | t0005 | g0037 | EUR | FIN | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | FIN | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0060 | AMR | PUR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0230 | AMR | PUR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01243 | hp1 | a0001 | c0001 | t0010 | g0240 | AMR | PUR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0182 | EUR | IBS | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0141 | AFR | ACB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0058 | AFR | ACB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02056 | hp1 | a0001 | c0001 | t0013 | g0116 | EAS | KHV | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02056 | hp2 | a0001 | c0005 | t0001 | g0211 | EAS | KHV | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PEL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CDX | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | ACB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | ACB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02300 | hp2 | a0001 | c0001 | t0005 | g0160 | AMR | PEL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | GWD | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0073 | AFR | GWD | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | GWD | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | GWD | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0235 | AFR | GWD | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0150 | AFR | GWD | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0128 | SAS | PJL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0143 | AFR | GWD | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | GWD | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0103 | AFR | ESN | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | ESN | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0142 | AFR | ESN | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0056 | AFR | MSL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | ESN | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | ESN | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ESN | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | MSL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | MSL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | PJL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | MSL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | ESN | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03540 | hp2 | a0001 | c0004 | t0001 | g0202 | AFR | GWD | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | MSL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0074 | AFR | MSL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | STU | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | BEB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0135 | SAS | BEB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | BEB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | STU | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | STU | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | STU | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | STU | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | STU | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0237 | AFR | YRI | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | YRI | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18947 | hp2 | a0001 | c0001 | t0007 | g0191 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18952 | hp1 | a0001 | c0006 | t0001 | g0067 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18961 | hp2 | a0001 | c0003 | t0001 | g0185 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18997 | hp1 | a0001 | c0001 | t0012 | g0055 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19000 | hp1 | a0001 | c0001 | t0008 | g0027 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19010 | hp2 | a0001 | c0001 | t0008 | g0027 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | LWK | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | LWK | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19064 | hp2 | a0001 | c0001 | t0014 | g0085 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19079 | hp2 | a0001 | c0001 | t0007 | g0195 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0057 | AFR | YRI | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | YRI | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ASW | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ASW | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0052 | EUR | TSI | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA20805 | hp1 | a0001 | c0001 | t0005 | g0037 | EUR | TSI | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0229 | EUR | TSI | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | GIH | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | ACB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0144 | AFR | MSL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18955 | hp1 | a0001 | c0001 | t0011 | g0196 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0238 | AFR | USA | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | USA | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | LWK | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | LWK | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0227 | REF | REF | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0189 | REF | REF | RNF19A_chr8_100252067_100314953 | RNF19A | chr8 | 100252067 | 100314953 |
| 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 |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:100258634 | G | A | 1 | a0001c0004 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.2439C>T | p.Gly813Gly | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 10/10 | 2619/4186 | 2439/2517 | 813/838 | chr8 | 100258634 | |||
| chr8:100259186 | G | A | 1 | a0001c0005 | 1 | HG02056.hp2 | synonymous_variant | LOW | c.1887C>T | p.His629His | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 10/10 | 2067/4186 | 1887/2517 | 629/838 | chr8 | 100259186 | |||
| chr8:100275116 | A | G | 1 | a0001c0003 | 1 | NA18961.hp2 | synonymous_variant | LOW | c.720T>C | p.Thr240Thr | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/10 | 900/4186 | 720/2517 | 240/838 | chr8 | 100275116 | |||
| chr8:100287584 | C | T | 1 | a0001c0002 | 3 | HG02055.hp2 HG03098.hp2 NA19240.hp1 |
synonymous_variant | LOW | c.591G>A | p.Leu197Leu | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/10 | 771/4186 | 591/2517 | 197/838 | chr8 | 100287584 | |||
| chr8:100287800 | T | C | 1 | a0001c0006 | 1 | NA18952.hp1 | synonymous_variant | LOW | c.375A>G | p.Gln125Gln | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/10 | 555/4186 | 375/2517 | 125/838 | chr8 | 100287800 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:100257157 | A | T | 1 | a0001c0001t0008 | 2 | NA19000.hp1 NA19010.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1399T>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 10/10 | 1399 | chr8 | 100257157 | ||||||
| chr8:100257352 | CCTG | C | 2 | a0001c0001t0002 a0001c0001t0004 |
48 | HG01081.hp2 HG01099.hp2 HG02055.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1201_*1203delCAG | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 10/10 | 1201 | chr8 | 100257352 | ||||||
| chr8:100257468 | T | C | 1 | a0001c0001t0013 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1088A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 10/10 | 1088 | chr8 | 100257468 | ||||||
| chr8:100257486 | T | G | 1 | a0001c0001t0012 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1070A>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 10/10 | 1070 | chr8 | 100257486 | ||||||
| chr8:100257643 | A | T | 1 | a0001c0001t0012 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*913T>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 10/10 | 913 | chr8 | 100257643 | ||||||
| chr8:100257644 | T | C | 1 | a0001c0001t0005 | 3 | HG00323.hp1 HG02300.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*912A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 10/10 | 912 | chr8 | 100257644 | ||||||
| chr8:100257743 | C | T | 1 | a0001c0001t0011 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*813G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 10/10 | 813 | chr8 | 100257743 | ||||||
| chr8:100257754 | G | C | 1 | a0001c0001t0010 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*802C>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 10/10 | 802 | chr8 | 100257754 | ||||||
| chr8:100257777 | A | C | 1 | a0001c0001t0009 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*779T>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 10/10 | 779 | chr8 | 100257777 | ||||||
| chr8:100257937 | C | T | 1 | a0001c0001t0010 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*619G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 10/10 | 619 | chr8 | 100257937 | ||||||
| chr8:100258056 | GA | G | 1 | a0001c0001t0002 | 42 | HG01081.hp2 HG02109.hp1 HG02148.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*499delT | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 10/10 | 499 | chr8 | 100258056 | ||||||
| chr8:100258095 | T | G | 1 | a0001c0001t0006 | 3 | HG02630.hp1 HG02922.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*461A>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 10/10 | 461 | chr8 | 100258095 | ||||||
| chr8:100258216 | C | T | 2 | a0001c0001t0003 a0001c0001t0009 |
11 | HG01109.hp2 HG01167.hp2 HG02258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*340G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 10/10 | 340 | chr8 | 100258216 | ||||||
| chr8:100258458 | G | A | 2 | a0001c0001t0008 a0001c0001t0014 |
3 | NA19000.hp1 NA19010.hp2 NA19064.hp2 |
3_prime_UTR_variant | MODIFIER | c.*98C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 10/10 | 98 | chr8 | 100258458 | ||||||
| chr8:100258517 | C | T | 1 | a0001c0001t0007 | 2 | NA18947.hp2 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*39G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 10/10 | 39 | chr8 | 100258517 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:100259593 | C | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(105): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.1826+261G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 9/9 | chr8 | 100259593 | |||||||
| chr8:100260190 | G | A | 18 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(15): Show |
26 | HG00733.hp2 HG00738.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1683-193C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 8/9 | chr8 | 100260190 | |||||||
| chr8:100260293 | C | T | 18 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(15): Show |
26 | HG00733.hp2 HG00738.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1683-296G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 8/9 | chr8 | 100260293 | |||||||
| chr8:100260459 | A | C | 3 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0058 |
3 | HG02055.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1683-462T>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 8/9 | chr8 | 100260459 | |||||||
| chr8:100260552 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0165 |
4 | HG01071.hp1 HG01074.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1683-555C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 8/9 | chr8 | 100260552 | |||||||
| chr8:100260775 | T | C | 8 | a0001c0001t0001g0019 a0001c0001t0001g0118 a0001c0001t0001g0119 others(5): Show |
10 | NA18977.hp1 NA18984.hp1 NA18995.hp1 others(7): Show |
intron_variant | MODIFIER | c.1682+767A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 8/9 | chr8 | 100260775 | |||||||
| chr8:100260864 | G | C | 1 | a0001c0001t0001g0098 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1682+678C>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 8/9 | chr8 | 100260864 | |||||||
| chr8:100261076 | G | C | 1 | a0001c0001t0001g0219 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1682+466C>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 8/9 | chr8 | 100261076 | |||||||
| chr8:100261204 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1682+338G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 8/9 | chr8 | 100261204 | |||||||
| chr8:100261243 | T | G | 3 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0058 |
3 | HG02055.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1682+299A>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 8/9 | chr8 | 100261243 | |||||||
| chr8:100261294 | C | T | 40 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(37): Show |
48 | HG01081.hp2 HG01099.hp2 HG02055.hp1 others(45): Show |
intron_variant | MODIFIER | c.1682+248G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 8/9 | chr8 | 100261294 | |||||||
| chr8:100261299 | T | C | 5 | a0001c0001t0004g0060 a0001c0001t0004g0142 a0001c0001t0004g0143 others(2): Show |
5 | HG01099.hp2 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1682+243A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 8/9 | chr8 | 100261299 | |||||||
| chr8:100261317 | C | G | 1 | a0001c0001t0001g0119 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1682+225G>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 8/9 | chr8 | 100261317 | |||||||
| chr8:100261378 | G | A | 34 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(31): Show |
42 | HG01081.hp2 HG02109.hp1 HG02148.hp1 others(39): Show |
intron_variant | MODIFIER | c.1682+164C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 8/9 | chr8 | 100261378 | |||||||
| chr8:100262164 | T | C | 18 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(15): Show |
26 | HG00733.hp2 HG00738.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1469-409A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 7/9 | chr8 | 100262164 | |||||||
| chr8:100262494 | C | A | 7 | a0001c0001t0001g0151 a0001c0001t0001g0161 a0001c0001t0001g0166 others(4): Show |
7 | HG01261.hp2 HG01346.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.1469-739G>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 7/9 | chr8 | 100262494 | |||||||
| chr8:100262806 | C | T | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(72): Show |
115 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.1469-1051G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 7/9 | chr8 | 100262806 | |||||||
| chr8:100263307 | GTA | G | 25 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0033 others(22): Show |
32 | HG01081.hp2 HG02109.hp1 HG02148.hp1 others(29): Show |
intron_variant | MODIFIER | c.1468+725_1468+726d others(4): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 7/9 | chr8 | 100263307 | |||||||
| chr8:100263435 | G | C | 20 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(17): Show |
33 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1468+599C>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 7/9 | chr8 | 100263435 | |||||||
| chr8:100263785 | T | A | 1 | a0001c0001t0001g0193 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1468+249A>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 7/9 | chr8 | 100263785 | |||||||
| chr8:100263990 | C | A | 1 | a0001c0001t0001g0209 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1468+44G>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 7/9 | chr8 | 100263990 | |||||||
| chr8:100264223 | AAAC | A | 2 | a0001c0001t0002g0032 a0001c0001t0002g0145 |
3 | HG03041.hp2 HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1307-31_1307-29del others(3): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 6/9 | chr8 | 100264223 | |||||||
| chr8:100264449 | C | T | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(172): Show |
242 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.1306+222G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 6/9 | chr8 | 100264449 | |||||||
| chr8:100264459 | T | C | 2 | a0001c0001t0001g0234 a0001c0001t0002g0127 |
2 | HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1306+212A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 6/9 | chr8 | 100264459 | |||||||
| chr8:100265151 | C | G | 3 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0216 |
5 | HG00099.hp2 HG03491.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.1192-366G>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100265151 | |||||||
| chr8:100265276 | T | C | 2 | a0001c0001t0001g0064 a0001c0001t0001g0122 |
2 | NA18992.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1192-491A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100265276 | |||||||
| chr8:100265314 | T | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | NA18995.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1192-529A>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100265314 | |||||||
| chr8:100265412 | T | C | 52 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(49): Show |
81 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1192-627A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100265412 | |||||||
| chr8:100265456 | T | C | 1 | a0001c0001t0002g0071 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1192-671A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100265456 | |||||||
| chr8:100265466 | TATC | T | 18 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(15): Show |
26 | HG00733.hp2 HG00738.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1192-684_1192-682d others(5): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100265466 | |||||||
| chr8:100265688 | T | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
117 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.1192-903A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100265688 | |||||||
| chr8:100265930 | A | G | 3 | a0001c0001t0001g0075 a0001c0001t0001g0078 a0001c0001t0001g0080 |
3 | NA18983.hp2 NA19058.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.1192-1145T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100265930 | |||||||
| chr8:100265955 | C | G | 1 | a0001c0001t0001g0110 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1192-1170G>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100265955 | |||||||
| chr8:100266037 | G | C | 1 | a0001c0001t0001g0079 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1192-1252C>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100266037 | |||||||
| chr8:100266180 | G | A | 3 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0058 |
3 | HG02055.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1192-1395C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100266180 | |||||||
| chr8:100266415 | C | G | 1 | a0001c0001t0001g0156 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1192-1630G>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100266415 | |||||||
| chr8:100266496 | T | A | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
117 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.1192-1711A>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100266496 | |||||||
| chr8:100266594 | T | G | 18 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(15): Show |
26 | HG00733.hp2 HG00738.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1192-1809A>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100266594 | |||||||
| chr8:100266761 | C | G | 1 | a0001c0001t0001g0047 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1192-1976G>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100266761 | |||||||
| chr8:100267070 | C | G | 56 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(53): Show |
72 | HG00733.hp2 HG00738.hp1 HG01081.hp2 others(69): Show |
intron_variant | MODIFIER | c.1191+1715G>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100267070 | |||||||
| chr8:100267293 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1191+1492G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100267293 | |||||||
| chr8:100267335 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG01884.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1191+1450G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100267335 | |||||||
| chr8:100267494 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1191+1291G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100267494 | |||||||
| chr8:100267543 | A | G | 1 | a0001c0001t0002g0139 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1191+1242T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100267543 | |||||||
| chr8:100267669 | T | C | 2 | a0001c0001t0001g0041 a0001c0001t0001g0218 |
3 | HG02145.hp1 HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1191+1116A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100267669 | |||||||
| chr8:100267678 | C | CT | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
124 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.1191+1106dupA | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100267678 | |||||||
| chr8:100267801 | C | T | 32 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(29): Show |
40 | HG01081.hp2 HG02109.hp1 HG02148.hp1 others(37): Show |
intron_variant | MODIFIER | c.1191+984G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100267801 | |||||||
| chr8:100267820 | A | C | 1 | a0001c0001t0001g0172 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1191+965T>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100267820 | |||||||
| chr8:100267884 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1191+901C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100267884 | |||||||
| chr8:100267943 | G | C | 1 | a0001c0001t0001g0094 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1191+842C>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100267943 | |||||||
| chr8:100268003 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1191+782A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100268003 | |||||||
| chr8:100268079 | T | A | 18 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(15): Show |
26 | HG00733.hp2 HG00738.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1191+706A>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100268079 | |||||||
| chr8:100268104 | C | CT | 18 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(15): Show |
26 | HG00733.hp2 HG00738.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1191+680dupA | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100268104 | |||||||
| chr8:100268302 | A | G | 1 | a0001c0001t0004g0060 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1191+483T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100268302 | |||||||
| chr8:100268305 | A | G | 18 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(15): Show |
26 | HG00733.hp2 HG00738.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1191+480T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100268305 | |||||||
| chr8:100268683 | T | TA | 6 | a0001c0001t0001g0051 a0001c0001t0001g0180 a0001c0001t0001g0190 others(3): Show |
6 | HG00140.hp2 HG02735.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.1191+101dupT | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100268683 | |||||||
| chr8:100268683 | TA | T | 47 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0018 others(44): Show |
60 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.1191+101delT | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100268683 | |||||||
| chr8:100268683 | TAA | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(91): Show |
140 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.1191+100_1191+101d others(4): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100268683 | |||||||
| chr8:100268683 | TAAA | T | 34 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0095 others(31): Show |
42 | HG01081.hp2 HG02109.hp1 HG02257.hp2 others(39): Show |
intron_variant | MODIFIER | c.1191+99_1191+101de others(4): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100268683 | |||||||
| chr8:100268733 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1191+52G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 5/9 | chr8 | 100268733 | |||||||
| chr8:100269010 | C | A | 178 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(175): Show |
245 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.1029-63G>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 4/9 | chr8 | 100269010 | |||||||
| chr8:100269034 | T | A | 18 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(15): Show |
26 | HG00733.hp2 HG00738.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1029-87A>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 4/9 | chr8 | 100269034 | |||||||
| chr8:100269043 | C | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
117 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.1029-96G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 4/9 | chr8 | 100269043 | |||||||
| chr8:100269430 | T | C | 38 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(35): Show |
46 | HG01081.hp2 HG01099.hp2 HG02055.hp1 others(43): Show |
intron_variant | MODIFIER | c.1028+439A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 4/9 | chr8 | 100269430 | |||||||
| chr8:100269516 | T | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0206 |
5 | NA18951.hp2 NA18971.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.1028+353A>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 4/9 | chr8 | 100269516 | |||||||
| chr8:100269516 | T | G | 1 | a0001c0001t0001g0193 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1028+353A>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 4/9 | chr8 | 100269516 | |||||||
| chr8:100269854 | C | T | 1 | a0001c0001t0004g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1028+15G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 4/9 | chr8 | 100269854 | |||||||
| chr8:100270070 | C | G | 1 | a0001c0004t0001g0202 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.884-57G>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100270070 | |||||||
| chr8:100270262 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.884-249T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100270262 | |||||||
| chr8:100270857 | C | T | 56 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(53): Show |
72 | HG00733.hp2 HG00738.hp1 HG01081.hp2 others(69): Show |
intron_variant | MODIFIER | c.884-844G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100270857 | |||||||
| chr8:100271102 | T | C | 3 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0058 |
3 | HG02055.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.884-1089A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100271102 | |||||||
| chr8:100271267 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.884-1254A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100271267 | |||||||
| chr8:100271331 | A | G | 1 | a0001c0001t0001g0199 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.884-1318T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100271331 | |||||||
| chr8:100271599 | T | C | 1 | a0001c0001t0002g0133 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.884-1586A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100271599 | |||||||
| chr8:100271680 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.884-1667T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100271680 | |||||||
| chr8:100271882 | C | T | 3 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0150 |
3 | HG02723.hp1 HG02809.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.884-1869G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100271882 | |||||||
| chr8:100271919 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.884-1906C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100271919 | |||||||
| chr8:100272030 | C | G | 13 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0041 others(10): Show |
18 | HG01257.hp2 HG01258.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.884-2017G>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100272030 | |||||||
| chr8:100272089 | G | A | 1 | a0001c0001t0002g0131 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.884-2076C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100272089 | |||||||
| chr8:100272094 | G | A | 18 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(15): Show |
26 | HG00733.hp2 HG00738.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.884-2081C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100272094 | |||||||
| chr8:100272095 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.884-2082C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100272095 | |||||||
| chr8:100272261 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0179 a0001c0001t0001g0209 |
6 | HG01433.hp2 HG01934.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.884-2248G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100272261 | |||||||
| chr8:100272368 | A | G | 2 | a0001c0001t0001g0154 a0001c0001t0001g0156 |
2 | HG01243.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.884-2355T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100272368 | |||||||
| chr8:100272458 | C | G | 1 | a0001c0001t0004g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.884-2445G>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100272458 | |||||||
| chr8:100272553 | A | T | 1 | a0001c0001t0004g0150 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.883+2400T>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100272553 | |||||||
| chr8:100272586 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.883+2367T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100272586 | |||||||
| chr8:100272605 | G | T | 56 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(53): Show |
72 | HG00733.hp2 HG00738.hp1 HG01081.hp2 others(69): Show |
intron_variant | MODIFIER | c.883+2348C>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100272605 | |||||||
| chr8:100272846 | A | G | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
192 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(189): Show |
intron_variant | MODIFIER | c.883+2107T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100272846 | |||||||
| chr8:100272847 | G | GC | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
117 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.883+2105dupG | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100272847 | |||||||
| chr8:100272851 | T | G | 3 | a0001c0001t0002g0016 a0001c0001t0002g0129 a0001c0001t0002g0137 |
5 | HG02109.hp1 HG02257.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.883+2102A>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100272851 | |||||||
| chr8:100272857 | C | A | 1 | a0001c0001t0001g0213 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.883+2096G>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100272857 | |||||||
| chr8:100273086 | C | T | 18 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(15): Show |
26 | HG00733.hp2 HG00738.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.883+1867G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100273086 | |||||||
| chr8:100273133 | C | T | 24 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(21): Show |
32 | HG00733.hp2 HG00738.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.883+1820G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100273133 | |||||||
| chr8:100273183 | C | G | 6 | a0001c0001t0001g0182 a0001c0001t0001g0186 a0001c0001t0001g0187 others(3): Show |
6 | HG01109.hp1 HG01517.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.883+1770G>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100273183 | |||||||
| chr8:100273213 | T | A | 1 | a0001c0001t0001g0156 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.883+1740A>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100273213 | |||||||
| chr8:100273489 | T | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0039 a0001c0001t0001g0040 others(3): Show |
11 | HG00099.hp2 HG01256.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.883+1464A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100273489 | |||||||
| chr8:100273621 | G | A | 13 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0041 others(10): Show |
18 | HG01257.hp2 HG01258.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.883+1332C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100273621 | |||||||
| chr8:100273781 | T | C | 1 | a0001c0001t0007g0195 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.883+1172A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100273781 | |||||||
| chr8:100273896 | C | T | 5 | a0001c0001t0001g0161 a0001c0001t0001g0166 a0001c0001t0001g0169 others(2): Show |
5 | HG01346.hp2 HG01981.hp2 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.883+1057G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100273896 | |||||||
| chr8:100274601 | T | C | 1 | a0001c0001t0001g0223 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.883+352A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100274601 | |||||||
| chr8:100274626 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.883+327G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 3/9 | chr8 | 100274626 | |||||||
| chr8:100275417 | T | C | 2 | a0001c0001t0001g0220 a0001c0001t0011g0196 |
2 | NA18955.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.675-256A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100275417 | |||||||
| chr8:100275590 | G | C | 38 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(35): Show |
46 | HG01081.hp2 HG01099.hp2 HG02055.hp1 others(43): Show |
intron_variant | MODIFIER | c.675-429C>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100275590 | |||||||
| chr8:100275836 | C | G | 1 | a0001c0001t0001g0168 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.675-675G>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100275836 | |||||||
| chr8:100275972 | A | C | 1 | a0001c0001t0001g0079 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.675-811T>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100275972 | |||||||
| chr8:100275990 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.675-829C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100275990 | |||||||
| chr8:100276123 | T | C | 32 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(29): Show |
40 | HG01081.hp2 HG02109.hp1 HG02148.hp1 others(37): Show |
intron_variant | MODIFIER | c.675-962A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100276123 | |||||||
| chr8:100276172 | A | C | 1 | a0001c0001t0001g0109 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.675-1011T>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100276172 | |||||||
| chr8:100276219 | T | C | 18 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(15): Show |
26 | HG00733.hp2 HG00738.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.675-1058A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100276219 | |||||||
| chr8:100276267 | A | C | 2 | a0001c0001t0002g0130 a0001c0001t0002g0146 |
2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.675-1106T>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100276267 | |||||||
| chr8:100276308 | CA | C | 3 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0058 |
3 | HG02055.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.675-1148delT | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100276308 | |||||||
| chr8:100276382 | T | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
117 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.675-1221A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100276382 | |||||||
| chr8:100276455 | T | C | 1 | a0001c0001t0001g0075 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.675-1294A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100276455 | |||||||
| chr8:100276723 | CA | C | 43 | a0001c0001t0001g0007 a0001c0001t0001g0117 a0001c0001t0001g0154 others(40): Show |
55 | HG00733.hp2 HG00738.hp1 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.675-1563delT | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100276723 | |||||||
| chr8:100276738 | A | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
117 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.675-1577T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100276738 | |||||||
| chr8:100276740 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.675-1579T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100276740 | |||||||
| chr8:100276876 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.675-1715C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100276876 | |||||||
| chr8:100277281 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.675-2120G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100277281 | |||||||
| chr8:100277608 | A | AT | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
193 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(190): Show |
intron_variant | MODIFIER | c.675-2448_675-2447i others(3): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100277608 | |||||||
| chr8:100277767 | C | G | 1 | a0001c0001t0001g0184 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.675-2606G>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100277767 | |||||||
| chr8:100277789 | AT | A | 45 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0023 others(42): Show |
56 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.675-2629delA | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100277789 | |||||||
| chr8:100277797 | T | A | 1 | a0001c0001t0001g0168 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.675-2636A>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100277797 | |||||||
| chr8:100277860 | C | T | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
192 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(189): Show |
intron_variant | MODIFIER | c.675-2699G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100277860 | |||||||
| chr8:100278166 | C | T | 1 | a0001c0001t0004g0060 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.675-3005G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100278166 | |||||||
| chr8:100278205 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.675-3044G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100278205 | |||||||
| chr8:100278219 | G | A | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
117 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.675-3058C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100278219 | |||||||
| chr8:100278436 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.675-3275G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100278436 | |||||||
| chr8:100278700 | T | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
192 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(189): Show |
intron_variant | MODIFIER | c.675-3539A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100278700 | |||||||
| chr8:100279020 | A | C | 3 | a0001c0001t0002g0127 a0001c0001t0002g0132 a0001c0001t0002g0149 |
3 | HG02280.hp1 HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.675-3859T>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100279020 | |||||||
| chr8:100279079 | T | C | 2 | a0001c0001t0001g0207 a0001c0001t0001g0213 |
2 | NA19064.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.675-3918A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100279079 | |||||||
| chr8:100279337 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.675-4176G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100279337 | |||||||
| chr8:100279409 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.675-4248G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100279409 | |||||||
| chr8:100279561 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.675-4400T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100279561 | |||||||
| chr8:100279616 | A | C | 1 | a0001c0001t0001g0101 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.675-4455T>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100279616 | |||||||
| chr8:100279647 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.675-4486C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100279647 | |||||||
| chr8:100279670 | C | T | 1 | a0001c0001t0002g0115 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.675-4509G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100279670 | |||||||
| chr8:100279746 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0001g0232 a0001c0001t0001g0233 others(7): Show |
14 | HG00733.hp2 HG00738.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.675-4585G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100279746 | |||||||
| chr8:100279787 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.675-4626T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100279787 | |||||||
| chr8:100279803 | A | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
117 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.675-4642T>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100279803 | |||||||
| chr8:100279935 | C | T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | NA18984.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.675-4774G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100279935 | |||||||
| chr8:100279959 | T | A | 1 | a0001c0001t0001g0158 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.675-4798A>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100279959 | |||||||
| chr8:100279978 | A | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
117 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.675-4817T>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100279978 | |||||||
| chr8:100279979 | A | T | 1 | a0001c0001t0001g0158 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.675-4818T>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100279979 | |||||||
| chr8:100280132 | A | G | 179 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
246 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.675-4971T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100280132 | |||||||
| chr8:100280252 | C | T | 2 | a0001c0001t0004g0060 a0001c0001t0004g0144 |
2 | HG01099.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.675-5091G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100280252 | |||||||
| chr8:100280293 | A | G | 1 | a0001c0001t0001g0203 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.675-5132T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100280293 | |||||||
| chr8:100280626 | A | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
117 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.675-5465T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100280626 | |||||||
| chr8:100280684 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.675-5523A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100280684 | |||||||
| chr8:100280733 | C | T | 18 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(15): Show |
26 | HG00733.hp2 HG00738.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.675-5572G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100280733 | |||||||
| chr8:100281097 | T | C | 3 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0058 |
3 | HG02055.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.675-5936A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100281097 | |||||||
| chr8:100281175 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.675-6014T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100281175 | |||||||
| chr8:100281231 | C | T | 1 | a0001c0001t0001g0039 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.675-6070G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100281231 | |||||||
| chr8:100281289 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.675-6128G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100281289 | |||||||
| chr8:100281324 | A | C | 1 | a0001c0001t0001g0182 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.675-6163T>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100281324 | |||||||
| chr8:100281336 | TTTTC | T | 4 | a0001c0001t0002g0032 a0001c0001t0002g0125 a0001c0001t0002g0126 others(1): Show |
5 | HG03041.hp2 HG03486.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.674+6161_674+6164d others(6): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100281336 | |||||||
| chr8:100281435 | T | G | 1 | a0001c0001t0002g0225 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.674+6066A>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100281435 | |||||||
| chr8:100281502 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.674+5999C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100281502 | |||||||
| chr8:100281661 | C | T | 3 | a0001c0001t0002g0127 a0001c0001t0002g0132 a0001c0001t0002g0149 |
3 | HG02280.hp1 HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.674+5840G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100281661 | |||||||
| chr8:100282510 | TTATAA | T | 18 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(15): Show |
26 | HG00733.hp2 HG00738.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.674+4986_674+4990d others(7): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100282510 | |||||||
| chr8:100282645 | GTTTTC | G | 38 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(35): Show |
46 | HG01081.hp2 HG01099.hp2 HG02055.hp1 others(43): Show |
intron_variant | MODIFIER | c.674+4851_674+4855d others(7): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100282645 | |||||||
| chr8:100282733 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.674+4768A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100282733 | |||||||
| chr8:100282771 | G | C | 56 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(53): Show |
72 | HG00733.hp2 HG00738.hp1 HG01081.hp2 others(69): Show |
intron_variant | MODIFIER | c.674+4730C>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100282771 | |||||||
| chr8:100283123 | A | C | 1 | a0001c0001t0001g0208 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.674+4378T>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100283123 | |||||||
| chr8:100283141 | G | A | 4 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0061 others(1): Show |
7 | HG00609.hp1 NA18940.hp1 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.674+4360C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100283141 | |||||||
| chr8:100283183 | G | A | 1 | a0001c0001t0001g0028 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.674+4318C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100283183 | |||||||
| chr8:100283215 | G | GTGGCCTT others(14): Show |
178 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(175): Show |
245 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.674+4265_674+4285d others(23): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100283215 | |||||||
| chr8:100283232 | A | AAACATGG others(14): Show |
1 | a0001c0001t0005g0160 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.674+4268_674+4269i others(23): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100283232 | |||||||
| chr8:100283240 | G | A | 1 | a0001c0001t0004g0144 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.674+4261C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100283240 | |||||||
| chr8:100283764 | T | A | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
117 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.674+3737A>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100283764 | |||||||
| chr8:100283789 | G | A | 3 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0058 |
3 | HG02055.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.674+3712C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100283789 | |||||||
| chr8:100283890 | G | A | 1 | a0001c0001t0004g0060 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.674+3611C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100283890 | |||||||
| chr8:100284064 | T | C | 38 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(35): Show |
46 | HG01081.hp2 HG01099.hp2 HG02055.hp1 others(43): Show |
intron_variant | MODIFIER | c.674+3437A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100284064 | |||||||
| chr8:100284137 | A | G | 1 | a0001c0001t0002g0130 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.674+3364T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100284137 | |||||||
| chr8:100284506 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.674+2995A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100284506 | |||||||
| chr8:100284864 | C | G | 18 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(15): Show |
26 | HG00733.hp2 HG00738.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.674+2637G>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100284864 | |||||||
| chr8:100284896 | T | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0041 a0001c0001t0001g0218 others(1): Show |
8 | HG02145.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.674+2605A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100284896 | |||||||
| chr8:100285000 | ACATCCCC others(4): Show |
A | 1 | a0001c0001t0001g0088 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.674+2490_674+2500d others(13): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100285000 | |||||||
| chr8:100285008 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.674+2493A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100285008 | |||||||
| chr8:100285260 | T | G | 1 | a0001c0001t0001g0089 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.674+2241A>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100285260 | |||||||
| chr8:100285498 | A | G | 25 | a0001c0001t0001g0018 a0001c0001t0001g0035 a0001c0001t0001g0036 others(22): Show |
31 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.674+2003T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100285498 | |||||||
| chr8:100285527 | T | C | 29 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(26): Show |
37 | HG01081.hp2 HG02109.hp1 HG02148.hp1 others(34): Show |
intron_variant | MODIFIER | c.674+1974A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100285527 | |||||||
| chr8:100285543 | C | G | 1 | a0001c0001t0003g0238 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.674+1958G>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100285543 | |||||||
| chr8:100285550 | GT | G | 32 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(29): Show |
40 | HG01081.hp2 HG02109.hp1 HG02148.hp1 others(37): Show |
intron_variant | MODIFIER | c.674+1950delA | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100285550 | |||||||
| chr8:100285577 | A | G | 1 | a0001c0004t0001g0202 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.674+1924T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100285577 | |||||||
| chr8:100285756 | T | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
192 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(189): Show |
intron_variant | MODIFIER | c.674+1745A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100285756 | |||||||
| chr8:100285916 | T | C | 3 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0058 |
3 | HG02055.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.674+1585A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100285916 | |||||||
| chr8:100286215 | C | A | 1 | a0001c0001t0001g0020 | 3 | NA18962.hp1 NA18998.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.674+1286G>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100286215 | |||||||
| chr8:100286244 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.674+1257C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100286244 | |||||||
| chr8:100286465 | T | C | 32 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(29): Show |
40 | HG01081.hp2 HG02109.hp1 HG02148.hp1 others(37): Show |
intron_variant | MODIFIER | c.674+1036A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100286465 | |||||||
| chr8:100286511 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.674+990A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100286511 | |||||||
| chr8:100286644 | T | C | 3 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0058 |
3 | HG02055.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.674+857A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100286644 | |||||||
| chr8:100287125 | G | T | 38 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(35): Show |
46 | HG01081.hp2 HG01099.hp2 HG02055.hp1 others(43): Show |
intron_variant | MODIFIER | c.674+376C>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100287125 | |||||||
| chr8:100287126 | T | C | 1 | a0001c0001t0001g0090 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.674+375A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100287126 | |||||||
| chr8:100287127 | C | T | 18 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(15): Show |
26 | HG00733.hp2 HG00738.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.674+374G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100287127 | |||||||
| chr8:100287330 | T | C | 18 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(15): Show |
26 | HG00733.hp2 HG00738.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.674+171A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 2/9 | chr8 | 100287330 | |||||||
| chr8:100288380 | G | T | 38 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(35): Show |
46 | HG01081.hp2 HG01099.hp2 HG02055.hp1 others(43): Show |
intron_variant | MODIFIER | c.-93-113C>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288380 | |||||||
| chr8:100288519 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-252G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288519 | |||||||
| chr8:100288525 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-258C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288525 | |||||||
| chr8:100288527 | C | A | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-260G>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288527 | |||||||
| chr8:100288528 | T | A | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-261A>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288528 | |||||||
| chr8:100288529 | T | A | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-262A>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288529 | |||||||
| chr8:100288530 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-263G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288530 | |||||||
| chr8:100288534 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-267C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288534 | |||||||
| chr8:100288537 | T | A | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-270A>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288537 | |||||||
| chr8:100288538 | T | A | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-271A>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288538 | |||||||
| chr8:100288539 | C | A | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-272G>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288539 | |||||||
| chr8:100288540 | T | C | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-273A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288540 | |||||||
| chr8:100288541 | C | A | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-274G>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288541 | |||||||
| chr8:100288542 | A | C | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-275T>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288542 | |||||||
| chr8:100288544 | T | A | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-277A>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288544 | |||||||
| chr8:100288545 | G | C | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-278C>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288545 | |||||||
| chr8:100288548 | T | C | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-281A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288548 | |||||||
| chr8:100288561 | T | C | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-294A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288561 | |||||||
| chr8:100288562 | T | A | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-295A>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288562 | |||||||
| chr8:100288563 | T | A | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-296A>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288563 | |||||||
| chr8:100288567 | G | C | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-300C>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288567 | |||||||
| chr8:100288570 | G | T | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-303C>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288570 | |||||||
| chr8:100288571 | T | A | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-304A>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288571 | |||||||
| chr8:100288572 | T | C | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-305A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288572 | |||||||
| chr8:100288599 | A | T | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-332T>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288599 | |||||||
| chr8:100288665 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-398G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288665 | |||||||
| chr8:100288668 | C | G | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-401G>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288668 | |||||||
| chr8:100288670 | G | C | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-403C>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288670 | |||||||
| chr8:100288677 | T | G | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-410A>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288677 | |||||||
| chr8:100288681 | T | A | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-414A>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288681 | |||||||
| chr8:100288683 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-416G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288683 | |||||||
| chr8:100288684 | T | C | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-417A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288684 | |||||||
| chr8:100288692 | T | TTCCGCCA others(9): Show |
1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-426_-93-425ins others(16): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288692 | |||||||
| chr8:100288694 | A | T | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-427T>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288694 | |||||||
| chr8:100288696 | A | T | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-429T>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288696 | |||||||
| chr8:100288701 | T | G | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-434A>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288701 | |||||||
| chr8:100288704 | A | C | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-437T>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288704 | |||||||
| chr8:100288705 | C | A | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-438G>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288705 | |||||||
| chr8:100288706 | A | G | 1 | a0001c0001t0001g0207 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93-439T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288706 | |||||||
| chr8:100288726 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-93-459C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288726 | |||||||
| chr8:100288925 | T | C | 3 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0058 |
3 | HG02055.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-93-658A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288925 | |||||||
| chr8:100288935 | C | T | 2 | a0001c0002t0001g0056 a0001c0002t0001g0057 |
2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-93-668G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288935 | |||||||
| chr8:100288977 | G | A | 3 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0058 |
3 | HG02055.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-93-710C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288977 | |||||||
| chr8:100288985 | G | A | 1 | a0001c0001t0002g0127 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-93-718C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100288985 | |||||||
| chr8:100289047 | G | A | 38 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(35): Show |
46 | HG01081.hp2 HG01099.hp2 HG02055.hp1 others(43): Show |
intron_variant | MODIFIER | c.-93-780C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100289047 | |||||||
| chr8:100289059 | C | CA | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(126): Show |
183 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(180): Show |
intron_variant | MODIFIER | c.-93-793dupT | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100289059 | |||||||
| chr8:100289059 | C | CAA | 6 | a0001c0001t0001g0234 a0001c0001t0002g0124 a0001c0001t0002g0129 others(3): Show |
6 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93-794_-93-793dup others(2): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100289059 | |||||||
| chr8:100289164 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-93-897A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100289164 | |||||||
| chr8:100289169 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-93-902A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100289169 | |||||||
| chr8:100289220 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-93-953G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100289220 | |||||||
| chr8:100289303 | A | C | 1 | a0001c0001t0001g0063 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-93-1036T>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100289303 | |||||||
| chr8:100289354 | T | C | 1 | a0001c0001t0002g0145 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-93-1087A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100289354 | |||||||
| chr8:100289403 | A | G | 1 | a0001c0001t0001g0026 | 2 | NA18964.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-93-1136T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100289403 | |||||||
| chr8:100289495 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-93-1228C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100289495 | |||||||
| chr8:100289532 | A | G | 1 | a0001c0001t0009g0235 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-93-1265T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100289532 | |||||||
| chr8:100289610 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-93-1343A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100289610 | |||||||
| chr8:100290222 | C | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0078 |
2 | NA19058.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.-93-1955G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100290222 | |||||||
| chr8:100290328 | C | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
117 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-93-2061G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100290328 | |||||||
| chr8:100290595 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0077 |
3 | HG01255.hp2 HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-93-2328C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100290595 | |||||||
| chr8:100290721 | T | C | 38 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(35): Show |
46 | HG01081.hp2 HG01099.hp2 HG02055.hp1 others(43): Show |
intron_variant | MODIFIER | c.-93-2454A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100290721 | |||||||
| chr8:100290907 | T | C | 2 | a0001c0001t0002g0070 a0001c0001t0002g0071 |
2 | NA18946.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.-93-2640A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100290907 | |||||||
| chr8:100291222 | A | G | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
192 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(189): Show |
intron_variant | MODIFIER | c.-93-2955T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100291222 | |||||||
| chr8:100291472 | C | T | 3 | a0001c0001t0002g0034 a0001c0001t0002g0148 a0001c0001t0002g0245 |
4 | NA18949.hp1 NA18975.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.-93-3205G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100291472 | |||||||
| chr8:100291473 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0159 |
3 | HG02109.hp2 HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-93-3206C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100291473 | |||||||
| chr8:100291474 | T | G | 1 | a0001c0001t0001g0095 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-93-3207A>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100291474 | |||||||
| chr8:100291493 | T | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
117 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-93-3226A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100291493 | |||||||
| chr8:100291539 | A | C | 1 | a0001c0001t0001g0217 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-93-3272T>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100291539 | |||||||
| chr8:100291704 | A | C | 7 | a0001c0001t0001g0023 a0001c0001t0001g0048 a0001c0001t0001g0049 others(4): Show |
8 | HG01257.hp2 HG01258.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.-93-3437T>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100291704 | |||||||
| chr8:100291708 | C | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
117 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-93-3441G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100291708 | |||||||
| chr8:100291820 | G | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
117 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-93-3553C>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100291820 | |||||||
| chr8:100291946 | T | TGAAAA | 10 | a0001c0001t0001g0007 a0001c0001t0001g0232 a0001c0001t0001g0233 others(7): Show |
14 | HG00733.hp2 HG00738.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93-3680_-93-3679i others(7): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100291946 | |||||||
| chr8:100291946 | T | TGAAGA | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
178 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.-93-3680_-93-3679i others(7): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100291946 | |||||||
| chr8:100291967 | C | CT | 73 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(70): Show |
113 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.-93-3701dupA | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100291967 | |||||||
| chr8:100291967 | CT | C | 64 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0036 others(61): Show |
79 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.-93-3701delA | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100291967 | |||||||
| chr8:100291967 | CTT | C | 19 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0038 others(16): Show |
23 | HG01071.hp1 HG01074.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.-93-3702_-93-3701d others(4): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100291967 | |||||||
| chr8:100291967 | CTTTT | C | 17 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(14): Show |
25 | HG00733.hp2 HG00738.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-93-3704_-93-3701d others(6): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100291967 | |||||||
| chr8:100292187 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-93-3920A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100292187 | |||||||
| chr8:100292433 | T | TGG | 6 | a0001c0001t0001g0018 a0001c0001t0001g0165 a0001c0001t0001g0172 others(3): Show |
8 | HG01071.hp1 HG01074.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.-93-4168_-93-4167d others(4): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100292433 | |||||||
| chr8:100292435 | G | GGGGGGT | 5 | a0001c0001t0001g0231 a0001c0001t0003g0044 a0001c0001t0003g0045 others(2): Show |
7 | HG01167.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-93-4169_-93-4168i others(8): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100292435 | |||||||
| chr8:100292435 | G | GGGGT | 5 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0162 others(2): Show |
5 | HG00735.hp2 HG01081.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93-4169_-93-4168i others(6): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100292435 | |||||||
| chr8:100292435 | G | GGGGTGT | 23 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0023 others(20): Show |
33 | HG00733.hp2 HG00738.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.-93-4169_-93-4168i others(8): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100292435 | |||||||
| chr8:100292435 | G | GGGGTGTG others(1): Show |
26 | a0001c0001t0001g0050 a0001c0001t0001g0233 a0001c0001t0001g0234 others(23): Show |
33 | HG01081.hp2 HG01099.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.-93-4169_-93-4168i others(10): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100292435 | |||||||
| chr8:100292435 | G | GGGGTGTG others(3): Show |
4 | a0001c0001t0001g0232 a0001c0001t0001g0239 a0001c0001t0002g0115 others(1): Show |
4 | HG02630.hp2 HG03195.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93-4169_-93-4168i others(12): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100292435 | |||||||
| chr8:100292435 | G | GGGGTGTG others(5): Show |
2 | a0001c0001t0004g0142 a0001c0001t0004g0150 |
2 | HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-93-4169_-93-4168i others(14): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100292435 | |||||||
| chr8:100292435 | G | GGGGTGTG others(7): Show |
1 | a0001c0001t0001g0218 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-93-4169_-93-4168i others(16): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100292435 | |||||||
| chr8:100292435 | G | GGT | 50 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(47): Show |
80 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.-93-4170_-93-4169d others(4): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100292435 | |||||||
| chr8:100292435 | G | GGTGT | 14 | a0001c0001t0001g0004 a0001c0001t0001g0062 a0001c0001t0001g0064 others(11): Show |
19 | HG01071.hp2 HG01167.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.-93-4172_-93-4169d others(6): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100292435 | |||||||
| chr8:100292435 | G | GGTGTGT | 4 | a0001c0001t0001g0025 a0001c0001t0001g0075 a0001c0001t0001g0076 others(1): Show |
5 | HG01255.hp2 HG02717.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.-93-4174_-93-4169d others(8): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100292435 | |||||||
| chr8:100292435 | G | GGTGTGTG others(1): Show |
5 | a0001c0001t0002g0130 a0001c0001t0002g0146 a0001c0001t0002g0147 others(2): Show |
5 | HG02148.hp1 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-93-4176_-93-4169d others(10): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100292435 | |||||||
| chr8:100292435 | G | GGTGTGTG others(3): Show |
3 | a0001c0001t0001g0113 a0001c0001t0006g0073 a0001c0001t0006g0103 |
3 | HG02630.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-93-4178_-93-4169d others(12): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100292435 | |||||||
| chr8:100292435 | G | GGTGTGTG others(5): Show |
1 | a0001c0001t0001g0072 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-93-4180_-93-4169d others(14): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100292435 | |||||||
| chr8:100292435 | GGT | G | 6 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0061 others(3): Show |
9 | HG01168.hp2 HG04115.hp2 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.-93-4170_-93-4169d others(4): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100292435 | |||||||
| chr8:100292437 | T | G | 20 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0038 others(17): Show |
24 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.-93-4170A>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100292437 | |||||||
| chr8:100292562 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-93-4295A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100292562 | |||||||
| chr8:100292787 | T | A | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
117 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-93-4520A>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100292787 | |||||||
| chr8:100292838 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-93-4571G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100292838 | |||||||
| chr8:100293004 | T | C | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG00323.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-93-4737A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100293004 | |||||||
| chr8:100293106 | G | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0206 |
5 | NA18951.hp2 NA18971.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.-93-4839C>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100293106 | |||||||
| chr8:100293143 | G | A | 2 | a0001c0001t0005g0037 a0001c0001t0005g0160 |
3 | HG00323.hp1 HG02300.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-93-4876C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100293143 | |||||||
| chr8:100293191 | A | G | 3 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0058 |
3 | HG02055.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-93-4924T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100293191 | |||||||
| chr8:100293363 | T | C | 1 | a0001c0001t0002g0126 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-93-5096A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100293363 | |||||||
| chr8:100293440 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG01884.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-93-5173G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100293440 | |||||||
| chr8:100293659 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-93-5392C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100293659 | |||||||
| chr8:100293668 | T | A | 1 | a0001c0001t0001g0098 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-93-5401A>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100293668 | |||||||
| chr8:100293952 | T | C | 1 | a0001c0001t0004g0060 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-93-5685A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100293952 | |||||||
| chr8:100294004 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-93-5737A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100294004 | |||||||
| chr8:100294173 | T | A | 25 | a0001c0001t0001g0018 a0001c0001t0001g0035 a0001c0001t0001g0036 others(22): Show |
31 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.-93-5906A>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100294173 | |||||||
| chr8:100294201 | C | G | 1 | a0001c0001t0002g0129 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-93-5934G>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100294201 | |||||||
| chr8:100294318 | G | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
117 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-93-6051C>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100294318 | |||||||
| chr8:100294549 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-93-6282A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100294549 | |||||||
| chr8:100294612 | CT | C | 179 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
246 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.-93-6346delA | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100294612 | |||||||
| chr8:100294672 | A | T | 1 | a0001c0001t0004g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-93-6405T>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100294672 | |||||||
| chr8:100294738 | A | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
117 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-93-6471T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100294738 | |||||||
| chr8:100294804 | C | T | 1 | a0001c0001t0002g0128 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-93-6537G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100294804 | |||||||
| chr8:100294937 | C | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0156 |
2 | HG01243.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-93-6670G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100294937 | |||||||
| chr8:100295083 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-93-6816A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100295083 | |||||||
| chr8:100295305 | G | A | 1 | a0001c0001t0001g0035 | 2 | HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-93-7038C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100295305 | |||||||
| chr8:100295311 | T | C | 1 | a0001c0001t0004g0144 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-93-7044A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100295311 | |||||||
| chr8:100295373 | C | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0157 |
2 | HG02145.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-93-7106G>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100295373 | |||||||
| chr8:100295455 | T | C | 32 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(29): Show |
40 | HG01081.hp2 HG02109.hp1 HG02148.hp1 others(37): Show |
intron_variant | MODIFIER | c.-93-7188A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100295455 | |||||||
| chr8:100295561 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0041 a0001c0001t0001g0218 others(1): Show |
8 | HG02145.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-93-7294C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100295561 | |||||||
| chr8:100295605 | T | C | 13 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0041 others(10): Show |
18 | HG01257.hp2 HG01258.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.-93-7338A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100295605 | |||||||
| chr8:100295749 | G | A | 1 | a0001c0004t0001g0202 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-93-7482C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100295749 | |||||||
| chr8:100295766 | A | G | 1 | a0001c0001t0002g0127 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-93-7499T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100295766 | |||||||
| chr8:100295808 | A | G | 1 | a0001c0001t0004g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-93-7541T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100295808 | |||||||
| chr8:100296085 | A | G | 1 | a0001c0001t0001g0214 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-93-7818T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100296085 | |||||||
| chr8:100296178 | C | CA | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
117 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-93-7912dupT | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100296178 | |||||||
| chr8:100296251 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-93-7984G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100296251 | |||||||
| chr8:100296304 | C | T | 2 | a0001c0001t0002g0070 a0001c0001t0002g0071 |
2 | NA18946.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.-93-8037G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100296304 | |||||||
| chr8:100296477 | A | T | 56 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(53): Show |
72 | HG00733.hp2 HG00738.hp1 HG01081.hp2 others(69): Show |
intron_variant | MODIFIER | c.-93-8210T>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100296477 | |||||||
| chr8:100296588 | A | AAT | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
117 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-93-8323_-93-8322d others(4): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100296588 | |||||||
| chr8:100296689 | C | T | 32 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(29): Show |
40 | HG01081.hp2 HG02109.hp1 HG02148.hp1 others(37): Show |
intron_variant | MODIFIER | c.-93-8422G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100296689 | |||||||
| chr8:100296744 | C | T | 3 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0058 |
3 | HG02055.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-93-8477G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100296744 | |||||||
| chr8:100296752 | A | C | 3 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0058 |
3 | HG02055.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-93-8485T>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100296752 | |||||||
| chr8:100296802 | AT | A | 38 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(35): Show |
46 | HG01081.hp2 HG01099.hp2 HG02055.hp1 others(43): Show |
intron_variant | MODIFIER | c.-93-8536delA | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100296802 | |||||||
| chr8:100296837 | G | T | 56 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(53): Show |
72 | HG00733.hp2 HG00738.hp1 HG01081.hp2 others(69): Show |
intron_variant | MODIFIER | c.-93-8570C>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100296837 | |||||||
| chr8:100296922 | A | T | 1 | a0001c0001t0001g0052 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-93-8655T>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100296922 | |||||||
| chr8:100297057 | A | C | 2 | a0001c0001t0001g0232 a0001c0001t0001g0239 |
2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-93-8790T>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100297057 | |||||||
| chr8:100297228 | T | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
243 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.-93-8961A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100297228 | |||||||
| chr8:100297249 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-93-8982A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100297249 | |||||||
| chr8:100297251 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-93-8984G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100297251 | |||||||
| chr8:100297262 | C | T | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
192 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(189): Show |
intron_variant | MODIFIER | c.-93-8995G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100297262 | |||||||
| chr8:100297268 | T | C | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG01884.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-93-9001A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100297268 | |||||||
| chr8:100297385 | A | G | 1 | a0001c0001t0013g0116 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-93-9118T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100297385 | |||||||
| chr8:100297426 | C | T | 3 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0058 |
3 | HG02055.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-93-9159G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100297426 | |||||||
| chr8:100297450 | A | C | 2 | a0001c0001t0002g0032 a0001c0001t0002g0145 |
3 | HG03041.hp2 HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-93-9183T>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100297450 | |||||||
| chr8:100297624 | A | G | 3 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0150 |
3 | HG02723.hp1 HG02809.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-93-9357T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100297624 | |||||||
| chr8:100297625 | A | C | 3 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0150 |
3 | HG02723.hp1 HG02809.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-93-9358T>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100297625 | |||||||
| chr8:100297761 | T | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
117 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-93-9494A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100297761 | |||||||
| chr8:100298052 | C | T | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
241 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.-93-9785G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100298052 | |||||||
| chr8:100298198 | T | TA | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(98): Show |
150 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.-93-9932dupT | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100298198 | |||||||
| chr8:100298198 | T | TAAAAA | 35 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(32): Show |
43 | HG01081.hp2 HG02109.hp1 HG02148.hp1 others(40): Show |
intron_variant | MODIFIER | c.-93-9936_-93-9932d others(7): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100298198 | |||||||
| chr8:100298339 | TATAA | T | 4 | a0001c0001t0002g0032 a0001c0001t0002g0125 a0001c0001t0002g0126 others(1): Show |
5 | HG03041.hp2 HG03486.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93-10076_-93-1007 others(8): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100298339 | |||||||
| chr8:100298421 | T | C | 6 | a0001c0001t0004g0060 a0001c0001t0004g0141 a0001c0001t0004g0142 others(3): Show |
6 | HG01099.hp2 HG02055.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93-10154A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100298421 | |||||||
| chr8:100298756 | C | G | 12 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0030 others(9): Show |
19 | HG00438.hp2 HG01943.hp1 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.-93-10489G>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100298756 | |||||||
| chr8:100298891 | A | C | 2 | a0001c0001t0005g0037 a0001c0001t0005g0160 |
3 | HG00323.hp1 HG02300.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-93-10624T>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100298891 | |||||||
| chr8:100298982 | C | T | 32 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(29): Show |
40 | HG01081.hp2 HG02109.hp1 HG02148.hp1 others(37): Show |
intron_variant | MODIFIER | c.-93-10715G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100298982 | |||||||
| chr8:100299089 | G | A | 38 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(35): Show |
46 | HG01081.hp2 HG01099.hp2 HG02055.hp1 others(43): Show |
intron_variant | MODIFIER | c.-94+10778C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100299089 | |||||||
| chr8:100299137 | T | C | 2 | a0001c0001t0001g0100 a0001c0001t0001g0111 |
2 | HG01167.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.-94+10730A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100299137 | |||||||
| chr8:100299513 | G | A | 3 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0058 |
3 | HG02055.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-94+10354C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100299513 | |||||||
| chr8:100299597 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-94+10270A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100299597 | |||||||
| chr8:100299732 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-94+10135G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100299732 | |||||||
| chr8:100299772 | GA | G | 13 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0041 others(10): Show |
18 | HG01257.hp2 HG01258.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.-94+10094delT | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100299772 | |||||||
| chr8:100299859 | C | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0159 |
3 | HG02109.hp2 HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-94+10008G>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100299859 | |||||||
| chr8:100299914 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-94+9953C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100299914 | |||||||
| chr8:100300247 | G | T | 3 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0058 |
3 | HG02055.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-94+9620C>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100300247 | |||||||
| chr8:100300269 | A | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
117 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-94+9598T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100300269 | |||||||
| chr8:100300287 | T | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
117 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-94+9580A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100300287 | |||||||
| chr8:100300437 | C | T | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
192 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(189): Show |
intron_variant | MODIFIER | c.-94+9430G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100300437 | |||||||
| chr8:100300480 | C | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG01884.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-94+9387G>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100300480 | |||||||
| chr8:100300577 | C | G | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-94+9290G>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100300577 | |||||||
| chr8:100300637 | A | C | 38 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(35): Show |
46 | HG01081.hp2 HG01099.hp2 HG02055.hp1 others(43): Show |
intron_variant | MODIFIER | c.-94+9230T>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100300637 | |||||||
| chr8:100300699 | C | A | 2 | a0001c0001t0001g0204 a0001c0001t0001g0222 |
2 | NA18971.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.-94+9168G>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100300699 | |||||||
| chr8:100301296 | A | C | 3 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0058 |
3 | HG02055.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-94+8571T>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100301296 | |||||||
| chr8:100301367 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-94+8500T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100301367 | |||||||
| chr8:100301447 | T | C | 1 | a0001c0001t0006g0103 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-94+8420A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100301447 | |||||||
| chr8:100301451 | A | C | 1 | a0001c0001t0003g0230 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-94+8416T>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100301451 | |||||||
| chr8:100301674 | G | A | 3 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0058 |
3 | HG02055.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-94+8193C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100301674 | |||||||
| chr8:100301920 | C | G | 1 | a0001c0001t0001g0159 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-94+7947G>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100301920 | |||||||
| chr8:100301942 | A | G | 1 | a0001c0001t0001g0052 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-94+7925T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100301942 | |||||||
| chr8:100302094 | G | A | 6 | a0001c0001t0004g0060 a0001c0001t0004g0141 a0001c0001t0004g0142 others(3): Show |
6 | HG01099.hp2 HG02055.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-94+7773C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100302094 | |||||||
| chr8:100302168 | G | T | 3 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0058 |
3 | HG02055.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-94+7699C>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100302168 | |||||||
| chr8:100302191 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-94+7676T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100302191 | |||||||
| chr8:100302706 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-94+7161G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100302706 | |||||||
| chr8:100302752 | G | A | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
117 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-94+7115C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100302752 | |||||||
| chr8:100302886 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-94+6981G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100302886 | |||||||
| chr8:100302983 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-94+6884A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100302983 | |||||||
| chr8:100303020 | A | G | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
192 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(189): Show |
intron_variant | MODIFIER | c.-94+6847T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100303020 | |||||||
| chr8:100303087 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-94+6780A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100303087 | |||||||
| chr8:100303338 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-94+6529C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100303338 | |||||||
| chr8:100303619 | G | A | 32 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(29): Show |
40 | HG01081.hp2 HG02109.hp1 HG02148.hp1 others(37): Show |
intron_variant | MODIFIER | c.-94+6248C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100303619 | |||||||
| chr8:100303756 | G | A | 38 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(35): Show |
46 | HG01081.hp2 HG01099.hp2 HG02055.hp1 others(43): Show |
intron_variant | MODIFIER | c.-94+6111C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100303756 | |||||||
| chr8:100303761 | T | TA | 43 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0021 others(40): Show |
56 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.-94+6105dupT | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100303761 | |||||||
| chr8:100303761 | TA | T | 44 | a0001c0001t0001g0007 a0001c0001t0001g0176 a0001c0001t0001g0177 others(41): Show |
59 | HG00544.hp1 HG00733.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.-94+6105delT | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100303761 | |||||||
| chr8:100303807 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-94+6060T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100303807 | |||||||
| chr8:100303824 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-94+6043C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100303824 | |||||||
| chr8:100303892 | GCGTCACT others(43): Show |
G | 1 | a0001c0001t0002g0245 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-94+5925_-94+5974d others(52): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100303892 | |||||||
| chr8:100304404 | T | C | 1 | a0001c0001t0002g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-94+5463A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100304404 | |||||||
| chr8:100304548 | C | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG01884.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-94+5319G>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100304548 | |||||||
| chr8:100304583 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-94+5284T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100304583 | |||||||
| chr8:100304653 | G | T | 56 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(53): Show |
72 | HG00733.hp2 HG00738.hp1 HG01081.hp2 others(69): Show |
intron_variant | MODIFIER | c.-94+5214C>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100304653 | |||||||
| chr8:100304982 | C | CTGGA | 2 | a0001c0001t0001g0023 a0001c0001t0001g0053 |
3 | HG01257.hp2 HG01258.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.-94+4881_-94+4884d others(6): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100304982 | |||||||
| chr8:100305003 | T | A | 1 | a0001c0001t0001g0114 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-94+4864A>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100305003 | |||||||
| chr8:100305011 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-94+4856G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100305011 | |||||||
| chr8:100305082 | C | G | 1 | a0001c0001t0001g0062 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-94+4785G>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100305082 | |||||||
| chr8:100305237 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-94+4630C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100305237 | |||||||
| chr8:100305438 | G | A | 25 | a0001c0001t0001g0018 a0001c0001t0001g0035 a0001c0001t0001g0036 others(22): Show |
31 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.-94+4429C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100305438 | |||||||
| chr8:100305462 | G | A | 1 | a0001c0001t0001g0214 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-94+4405C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100305462 | |||||||
| chr8:100305487 | A | G | 178 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(175): Show |
245 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.-94+4380T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100305487 | |||||||
| chr8:100305535 | T | C | 1 | a0001c0001t0001g0030 | 2 | NA19070.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-94+4332A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100305535 | |||||||
| chr8:100305574 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-94+4293A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100305574 | |||||||
| chr8:100305600 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-94+4267A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100305600 | |||||||
| chr8:100305724 | A | G | 178 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(175): Show |
245 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.-94+4143T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100305724 | |||||||
| chr8:100305787 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-94+4080G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100305787 | |||||||
| chr8:100305851 | T | C | 1 | a0001c0001t0001g0216 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-94+4016A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100305851 | |||||||
| chr8:100305873 | C | T | 3 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0058 |
3 | HG02055.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-94+3994G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100305873 | |||||||
| chr8:100306078 | T | A | 1 | a0001c0001t0004g0150 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-94+3789A>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100306078 | |||||||
| chr8:100306311 | A | C | 38 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(35): Show |
46 | HG01081.hp2 HG01099.hp2 HG02055.hp1 others(43): Show |
intron_variant | MODIFIER | c.-94+3556T>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100306311 | |||||||
| chr8:100306578 | AC | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0041 a0001c0001t0001g0218 others(1): Show |
8 | HG02145.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-94+3288delG | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100306578 | |||||||
| chr8:100306653 | TA | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0152 a0001c0001t0001g0153 |
4 | HG02486.hp2 HG02572.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-94+3213delT | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100306653 | |||||||
| chr8:100306779 | T | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0041 a0001c0001t0001g0047 others(3): Show |
10 | HG02145.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-94+3088A>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100306779 | |||||||
| chr8:100306807 | A | G | 2 | a0001c0001t0002g0123 a0001c0001t0002g0124 |
2 | NA18983.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-94+3060T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100306807 | |||||||
| chr8:100307098 | G | A | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
117 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-94+2769C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100307098 | |||||||
| chr8:100307148 | T | C | 56 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(53): Show |
72 | HG00733.hp2 HG00738.hp1 HG01081.hp2 others(69): Show |
intron_variant | MODIFIER | c.-94+2719A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100307148 | |||||||
| chr8:100307416 | C | A | 2 | a0001c0001t0001g0117 a0001c0001t0013g0116 |
2 | HG02056.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.-94+2451G>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100307416 | |||||||
| chr8:100307512 | A | C | 18 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(15): Show |
26 | HG00733.hp2 HG00738.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.-94+2355T>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100307512 | |||||||
| chr8:100307518 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-94+2349T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100307518 | |||||||
| chr8:100307547 | C | CA | 21 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(18): Show |
29 | HG00733.hp2 HG00738.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.-94+2319dupT | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100307547 | |||||||
| chr8:100307602 | G | A | 1 | a0001c0001t0001g0223 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-94+2265C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100307602 | |||||||
| chr8:100307710 | G | C | 1 | a0001c0001t0001g0224 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-94+2157C>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100307710 | |||||||
| chr8:100307768 | C | T | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
192 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(189): Show |
intron_variant | MODIFIER | c.-94+2099G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100307768 | |||||||
| chr8:100308351 | TTTA | T | 3 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 |
3 | NA18995.hp1 NA19068.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-94+1513_-94+1515d others(5): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100308351 | |||||||
| chr8:100308447 | A | G | 18 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(15): Show |
26 | HG00733.hp2 HG00738.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.-94+1420T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100308447 | |||||||
| chr8:100308477 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-94+1390A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100308477 | |||||||
| chr8:100308506 | C | T | 1 | a0001c0001t0003g0044 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-94+1361G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100308506 | |||||||
| chr8:100308637 | T | C | 1 | a0001c0001t0002g0225 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-94+1230A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100308637 | |||||||
| chr8:100308662 | T | TA | 3 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0053 |
4 | HG01257.hp2 HG01258.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.-94+1204dupT | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100308662 | |||||||
| chr8:100308689 | TA | T | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(72): Show |
114 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.-94+1177delT | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100308689 | |||||||
| chr8:100308908 | A | G | 3 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0058 |
3 | HG02055.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-94+959T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100308908 | |||||||
| chr8:100308977 | T | C | 6 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0226 others(3): Show |
8 | HG00741.hp2 HG01074.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-94+890A>G | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100308977 | |||||||
| chr8:100309145 | G | T | 18 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(15): Show |
26 | HG00733.hp2 HG00738.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.-94+722C>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100309145 | |||||||
| chr8:100309232 | C | A | 18 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(15): Show |
26 | HG00733.hp2 HG00738.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.-94+635G>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100309232 | |||||||
| chr8:100309311 | C | T | 1 | a0001c0001t0004g0060 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-94+556G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100309311 | |||||||
| chr8:100309341 | C | A | 1 | a0001c0001t0001g0244 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-94+526G>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100309341 | |||||||
| chr8:100309389 | A | G | 1 | a0001c0001t0001g0059 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-94+478T>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100309389 | |||||||
| chr8:100309474 | C | A | 1 | a0001c0001t0002g0046 | 2 | NA18966.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.-94+393G>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100309474 | |||||||
| chr8:100309474 | C | G | 3 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0058 |
3 | HG02055.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-94+393G>C | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100309474 | |||||||
| chr8:100309577 | T | TGGGGGGG others(32): Show |
1 | a0001c0001t0002g0245 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-94+289_-94+290ins others(39): Show |
RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100309577 | |||||||
| chr8:100309623 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-94+244C>T | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100309623 | |||||||
| chr8:100309649 | C | T | 1 | a0001c0001t0012g0055 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-94+218G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100309649 | |||||||
| chr8:100309670 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-94+197G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100309670 | |||||||
| chr8:100309738 | C | T | 7 | a0001c0001t0001g0023 a0001c0001t0001g0048 a0001c0001t0001g0049 others(4): Show |
8 | HG01257.hp2 HG01258.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.-94+129G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100309738 | |||||||
| chr8:100309760 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-94+107G>A | RNF19A | ENSG00000034677.13 | transcript | ENST00000341084.7 | protein_coding | 1/9 | chr8 | 100309760 |