Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 152006 |
| ensemblid | ENSG00000137075.18 |
| hgncid | 18052 |
| symbol | RNF38 |
| name | ring finger protein 38 |
| refseq_nuc | NM_022781.5 |
| refseq_prot | NP_073618.3 |
| ensembl_nuc | ENST00000259605.11 |
| ensembl_prot | ENSP00000259605.6 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 36336400 |
| end | 36400269 |
| strand | - |
| ver | v1.2 |
| region | chr9:36336400-36400269 |
| region5000 | chr9:36331400-36405269 |
| regionname0 | RNF38_chr9_36336400_36400269 |
| regionname5000 | RNF38_chr9_36331400_36405269 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1545 | 400 | 88 | 76 | 178 | 14 | 42 | RNF38_chr9_36331400_36405269 | RNF38 | ATGGC others(1540): Show |
chr9 | 36331400 | 36405269 | ||
| a0001c0002 | 0/0 | 1545 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | ATGGC others(1540): Show |
chr9 | 36331400 | 36405269 | ||
| a0001c0003 | 0/0 | 1545 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | ATGGC others(1540): Show |
chr9 | 36331400 | 36405269 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5061 | 268 | 59 | 43 | 133 | 3 | 29 | RNF38_chr9_36331400_36405269 | RNF38 | GTCCT others(5056): Show |
chr9 | 36331400 | 36405269 |
| a0001c0001t0002 | 0/0 | 5062 | 56 | 1 | 13 | 27 | 7 | 8 | RNF38_chr9_36331400_36405269 | RNF38 | GTCCT others(5057): Show |
chr9 | 36331400 | 36405269 |
| a0001c0001t0003 | 0/0 | 5062 | 29 | 0 | 17 | 7 | 2 | 3 | RNF38_chr9_36331400_36405269 | RNF38 | GTCCT others(5057): Show |
chr9 | 36331400 | 36405269 |
| a0001c0001t0004 | 0/0 | 5062 | 9 | 8 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | GTCCT others(5057): Show |
chr9 | 36331400 | 36405269 |
| a0001c0001t0005 | 0/0 | 5061 | 7 | 7 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | GTCCT others(5056): Show |
chr9 | 36331400 | 36405269 |
| a0001c0001t0006 | 0/0 | 5061 | 4 | 4 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | GTCCT others(5056): Show |
chr9 | 36331400 | 36405269 |
| a0001c0001t0007 | 0/0 | 5061 | 4 | 0 | 0 | 4 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | GTCCT others(5056): Show |
chr9 | 36331400 | 36405269 |
| a0001c0001t0008 | 0/0 | 5058 | 3 | 3 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | GTCCT others(5053): Show |
chr9 | 36331400 | 36405269 |
| a0001c0001t0009 | 0/0 | 5062 | 3 | 0 | 0 | 0 | 2 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | GTCCT others(5057): Show |
chr9 | 36331400 | 36405269 |
| a0001c0001t0010 | 0/0 | 5061 | 2 | 2 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | GTCCT others(5056): Show |
chr9 | 36331400 | 36405269 |
| a0001c0001t0011 | 0/0 | 5061 | 2 | 0 | 0 | 2 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | GTCCT others(5056): Show |
chr9 | 36331400 | 36405269 |
| a0001c0001t0012 | 0/0 | 5061 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | GTCCT others(5056): Show |
chr9 | 36331400 | 36405269 |
| a0001c0001t0013 | 0/0 | 5061 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | GTCCT others(5056): Show |
chr9 | 36331400 | 36405269 |
| a0001c0001t0014 | 0/0 | 5062 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | GTCCT others(5057): Show |
chr9 | 36331400 | 36405269 |
| a0001c0001t0015 | 0/0 | 5061 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | GTCCT others(5056): Show |
chr9 | 36331400 | 36405269 |
| a0001c0001t0016 | 0/0 | 5061 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | GTCCT others(5056): Show |
chr9 | 36331400 | 36405269 |
| a0001c0001t0017 | 0/0 | 5061 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | GTCCT others(5056): Show |
chr9 | 36331400 | 36405269 |
| a0001c0001t0018 | 0/0 | 5061 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | GTCCT others(5056): Show |
chr9 | 36331400 | 36405269 |
| a0001c0001t0019 | 0/0 | 5061 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | GTCCT others(5056): Show |
chr9 | 36331400 | 36405269 |
| a0001c0001t0020 | 0/0 | 5062 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | GTCCT others(5057): Show |
chr9 | 36331400 | 36405269 |
| a0001c0001t0021 | 0/0 | 5062 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | GTCCT others(5057): Show |
chr9 | 36331400 | 36405269 |
| a0001c0001t0022 | 0/0 | 5062 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | GTCCT others(5057): Show |
chr9 | 36331400 | 36405269 |
| a0001c0001t0023 | 1/0 | 5061 | 1 | 0 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | GTCCT others(5056): Show |
chr9 | 36331400 | 36405269 |
| a0001c0001t0024 | 0/0 | 5061 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | GTCCT others(5056): Show |
chr9 | 36331400 | 36405269 |
| a0001c0002t0001 | 0/0 | 5061 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | GTCCT others(5056): Show |
chr9 | 36331400 | 36405269 |
| a0001c0003t0005 | 0/0 | 5061 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | GTCCT others(5056): Show |
chr9 | 36331400 | 36405269 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0005 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0313 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0001g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0003 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0004 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0002g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0003g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0006g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0007g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0007g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0007g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0007g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0008g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0008g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0008g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0009g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0009g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0009g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0010g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0010g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0011g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0011g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0012g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0013g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0014g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0015g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0016g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0017g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0018g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0019g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0020g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0021g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0022g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0023g0247 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0001t0024g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| a0001c0003t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0194 | EUR | GBR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00099 | hp2 | a0001 | c0001 | t0009 | g0171 | EUR | GBR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0091 | EUR | GBR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0306 | EUR | GBR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0170 | EUR | FIN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0049 | EUR | FIN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00408 | hp1 | a0001 | c0001 | t0020 | g0102 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0332 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0190 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0156 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0124 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0188 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0373 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0374 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0165 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0174 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0169 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0353 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0370 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0168 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0366 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0167 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0186 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0166 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01346 | hp2 | a0001 | c0001 | t0024 | g0266 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0220 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0173 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0189 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0035 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01515 | hp1 | a0001 | c0001 | t0009 | g0115 | EUR | IBS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | IBS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0162 | EUR | IBS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0104 | EUR | IBS | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01891 | hp2 | a0001 | c0001 | t0015 | g0077 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0350 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0336 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0351 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0200 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0330 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0356 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02027 | hp1 | a0001 | c0001 | t0018 | g0057 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0365 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0364 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02293 | hp2 | a0001 | c0001 | t0016 | g0291 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0354 | AMR | PEL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0040 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0037 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0041 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0033 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02647 | hp2 | a0001 | c0001 | t0008 | g0333 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0034 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0082 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02738 | hp1 | a0001 | c0001 | t0009 | g0085 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0157 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0025 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0032 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02965 | hp1 | a0001 | c0003 | t0005 | g0027 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0334 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | MSL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0036 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0029 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0042 | AFR | MSL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | MSL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | MSL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0337 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0367 | AFR | MSL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03453 | hp2 | a0001 | c0001 | t0010 | g0044 | AFR | MSL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0026 | AFR | MSL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0361 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0185 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0098 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0023 | AFR | ESN | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0369 | AFR | MSL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03579 | hp2 | a0001 | c0001 | t0008 | g0335 | AFR | MSL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0352 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | STU | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | STU | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0088 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0324 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | BEB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | BEB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | STU | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | STU | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0123 | SAS | BEB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | STU | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | STU | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG04228 | hp1 | a0001 | c0001 | t0014 | g0045 | SAS | STU | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0360 | SAS | STU | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0368 | AFR | YRI | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | YRI | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0357 | EAS | CHB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | CHB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | CHB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18906 | hp1 | a0001 | c0001 | t0013 | g0043 | AFR | YRI | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18906 | hp2 | a0001 | c0001 | t0010 | g0021 | AFR | YRI | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18943 | hp2 | a0001 | c0001 | t0022 | g0112 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18949 | hp1 | a0001 | c0001 | t0007 | g0071 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18966 | hp1 | a0001 | c0001 | t0019 | g0203 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18983 | hp1 | a0001 | c0001 | t0007 | g0070 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18990 | hp1 | a0001 | c0001 | t0017 | g0149 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18999 | hp2 | a0001 | c0001 | t0007 | g0072 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19002 | hp2 | a0001 | c0001 | t0011 | g0228 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19030 | hp1 | a0001 | c0001 | t0012 | g0020 | AFR | LWK | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | LWK | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | LWK | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | LWK | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19054 | hp1 | a0001 | c0001 | t0011 | g0232 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0362 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19086 | hp2 | a0001 | c0001 | t0007 | g0069 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | YRI | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | YRI | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0039 | AFR | ASW | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0371 | AFR | ASW | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0092 | EUR | TSI | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0128 | EUR | TSI | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0125 | EUR | TSI | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0267 | EUR | TSI | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | GIH | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | GIH | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0164 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | CLM | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0372 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | MSL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0363 | AFR | USA | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0028 | AFR | USA | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | USA | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | USA | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA21309 | hp1 | a0001 | c0001 | t0021 | g0047 | AFR | LWK | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | LWK | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0313 | REF | REF | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0023 | g0247 | REF | REF | RNF38_chr9_36331400_36405269 | RNF38 | chr9 | 36331400 | 36405269 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:36344867 | C | T | 1 | a0001c0002 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.1350G>A | p.Arg450Arg | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/12 | 1511/5061 | 1350/1548 | 450/515 | chr9 | 36344867 | |||
| chr9:36353221 | G | A | 1 | a0001c0003 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.1020C>T | p.Pro340Pro | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 7/12 | 1181/5061 | 1020/1548 | 340/515 | chr9 | 36353221 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:36336677 | C | A | 1 | a0001c0001t0007 | 4 | NA18949.hp1 NA18983.hp1 NA18999.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3075G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 3075 | chr9 | 36336677 | ||||||
| chr9:36337073 | A | G | 2 | a0001c0001t0013 a0001c0001t0020 |
2 | HG00408.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2679T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 2679 | chr9 | 36337073 | ||||||
| chr9:36337183 | C | T | 1 | a0001c0001t0007 | 4 | NA18949.hp1 NA18983.hp1 NA18999.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2569G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 2569 | chr9 | 36337183 | ||||||
| chr9:36337191 | A | G | 2 | a0001c0001t0005 a0001c0003t0005 |
8 | HG02723.hp2 HG02809.hp2 HG02965.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2561T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 2561 | chr9 | 36337191 | ||||||
| chr9:36337256 | T | G | 1 | a0001c0001t0009 | 3 | HG00099.hp2 HG01515.hp1 HG02738.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2496A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 2496 | chr9 | 36337256 | ||||||
| chr9:36337395 | T | C | 1 | a0001c0001t0021 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2357A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 2357 | chr9 | 36337395 | ||||||
| chr9:36337470 | T | C | 1 | a0001c0001t0017 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2282A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 2282 | chr9 | 36337470 | ||||||
| chr9:36337503 | T | C | 1 | a0001c0001t0022 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2249A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 2249 | chr9 | 36337503 | ||||||
| chr9:36337649 | A | AT | 2 | a0001c0001t0003 a0001c0001t0014 |
30 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2102dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 2102 | chr9 | 36337649 | ||||||
| chr9:36337775 | A | G | 1 | a0001c0001t0014 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1977T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 1977 | chr9 | 36337775 | ||||||
| chr9:36337790 | A | T | 1 | a0001c0001t0014 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1962T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 1962 | chr9 | 36337790 | ||||||
| chr9:36337961 | G | A | 1 | a0001c0001t0018 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1791C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 1791 | chr9 | 36337961 | ||||||
| chr9:36338025 | A | G | 23 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(20): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
3_prime_UTR_variant | MODIFIER | c.*1727T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 1727 | chr9 | 36338025 | ||||||
| chr9:36338488 | C | T | 1 | a0001c0001t0019 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1264G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 1264 | chr9 | 36338488 | ||||||
| chr9:36338512 | G | T | 1 | a0001c0001t0011 | 2 | NA19002.hp2 NA19054.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1240C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 1240 | chr9 | 36338512 | ||||||
| chr9:36338570 | T | TA | 1 | a0001c0001t0004 | 9 | HG01496.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1181dupT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 1181 | chr9 | 36338570 | ||||||
| chr9:36338589 | T | C | 1 | a0001c0001t0019 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1163A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 1163 | chr9 | 36338589 | ||||||
| chr9:36338760 | T | TA | 5 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0020 others(2): Show |
62 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*991dupT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 991 | chr9 | 36338760 | ||||||
| chr9:36338958 | C | T | 23 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(20): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
3_prime_UTR_variant | MODIFIER | c.*794G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 794 | chr9 | 36338958 | ||||||
| chr9:36339133 | C | T | 1 | a0001c0001t0016 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*619G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 619 | chr9 | 36339133 | ||||||
| chr9:36339396 | TATC | T | 1 | a0001c0001t0008 | 3 | HG02647.hp2 HG03041.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*353_*355delGAT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 353 | chr9 | 36339396 | ||||||
| chr9:36339643 | C | T | 1 | a0001c0001t0015 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*109G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 109 | chr9 | 36339643 | ||||||
| chr9:36339699 | G | A | 1 | a0001c0001t0024 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*53C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 12/12 | 53 | chr9 | 36339699 | ||||||
| chr9:36400159 | C | T | 7 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(4): Show |
25 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-51G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/12 | 51 | chr9 | 36400159 | ||||||
| chr9:36400220 | C | T | 1 | a0001c0001t0012 | 1 | NA19030.hp1 | 5_prime_UTR_variant | MODIFIER | c.-112G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/12 | 112 | chr9 | 36400220 | ||||||
| chr9:36400242 | A | G | 8 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(5): Show |
26 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(23): Show |
5_prime_UTR_variant | MODIFIER | c.-134T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/12 | 134 | chr9 | 36400242 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:36339823 | C | A | 1 | a0001c0001t0001g0079 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1486-9G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36339823 | |||||||
| chr9:36339880 | G | C | 1 | a0001c0001t0002g0090 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1486-66C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36339880 | |||||||
| chr9:36339986 | AT | A | 365 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(362): Show |
393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.1486-173delA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36339986 | |||||||
| chr9:36340092 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1486-278C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36340092 | |||||||
| chr9:36340138 | C | A | 1 | a0001c0001t0001g0246 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1486-324G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36340138 | |||||||
| chr9:36340168 | G | A | 1 | a0001c0001t0003g0138 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1486-354C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36340168 | |||||||
| chr9:36340248 | G | A | 1 | a0001c0001t0003g0164 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1486-434C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36340248 | |||||||
| chr9:36340296 | G | A | 1 | a0001c0001t0002g0129 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1486-482C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36340296 | |||||||
| chr9:36340393 | C | T | 1 | a0001c0001t0001g0019 | 2 | NA18962.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1486-579G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36340393 | |||||||
| chr9:36340452 | C | T | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | NA18974.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1486-638G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36340452 | |||||||
| chr9:36340464 | G | C | 4 | a0001c0001t0001g0329 a0001c0001t0001g0341 a0001c0001t0001g0342 others(1): Show |
4 | HG03195.hp1 HG03225.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1486-650C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36340464 | |||||||
| chr9:36340503 | C | G | 1 | a0001c0001t0008g0335 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1486-689G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36340503 | |||||||
| chr9:36340638 | T | C | 1 | a0001c0001t0001g0299 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1486-824A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36340638 | |||||||
| chr9:36340721 | C | T | 2 | a0001c0001t0010g0021 a0001c0001t0014g0045 |
2 | HG04228.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1486-907G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36340721 | |||||||
| chr9:36340914 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1486-1100G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36340914 | |||||||
| chr9:36340943 | T | C | 3 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0098 |
3 | HG03491.hp2 HG03492.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1486-1129A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36340943 | |||||||
| chr9:36341092 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0180 |
3 | HG02735.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1485+1233C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341092 | |||||||
| chr9:36341120 | CGCTTCAG others(4): Show |
C | 1 | a0001c0001t0014g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1485+1194_1485+120 others(15): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341120 | |||||||
| chr9:36341201 | C | T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0221 a0001c0001t0001g0222 others(1): Show |
4 | HG00609.hp1 HG02083.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.1485+1124G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341201 | |||||||
| chr9:36341217 | G | A | 1 | a0001c0001t0001g0339 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1485+1108C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341217 | |||||||
| chr9:36341227 | G | A | 1 | a0001c0001t0001g0006 | 3 | HG03654.hp1 HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1485+1098C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341227 | |||||||
| chr9:36341249 | C | T | 1 | a0001c0001t0001g0340 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1485+1076G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341249 | |||||||
| chr9:36341250 | G | A | 11 | a0001c0001t0002g0004 a0001c0001t0002g0048 a0001c0001t0002g0049 others(8): Show |
13 | HG00280.hp2 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.1485+1075C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341250 | |||||||
| chr9:36341384 | T | G | 1 | a0001c0001t0002g0090 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1485+941A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341384 | |||||||
| chr9:36341387 | T | G | 1 | a0001c0001t0002g0090 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1485+938A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341387 | |||||||
| chr9:36341391 | G | A | 1 | a0001c0001t0002g0090 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1485+934C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341391 | |||||||
| chr9:36341393 | T | A | 1 | a0001c0001t0002g0090 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1485+932A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341393 | |||||||
| chr9:36341455 | T | G | 1 | a0001c0001t0015g0077 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1485+870A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341455 | |||||||
| chr9:36341514 | A | G | 1 | a0001c0001t0015g0077 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1485+811T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341514 | |||||||
| chr9:36341521 | T | C | 1 | a0001c0001t0001g0332 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1485+804A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341521 | |||||||
| chr9:36341679 | C | T | 3 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0289 |
3 | HG03688.hp1 HG03834.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1485+646G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341679 | |||||||
| chr9:36341721 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1485+604C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341721 | |||||||
| chr9:36341751 | G | A | 2 | a0001c0001t0002g0373 a0001c0001t0002g0374 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1485+574C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341751 | |||||||
| chr9:36341793 | A | AATATATA others(15): Show |
1 | a0001c0002t0001g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1485+510_1485+531d others(24): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341793 | |||||||
| chr9:36341793 | AATATATA others(3): Show |
A | 1 | a0001c0001t0014g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1485+522_1485+531d others(12): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341793 | |||||||
| chr9:36341793 | AATATATA others(9): Show |
A | 1 | a0001c0001t0006g0041 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1485+516_1485+531d others(18): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341793 | |||||||
| chr9:36341793 | AATATATA others(15): Show |
A | 1 | a0001c0001t0006g0040 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1485+510_1485+531d others(24): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341793 | |||||||
| chr9:36341793 | AATATATA others(17): Show |
A | 3 | a0001c0001t0001g0341 a0001c0001t0006g0042 a0001c0001t0013g0043 |
3 | HG03209.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1485+508_1485+531d others(26): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341793 | |||||||
| chr9:36341793 | AATATATA others(19): Show |
A | 2 | a0001c0001t0001g0329 a0001c0001t0001g0363 |
2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1485+506_1485+531d others(28): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341793 | |||||||
| chr9:36341793 | AATATATA others(21): Show |
A | 1 | a0001c0001t0005g0025 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1485+504_1485+531d others(30): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341793 | |||||||
| chr9:36341793 | AATATATA others(25): Show |
A | 2 | a0001c0001t0005g0022 a0001c0001t0010g0021 |
2 | HG02723.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1485+500_1485+531d others(34): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341793 | |||||||
| chr9:36341793 | AATATATA others(29): Show |
A | 1 | a0001c0001t0006g0039 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1485+496_1485+531d others(38): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341793 | |||||||
| chr9:36341793 | AATATATA others(31): Show |
A | 4 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0034 others(1): Show |
4 | HG02717.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1485+494_1485+531d others(40): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341793 | |||||||
| chr9:36341793 | AATATATA others(35): Show |
A | 4 | a0001c0001t0004g0035 a0001c0001t0005g0026 a0001c0001t0005g0028 others(1): Show |
4 | HG01496.hp2 HG03195.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1485+490_1485+531d others(44): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341793 | |||||||
| chr9:36341793 | AATATATA others(37): Show |
A | 6 | a0001c0001t0004g0031 a0001c0001t0004g0033 a0001c0001t0004g0036 others(3): Show |
6 | HG02258.hp2 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1485+488_1485+531d others(46): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341793 | |||||||
| chr9:36341793 | AATATATA others(49): Show |
A | 1 | a0001c0001t0001g0342 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1485+476_1485+531d others(58): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341793 | |||||||
| chr9:36341807 | TATATATA others(53): Show |
T | 161 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(158): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.1485+458_1485+517d others(62): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341807 | |||||||
| chr9:36341809 | TATATATA others(51): Show |
T | 145 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(142): Show |
152 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.1485+458_1485+515d others(60): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341809 | |||||||
| chr9:36341811 | TATATATA others(49): Show |
T | 1 | a0001c0001t0001g0306 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1485+458_1485+513d others(58): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341811 | |||||||
| chr9:36341815 | TATATATA others(45): Show |
T | 32 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(29): Show |
39 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.1485+458_1485+509d others(54): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341815 | |||||||
| chr9:36341817 | TATATATA others(43): Show |
T | 1 | a0001c0001t0001g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1485+458_1485+507d others(52): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341817 | |||||||
| chr9:36341823 | TATATATA others(37): Show |
T | 1 | a0001c0001t0015g0077 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1485+458_1485+501d others(46): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341823 | |||||||
| chr9:36341825 | T | C | 1 | a0001c0001t0014g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1485+500A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341825 | |||||||
| chr9:36341827 | TATATATA others(33): Show |
T | 1 | a0001c0001t0005g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1485+458_1485+497d others(42): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341827 | |||||||
| chr9:36341829 | TATATATA others(31): Show |
T | 1 | a0001c0001t0005g0024 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1485+458_1485+495d others(40): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341829 | |||||||
| chr9:36341867 | A | T | 1 | a0001c0002t0001g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1485+458T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341867 | |||||||
| chr9:36341986 | AT | A | 9 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(6): Show |
9 | HG01496.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1485+338delA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36341986 | |||||||
| chr9:36342046 | A | C | 4 | a0001c0001t0001g0329 a0001c0001t0001g0341 a0001c0001t0001g0342 others(1): Show |
4 | HG03195.hp1 HG03225.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1485+279T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36342046 | |||||||
| chr9:36342178 | G | T | 1 | a0001c0001t0001g0339 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1485+147C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36342178 | |||||||
| chr9:36342184 | T | TCTC | 367 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(364): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.1485+138_1485+140d others(5): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36342184 | |||||||
| chr9:36342306 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1485+19T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 11/11 | chr9 | 36342306 | |||||||
| chr9:36342668 | T | C | 162 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(159): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.1386-244A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36342668 | |||||||
| chr9:36342673 | A | T | 343 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(340): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.1386-249T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36342673 | |||||||
| chr9:36342674 | A | T | 1 | a0001c0001t0014g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1386-250T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36342674 | |||||||
| chr9:36342683 | G | C | 4 | a0001c0001t0001g0329 a0001c0001t0001g0341 a0001c0001t0001g0342 others(1): Show |
4 | HG03195.hp1 HG03225.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1386-259C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36342683 | |||||||
| chr9:36342699 | G | T | 1 | a0001c0001t0001g0304 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1386-275C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36342699 | |||||||
| chr9:36342742 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1386-318A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36342742 | |||||||
| chr9:36342825 | T | G | 1 | a0001c0002t0001g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1386-401A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36342825 | |||||||
| chr9:36342889 | G | C | 343 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(340): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.1386-465C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36342889 | |||||||
| chr9:36343095 | A | G | 1 | a0001c0001t0001g0073 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1386-671T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36343095 | |||||||
| chr9:36343167 | T | C | 163 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(160): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.1386-743A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36343167 | |||||||
| chr9:36343489 | G | A | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1386-1065C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36343489 | |||||||
| chr9:36343568 | T | C | 348 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(345): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.1386-1144A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36343568 | |||||||
| chr9:36343585 | A | G | 1 | a0001c0001t0004g0036 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1386-1161T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36343585 | |||||||
| chr9:36343646 | A | G | 58 | a0001c0001t0001g0086 a0001c0001t0001g0113 a0001c0001t0002g0003 others(55): Show |
63 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.1385+1186T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36343646 | |||||||
| chr9:36343677 | T | C | 356 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(353): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.1385+1155A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36343677 | |||||||
| chr9:36343767 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1385+1065C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36343767 | |||||||
| chr9:36343876 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1385+956T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36343876 | |||||||
| chr9:36343895 | A | T | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1385+937T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36343895 | |||||||
| chr9:36343996 | C | A | 1 | a0001c0001t0012g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1385+836G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36343996 | |||||||
| chr9:36344104 | C | A | 9 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(6): Show |
9 | HG01496.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1385+728G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36344104 | |||||||
| chr9:36344235 | A | C | 1 | a0001c0001t0003g0220 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1385+597T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36344235 | |||||||
| chr9:36344331 | A | T | 1 | a0001c0001t0001g0176 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1385+501T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36344331 | |||||||
| chr9:36344387 | A | T | 1 | a0001c0001t0001g0293 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1385+445T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36344387 | |||||||
| chr9:36344503 | A | G | 2 | a0001c0001t0001g0341 a0001c0001t0001g0363 |
2 | HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1385+329T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36344503 | |||||||
| chr9:36344633 | A | G | 1 | a0001c0001t0003g0156 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1385+199T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36344633 | |||||||
| chr9:36344715 | G | A | 1 | a0001c0002t0001g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1385+117C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 10/11 | chr9 | 36344715 | |||||||
| chr9:36344961 | G | A | 1 | a0001c0001t0002g0094 | 1 | HG00544.hp1 | splice_region_variant&intron_variant | LOW | c.1264-8C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36344961 | |||||||
| chr9:36344971 | G | A | 5 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(2): Show |
5 | HG01074.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1264-18C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36344971 | |||||||
| chr9:36345010 | CT | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(30): Show |
40 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.1264-58delA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36345010 | |||||||
| chr9:36345154 | C | T | 137 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(134): Show |
144 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.1264-201G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36345154 | |||||||
| chr9:36345160 | T | C | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1264-207A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36345160 | |||||||
| chr9:36345349 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1264-396C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36345349 | |||||||
| chr9:36345357 | G | A | 4 | a0001c0001t0001g0329 a0001c0001t0001g0341 a0001c0001t0001g0342 others(1): Show |
4 | HG03195.hp1 HG03225.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264-404C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36345357 | |||||||
| chr9:36345399 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1264-446T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36345399 | |||||||
| chr9:36345438 | C | T | 4 | a0001c0001t0001g0332 a0001c0001t0001g0359 a0001c0001t0001g0362 others(1): Show |
4 | HG00642.hp2 NA18951.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1264-485G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36345438 | |||||||
| chr9:36345514 | C | G | 1 | a0001c0001t0003g0190 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1264-561G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36345514 | |||||||
| chr9:36345774 | TGGCCTAA others(8): Show |
T | 1 | a0001c0001t0001g0006 | 3 | HG03654.hp1 HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1264-836_1264-822d others(17): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36345774 | |||||||
| chr9:36345799 | T | C | 1 | a0001c0001t0008g0333 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1264-846A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36345799 | |||||||
| chr9:36345837 | G | A | 1 | a0001c0001t0010g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1264-884C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36345837 | |||||||
| chr9:36345962 | C | T | 3 | a0001c0001t0004g0033 a0001c0001t0004g0037 a0001c0001t0004g0038 |
3 | HG02572.hp2 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1264-1009G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36345962 | |||||||
| chr9:36346013 | T | C | 2 | a0001c0001t0001g0198 a0001c0001t0001g0212 |
2 | HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1264-1060A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36346013 | |||||||
| chr9:36346019 | C | A | 5 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(2): Show |
5 | HG01074.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1264-1066G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36346019 | |||||||
| chr9:36346104 | T | C | 1 | a0001c0002t0001g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1264-1151A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36346104 | |||||||
| chr9:36346108 | G | A | 1 | a0001c0002t0001g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1264-1155C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36346108 | |||||||
| chr9:36346284 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0152 |
2 | HG02056.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1264-1331G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36346284 | |||||||
| chr9:36346308 | C | T | 137 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(134): Show |
144 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.1264-1355G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36346308 | |||||||
| chr9:36346384 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1264-1431A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36346384 | |||||||
| chr9:36346530 | C | T | 311 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(308): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1264-1577G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36346530 | |||||||
| chr9:36346692 | T | TGTG | 366 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(363): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.1264-1740_1264-173 others(7): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36346692 | |||||||
| chr9:36347120 | CGGGGGGG others(3): Show |
C | 17 | a0001c0001t0001g0079 a0001c0001t0001g0176 a0001c0001t0001g0241 others(14): Show |
17 | HG00408.hp1 HG01192.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.1264-2177_1264-216 others(14): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347120 | |||||||
| chr9:36347120 | CGGGGGGG others(4): Show |
C | 28 | a0001c0001t0001g0016 a0001c0001t0001g0051 a0001c0001t0001g0074 others(25): Show |
29 | HG00673.hp2 HG01109.hp1 HG01346.hp2 others(26): Show |
intron_variant | MODIFIER | c.1264-2178_1264-216 others(15): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347120 | |||||||
| chr9:36347120 | CGGGGGGG others(5): Show |
C | 36 | a0001c0001t0001g0014 a0001c0001t0001g0239 a0001c0001t0001g0245 others(33): Show |
37 | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.1264-2179_1264-216 others(16): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347120 | |||||||
| chr9:36347120 | CGGGGGGG others(6): Show |
C | 26 | a0001c0001t0001g0013 a0001c0001t0001g0060 a0001c0001t0001g0064 others(23): Show |
27 | HG01071.hp2 HG01074.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.1264-2180_1264-216 others(17): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347120 | |||||||
| chr9:36347120 | CGGGGGGG others(7): Show |
C | 41 | a0001c0001t0001g0063 a0001c0001t0001g0078 a0001c0001t0001g0161 others(38): Show |
41 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.1264-2181_1264-216 others(18): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347120 | |||||||
| chr9:36347120 | CGGGGGGG others(8): Show |
C | 51 | a0001c0001t0001g0008 a0001c0001t0001g0061 a0001c0001t0001g0062 others(48): Show |
57 | HG00099.hp2 HG00408.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.1264-2182_1264-216 others(19): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347120 | |||||||
| chr9:36347120 | CGGGGGGG others(9): Show |
C | 71 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0011 others(68): Show |
76 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.1264-2183_1264-216 others(20): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347120 | |||||||
| chr9:36347120 | CGGGGGGG others(10): Show |
C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(57): Show |
70 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1264-2184_1264-216 others(21): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347120 | |||||||
| chr9:36347120 | CGGGGGGG others(11): Show |
C | 2 | a0001c0001t0001g0054 a0001c0001t0006g0039 |
2 | NA19012.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1264-2185_1264-216 others(22): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347120 | |||||||
| chr9:36347120 | CGGGGGGG others(14): Show |
C | 1 | a0001c0001t0001g0271 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1264-2188_1264-216 others(25): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347120 | |||||||
| chr9:36347136 | GGGGGGGG others(7): Show |
G | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1264-2197_1264-218 others(18): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347136 | |||||||
| chr9:36347138 | G | T | 3 | a0001c0001t0002g0004 a0001c0001t0002g0124 a0001c0001t0002g0126 |
3 | HG00741.hp1 HG01433.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.1264-2185C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347138 | |||||||
| chr9:36347138 | GGGGGGGG others(5): Show |
G | 1 | a0001c0001t0001g0327 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1264-2197_1264-218 others(16): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347138 | |||||||
| chr9:36347139 | G | T | 1 | a0001c0001t0015g0077 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1264-2186C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347139 | |||||||
| chr9:36347139 | GGGGGGGG others(4): Show |
G | 4 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0323 others(1): Show |
4 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1264-2197_1264-218 others(15): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347139 | |||||||
| chr9:36347183 | TATAAAAT others(4): Show |
T | 1 | a0001c0001t0002g0099 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1264-2241_1264-223 others(15): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347183 | |||||||
| chr9:36347213 | T | C | 1 | a0001c0001t0001g0300 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1264-2260A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347213 | |||||||
| chr9:36347218 | A | C | 312 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(309): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1264-2265T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347218 | |||||||
| chr9:36347645 | C | T | 4 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0303 others(1): Show |
4 | HG01243.hp2 HG01261.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264-2692G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347645 | |||||||
| chr9:36347904 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1264-2951C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347904 | |||||||
| chr9:36347932 | C | T | 1 | a0001c0001t0001g0372 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1264-2979G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347932 | |||||||
| chr9:36347946 | G | A | 2 | a0001c0001t0001g0355 a0001c0001t0001g0361 |
2 | HG02071.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1264-2993C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36347946 | |||||||
| chr9:36348008 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1264-3055C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36348008 | |||||||
| chr9:36348025 | G | A | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(344): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.1264-3072C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36348025 | |||||||
| chr9:36348129 | A | G | 2 | a0001c0001t0001g0337 a0001c0001t0001g0360 |
2 | HG03239.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1263+2986T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36348129 | |||||||
| chr9:36348182 | T | C | 2 | a0001c0001t0009g0085 a0001c0001t0009g0171 |
2 | HG00099.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1263+2933A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36348182 | |||||||
| chr9:36348285 | A | C | 1 | a0001c0001t0001g0302 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1263+2830T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36348285 | |||||||
| chr9:36348828 | T | C | 2 | a0001c0001t0001g0326 a0001c0001t0001g0327 |
2 | HG01175.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1263+2287A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36348828 | |||||||
| chr9:36348848 | A | C | 1 | a0001c0001t0001g0327 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1263+2267T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36348848 | |||||||
| chr9:36348958 | GCTGA | G | 25 | a0001c0001t0001g0330 a0001c0001t0001g0332 a0001c0001t0001g0336 others(22): Show |
25 | HG00609.hp2 HG00642.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.1263+2153_1263+215 others(8): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36348958 | |||||||
| chr9:36349376 | G | A | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1263+1739C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36349376 | |||||||
| chr9:36349384 | G | A | 1 | a0001c0001t0014g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1263+1731C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36349384 | |||||||
| chr9:36349564 | C | T | 1 | a0001c0001t0003g0164 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1263+1551G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36349564 | |||||||
| chr9:36349589 | G | A | 3 | a0001c0001t0008g0333 a0001c0001t0008g0334 a0001c0001t0008g0335 |
3 | HG02647.hp2 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1263+1526C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36349589 | |||||||
| chr9:36349663 | A | G | 355 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(352): Show |
383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.1263+1452T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36349663 | |||||||
| chr9:36349720 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1263+1395G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36349720 | |||||||
| chr9:36349876 | A | G | 1 | a0001c0001t0015g0077 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1263+1239T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36349876 | |||||||
| chr9:36349921 | G | T | 1 | a0001c0001t0001g0217 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1263+1194C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36349921 | |||||||
| chr9:36349975 | C | T | 1 | a0001c0001t0001g0259 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1263+1140G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36349975 | |||||||
| chr9:36349980 | C | T | 346 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(343): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.1263+1135G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36349980 | |||||||
| chr9:36350007 | G | A | 3 | a0001c0001t0001g0329 a0001c0001t0001g0341 a0001c0001t0001g0363 |
3 | HG03195.hp1 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1263+1108C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36350007 | |||||||
| chr9:36350023 | G | T | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1263+1092C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36350023 | |||||||
| chr9:36350037 | C | T | 1 | a0001c0001t0010g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1263+1078G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36350037 | |||||||
| chr9:36350108 | C | T | 8 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(5): Show |
8 | HG01109.hp1 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1263+1007G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36350108 | |||||||
| chr9:36350267 | T | A | 1 | a0001c0001t0001g0324 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1263+848A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36350267 | |||||||
| chr9:36350315 | T | A | 1 | a0001c0001t0001g0215 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1263+800A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36350315 | |||||||
| chr9:36350552 | A | C | 1 | a0001c0001t0001g0253 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1263+563T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36350552 | |||||||
| chr9:36350567 | A | T | 1 | a0001c0001t0001g0254 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1263+548T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36350567 | |||||||
| chr9:36351077 | C | T | 30 | a0001c0001t0001g0006 a0001c0001t0001g0158 a0001c0001t0001g0184 others(27): Show |
32 | HG00438.hp1 HG00544.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1263+38G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36351077 | |||||||
| chr9:36351084 | C | T | 1 | a0001c0001t0002g0116 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1263+31G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 9/11 | chr9 | 36351084 | |||||||
| chr9:36351229 | A | G | 11 | a0001c0001t0001g0012 a0001c0001t0001g0225 a0001c0001t0001g0227 others(8): Show |
12 | HG02071.hp1 HG02523.hp2 NA18948.hp1 others(9): Show |
intron_variant | MODIFIER | c.1179-30T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 8/11 | chr9 | 36351229 | |||||||
| chr9:36351638 | G | A | 1 | a0001c0001t0006g0041 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1179-439C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 8/11 | chr9 | 36351638 | |||||||
| chr9:36351662 | G | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0074 |
2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1179-463C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 8/11 | chr9 | 36351662 | |||||||
| chr9:36351697 | G | A | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(170): Show |
187 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(184): Show |
intron_variant | MODIFIER | c.1179-498C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 8/11 | chr9 | 36351697 | |||||||
| chr9:36351803 | C | T | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(169): Show |
186 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.1179-604G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 8/11 | chr9 | 36351803 | |||||||
| chr9:36352026 | G | A | 4 | a0001c0001t0005g0026 a0001c0001t0005g0028 a0001c0001t0005g0029 others(1): Show |
4 | HG02965.hp1 HG03195.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1178+716C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 8/11 | chr9 | 36352026 | |||||||
| chr9:36352070 | T | C | 1 | a0001c0001t0002g0049 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1178+672A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 8/11 | chr9 | 36352070 | |||||||
| chr9:36352320 | A | C | 1 | a0001c0002t0001g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1178+422T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 8/11 | chr9 | 36352320 | |||||||
| chr9:36352356 | C | T | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1178+386G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 8/11 | chr9 | 36352356 | |||||||
| chr9:36352584 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1178+158G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 8/11 | chr9 | 36352584 | |||||||
| chr9:36352690 | G | T | 9 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(6): Show |
9 | HG01496.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1178+52C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 8/11 | chr9 | 36352690 | |||||||
| chr9:36352916 | T | C | 1 | a0001c0001t0003g0173 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1072-68A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 7/11 | chr9 | 36352916 | |||||||
| chr9:36353130 | C | T | 2 | a0001c0001t0001g0365 a0001c0001t0003g0366 |
2 | HG01255.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1071+40G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 7/11 | chr9 | 36353130 | |||||||
| chr9:36353139 | G | C | 2 | a0001c0001t0002g0093 a0001c0001t0002g0095 |
2 | NA18954.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1071+31C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 7/11 | chr9 | 36353139 | |||||||
| chr9:36353343 | GA | G | 5 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(2): Show |
5 | HG01074.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.910-13delT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36353343 | |||||||
| chr9:36353344 | A | G | 2 | a0001c0001t0001g0337 a0001c0001t0001g0360 |
2 | HG03239.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.910-13T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36353344 | |||||||
| chr9:36353405 | A | C | 1 | a0001c0001t0001g0370 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.910-74T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36353405 | |||||||
| chr9:36353462 | T | G | 3 | a0001c0001t0008g0333 a0001c0001t0008g0334 a0001c0001t0008g0335 |
3 | HG02647.hp2 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.910-131A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36353462 | |||||||
| chr9:36353625 | C | T | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | NA18965.hp2 NA19060.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.910-294G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36353625 | |||||||
| chr9:36353670 | A | G | 1 | a0001c0001t0001g0330 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.910-339T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36353670 | |||||||
| chr9:36353677 | T | C | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG01891.hp1 HG02451.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.910-346A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36353677 | |||||||
| chr9:36353698 | A | T | 19 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(16): Show |
26 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.910-367T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36353698 | |||||||
| chr9:36353859 | G | C | 1 | a0001c0001t0001g0292 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.910-528C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36353859 | |||||||
| chr9:36353879 | C | T | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.910-548G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36353879 | |||||||
| chr9:36354047 | A | C | 1 | a0001c0001t0002g0110 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.910-716T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354047 | |||||||
| chr9:36354074 | T | G | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.910-743A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354074 | |||||||
| chr9:36354116 | T | C | 133 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(130): Show |
140 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.910-785A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354116 | |||||||
| chr9:36354187 | C | T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0212 |
2 | HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.910-856G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354187 | |||||||
| chr9:36354215 | A | T | 1 | a0001c0001t0001g0263 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.910-884T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354215 | |||||||
| chr9:36354253 | C | T | 9 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(6): Show |
9 | HG01496.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.910-922G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354253 | |||||||
| chr9:36354255 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.910-924G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354255 | |||||||
| chr9:36354448 | C | T | 19 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(16): Show |
26 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.910-1117G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354448 | |||||||
| chr9:36354493 | G | A | 2 | a0001c0001t0001g0278 a0001c0001t0016g0291 |
2 | HG02293.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.910-1162C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354493 | |||||||
| chr9:36354502 | A | C | 1 | a0001c0001t0001g0219 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.910-1171T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354502 | |||||||
| chr9:36354599 | A | G | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG00558.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.910-1268T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354599 | |||||||
| chr9:36354616 | A | G | 174 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(171): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.910-1285T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354616 | |||||||
| chr9:36354721 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.910-1390A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354721 | |||||||
| chr9:36354754 | T | C | 8 | a0001c0001t0005g0022 a0001c0001t0005g0023 a0001c0001t0005g0024 others(5): Show |
8 | HG02723.hp2 HG02809.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.910-1423A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354754 | |||||||
| chr9:36354832 | T | C | 10 | a0001c0001t0003g0010 a0001c0001t0003g0164 a0001c0001t0003g0165 others(7): Show |
11 | HG00741.hp2 HG01099.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.909+1471A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354832 | |||||||
| chr9:36354938 | T | C | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.909+1365A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36354938 | |||||||
| chr9:36355107 | C | T | 2 | a0001c0001t0002g0130 a0001c0001t0002g0131 |
2 | HG01071.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.909+1196G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36355107 | |||||||
| chr9:36355149 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.909+1154T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36355149 | |||||||
| chr9:36355274 | C | T | 1 | a0001c0001t0001g0324 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.909+1029G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36355274 | |||||||
| chr9:36355338 | C | T | 89 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(86): Show |
96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.909+965G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36355338 | |||||||
| chr9:36355385 | T | C | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.909+918A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36355385 | |||||||
| chr9:36355387 | T | C | 1 | a0001c0001t0006g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.909+916A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36355387 | |||||||
| chr9:36355499 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.909+804A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36355499 | |||||||
| chr9:36355563 | A | G | 1 | a0001c0001t0004g0034 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.909+740T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36355563 | |||||||
| chr9:36355565 | G | T | 1 | a0001c0001t0002g0114 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.909+738C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36355565 | |||||||
| chr9:36355853 | T | C | 120 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(117): Show |
129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.909+450A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36355853 | |||||||
| chr9:36355865 | G | A | 29 | a0001c0001t0001g0274 a0001c0001t0001g0330 a0001c0001t0001g0332 others(26): Show |
29 | HG00609.hp2 HG00621.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.909+438C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36355865 | |||||||
| chr9:36355943 | T | G | 8 | a0001c0001t0005g0022 a0001c0001t0005g0023 a0001c0001t0005g0024 others(5): Show |
8 | HG02723.hp2 HG02809.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.909+360A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36355943 | |||||||
| chr9:36356022 | C | T | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(344): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.909+281G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36356022 | |||||||
| chr9:36356045 | C | T | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(344): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.909+258G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36356045 | |||||||
| chr9:36356135 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.909+168G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 6/11 | chr9 | 36356135 | |||||||
| chr9:36356625 | A | C | 1 | a0001c0001t0001g0249 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.739-152T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 5/11 | chr9 | 36356625 | |||||||
| chr9:36356747 | T | TG | 158 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(155): Show |
170 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.739-275dupC | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 5/11 | chr9 | 36356747 | |||||||
| chr9:36356756 | C | G | 2 | a0001c0001t0001g0323 a0001c0001t0002g0099 |
2 | HG00423.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.739-283G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 5/11 | chr9 | 36356756 | |||||||
| chr9:36356883 | A | G | 8 | a0001c0001t0005g0022 a0001c0001t0005g0023 a0001c0001t0005g0024 others(5): Show |
8 | HG02723.hp2 HG02809.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.739-410T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 5/11 | chr9 | 36356883 | |||||||
| chr9:36357135 | T | A | 1 | a0001c0001t0001g0235 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.738+640A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 5/11 | chr9 | 36357135 | |||||||
| chr9:36357158 | G | A | 1 | a0001c0001t0014g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.738+617C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 5/11 | chr9 | 36357158 | |||||||
| chr9:36357436 | C | G | 2 | a0001c0001t0001g0250 a0001c0001t0001g0255 |
2 | NA18944.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.738+339G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 5/11 | chr9 | 36357436 | |||||||
| chr9:36357537 | C | T | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.738+238G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 5/11 | chr9 | 36357537 | |||||||
| chr9:36357541 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.738+234A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 5/11 | chr9 | 36357541 | |||||||
| chr9:36357570 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.738+205T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 5/11 | chr9 | 36357570 | |||||||
| chr9:36357582 | T | C | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.738+193A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 5/11 | chr9 | 36357582 | |||||||
| chr9:36357609 | C | A | 13 | a0001c0001t0001g0013 a0001c0001t0001g0249 a0001c0001t0001g0250 others(10): Show |
14 | HG01123.hp2 HG01433.hp1 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.738+166G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 5/11 | chr9 | 36357609 | |||||||
| chr9:36357678 | C | A | 7 | a0001c0001t0001g0239 a0001c0001t0001g0318 a0001c0001t0001g0319 others(4): Show |
7 | HG00423.hp2 NA18946.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.738+97G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 5/11 | chr9 | 36357678 | |||||||
| chr9:36357713 | A | C | 1 | a0001c0001t0014g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.738+62T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 5/11 | chr9 | 36357713 | |||||||
| chr9:36357962 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.571-20A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36357962 | |||||||
| chr9:36358055 | C | CA | 19 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(16): Show |
26 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.571-114dupT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36358055 | |||||||
| chr9:36358246 | G | C | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.571-304C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36358246 | |||||||
| chr9:36358332 | T | C | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 |
3 | HG02970.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.571-390A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36358332 | |||||||
| chr9:36358535 | T | C | 1 | a0001c0001t0001g0068 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.571-593A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36358535 | |||||||
| chr9:36358566 | T | C | 1 | a0001c0001t0001g0230 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.571-624A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36358566 | |||||||
| chr9:36358632 | A | C | 174 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(171): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.571-690T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36358632 | |||||||
| chr9:36358705 | C | T | 1 | a0001c0002t0001g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.571-763G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36358705 | |||||||
| chr9:36358811 | G | A | 348 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(345): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.571-869C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36358811 | |||||||
| chr9:36358839 | G | A | 9 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(6): Show |
9 | HG01496.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.571-897C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36358839 | |||||||
| chr9:36358852 | A | G | 5 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(2): Show |
5 | HG01891.hp2 HG04115.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-910T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36358852 | |||||||
| chr9:36358855 | C | G | 117 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(114): Show |
126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.571-913G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36358855 | |||||||
| chr9:36358867 | T | A | 133 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(130): Show |
140 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.571-925A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36358867 | |||||||
| chr9:36358930 | G | A | 3 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0289 |
3 | HG03688.hp1 HG03834.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.571-988C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36358930 | |||||||
| chr9:36359161 | T | A | 1 | a0001c0001t0003g0157 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.571-1219A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36359161 | |||||||
| chr9:36359279 | AT | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(30): Show |
40 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.571-1338delA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36359279 | |||||||
| chr9:36359314 | G | C | 1 | a0001c0001t0001g0230 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.571-1372C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36359314 | |||||||
| chr9:36359379 | G | A | 57 | a0001c0001t0001g0086 a0001c0001t0001g0113 a0001c0001t0002g0003 others(54): Show |
62 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.571-1437C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36359379 | |||||||
| chr9:36359550 | C | T | 367 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(364): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.571-1608G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36359550 | |||||||
| chr9:36359624 | T | C | 1 | a0001c0001t0005g0025 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.571-1682A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36359624 | |||||||
| chr9:36359644 | C | T | 43 | a0001c0001t0001g0086 a0001c0001t0001g0113 a0001c0001t0002g0003 others(40): Show |
46 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.571-1702G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36359644 | |||||||
| chr9:36359737 | A | AT | 356 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(353): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.571-1796dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36359737 | |||||||
| chr9:36359737 | A | ATT | 8 | a0001c0001t0001g0178 a0001c0001t0001g0261 a0001c0001t0001g0352 others(5): Show |
8 | HG00280.hp1 HG02055.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.571-1797_571-1796d others(4): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36359737 | |||||||
| chr9:36359912 | C | CT | 115 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(112): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.571-1971dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36359912 | |||||||
| chr9:36360035 | G | A | 1 | a0001c0001t0007g0072 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.571-2093C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36360035 | |||||||
| chr9:36360097 | C | T | 33 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(30): Show |
40 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.571-2155G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36360097 | |||||||
| chr9:36360153 | GA | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(169): Show |
186 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.571-2212delT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36360153 | |||||||
| chr9:36360165 | T | C | 1 | a0001c0001t0001g0250 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.571-2223A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36360165 | |||||||
| chr9:36360336 | A | T | 1 | a0001c0001t0006g0039 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.571-2394T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36360336 | |||||||
| chr9:36360461 | G | T | 1 | a0001c0001t0008g0333 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.571-2519C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36360461 | |||||||
| chr9:36360504 | C | T | 4 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(1): Show |
4 | HG04115.hp1 NA18612.hp1 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-2562G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36360504 | |||||||
| chr9:36360612 | G | A | 346 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(343): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.571-2670C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36360612 | |||||||
| chr9:36360848 | T | C | 13 | a0001c0001t0001g0013 a0001c0001t0001g0249 a0001c0001t0001g0250 others(10): Show |
14 | HG01123.hp2 HG01433.hp1 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.571-2906A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36360848 | |||||||
| chr9:36360891 | G | A | 1 | a0001c0001t0002g0109 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.571-2949C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36360891 | |||||||
| chr9:36361007 | G | C | 1 | a0001c0001t0002g0109 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.571-3065C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361007 | |||||||
| chr9:36361059 | T | C | 348 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(345): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.571-3117A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361059 | |||||||
| chr9:36361138 | C | T | 1 | a0001c0001t0002g0126 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.571-3196G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361138 | |||||||
| chr9:36361151 | T | C | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.571-3209A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361151 | |||||||
| chr9:36361298 | C | G | 1 | a0001c0001t0001g0063 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.571-3356G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361298 | |||||||
| chr9:36361306 | C | A | 133 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(130): Show |
140 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.571-3364G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361306 | |||||||
| chr9:36361339 | T | TTTTTTTT others(174): Show |
1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.571-3398_571-3397i others(183): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361339 | |||||||
| chr9:36361354 | A | G | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.571-3412T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361354 | |||||||
| chr9:36361364 | C | T | 1 | a0001c0001t0003g0170 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.571-3422G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361364 | |||||||
| chr9:36361367 | G | T | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.571-3425C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361367 | |||||||
| chr9:36361374 | A | G | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.571-3432T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361374 | |||||||
| chr9:36361399 | G | A | 3 | a0001c0001t0008g0333 a0001c0001t0008g0334 a0001c0001t0008g0335 |
3 | HG02647.hp2 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.571-3457C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361399 | |||||||
| chr9:36361438 | T | C | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.571-3496A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361438 | |||||||
| chr9:36361441 | A | G | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.571-3499T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361441 | |||||||
| chr9:36361442 | CG | C | 346 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(343): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.571-3501delC | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361442 | |||||||
| chr9:36361454 | C | T | 1 | a0001c0001t0014g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.571-3512G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361454 | |||||||
| chr9:36361538 | A | G | 1 | a0001c0001t0003g0189 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.571-3596T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361538 | |||||||
| chr9:36361745 | C | T | 2 | a0001c0001t0001g0299 a0001c0001t0003g0281 |
2 | NA18747.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.571-3803G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361745 | |||||||
| chr9:36361907 | ATG | A | 1 | a0001c0001t0001g0006 | 3 | HG03654.hp1 HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.571-3967_571-3966d others(4): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36361907 | |||||||
| chr9:36362005 | C | T | 365 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(362): Show |
393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.571-4063G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362005 | |||||||
| chr9:36362018 | T | C | 1 | a0001c0001t0001g0267 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.571-4076A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362018 | |||||||
| chr9:36362078 | C | T | 1 | a0001c0001t0001g0369 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.571-4136G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362078 | |||||||
| chr9:36362095 | G | A | 10 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0204 others(7): Show |
10 | HG00438.hp1 HG00544.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.571-4153C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362095 | |||||||
| chr9:36362301 | T | A | 1 | a0001c0001t0002g0121 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.571-4359A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362301 | |||||||
| chr9:36362312 | C | T | 1 | a0001c0001t0001g0351 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.571-4370G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362312 | |||||||
| chr9:36362319 | T | C | 8 | a0001c0001t0005g0022 a0001c0001t0005g0023 a0001c0001t0005g0024 others(5): Show |
8 | HG02723.hp2 HG02809.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.571-4377A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362319 | |||||||
| chr9:36362354 | G | A | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.571-4412C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362354 | |||||||
| chr9:36362470 | CA | C | 349 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(346): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.571-4529delT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362470 | |||||||
| chr9:36362627 | T | C | 1 | a0001c0001t0002g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.571-4685A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362627 | |||||||
| chr9:36362653 | A | AT | 6 | a0001c0001t0001g0054 a0001c0001t0001g0137 a0001c0001t0001g0191 others(3): Show |
6 | HG01109.hp2 HG03225.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-4712dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362653 | |||||||
| chr9:36362660 | T | A | 1 | a0001c0001t0012g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.571-4718A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362660 | |||||||
| chr9:36362884 | GGCCTCCC others(1191): Show |
G | 174 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(171): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.570+5637_571-4943d others(2): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362884 | |||||||
| chr9:36362904 | T | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(170): Show |
187 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(184): Show |
intron_variant | MODIFIER | c.571-4962A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362904 | |||||||
| chr9:36362934 | A | C | 1 | a0001c0001t0014g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.571-4992T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36362934 | |||||||
| chr9:36363020 | G | A | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.571-5078C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36363020 | |||||||
| chr9:36363162 | C | T | 1 | a0001c0001t0001g0325 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.571-5220G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36363162 | |||||||
| chr9:36363302 | A | AT | 10 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0248 others(7): Show |
12 | NA18950.hp1 NA18955.hp1 NA18959.hp1 others(9): Show |
intron_variant | MODIFIER | c.571-5361dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36363302 | |||||||
| chr9:36363356 | T | C | 1 | a0001c0002t0001g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.571-5414A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36363356 | |||||||
| chr9:36363487 | G | A | 1 | a0001c0002t0001g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.571-5545C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36363487 | |||||||
| chr9:36363859 | C | G | 1 | a0001c0001t0001g0055 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.570+5860G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36363859 | |||||||
| chr9:36363873 | A | AT | 24 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0050 others(21): Show |
24 | HG00597.hp2 HG01175.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.570+5845dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36363873 | |||||||
| chr9:36363873 | AT | A | 6 | a0001c0001t0001g0242 a0001c0001t0001g0258 a0001c0001t0001g0290 others(3): Show |
6 | HG00140.hp2 HG01168.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.570+5845delA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36363873 | |||||||
| chr9:36363980 | A | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(171): Show |
188 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(185): Show |
intron_variant | MODIFIER | c.570+5739T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36363980 | |||||||
| chr9:36364021 | G | A | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.570+5698C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36364021 | |||||||
| chr9:36364119 | C | T | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 |
3 | HG02970.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.570+5600G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36364119 | |||||||
| chr9:36364164 | C | T | 137 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(134): Show |
144 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.570+5555G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36364164 | |||||||
| chr9:36364188 | A | G | 356 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(353): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.570+5531T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36364188 | |||||||
| chr9:36364423 | G | A | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.570+5296C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36364423 | |||||||
| chr9:36364516 | T | C | 9 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(6): Show |
9 | HG01496.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.570+5203A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36364516 | |||||||
| chr9:36364567 | G | T | 97 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(94): Show |
104 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.570+5152C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36364567 | |||||||
| chr9:36364786 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.570+4933G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36364786 | |||||||
| chr9:36364826 | G | A | 4 | a0001c0001t0007g0069 a0001c0001t0007g0070 a0001c0001t0007g0071 others(1): Show |
4 | NA18949.hp1 NA18983.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+4893C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36364826 | |||||||
| chr9:36364873 | C | A | 1 | a0001c0001t0003g0173 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.570+4846G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36364873 | |||||||
| chr9:36365149 | C | G | 2 | a0001c0001t0001g0175 a0001c0001t0001g0216 |
2 | HG02027.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.570+4570G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365149 | |||||||
| chr9:36365152 | G | GT | 6 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(3): Show |
6 | HG01891.hp1 HG02451.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+4566dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365152 | |||||||
| chr9:36365202 | T | C | 1 | a0001c0001t0002g0121 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.570+4517A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365202 | |||||||
| chr9:36365231 | TA | T | 367 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(364): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.570+4487delT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365231 | |||||||
| chr9:36365268 | T | C | 1 | a0001c0001t0003g0165 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.570+4451A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365268 | |||||||
| chr9:36365493 | G | C | 2 | a0001c0001t0002g0094 a0001c0001t0002g0105 |
2 | HG00544.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.570+4226C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365493 | |||||||
| chr9:36365537 | C | T | 3 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0098 |
3 | HG03491.hp2 HG03492.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.570+4182G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365537 | |||||||
| chr9:36365551 | C | T | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.570+4168G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365551 | |||||||
| chr9:36365662 | G | GT | 16 | a0001c0001t0001g0081 a0001c0001t0001g0161 a0001c0001t0001g0197 others(13): Show |
16 | HG02074.hp1 HG02723.hp2 HG02809.hp2 others(13): Show |
intron_variant | MODIFIER | c.570+4056dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365662 | |||||||
| chr9:36365662 | G | GTT | 264 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(261): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.570+4055_570+4056d others(4): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365662 | |||||||
| chr9:36365662 | G | GTTT | 48 | a0001c0001t0001g0080 a0001c0001t0001g0136 a0001c0001t0001g0155 others(45): Show |
48 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.570+4054_570+4056d others(5): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365662 | |||||||
| chr9:36365662 | G | GTTTT | 22 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(19): Show |
29 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.570+4053_570+4056d others(6): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365662 | |||||||
| chr9:36365662 | G | GTTTTT | 14 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(11): Show |
14 | HG00597.hp2 HG01934.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.570+4052_570+4056d others(7): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365662 | |||||||
| chr9:36365752 | G | A | 3 | a0001c0001t0008g0333 a0001c0001t0008g0334 a0001c0001t0008g0335 |
3 | HG02647.hp2 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.570+3967C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365752 | |||||||
| chr9:36365815 | G | A | 1 | a0001c0001t0014g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.570+3904C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365815 | |||||||
| chr9:36365815 | G | GCCA | 9 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(6): Show |
9 | HG01496.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.570+3901_570+3903d others(5): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365815 | |||||||
| chr9:36365832 | A | C | 1 | a0001c0002t0001g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.570+3887T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365832 | |||||||
| chr9:36365933 | G | A | 1 | a0001c0001t0002g0049 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.570+3786C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36365933 | |||||||
| chr9:36366067 | G | A | 1 | a0001c0001t0009g0115 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.570+3652C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36366067 | |||||||
| chr9:36366068 | C | G | 365 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(362): Show |
393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.570+3651G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36366068 | |||||||
| chr9:36366132 | T | C | 4 | a0001c0001t0005g0026 a0001c0001t0005g0028 a0001c0001t0005g0029 others(1): Show |
4 | HG02965.hp1 HG03195.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+3587A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36366132 | |||||||
| chr9:36366260 | A | G | 3 | a0001c0001t0001g0329 a0001c0001t0001g0341 a0001c0001t0001g0363 |
3 | HG03195.hp1 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.570+3459T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36366260 | |||||||
| chr9:36366700 | G | A | 1 | a0001c0002t0001g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.570+3019C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36366700 | |||||||
| chr9:36366838 | T | C | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 |
3 | HG02970.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.570+2881A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36366838 | |||||||
| chr9:36367004 | T | A | 1 | a0001c0001t0002g0089 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.570+2715A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367004 | |||||||
| chr9:36367125 | C | T | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(232): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.570+2594G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367125 | |||||||
| chr9:36367256 | T | C | 1 | a0001c0001t0001g0214 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.570+2463A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367256 | |||||||
| chr9:36367340 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.570+2379G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367340 | |||||||
| chr9:36367341 | G | A | 57 | a0001c0001t0001g0086 a0001c0001t0001g0113 a0001c0001t0002g0003 others(54): Show |
62 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.570+2378C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367341 | |||||||
| chr9:36367559 | C | T | 1 | a0001c0001t0012g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.570+2160G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367559 | |||||||
| chr9:36367579 | CT | C | 12 | a0001c0001t0002g0004 a0001c0001t0002g0048 a0001c0001t0002g0049 others(9): Show |
14 | HG00280.hp2 HG00733.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.570+2139delA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367579 | |||||||
| chr9:36367656 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.570+2063C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367656 | |||||||
| chr9:36367659 | T | G | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.570+2060A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367659 | |||||||
| chr9:36367673 | T | C | 1 | a0001c0001t0012g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.570+2046A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367673 | |||||||
| chr9:36367716 | T | C | 27 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(24): Show |
34 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.570+2003A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367716 | |||||||
| chr9:36367883 | G | A | 2 | a0001c0001t0001g0326 a0001c0001t0001g0327 |
2 | HG01175.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.570+1836C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367883 | |||||||
| chr9:36367885 | T | C | 5 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(2): Show |
5 | HG01074.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.570+1834A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367885 | |||||||
| chr9:36367927 | C | A | 1 | a0001c0001t0001g0329 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.570+1792G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367927 | |||||||
| chr9:36367939 | C | T | 1 | a0001c0001t0001g0345 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.570+1780G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367939 | |||||||
| chr9:36367954 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.570+1765G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367954 | |||||||
| chr9:36367980 | T | C | 1 | a0001c0001t0002g0093 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.570+1739A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36367980 | |||||||
| chr9:36368477 | A | T | 1 | a0001c0001t0001g0362 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.570+1242T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36368477 | |||||||
| chr9:36368674 | T | A | 3 | a0001c0001t0001g0290 a0001c0001t0001g0302 a0001c0001t0001g0306 |
3 | HG00140.hp2 HG01168.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.570+1045A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36368674 | |||||||
| chr9:36368763 | G | GA | 8 | a0001c0001t0005g0022 a0001c0001t0005g0023 a0001c0001t0005g0024 others(5): Show |
8 | HG02723.hp2 HG02809.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.570+955dupT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36368763 | |||||||
| chr9:36368768 | T | C | 8 | a0001c0001t0005g0022 a0001c0001t0005g0023 a0001c0001t0005g0024 others(5): Show |
8 | HG02723.hp2 HG02809.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.570+951A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36368768 | |||||||
| chr9:36368810 | G | T | 3 | a0001c0001t0007g0069 a0001c0001t0007g0070 a0001c0001t0007g0071 |
3 | NA18949.hp1 NA18983.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.570+909C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36368810 | |||||||
| chr9:36368857 | T | A | 1 | a0001c0001t0001g0007 | 2 | HG00673.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.570+862A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36368857 | |||||||
| chr9:36368867 | G | T | 1 | a0001c0001t0001g0194 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.570+852C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36368867 | |||||||
| chr9:36368886 | C | CT | 23 | a0001c0001t0001g0006 a0001c0001t0001g0178 a0001c0001t0001g0184 others(20): Show |
25 | HG00438.hp1 HG00544.hp2 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.570+832dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36368886 | |||||||
| chr9:36369029 | T | A | 5 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(2): Show |
5 | HG02572.hp1 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.570+690A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36369029 | |||||||
| chr9:36369262 | C | T | 3 | a0001c0001t0008g0333 a0001c0001t0008g0334 a0001c0001t0008g0335 |
3 | HG02647.hp2 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.570+457G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36369262 | |||||||
| chr9:36369295 | C | T | 1 | a0001c0001t0004g0036 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.570+424G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36369295 | |||||||
| chr9:36369377 | C | CA | 3 | a0001c0001t0001g0260 a0001c0001t0001g0271 a0001c0001t0001g0272 |
3 | HG02109.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.570+341dupT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36369377 | |||||||
| chr9:36369437 | G | A | 4 | a0001c0001t0003g0166 a0001c0001t0003g0167 a0001c0001t0003g0168 others(1): Show |
4 | HG00741.hp2 HG01255.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+282C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36369437 | |||||||
| chr9:36369490 | T | C | 57 | a0001c0001t0001g0086 a0001c0001t0001g0113 a0001c0001t0002g0003 others(54): Show |
62 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.570+229A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36369490 | |||||||
| chr9:36369498 | T | C | 9 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(6): Show |
9 | HG01496.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.570+221A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36369498 | |||||||
| chr9:36369516 | C | T | 1 | a0001c0001t0002g0124 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.570+203G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36369516 | |||||||
| chr9:36369610 | A | G | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.570+109T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36369610 | |||||||
| chr9:36369649 | CA | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(217): Show |
240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.570+69delT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36369649 | |||||||
| chr9:36369649 | CAA | C | 19 | a0001c0001t0001g0052 a0001c0001t0001g0217 a0001c0001t0001g0218 others(16): Show |
20 | HG00741.hp2 HG01099.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.570+68_570+69delTT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 4/11 | chr9 | 36369649 | |||||||
| chr9:36369935 | G | A | 1 | a0001c0001t0001g0251 | 1 | NA18986.hp2 | splice_region_variant&intron_variant | LOW | c.357-3C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36369935 | |||||||
| chr9:36370008 | T | A | 1 | a0001c0001t0001g0276 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.357-76A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36370008 | |||||||
| chr9:36370386 | C | T | 2 | a0001c0001t0003g0174 a0001c0001t0003g0189 |
2 | HG01167.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.357-454G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36370386 | |||||||
| chr9:36370568 | G | C | 1 | a0001c0001t0001g0202 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.357-636C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36370568 | |||||||
| chr9:36370576 | C | G | 4 | a0001c0001t0001g0329 a0001c0001t0001g0341 a0001c0001t0001g0342 others(1): Show |
4 | HG03195.hp1 HG03225.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.357-644G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36370576 | |||||||
| chr9:36370580 | G | C | 1 | a0001c0001t0001g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.357-648C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36370580 | |||||||
| chr9:36370646 | C | T | 1 | a0001c0001t0002g0096 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.357-714G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36370646 | |||||||
| chr9:36370675 | G | A | 5 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(2): Show |
5 | HG01074.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.357-743C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36370675 | |||||||
| chr9:36370685 | C | T | 1 | a0001c0001t0006g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.357-753G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36370685 | |||||||
| chr9:36370849 | T | TA | 31 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(28): Show |
38 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.357-918dupT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36370849 | |||||||
| chr9:36370905 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0152 |
2 | HG02056.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.357-973A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36370905 | |||||||
| chr9:36370919 | G | T | 1 | a0001c0001t0001g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.357-987C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36370919 | |||||||
| chr9:36370969 | A | G | 1 | a0001c0001t0002g0106 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.357-1037T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36370969 | |||||||
| chr9:36371259 | C | A | 1 | a0001c0001t0001g0081 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.357-1327G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36371259 | |||||||
| chr9:36371358 | A | G | 1 | a0001c0001t0002g0116 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.357-1426T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36371358 | |||||||
| chr9:36371436 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.357-1504G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36371436 | |||||||
| chr9:36371443 | C | CT | 13 | a0001c0001t0001g0054 a0001c0001t0001g0141 a0001c0001t0001g0150 others(10): Show |
13 | HG02056.hp2 HG02723.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.357-1512dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36371443 | |||||||
| chr9:36371443 | CT | C | 13 | a0001c0001t0001g0066 a0001c0001t0001g0075 a0001c0001t0001g0152 others(10): Show |
13 | HG01496.hp2 HG01975.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.357-1512delA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36371443 | |||||||
| chr9:36371516 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.357-1584C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36371516 | |||||||
| chr9:36371728 | A | G | 1 | a0001c0001t0003g0162 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.357-1796T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36371728 | |||||||
| chr9:36371760 | T | C | 1 | a0001c0001t0002g0128 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.357-1828A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36371760 | |||||||
| chr9:36371834 | C | G | 1 | a0001c0001t0002g0046 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.357-1902G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36371834 | |||||||
| chr9:36371934 | C | CT | 12 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(9): Show |
12 | HG01106.hp2 HG01243.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.357-2003dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36371934 | |||||||
| chr9:36371934 | C | CTT | 7 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(4): Show |
7 | HG02572.hp1 HG02630.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.357-2004_357-2003d others(4): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36371934 | |||||||
| chr9:36371971 | G | C | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(236): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.357-2039C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36371971 | |||||||
| chr9:36372183 | C | T | 1 | a0001c0001t0002g0048 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.357-2251G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36372183 | |||||||
| chr9:36372419 | T | C | 5 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(2): Show |
5 | HG01891.hp2 HG04115.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.357-2487A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36372419 | |||||||
| chr9:36372465 | G | A | 1 | a0001c0001t0001g0343 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.357-2533C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36372465 | |||||||
| chr9:36372651 | C | A | 1 | a0001c0001t0014g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.357-2719G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36372651 | |||||||
| chr9:36372740 | C | A | 174 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(171): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.357-2808G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36372740 | |||||||
| chr9:36372762 | A | G | 4 | a0001c0001t0005g0022 a0001c0001t0005g0023 a0001c0001t0005g0024 others(1): Show |
4 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357-2830T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36372762 | |||||||
| chr9:36372808 | C | A | 16 | a0001c0001t0001g0006 a0001c0001t0001g0184 a0001c0001t0001g0187 others(13): Show |
18 | HG00438.hp1 HG00544.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.357-2876G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36372808 | |||||||
| chr9:36372846 | T | C | 1 | a0001c0001t0016g0291 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.357-2914A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36372846 | |||||||
| chr9:36373082 | C | CT | 7 | a0001c0001t0001g0008 a0001c0001t0001g0146 a0001c0001t0001g0147 others(4): Show |
8 | HG00408.hp2 HG02602.hp2 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.356+2851dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373082 | |||||||
| chr9:36373084 | G | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0146 a0001c0001t0001g0147 others(4): Show |
8 | HG00408.hp2 HG02602.hp2 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.356+2850C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373084 | |||||||
| chr9:36373142 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.356+2792C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373142 | |||||||
| chr9:36373332 | T | C | 200 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(197): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.356+2602A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373332 | |||||||
| chr9:36373342 | A | G | 1 | a0001c0001t0014g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.356+2592T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373342 | |||||||
| chr9:36373410 | C | T | 275 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(272): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.356+2524G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373410 | |||||||
| chr9:36373489 | C | A | 174 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(171): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.356+2445G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373489 | |||||||
| chr9:36373513 | C | T | 1 | a0001c0001t0002g0095 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.356+2421G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373513 | |||||||
| chr9:36373544 | A | C | 2 | a0001c0001t0005g0022 a0001c0001t0005g0025 |
2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.356+2390T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373544 | |||||||
| chr9:36373589 | C | CT | 17 | a0001c0001t0001g0019 a0001c0001t0001g0237 a0001c0001t0001g0238 others(14): Show |
18 | HG00438.hp2 HG02615.hp2 HG02647.hp2 others(15): Show |
intron_variant | MODIFIER | c.356+2344dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373589 | |||||||
| chr9:36373589 | CT | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(212): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.356+2344delA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373589 | |||||||
| chr9:36373590 | T | C | 1 | a0001c0001t0001g0324 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.356+2344A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373590 | |||||||
| chr9:36373591 | T | C | 1 | a0001c0001t0013g0043 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.356+2343A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373591 | |||||||
| chr9:36373608 | T | A | 2 | a0001c0001t0007g0069 a0001c0001t0007g0071 |
2 | NA18949.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.356+2326A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373608 | |||||||
| chr9:36373638 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.356+2296G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373638 | |||||||
| chr9:36373658 | C | T | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG02132.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.356+2276G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373658 | |||||||
| chr9:36373695 | G | A | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG00639.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.356+2239C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373695 | |||||||
| chr9:36373739 | C | T | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.356+2195G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373739 | |||||||
| chr9:36373817 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.356+2117C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373817 | |||||||
| chr9:36373853 | G | A | 1 | a0001c0001t0003g0138 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.356+2081C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373853 | |||||||
| chr9:36373982 | C | T | 1 | a0001c0001t0002g0093 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.356+1952G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36373982 | |||||||
| chr9:36374159 | G | T | 6 | a0001c0001t0001g0365 a0001c0001t0001g0367 a0001c0001t0001g0369 others(3): Show |
6 | HG01255.hp2 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.356+1775C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36374159 | |||||||
| chr9:36374171 | T | C | 1 | a0001c0001t0014g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.356+1763A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36374171 | |||||||
| chr9:36374207 | A | G | 174 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(171): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.356+1727T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36374207 | |||||||
| chr9:36374216 | A | C | 1 | a0001c0001t0001g0253 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.356+1718T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36374216 | |||||||
| chr9:36374621 | C | G | 1 | a0001c0001t0002g0107 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.356+1313G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36374621 | |||||||
| chr9:36374678 | C | A | 5 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(2): Show |
5 | HG02572.hp1 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.356+1256G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36374678 | |||||||
| chr9:36374724 | C | T | 27 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(24): Show |
34 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.356+1210G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36374724 | |||||||
| chr9:36374835 | A | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(30): Show |
40 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.356+1099T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36374835 | |||||||
| chr9:36374943 | A | G | 1 | a0001c0002t0001g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.356+991T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36374943 | |||||||
| chr9:36375340 | G | A | 1 | a0001c0001t0001g0340 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.356+594C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36375340 | |||||||
| chr9:36375412 | G | A | 9 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(6): Show |
9 | HG01496.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.356+522C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36375412 | |||||||
| chr9:36375462 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.356+472C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36375462 | |||||||
| chr9:36375650 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.356+284C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36375650 | |||||||
| chr9:36375686 | T | G | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.356+248A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36375686 | |||||||
| chr9:36375712 | G | C | 57 | a0001c0001t0001g0086 a0001c0001t0001g0113 a0001c0001t0002g0003 others(54): Show |
62 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.356+222C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36375712 | |||||||
| chr9:36375878 | T | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 |
3 | HG01074.hp1 HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.356+56A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 3/11 | chr9 | 36375878 | |||||||
| chr9:36376204 | G | C | 1 | a0001c0001t0001g0369 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.163-77C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376204 | |||||||
| chr9:36376335 | G | C | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(236): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.163-208C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376335 | |||||||
| chr9:36376385 | G | T | 1 | a0001c0001t0001g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.163-258C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376385 | |||||||
| chr9:36376398 | G | A | 1 | a0001c0001t0003g0174 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.163-271C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376398 | |||||||
| chr9:36376595 | C | G | 25 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(22): Show |
25 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(22): Show |
intron_variant | MODIFIER | c.163-468G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376595 | |||||||
| chr9:36376648 | G | A | 1 | a0001c0002t0001g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.163-521C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376648 | |||||||
| chr9:36376674 | C | T | 1 | a0001c0001t0014g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.163-547G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376674 | |||||||
| chr9:36376760 | T | C | 1 | a0001c0001t0014g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.163-633A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376760 | |||||||
| chr9:36376790 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.163-663C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376790 | |||||||
| chr9:36376877 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.163-750C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376877 | |||||||
| chr9:36376888 | G | T | 26 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(23): Show |
26 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.163-761C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376888 | |||||||
| chr9:36376912 | G | GT | 4 | a0001c0001t0002g0083 a0001c0001t0002g0084 a0001c0001t0002g0106 others(1): Show |
4 | HG02074.hp2 NA18944.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-786dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376912 | |||||||
| chr9:36376926 | C | CA | 14 | a0001c0001t0001g0250 a0001c0001t0001g0276 a0001c0001t0001g0294 others(11): Show |
14 | HG01261.hp2 HG01934.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.163-800dupT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376926 | |||||||
| chr9:36376926 | CA | C | 74 | a0001c0001t0001g0053 a0001c0001t0001g0058 a0001c0001t0001g0059 others(71): Show |
79 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.163-800delT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376926 | |||||||
| chr9:36376926 | CAA | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(141): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.163-801_163-800del others(2): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376926 | |||||||
| chr9:36376926 | CAAA | C | 7 | a0001c0001t0001g0066 a0001c0001t0001g0158 a0001c0001t0001g0176 others(4): Show |
7 | HG01975.hp1 HG02976.hp2 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.163-802_163-800del others(3): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376926 | |||||||
| chr9:36376996 | G | T | 28 | a0001c0001t0001g0330 a0001c0001t0001g0332 a0001c0001t0001g0336 others(25): Show |
28 | HG00609.hp2 HG00621.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.163-869C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36376996 | |||||||
| chr9:36377070 | A | G | 1 | a0001c0001t0001g0277 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.163-943T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36377070 | |||||||
| chr9:36377300 | T | A | 2 | a0001c0001t0001g0296 a0001c0001t0001g0304 |
2 | NA18747.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.163-1173A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36377300 | |||||||
| chr9:36377625 | A | C | 5 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(2): Show |
5 | HG01074.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.163-1498T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36377625 | |||||||
| chr9:36377733 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.163-1606G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36377733 | |||||||
| chr9:36377760 | A | T | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.163-1633T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36377760 | |||||||
| chr9:36377802 | A | G | 2 | a0001c0001t0002g0091 a0001c0001t0002g0092 |
2 | HG00140.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.163-1675T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36377802 | |||||||
| chr9:36377824 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.163-1697T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36377824 | |||||||
| chr9:36377933 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.163-1806G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36377933 | |||||||
| chr9:36377983 | GAAAGTTA others(19): Show |
G | 8 | a0001c0001t0001g0365 a0001c0001t0001g0367 a0001c0001t0001g0368 others(5): Show |
8 | HG01243.hp1 HG01255.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-1882_163-1857d others(28): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36377983 | |||||||
| chr9:36378012 | AACTTAAA others(25): Show |
A | 1 | a0001c0001t0005g0022 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.163-1917_163-1886d others(34): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36378012 | |||||||
| chr9:36378016 | T | TA | 7 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(4): Show |
7 | HG02572.hp1 HG02630.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-1890dupT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36378016 | |||||||
| chr9:36378057 | A | AT | 7 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(4): Show |
7 | HG02572.hp1 HG02630.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-1931dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36378057 | |||||||
| chr9:36378169 | C | CT | 70 | a0001c0001t0001g0012 a0001c0001t0001g0140 a0001c0001t0001g0160 others(67): Show |
71 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.163-2043dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36378169 | |||||||
| chr9:36378169 | CT | C | 36 | a0001c0001t0001g0013 a0001c0001t0001g0052 a0001c0001t0001g0053 others(33): Show |
37 | HG00609.hp1 HG01123.hp2 HG01433.hp1 others(34): Show |
intron_variant | MODIFIER | c.163-2043delA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36378169 | |||||||
| chr9:36378169 | CTT | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
44 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.163-2044_163-2043d others(4): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36378169 | |||||||
| chr9:36378192 | T | G | 4 | a0001c0001t0001g0051 a0001c0001t0001g0060 a0001c0001t0001g0074 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-2065A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36378192 | |||||||
| chr9:36378192 | T | TG | 4 | a0001c0001t0002g0116 a0001c0001t0002g0117 a0001c0001t0002g0118 others(1): Show |
4 | NA18965.hp1 NA18978.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-2066dupC | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36378192 | |||||||
| chr9:36378200 | G | T | 1 | a0001c0001t0014g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.163-2073C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36378200 | |||||||
| chr9:36378413 | T | C | 1 | a0001c0001t0010g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.163-2286A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36378413 | |||||||
| chr9:36378643 | T | C | 7 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(4): Show |
7 | HG02572.hp1 HG02630.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-2516A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36378643 | |||||||
| chr9:36378856 | G | A | 57 | a0001c0001t0001g0086 a0001c0001t0001g0113 a0001c0001t0002g0003 others(54): Show |
62 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.163-2729C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36378856 | |||||||
| chr9:36378904 | C | CT | 177 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(174): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.163-2778dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36378904 | |||||||
| chr9:36379086 | G | C | 1 | a0001c0001t0001g0297 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.163-2959C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36379086 | |||||||
| chr9:36379143 | G | A | 1 | a0001c0001t0003g0157 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.163-3016C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36379143 | |||||||
| chr9:36379147 | G | A | 2 | a0001c0001t0008g0334 a0001c0001t0008g0335 |
2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.163-3020C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36379147 | |||||||
| chr9:36379201 | A | G | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.163-3074T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36379201 | |||||||
| chr9:36379652 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.163-3525G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36379652 | |||||||
| chr9:36380359 | CCTG | C | 5 | a0001c0001t0001g0329 a0001c0001t0001g0340 a0001c0001t0001g0341 others(2): Show |
5 | HG03098.hp1 HG03195.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-4235_163-4233d others(5): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36380359 | |||||||
| chr9:36380501 | G | GT | 10 | a0001c0001t0001g0014 a0001c0001t0001g0262 a0001c0001t0001g0263 others(7): Show |
11 | HG00639.hp2 HG00738.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-4375dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36380501 | |||||||
| chr9:36380519 | G | A | 1 | a0001c0001t0003g0190 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.163-4392C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36380519 | |||||||
| chr9:36380694 | A | G | 8 | a0001c0001t0005g0022 a0001c0001t0005g0023 a0001c0001t0005g0024 others(5): Show |
8 | HG02723.hp2 HG02809.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.163-4567T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36380694 | |||||||
| chr9:36380866 | G | C | 10 | a0001c0001t0002g0004 a0001c0001t0002g0123 a0001c0001t0002g0124 others(7): Show |
12 | HG00733.hp2 HG00741.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.163-4739C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36380866 | |||||||
| chr9:36380941 | C | T | 1 | a0001c0001t0005g0022 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.163-4814G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36380941 | |||||||
| chr9:36381028 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.163-4901G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36381028 | |||||||
| chr9:36381034 | T | C | 38 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(35): Show |
45 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.163-4907A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36381034 | |||||||
| chr9:36381118 | C | T | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | NA18965.hp2 NA19060.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.163-4991G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36381118 | |||||||
| chr9:36381141 | G | A | 9 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(6): Show |
9 | HG01496.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.163-5014C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36381141 | |||||||
| chr9:36381229 | T | C | 1 | a0001c0002t0001g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.163-5102A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36381229 | |||||||
| chr9:36381583 | G | A | 1 | a0001c0001t0006g0040 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.163-5456C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36381583 | |||||||
| chr9:36381740 | G | C | 1 | a0001c0001t0019g0203 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.163-5613C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36381740 | |||||||
| chr9:36381801 | T | A | 28 | a0001c0001t0001g0330 a0001c0001t0001g0332 a0001c0001t0001g0336 others(25): Show |
28 | HG00609.hp2 HG00621.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.163-5674A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36381801 | |||||||
| chr9:36381905 | C | T | 349 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(346): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.163-5778G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36381905 | |||||||
| chr9:36381918 | C | A | 1 | a0001c0001t0001g0212 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.163-5791G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36381918 | |||||||
| chr9:36382074 | G | C | 28 | a0001c0001t0001g0330 a0001c0001t0001g0332 a0001c0001t0001g0336 others(25): Show |
28 | HG00609.hp2 HG00621.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.163-5947C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36382074 | |||||||
| chr9:36382079 | T | C | 1 | a0001c0002t0001g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.163-5952A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36382079 | |||||||
| chr9:36382240 | T | C | 1 | a0001c0001t0002g0123 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.163-6113A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36382240 | |||||||
| chr9:36382311 | C | T | 1 | a0001c0002t0001g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.163-6184G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36382311 | |||||||
| chr9:36382392 | T | C | 5 | a0001c0001t0001g0019 a0001c0001t0001g0309 a0001c0001t0001g0310 others(2): Show |
6 | NA18962.hp1 NA18971.hp1 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-6265A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36382392 | |||||||
| chr9:36382427 | C | T | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | NA18977.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.163-6300G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36382427 | |||||||
| chr9:36382793 | A | G | 27 | a0001c0001t0003g0010 a0001c0001t0003g0138 a0001c0001t0003g0139 others(24): Show |
28 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.163-6666T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36382793 | |||||||
| chr9:36382857 | C | T | 4 | a0001c0001t0001g0329 a0001c0001t0001g0341 a0001c0001t0001g0342 others(1): Show |
4 | HG03195.hp1 HG03225.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-6730G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36382857 | |||||||
| chr9:36382865 | C | T | 26 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(23): Show |
26 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.163-6738G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36382865 | |||||||
| chr9:36383069 | G | A | 1 | a0001c0001t0012g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.163-6942C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36383069 | |||||||
| chr9:36383195 | A | T | 1 | a0001c0001t0007g0072 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.163-7068T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36383195 | |||||||
| chr9:36383196 | C | A | 1 | a0001c0001t0007g0072 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.163-7069G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36383196 | |||||||
| chr9:36383296 | G | C | 2 | a0001c0001t0001g0198 a0001c0001t0001g0212 |
2 | HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.163-7169C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36383296 | |||||||
| chr9:36383372 | T | C | 1 | a0001c0001t0021g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.162+7095A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36383372 | |||||||
| chr9:36383433 | G | A | 1 | a0001c0001t0001g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.162+7034C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36383433 | |||||||
| chr9:36383445 | C | T | 1 | a0001c0001t0002g0090 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.162+7022G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36383445 | |||||||
| chr9:36383499 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.162+6968A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36383499 | |||||||
| chr9:36383718 | AATGTTGT others(14): Show |
A | 1 | a0001c0001t0001g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.162+6728_162+6748d others(23): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36383718 | |||||||
| chr9:36383738 | C | A | 25 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(22): Show |
25 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(22): Show |
intron_variant | MODIFIER | c.162+6729G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36383738 | |||||||
| chr9:36383892 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.162+6575C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36383892 | |||||||
| chr9:36384057 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.162+6410T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36384057 | |||||||
| chr9:36384505 | T | C | 1 | a0001c0001t0003g0185 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.162+5962A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36384505 | |||||||
| chr9:36384565 | A | G | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(236): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.162+5902T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36384565 | |||||||
| chr9:36384649 | T | C | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.162+5818A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36384649 | |||||||
| chr9:36384658 | G | A | 118 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(115): Show |
127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.162+5809C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36384658 | |||||||
| chr9:36384684 | TA | T | 6 | a0001c0001t0001g0344 a0001c0001t0001g0345 a0001c0001t0001g0346 others(3): Show |
6 | HG00621.hp1 NA18949.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+5782delT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36384684 | |||||||
| chr9:36385083 | A | G | 1 | a0001c0001t0001g0340 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.162+5384T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36385083 | |||||||
| chr9:36385144 | T | TA | 8 | a0001c0001t0001g0187 a0001c0001t0001g0201 a0001c0001t0001g0202 others(5): Show |
8 | HG00438.hp1 HG00544.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.162+5322_162+5323i others(3): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36385144 | |||||||
| chr9:36385145 | T | A | 173 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(170): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.162+5322A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36385145 | |||||||
| chr9:36385145 | T | TA | 25 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(22): Show |
25 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(22): Show |
intron_variant | MODIFIER | c.162+5321dupT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36385145 | |||||||
| chr9:36385380 | C | CT | 87 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(84): Show |
92 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.162+5086dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36385380 | |||||||
| chr9:36385380 | C | CTT | 25 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(22): Show |
32 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.162+5085_162+5086d others(4): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36385380 | |||||||
| chr9:36385439 | C | T | 1 | a0001c0001t0001g0318 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.162+5028G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36385439 | |||||||
| chr9:36385442 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.162+5025C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36385442 | |||||||
| chr9:36385536 | A | T | 1 | a0001c0001t0001g0213 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.162+4931T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36385536 | |||||||
| chr9:36385885 | A | C | 2 | a0001c0001t0005g0026 a0001c0003t0005g0027 |
2 | HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.162+4582T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36385885 | |||||||
| chr9:36385903 | G | A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0212 |
2 | HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.162+4564C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36385903 | |||||||
| chr9:36386039 | G | A | 2 | a0001c0001t0002g0130 a0001c0001t0002g0131 |
2 | HG01071.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.162+4428C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36386039 | |||||||
| chr9:36386060 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.162+4407C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36386060 | |||||||
| chr9:36386086 | G | C | 4 | a0001c0001t0007g0069 a0001c0001t0007g0070 a0001c0001t0007g0071 others(1): Show |
4 | NA18949.hp1 NA18983.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+4381C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36386086 | |||||||
| chr9:36386145 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.162+4322G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36386145 | |||||||
| chr9:36386170 | C | T | 1 | a0001c0002t0001g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.162+4297G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36386170 | |||||||
| chr9:36386221 | T | C | 14 | a0001c0001t0001g0012 a0001c0001t0001g0224 a0001c0001t0001g0225 others(11): Show |
15 | HG01106.hp1 HG02071.hp1 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.162+4246A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36386221 | |||||||
| chr9:36386296 | A | G | 1 | a0001c0001t0001g0328 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.162+4171T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36386296 | |||||||
| chr9:36386413 | C | T | 1 | a0001c0001t0008g0334 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.162+4054G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36386413 | |||||||
| chr9:36386585 | C | T | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG00609.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.162+3882G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36386585 | |||||||
| chr9:36386590 | C | A | 200 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(197): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.162+3877G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36386590 | |||||||
| chr9:36386604 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.162+3863T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36386604 | |||||||
| chr9:36386844 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.162+3623G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36386844 | |||||||
| chr9:36386868 | T | G | 13 | a0001c0001t0001g0013 a0001c0001t0001g0249 a0001c0001t0001g0250 others(10): Show |
14 | HG01123.hp2 HG01433.hp1 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.162+3599A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36386868 | |||||||
| chr9:36387018 | A | G | 200 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(197): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.162+3449T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387018 | |||||||
| chr9:36387045 | C | T | 1 | a0001c0001t0014g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.162+3422G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387045 | |||||||
| chr9:36387052 | T | C | 26 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(23): Show |
26 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.162+3415A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387052 | |||||||
| chr9:36387058 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.162+3409G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387058 | |||||||
| chr9:36387154 | A | G | 1 | a0001c0001t0002g0088 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.162+3313T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387154 | |||||||
| chr9:36387198 | G | C | 1 | a0001c0001t0001g0299 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.162+3269C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387198 | |||||||
| chr9:36387242 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.162+3225A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387242 | |||||||
| chr9:36387286 | C | T | 1 | a0001c0001t0001g0259 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.162+3181G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387286 | |||||||
| chr9:36387342 | A | G | 1 | a0001c0001t0001g0343 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.162+3125T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387342 | |||||||
| chr9:36387384 | TA | T | 4 | a0001c0001t0005g0022 a0001c0001t0005g0023 a0001c0001t0005g0024 others(1): Show |
4 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+3082delT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387384 | |||||||
| chr9:36387386 | A | G | 4 | a0001c0001t0005g0022 a0001c0001t0005g0023 a0001c0001t0005g0024 others(1): Show |
4 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+3081T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387386 | |||||||
| chr9:36387388 | G | T | 4 | a0001c0001t0005g0022 a0001c0001t0005g0023 a0001c0001t0005g0024 others(1): Show |
4 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+3079C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387388 | |||||||
| chr9:36387683 | G | A | 3 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0246 |
3 | HG02257.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.162+2784C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387683 | |||||||
| chr9:36387750 | C | T | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.162+2717G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387750 | |||||||
| chr9:36387891 | CA | C | 10 | a0001c0001t0001g0013 a0001c0001t0001g0250 a0001c0001t0001g0251 others(7): Show |
11 | HG01433.hp1 HG01981.hp2 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.162+2575delT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36387891 | |||||||
| chr9:36388146 | C | A | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.162+2321G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36388146 | |||||||
| chr9:36388246 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.162+2221C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36388246 | |||||||
| chr9:36388353 | A | G | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(236): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.162+2114T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36388353 | |||||||
| chr9:36388470 | G | T | 1 | a0001c0001t0001g0363 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.162+1997C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36388470 | |||||||
| chr9:36388587 | T | C | 1 | a0001c0001t0014g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.162+1880A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36388587 | |||||||
| chr9:36388616 | C | T | 6 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(3): Show |
6 | HG01891.hp1 HG02451.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+1851G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36388616 | |||||||
| chr9:36388719 | G | A | 1 | a0001c0002t0001g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.162+1748C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36388719 | |||||||
| chr9:36388729 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.162+1738A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36388729 | |||||||
| chr9:36389107 | T | C | 4 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(1): Show |
4 | HG04115.hp1 NA18612.hp1 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+1360A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36389107 | |||||||
| chr9:36389210 | C | G | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.162+1257G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36389210 | |||||||
| chr9:36389328 | T | G | 1 | a0001c0001t0004g0038 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.162+1139A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36389328 | |||||||
| chr9:36389344 | C | CA | 35 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(32): Show |
35 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.162+1122dupT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36389344 | |||||||
| chr9:36389344 | CA | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(216): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.162+1122delT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36389344 | |||||||
| chr9:36389344 | CAA | C | 6 | a0001c0001t0001g0225 a0001c0001t0007g0069 a0001c0001t0007g0070 others(3): Show |
6 | HG02071.hp1 NA18906.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+1121_162+1122d others(4): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36389344 | |||||||
| chr9:36389356 | A | C | 57 | a0001c0001t0001g0086 a0001c0001t0001g0113 a0001c0001t0002g0003 others(54): Show |
62 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.162+1111T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36389356 | |||||||
| chr9:36389368 | T | C | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 |
3 | HG02970.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.162+1099A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36389368 | |||||||
| chr9:36389386 | G | A | 8 | a0001c0001t0005g0022 a0001c0001t0005g0023 a0001c0001t0005g0024 others(5): Show |
8 | HG02723.hp2 HG02809.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.162+1081C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36389386 | |||||||
| chr9:36389556 | G | A | 1 | a0001c0001t0001g0327 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.162+911C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36389556 | |||||||
| chr9:36389596 | C | G | 1 | a0001c0001t0001g0326 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.162+871G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36389596 | |||||||
| chr9:36389676 | A | G | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG00609.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.162+791T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36389676 | |||||||
| chr9:36389872 | C | T | 1 | a0001c0001t0002g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.162+595G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36389872 | |||||||
| chr9:36390009 | T | A | 4 | a0001c0001t0001g0225 a0001c0001t0001g0233 a0001c0001t0001g0234 others(1): Show |
4 | HG02071.hp1 HG02523.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+458A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 2/11 | chr9 | 36390009 | |||||||
| chr9:36390751 | T | C | 2 | a0001c0001t0001g0326 a0001c0001t0001g0327 |
2 | HG01175.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.13-135A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36390751 | |||||||
| chr9:36390828 | C | T | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.13-212G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36390828 | |||||||
| chr9:36390912 | A | G | 1 | a0001c0001t0002g0087 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.13-296T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36390912 | |||||||
| chr9:36391274 | A | C | 1 | a0001c0001t0001g0252 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.13-658T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391274 | |||||||
| chr9:36391297 | T | C | 9 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(6): Show |
9 | HG01496.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.13-681A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391297 | |||||||
| chr9:36391328 | T | C | 1 | a0001c0001t0019g0203 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.13-712A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391328 | |||||||
| chr9:36391361 | A | G | 1 | a0001c0001t0001g0251 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.13-745T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391361 | |||||||
| chr9:36391462 | G | A | 1 | a0001c0002t0001g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.13-846C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391462 | |||||||
| chr9:36391540 | T | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG00099.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.13-924A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391540 | |||||||
| chr9:36391548 | A | G | 1 | a0001c0001t0001g0250 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.13-932T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391548 | |||||||
| chr9:36391587 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG00558.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.13-971G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391587 | |||||||
| chr9:36391612 | C | CT | 12 | a0001c0001t0001g0086 a0001c0001t0001g0143 a0001c0001t0001g0158 others(9): Show |
12 | HG00738.hp1 HG01934.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.13-997dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391612 | |||||||
| chr9:36391612 | CT | C | 10 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0196 others(7): Show |
10 | HG00140.hp2 HG02559.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.13-997delA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391612 | |||||||
| chr9:36391613 | T | C | 1 | a0001c0001t0014g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.13-997A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391613 | |||||||
| chr9:36391637 | T | C | 26 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(23): Show |
26 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.13-1021A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391637 | |||||||
| chr9:36391673 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.13-1057A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391673 | |||||||
| chr9:36391751 | C | T | 1 | a0001c0001t0014g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.13-1135G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391751 | |||||||
| chr9:36391771 | G | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0074 |
2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.13-1155C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391771 | |||||||
| chr9:36391860 | G | A | 5 | a0001c0001t0001g0019 a0001c0001t0001g0309 a0001c0001t0001g0310 others(2): Show |
6 | NA18962.hp1 NA18971.hp1 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.13-1244C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391860 | |||||||
| chr9:36391873 | G | A | 26 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(23): Show |
26 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.13-1257C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36391873 | |||||||
| chr9:36392090 | C | A | 4 | a0001c0001t0007g0069 a0001c0001t0007g0070 a0001c0001t0007g0071 others(1): Show |
4 | NA18949.hp1 NA18983.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.13-1474G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36392090 | |||||||
| chr9:36392098 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.13-1482G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36392098 | |||||||
| chr9:36392690 | A | C | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0019g0203 |
3 | HG00438.hp1 HG00544.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.13-2074T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36392690 | |||||||
| chr9:36392748 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.13-2132A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36392748 | |||||||
| chr9:36392806 | G | A | 2 | a0001c0001t0008g0334 a0001c0001t0008g0335 |
2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.13-2190C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36392806 | |||||||
| chr9:36392892 | A | C | 57 | a0001c0001t0001g0086 a0001c0001t0001g0113 a0001c0001t0002g0003 others(54): Show |
62 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.13-2276T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36392892 | |||||||
| chr9:36392908 | A | C | 24 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(21): Show |
24 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(21): Show |
intron_variant | MODIFIER | c.13-2292T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36392908 | |||||||
| chr9:36393082 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.13-2466G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393082 | |||||||
| chr9:36393110 | C | T | 1 | a0001c0001t0010g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.13-2494G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393110 | |||||||
| chr9:36393433 | G | T | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.13-2817C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393433 | |||||||
| chr9:36393473 | CACATTGT others(4): Show |
C | 1 | a0001c0001t0003g0199 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.13-2868_13-2858del others(11): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393473 | |||||||
| chr9:36393475 | CA | C | 16 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(13): Show |
19 | HG00558.hp1 HG01175.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.13-2860delT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393475 | |||||||
| chr9:36393475 | CATT | C | 27 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0133 others(24): Show |
27 | HG00099.hp1 HG00544.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.13-2862_13-2860del others(3): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393475 | |||||||
| chr9:36393475 | CATTGT | C | 45 | a0001c0001t0001g0012 a0001c0001t0001g0192 a0001c0001t0001g0193 others(42): Show |
46 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.13-2864_13-2860del others(5): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393475 | |||||||
| chr9:36393475 | CATTGTGT | C | 8 | a0001c0001t0001g0009 a0001c0001t0001g0150 a0001c0001t0001g0152 others(5): Show |
8 | HG00639.hp1 HG01255.hp1 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.13-2866_13-2860del others(7): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393475 | |||||||
| chr9:36393475 | CATTGTGT others(2): Show |
C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0146 a0001c0001t0001g0147 others(3): Show |
7 | HG00408.hp2 NA18943.hp1 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.13-2868_13-2860del others(9): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393475 | |||||||
| chr9:36393476 | A | G | 18 | a0001c0001t0001g0005 a0001c0001t0001g0135 a0001c0001t0001g0136 others(15): Show |
18 | HG00438.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.13-2860T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393476 | |||||||
| chr9:36393477 | T | G | 16 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(13): Show |
19 | HG00558.hp1 HG01175.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.13-2861A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | |||||||
| chr9:36393477 | T | TG | 12 | a0001c0001t0001g0005 a0001c0001t0001g0140 a0001c0001t0001g0141 others(9): Show |
12 | HG00438.hp1 HG01255.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.13-2862_13-2861ins others(1): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | |||||||
| chr9:36393477 | T | TGTGTGTG others(4): Show |
1 | a0001c0001t0001g0177 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.13-2862_13-2861ins others(11): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | |||||||
| chr9:36393477 | T | TTG | 32 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0073 others(29): Show |
33 | HG00673.hp2 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.13-2863_13-2862dup others(2): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | |||||||
| chr9:36393477 | T | TTGTG | 52 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(49): Show |
55 | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.13-2865_13-2862dup others(4): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | |||||||
| chr9:36393477 | T | TTGTGTG | 31 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0050 others(28): Show |
32 | HG00558.hp2 HG00642.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.13-2867_13-2862dup others(6): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | |||||||
| chr9:36393477 | T | TTGTGTGT others(1): Show |
30 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0051 others(27): Show |
30 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.13-2869_13-2862dup others(8): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | |||||||
| chr9:36393477 | T | TTGTGTGT others(3): Show |
12 | a0001c0001t0001g0019 a0001c0001t0001g0250 a0001c0001t0001g0284 others(9): Show |
12 | HG00609.hp2 HG01993.hp1 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.13-2871_13-2862dup others(10): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | |||||||
| chr9:36393477 | T | TTGTGTGT others(5): Show |
8 | a0001c0001t0001g0074 a0001c0001t0001g0330 a0001c0001t0001g0352 others(5): Show |
8 | HG01981.hp1 HG02040.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.13-2873_13-2862dup others(12): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | |||||||
| chr9:36393477 | T | TTGTGTGT others(7): Show |
5 | a0001c0001t0001g0359 a0001c0001t0001g0362 a0001c0001t0002g0090 others(2): Show |
5 | HG00423.hp1 NA18951.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-2875_13-2862dup others(14): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | |||||||
| chr9:36393477 | T | TTGTGTGT others(9): Show |
3 | a0001c0001t0001g0310 a0001c0001t0002g0003 a0001c0001t0002g0089 |
3 | NA18969.hp1 NA18971.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.13-2877_13-2862dup others(16): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | |||||||
| chr9:36393477 | T | TTGTGTGT others(11): Show |
2 | a0001c0001t0001g0058 a0001c0001t0002g0003 |
2 | NA18972.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.13-2879_13-2862dup others(18): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | |||||||
| chr9:36393477 | TTGTGTGT others(1): Show |
T | 3 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0036 |
3 | HG02896.hp2 HG02897.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.13-2869_13-2862del others(8): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | |||||||
| chr9:36393477 | TTGTGTGT others(3): Show |
T | 6 | a0001c0001t0004g0031 a0001c0001t0004g0033 a0001c0001t0004g0034 others(3): Show |
6 | HG01496.hp2 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.13-2871_13-2862del others(10): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | |||||||
| chr9:36393477 | TTGTGTGT others(5): Show |
T | 2 | a0001c0001t0001g0258 a0001c0002t0001g0082 |
2 | HG01981.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.13-2873_13-2862del others(12): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | |||||||
| chr9:36393477 | TTGTGTGT others(7): Show |
T | 4 | a0001c0001t0001g0288 a0001c0001t0001g0293 a0001c0001t0001g0294 others(1): Show |
4 | HG02615.hp2 HG03139.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.13-2875_13-2862del others(14): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393477 | |||||||
| chr9:36393485 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.13-2869C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393485 | |||||||
| chr9:36393512 | TGTGTGTG others(5): Show |
T | 4 | a0001c0001t0002g0123 a0001c0001t0005g0022 a0001c0001t0005g0023 others(1): Show |
4 | HG02723.hp2 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.13-2908_13-2897del others(12): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393512 | |||||||
| chr9:36393514 | TGTGTGTG others(3): Show |
T | 5 | a0001c0001t0005g0025 a0001c0001t0005g0026 a0001c0001t0005g0028 others(2): Show |
5 | HG02809.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-2908_13-2899del others(10): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393514 | |||||||
| chr9:36393520 | TGTGG | T | 5 | a0001c0001t0001g0054 a0001c0001t0001g0075 a0001c0001t0001g0076 others(2): Show |
5 | HG01433.hp2 HG02559.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.13-2908_13-2905del others(4): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393520 | |||||||
| chr9:36393522 | T | G | 1 | a0001c0001t0001g0280 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.13-2906A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393522 | |||||||
| chr9:36393522 | TGG | T | 10 | a0001c0001t0001g0007 a0001c0001t0001g0052 a0001c0001t0001g0061 others(7): Show |
10 | HG00140.hp1 HG00280.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.13-2908_13-2907del others(2): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393522 | |||||||
| chr9:36393523 | G | GTGTGTGT others(4): Show |
1 | a0001c0001t0001g0360 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.13-2908_13-2907ins others(11): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393523 | |||||||
| chr9:36393523 | G | GTGTGTGT others(10): Show |
1 | a0001c0001t0001g0332 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.13-2908_13-2907ins others(17): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393523 | |||||||
| chr9:36393524 | G | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(211): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.13-2908C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393524 | |||||||
| chr9:36393539 | T | C | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.13-2923A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393539 | |||||||
| chr9:36393577 | C | T | 5 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(2): Show |
5 | HG02572.hp1 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.13-2961G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393577 | |||||||
| chr9:36393580 | T | G | 2 | a0001c0001t0001g0314 a0001c0001t0001g0315 |
2 | HG00438.hp2 HG00597.hp1 |
intron_variant | MODIFIER | c.13-2964A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393580 | |||||||
| chr9:36393747 | A | G | 1 | a0001c0002t0001g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.13-3131T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393747 | |||||||
| chr9:36393976 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.13-3360C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36393976 | |||||||
| chr9:36394009 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.13-3393C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36394009 | |||||||
| chr9:36394010 | C | A | 1 | a0001c0001t0001g0155 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.13-3394G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36394010 | |||||||
| chr9:36394042 | C | T | 16 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(13): Show |
20 | HG00408.hp2 HG00558.hp1 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.13-3426G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36394042 | |||||||
| chr9:36394231 | T | C | 275 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(272): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.13-3615A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36394231 | |||||||
| chr9:36394523 | G | C | 1 | a0001c0001t0002g0121 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.13-3907C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36394523 | |||||||
| chr9:36394594 | C | T | 1 | a0001c0001t0021g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.13-3978G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36394594 | |||||||
| chr9:36394716 | G | A | 1 | a0001c0002t0001g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.13-4100C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36394716 | |||||||
| chr9:36394971 | G | C | 174 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(171): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.13-4355C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36394971 | |||||||
| chr9:36395105 | G | A | 1 | a0001c0001t0001g0236 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.13-4489C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36395105 | |||||||
| chr9:36395164 | C | G | 3 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 |
3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.13-4548G>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36395164 | |||||||
| chr9:36395228 | T | C | 2 | a0001c0001t0002g0130 a0001c0001t0002g0131 |
2 | HG01071.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.13-4612A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36395228 | |||||||
| chr9:36395241 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.13-4625G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36395241 | |||||||
| chr9:36395396 | T | C | 8 | a0001c0001t0005g0022 a0001c0001t0005g0023 a0001c0001t0005g0024 others(5): Show |
8 | HG02723.hp2 HG02809.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+4701A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36395396 | |||||||
| chr9:36395400 | G | A | 1 | a0001c0001t0001g0362 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.12+4697C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36395400 | |||||||
| chr9:36395429 | G | A | 1 | a0001c0001t0002g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.12+4668C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36395429 | |||||||
| chr9:36395678 | AATCTCTA others(18): Show |
A | 1 | a0001c0001t0001g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.12+4394_12+4418del others(25): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36395678 | |||||||
| chr9:36395754 | C | A | 1 | a0001c0001t0003g0200 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.12+4343G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36395754 | |||||||
| chr9:36395892 | T | C | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG00621.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.12+4205A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36395892 | |||||||
| chr9:36395949 | G | A | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(236): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.12+4148C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36395949 | |||||||
| chr9:36395960 | C | A | 11 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0204 others(8): Show |
11 | HG00438.hp1 HG00544.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.12+4137G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36395960 | |||||||
| chr9:36396197 | T | C | 1 | a0001c0001t0003g0139 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.12+3900A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36396197 | |||||||
| chr9:36396198 | G | GT | 6 | a0001c0001t0001g0239 a0001c0001t0001g0318 a0001c0001t0001g0319 others(3): Show |
6 | NA18946.hp2 NA18974.hp1 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+3898dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36396198 | |||||||
| chr9:36396229 | A | C | 1 | a0001c0001t0001g0248 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.12+3868T>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36396229 | |||||||
| chr9:36396422 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.12+3675A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36396422 | |||||||
| chr9:36396551 | G | A | 25 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(22): Show |
25 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(22): Show |
intron_variant | MODIFIER | c.12+3546C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36396551 | |||||||
| chr9:36396772 | T | C | 200 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(197): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.12+3325A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36396772 | |||||||
| chr9:36396775 | T | C | 2 | a0001c0001t0006g0042 a0001c0001t0013g0043 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.12+3322A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36396775 | |||||||
| chr9:36396786 | T | TAAAAAAA others(2734): Show |
1 | a0001c0001t0001g0051 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.12+3310_12+3311ins others(2741): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36396786 | |||||||
| chr9:36396786 | T | TAAAAAAA others(2760): Show |
1 | a0001c0001t0001g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.12+3310_12+3311ins others(2767): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36396786 | |||||||
| chr9:36396835 | T | C | 7 | a0001c0001t0001g0239 a0001c0001t0001g0318 a0001c0001t0001g0319 others(4): Show |
7 | HG00423.hp2 NA18946.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.12+3262A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36396835 | |||||||
| chr9:36396919 | G | A | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(236): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.12+3178C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36396919 | |||||||
| chr9:36396979 | TCACTA | T | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG02055.hp2 HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.12+3113_12+3117del others(5): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36396979 | |||||||
| chr9:36397011 | ATG | A | 360 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(357): Show |
388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.12+3084_12+3085del others(2): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397011 | |||||||
| chr9:36397013 | GTGTGTGT others(51): Show |
G | 1 | a0001c0001t0001g0370 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.12+3026_12+3083del others(58): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397013 | |||||||
| chr9:36397019 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.12+3078C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397019 | |||||||
| chr9:36397021 | G | GTGTATAT others(21): Show |
2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG01358.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.12+3075_12+3076ins others(28): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397021 | |||||||
| chr9:36397021 | G | GTGTATAT others(21): Show |
1 | a0001c0001t0001g0213 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.12+3075_12+3076ins others(28): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397021 | |||||||
| chr9:36397022 | TGTGTATA others(3): Show |
T | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.12+3065_12+3074del others(10): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397022 | |||||||
| chr9:36397025 | G | A | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 |
3 | HG01358.hp1 NA18977.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.12+3072C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397025 | |||||||
| chr9:36397071 | A | ATG | 115 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(112): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.12+3024_12+3025dup others(2): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397071 | |||||||
| chr9:36397081 | G | GTA | 7 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(4): Show |
7 | HG01109.hp1 HG02257.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.12+3014_12+3015dup others(2): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397081 | |||||||
| chr9:36397081 | G | GTGTA | 11 | a0001c0001t0001g0216 a0001c0001t0002g0004 a0001c0001t0002g0123 others(8): Show |
13 | HG00733.hp2 HG00741.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.12+3015_12+3016ins others(4): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397081 | |||||||
| chr9:36397081 | G | GTGTATA | 45 | a0001c0001t0001g0086 a0001c0001t0001g0113 a0001c0001t0002g0003 others(42): Show |
48 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.12+3015_12+3016ins others(6): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397081 | |||||||
| chr9:36397081 | GTA | G | 3 | a0001c0001t0008g0333 a0001c0001t0008g0334 a0001c0001t0008g0335 |
3 | HG02647.hp2 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.12+3014_12+3015del others(2): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397081 | |||||||
| chr9:36397081 | GTATA | G | 26 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(23): Show |
26 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.12+3012_12+3015del others(4): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397081 | |||||||
| chr9:36397083 | A | G | 35 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(32): Show |
42 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.12+3014T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397083 | |||||||
| chr9:36397085 | A | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG01192.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.12+3012T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397085 | |||||||
| chr9:36397104 | G | GT | 6 | a0001c0001t0001g0065 a0001c0001t0001g0258 a0001c0001t0001g0300 others(3): Show |
6 | HG01891.hp2 HG01981.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.12+2992dupA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397104 | |||||||
| chr9:36397104 | G | T | 1 | a0001c0001t0001g0259 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.12+2993C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397104 | |||||||
| chr9:36397104 | GT | G | 161 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(158): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.12+2992delA | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397104 | |||||||
| chr9:36397104 | GTT | G | 24 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(21): Show |
24 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(21): Show |
intron_variant | MODIFIER | c.12+2991_12+2992del others(2): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397104 | |||||||
| chr9:36397106 | T | G | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.12+2991A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397106 | |||||||
| chr9:36397236 | C | A | 1 | a0001c0001t0001g0219 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.12+2861G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397236 | |||||||
| chr9:36397240 | A | G | 1 | a0001c0001t0001g0330 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.12+2857T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397240 | |||||||
| chr9:36397287 | T | C | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 |
3 | HG02970.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.12+2810A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397287 | |||||||
| chr9:36397424 | T | C | 1 | a0001c0001t0001g0324 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.12+2673A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397424 | |||||||
| chr9:36397461 | A | G | 174 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(171): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.12+2636T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397461 | |||||||
| chr9:36397543 | T | C | 1 | a0001c0001t0014g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.12+2554A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397543 | |||||||
| chr9:36397578 | T | A | 1 | a0001c0001t0001g0325 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.12+2519A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397578 | |||||||
| chr9:36397579 | C | A | 2 | a0001c0001t0001g0326 a0001c0001t0001g0327 |
2 | HG01175.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.12+2518G>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397579 | |||||||
| chr9:36397612 | C | T | 25 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(22): Show |
25 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(22): Show |
intron_variant | MODIFIER | c.12+2485G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397612 | |||||||
| chr9:36397701 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.12+2396G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397701 | |||||||
| chr9:36397781 | CTT | C | 43 | a0001c0001t0001g0086 a0001c0001t0001g0113 a0001c0001t0002g0003 others(40): Show |
46 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.12+2314_12+2315del others(2): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397781 | |||||||
| chr9:36397874 | G | T | 1 | a0001c0001t0010g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.12+2223C>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397874 | |||||||
| chr9:36397889 | T | G | 1 | a0001c0001t0010g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.12+2208A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397889 | |||||||
| chr9:36397938 | A | T | 8 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(5): Show |
8 | HG01109.hp1 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+2159T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36397938 | |||||||
| chr9:36398248 | G | A | 25 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(22): Show |
25 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(22): Show |
intron_variant | MODIFIER | c.12+1849C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36398248 | |||||||
| chr9:36398426 | A | T | 1 | a0001c0001t0001g0239 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.12+1671T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36398426 | |||||||
| chr9:36398427 | T | A | 6 | a0001c0001t0001g0364 a0001c0001t0006g0039 a0001c0001t0006g0040 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+1670A>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36398427 | |||||||
| chr9:36398566 | G | C | 1 | a0001c0001t0003g0220 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.12+1531C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36398566 | |||||||
| chr9:36398577 | C | T | 2 | a0001c0001t0003g0138 a0001c0001t0003g0139 |
2 | NA18954.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.12+1520G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36398577 | |||||||
| chr9:36398706 | T | C | 111 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(108): Show |
120 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.12+1391A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36398706 | |||||||
| chr9:36398751 | T | C | 10 | a0001c0001t0002g0004 a0001c0001t0002g0123 a0001c0001t0002g0124 others(7): Show |
12 | HG00733.hp2 HG00741.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.12+1346A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36398751 | |||||||
| chr9:36398935 | T | C | 16 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(13): Show |
16 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+1162A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36398935 | |||||||
| chr9:36399023 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(273): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.12+1074A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36399023 | |||||||
| chr9:36399039 | G | C | 1 | a0001c0001t0001g0238 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.12+1058C>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36399039 | |||||||
| chr9:36399213 | G | A | 117 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(114): Show |
126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.12+884C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36399213 | |||||||
| chr9:36399295 | T | C | 3 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 |
3 | HG00609.hp1 HG02083.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.12+802A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36399295 | |||||||
| chr9:36399442 | A | T | 2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+655T>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36399442 | |||||||
| chr9:36399493 | A | AAC | 14 | a0001c0001t0001g0012 a0001c0001t0001g0224 a0001c0001t0001g0225 others(11): Show |
15 | HG01106.hp1 HG02071.hp1 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.12+603_12+604insGT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36399493 | |||||||
| chr9:36399493 | A | AAT | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(221): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.12+602_12+603dupAT | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36399493 | |||||||
| chr9:36399493 | A | AATATATA others(32): Show |
1 | a0001c0001t0010g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.12+603_12+604insAT others(37): Show |
RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36399493 | |||||||
| chr9:36399529 | T | C | 25 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(22): Show |
25 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(22): Show |
intron_variant | MODIFIER | c.12+568A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36399529 | |||||||
| chr9:36399536 | T | C | 2 | a0001c0001t0001g0371 a0001c0001t0001g0372 |
2 | HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.12+561A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36399536 | |||||||
| chr9:36399542 | T | G | 8 | a0001c0001t0001g0365 a0001c0001t0001g0367 a0001c0001t0001g0368 others(5): Show |
8 | HG01243.hp1 HG01255.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.12+555A>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36399542 | |||||||
| chr9:36399563 | A | G | 26 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(23): Show |
26 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.12+534T>C | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36399563 | |||||||
| chr9:36399751 | T | C | 2 | a0001c0001t0002g0373 a0001c0001t0002g0374 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.12+346A>G | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36399751 | |||||||
| chr9:36399826 | C | T | 26 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(23): Show |
26 | HG01496.hp2 HG02258.hp2 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.12+271G>A | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36399826 | |||||||
| chr9:36400026 | G | A | 1 | a0001c0001t0010g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.12+71C>T | RNF38 | ENSG00000137075.18 | transcript | ENST00000259605.11 | protein_coding | 1/11 | chr9 | 36400026 |