Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10193 |
| ensemblid | ENSG00000181852.18 |
| hgncid | 18401 |
| symbol | RNF41 |
| name | ring finger protein 41 |
| refseq_nuc | NM_005785.4 |
| refseq_prot | NP_005776.1 |
| ensembl_nuc | ENST00000345093.9 |
| ensembl_prot | ENSP00000342755.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 56202179 |
| end | 56221922 |
| strand | - |
| ver | v1.2 |
| region | chr12:56202179-56221922 |
| region5000 | chr12:56197179-56226922 |
| regionname0 | RNF41_chr12_56202179_56221922 |
| regionname5000 | RNF41_chr12_56197179_56226922 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 317 | 333 | 86 | 58 | 153 | 12 | 22 | 117 | RNF41_chr12_56197179_56226922 | RNF41 | MGYDV others(312): Show |
chr12 | 56197179 | 56226922 |
| a0002 | 0/0 | 317 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | MGYDV others(312): Show |
chr12 | 56197179 | 56226922 |
| a0003 | 0/0 | 317 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF41_chr12_56197179_56226922 | RNF41 | MGYDV others(312): Show |
chr12 | 56197179 | 56226922 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 951 | 330 | 84 | 57 | 153 | 12 | 22 | RNF41_chr12_56197179_56226922 | RNF41 | ATGGG others(946): Show |
chr12 | 56197179 | 56226922 | ||
| a0001c0003 | 0/0 | 951 | 2 | 2 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | ATGGG others(946): Show |
chr12 | 56197179 | 56226922 | ||
| a0001c0004 | 0/0 | 951 | 1 | 0 | 1 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | ATGGG others(946): Show |
chr12 | 56197179 | 56226922 | ||
| a0002c0002 | 0/0 | 951 | 2 | 2 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | ATGGG others(946): Show |
chr12 | 56197179 | 56226922 | ||
| a0003c0005 | 0/0 | 951 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | ATGGG others(946): Show |
chr12 | 56197179 | 56226922 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5593 | 202 | 31 | 40 | 104 | 10 | 17 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5588): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0002 | 0/0 | 5593 | 20 | 0 | 5 | 15 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5588): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0003 | 0/0 | 5592 | 13 | 12 | 1 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5587): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0004 | 0/0 | 5594 | 8 | 1 | 3 | 4 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5589): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0005 | 0/0 | 5594 | 7 | 0 | 4 | 0 | 0 | 3 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5589): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0006 | 0/0 | 5594 | 5 | 5 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5589): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0007 | 0/0 | 5591 | 5 | 5 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5586): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0008 | 1/0 | 5593 | 4 | 3 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5588): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0009 | 0/0 | 5593 | 4 | 0 | 0 | 4 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5588): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0010 | 0/0 | 5593 | 3 | 0 | 0 | 3 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5588): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0011 | 0/0 | 5592 | 3 | 1 | 0 | 2 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5587): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0012 | 0/0 | 5592 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5587): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0013 | 0/0 | 5592 | 3 | 0 | 0 | 3 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5587): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0014 | 0/0 | 5594 | 3 | 3 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5589): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0015 | 0/0 | 5593 | 3 | 3 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5588): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0016 | 0/0 | 5593 | 3 | 3 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5588): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0017 | 0/0 | 5594 | 2 | 0 | 0 | 1 | 1 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5589): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0018 | 0/0 | 5594 | 2 | 0 | 1 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5589): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0019 | 0/0 | 5593 | 2 | 0 | 0 | 2 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5588): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0020 | 0/0 | 5594 | 2 | 0 | 0 | 2 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5589): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0021 | 0/0 | 5591 | 2 | 2 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5586): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0022 | 0/0 | 5593 | 2 | 2 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5588): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0023 | 0/0 | 5593 | 2 | 2 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5588): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0025 | 0/0 | 5592 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5587): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0026 | 0/0 | 5593 | 1 | 0 | 1 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5588): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0027 | 0/0 | 5593 | 1 | 0 | 0 | 0 | 0 | 1 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5588): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0028 | 0/0 | 5595 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5590): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0029 | 0/0 | 5595 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5590): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0030 | 0/0 | 5594 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5589): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0031 | 0/0 | 5593 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5588): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0032 | 0/0 | 5593 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5588): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0033 | 0/0 | 5592 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5587): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0034 | 0/1 | 5591 | 1 | 0 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5586): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0035 | 0/0 | 5593 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5588): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0036 | 0/0 | 5593 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5588): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0037 | 0/0 | 5593 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5588): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0038 | 0/0 | 5593 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5588): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0039 | 0/0 | 5594 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5589): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0040 | 0/0 | 5593 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5588): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0041 | 0/0 | 5593 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5588): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0042 | 0/0 | 5594 | 1 | 0 | 0 | 0 | 0 | 1 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5589): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0043 | 0/0 | 5593 | 1 | 0 | 0 | 0 | 1 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5588): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0044 | 0/0 | 5593 | 1 | 0 | 1 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5588): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0045 | 0/0 | 5594 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5589): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0046 | 0/0 | 5594 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5589): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0047 | 0/0 | 5594 | 1 | 0 | 1 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5589): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0048 | 0/0 | 5593 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5588): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0049 | 0/0 | 5594 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5589): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0051 | 0/0 | 5594 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5589): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0052 | 0/0 | 5594 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5589): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0053 | 0/0 | 5592 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5587): Show |
chr12 | 56197179 | 56226922 |
| a0001c0001t0054 | 0/0 | 5591 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5586): Show |
chr12 | 56197179 | 56226922 |
| a0001c0003t0012 | 0/0 | 5592 | 2 | 2 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5587): Show |
chr12 | 56197179 | 56226922 |
| a0001c0004t0001 | 0/0 | 5593 | 1 | 0 | 1 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5588): Show |
chr12 | 56197179 | 56226922 |
| a0002c0002t0024 | 0/0 | 5593 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5588): Show |
chr12 | 56197179 | 56226922 |
| a0002c0002t0050 | 0/0 | 5592 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5587): Show |
chr12 | 56197179 | 56226922 |
| a0003c0005t0002 | 0/0 | 5593 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | GTCTG others(5588): Show |
chr12 | 56197179 | 56226922 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 20 | 2 | 5 | 9 | 3 | 1 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0002 | 0/0 | 18 | 2 | 10 | 6 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0003 | 0/0 | 17 | 2 | 0 | 13 | 0 | 2 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0005 | 0/0 | 15 | 0 | 3 | 12 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0006 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0007 | 0/0 | 8 | 0 | 4 | 2 | 1 | 1 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 3 | 0 | 2 | 1 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0029 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0002g0004 | 0/0 | 15 | 0 | 5 | 10 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0003g0009 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0003g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0004g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0005g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0005g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0005g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0005g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0006g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0007g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0007g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0008g0014 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0008g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0009g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0009g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0010g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0011g0032 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0011g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0012g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0013g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0014g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0014g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0014g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0015g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0015g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0015g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0016g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0017g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0017g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0018g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0018g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0019g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0019g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0020g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0020g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0021g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0022g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0022g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0023g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0023g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0025g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0026g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0027g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0028g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0029g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0030g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0031g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0032g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0033g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0034g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0035g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0036g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0037g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0038g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0039g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0040g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0041g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0042g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0043g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0044g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0045g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0046g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0047g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0048g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0049g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0051g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0052g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0053g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0001t0054g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0003t0012g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0001c0004t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0002c0002t0024g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0002c0002t0050g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| a0003c0005t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0081 | EUR | FIN | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0093 | EUR | FIN | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG00323 | hp1 | a0001 | c0001 | t0017 | g0106 | EUR | FIN | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0086 | EUR | FIN | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG00423 | hp2 | a0001 | c0001 | t0039 | g0111 | EAS | CHS | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG00558 | hp2 | a0001 | c0001 | t0032 | g0102 | EAS | CHS | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | CHS | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG00733 | hp1 | a0001 | c0001 | t0005 | g0015 | AMR | PUR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0080 | AMR | PUR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0015 | AMR | PUR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0031 | AMR | PUR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0015 | AMR | PUR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01081 | hp2 | a0001 | c0004 | t0001 | g0096 | AMR | PUR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01169 | hp1 | a0001 | c0001 | t0044 | g0060 | AMR | PUR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01169 | hp2 | a0001 | c0001 | t0026 | g0104 | AMR | PUR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0159 | AMR | PUR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0087 | AMR | PUR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01433 | hp2 | a0001 | c0001 | t0047 | g0144 | AMR | CLM | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0024 | AFR | ACB | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0045 | AFR | ACB | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01891 | hp2 | a0001 | c0001 | t0049 | g0166 | AFR | ACB | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02027 | hp1 | a0001 | c0001 | t0010 | g0017 | EAS | KHV | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02040 | hp1 | a0001 | c0001 | t0011 | g0032 | EAS | KHV | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02040 | hp2 | a0001 | c0001 | t0011 | g0099 | EAS | KHV | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02055 | hp1 | a0001 | c0001 | t0012 | g0047 | AFR | ACB | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02056 | hp2 | a0001 | c0001 | t0019 | g0157 | EAS | KHV | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | KHV | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02135 | hp1 | a0001 | c0001 | t0019 | g0108 | EAS | KHV | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02145 | hp1 | a0001 | c0001 | t0051 | g0175 | AFR | ACB | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02145 | hp2 | a0001 | c0001 | t0029 | g0065 | AFR | ACB | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02148 | hp1 | a0001 | c0001 | t0018 | g0107 | AMR | PEL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02165 | hp1 | a0001 | c0001 | t0010 | g0017 | EAS | CDX | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0044 | AFR | ACB | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | ACB | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0013 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02615 | hp2 | a0001 | c0001 | t0052 | g0168 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02630 | hp1 | a0001 | c0001 | t0014 | g0171 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02647 | hp2 | a0001 | c0001 | t0008 | g0052 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02717 | hp2 | a0001 | c0001 | t0045 | g0054 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0013 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02818 | hp1 | a0001 | c0001 | t0014 | g0177 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02895 | hp1 | a0001 | c0001 | t0022 | g0164 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02895 | hp2 | a0001 | c0001 | t0016 | g0022 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02896 | hp2 | a0001 | c0001 | t0008 | g0014 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02897 | hp2 | a0001 | c0001 | t0022 | g0165 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0053 | AFR | ESN | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0043 | AFR | ESN | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0024 | AFR | ESN | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0046 | AFR | ESN | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03017 | hp1 | a0001 | c0001 | t0005 | g0031 | SAS | PJL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0075 | SAS | PJL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03041 | hp1 | a0001 | c0001 | t0015 | g0167 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03041 | hp2 | a0001 | c0001 | t0014 | g0176 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03098 | hp1 | a0001 | c0003 | t0012 | g0025 | AFR | MSL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | MSL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03130 | hp1 | a0001 | c0001 | t0021 | g0037 | AFR | ESN | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03130 | hp2 | a0001 | c0001 | t0054 | g0179 | AFR | ESN | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03139 | hp1 | a0001 | c0003 | t0012 | g0025 | AFR | ESN | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03139 | hp2 | a0002 | c0002 | t0024 | g0143 | AFR | ESN | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03209 | hp1 | a0001 | c0001 | t0023 | g0174 | AFR | MSL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03209 | hp2 | a0001 | c0001 | t0023 | g0178 | AFR | MSL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03225 | hp1 | a0001 | c0001 | t0031 | g0063 | AFR | MSL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03225 | hp2 | a0001 | c0001 | t0016 | g0022 | AFR | MSL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03453 | hp1 | a0001 | c0001 | t0016 | g0022 | AFR | MSL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | MSL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03486 | hp1 | a0001 | c0001 | t0015 | g0173 | AFR | MSL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03486 | hp2 | a0001 | c0001 | t0048 | g0163 | AFR | MSL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03516 | hp1 | a0001 | c0001 | t0021 | g0037 | AFR | ESN | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0098 | AFR | ESN | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0013 | AFR | GWD | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03579 | hp1 | a0002 | c0002 | t0050 | g0170 | AFR | MSL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03579 | hp2 | a0001 | c0001 | t0008 | g0014 | AFR | MSL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03688 | hp1 | a0001 | c0001 | t0042 | g0058 | SAS | STU | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG04199 | hp2 | a0001 | c0001 | t0027 | g0120 | SAS | STU | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0101 | SAS | STU | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18522 | hp2 | a0001 | c0001 | t0025 | g0142 | AFR | YRI | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHB | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHB | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | YRI | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18941 | hp2 | a0001 | c0001 | t0020 | g0074 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18945 | hp2 | a0001 | c0001 | t0040 | g0069 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18946 | hp1 | a0001 | c0001 | t0041 | g0071 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18948 | hp1 | a0001 | c0001 | t0020 | g0103 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18957 | hp1 | a0001 | c0001 | t0036 | g0109 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18962 | hp1 | a0001 | c0001 | t0018 | g0100 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18964 | hp1 | a0001 | c0001 | t0009 | g0023 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18966 | hp2 | a0001 | c0001 | t0013 | g0016 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0154 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18975 | hp1 | a0001 | c0001 | t0017 | g0088 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18981 | hp1 | a0001 | c0001 | t0013 | g0016 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18985 | hp1 | a0001 | c0001 | t0030 | g0136 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18985 | hp2 | a0001 | c0001 | t0028 | g0105 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18998 | hp1 | a0001 | c0001 | t0038 | g0117 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18998 | hp2 | a0001 | c0001 | t0009 | g0180 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18999 | hp2 | a0003 | c0005 | t0002 | g0110 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19004 | hp1 | a0001 | c0001 | t0037 | g0134 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19010 | hp2 | a0001 | c0001 | t0010 | g0017 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0133 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | LWK | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | LWK | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19043 | hp2 | a0001 | c0001 | t0053 | g0172 | AFR | LWK | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19056 | hp2 | a0001 | c0001 | t0035 | g0141 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19062 | hp1 | a0001 | c0001 | t0033 | g0095 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19064 | hp1 | a0001 | c0001 | t0013 | g0016 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19080 | hp1 | a0001 | c0001 | t0009 | g0023 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19081 | hp2 | a0001 | c0001 | t0046 | g0070 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19088 | hp1 | a0001 | c0001 | t0009 | g0023 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | YRI | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA19240 | hp2 | a0001 | c0001 | t0015 | g0169 | AFR | YRI | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ASW | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA20752 | hp1 | a0001 | c0001 | t0043 | g0160 | EUR | TSI | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0067 | EUR | TSI | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | GIH | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | GIH | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0048 | AFR | ACB | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | USA | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA21309 | hp1 | a0001 | c0001 | t0011 | g0032 | AFR | LWK | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0034 | g0076 | REF | REF | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0008 | g0014 | REF | REF | RNF41_chr12_56197179_56226922 | RNF41 | chr12 | 56197179 | 56226922 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:56208197 | G | A | 1 | a0003 | 1 | NA18999.hp2 | missense_variant | MODERATE | c.464C>T | p.Thr155Met | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 5/7 | 835/5593 | 464/954 | 155/317 | chr12 | 56208197 | |||
| chr12:56208253 | C | G | 1 | a0002 | 2 | HG03139.hp2 HG03579.hp1 |
missense_variant | MODERATE | c.408G>C | p.Lys136Asn | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 5/7 | 779/5593 | 408/954 | 136/317 | chr12 | 56208253 | |||
| chr12:56216611 | A | T | 1 | a0001 | 3 | HG02027.hp1 HG02165.hp1 NA19010.hp2 |
splice_region_variant | LOW | c.-206T>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 2/7 | chr12 | 56216611 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:56206744 | C | T | 1 | a0001c0004 | 1 | HG01081.hp2 | synonymous_variant | LOW | c.657G>A | p.Ser219Ser | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 1028/5593 | 657/954 | 219/317 | chr12 | 56206744 | |||
| chr12:56208214 | G | A | 1 | a0001c0003 | 2 | HG03098.hp1 HG03139.hp1 |
synonymous_variant | LOW | c.447C>T | p.Ile149Ile | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 5/7 | 818/5593 | 447/954 | 149/317 | chr12 | 56208214 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:56202202 | T | A | 1 | a0001c0001t0032 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4245A>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 4245 | chr12 | 56202202 | ||||||
| chr12:56202207 | C | A | 53 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(50): Show |
317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
3_prime_UTR_variant | MODIFIER | c.*4240G>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 4240 | chr12 | 56202207 | ||||||
| chr12:56203037 | A | C | 1 | a0001c0001t0039 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3410T>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 3410 | chr12 | 56203037 | ||||||
| chr12:56203061 | C | CT | 44 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(41): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
3_prime_UTR_variant | MODIFIER | c.*3385dupA | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 3385 | chr12 | 56203061 | ||||||
| chr12:56203127 | A | G | 1 | a0001c0001t0031 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3320T>C | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 3320 | chr12 | 56203127 | ||||||
| chr12:56203185 | CTT | C | 30 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(27): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
3_prime_UTR_variant | MODIFIER | c.*3260_*3261delAA | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 3260 | chr12 | 56203185 | ||||||
| chr12:56203187 | T | C | 1 | a0001c0001t0030 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3260A>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 3260 | chr12 | 56203187 | ||||||
| chr12:56203191 | T | C | 1 | a0001c0001t0035 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3256A>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 3256 | chr12 | 56203191 | ||||||
| chr12:56203195 | T | C | 31 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(28): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*3252A>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 3252 | chr12 | 56203195 | ||||||
| chr12:56203196 | T | C | 1 | a0001c0001t0035 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3251A>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 3251 | chr12 | 56203196 | ||||||
| chr12:56203372 | A | G | 1 | a0001c0001t0021 | 2 | HG03130.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3075T>C | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 3075 | chr12 | 56203372 | ||||||
| chr12:56203398 | TG | T | 28 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(25): Show |
268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
3_prime_UTR_variant | MODIFIER | c.*3048delC | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 3048 | chr12 | 56203398 | ||||||
| chr12:56203399 | GGT | G | 13 | a0001c0001t0006 a0001c0001t0014 a0001c0001t0015 others(10): Show |
24 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3046_*3047delAC | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 3046 | chr12 | 56203399 | ||||||
| chr12:56203400 | G | T | 7 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0028 others(4): Show |
14 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3047C>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 3047 | chr12 | 56203400 | ||||||
| chr12:56203403 | T | G | 4 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0028 others(1): Show |
11 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3044A>C | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 3044 | chr12 | 56203403 | ||||||
| chr12:56203404 | T | G | 26 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(23): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
3_prime_UTR_variant | MODIFIER | c.*3043A>C | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 3043 | chr12 | 56203404 | ||||||
| chr12:56203405 | T | G | 1 | a0001c0001t0020 | 2 | NA18941.hp2 NA18948.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3042A>C | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 3042 | chr12 | 56203405 | ||||||
| chr12:56203572 | T | C | 1 | a0001c0001t0036 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2875A>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2875 | chr12 | 56203572 | ||||||
| chr12:56203596 | A | G | 1 | a0001c0001t0021 | 2 | HG03130.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2851T>C | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2851 | chr12 | 56203596 | ||||||
| chr12:56203685 | T | C | 1 | a0001c0001t0037 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2762A>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2762 | chr12 | 56203685 | ||||||
| chr12:56203702 | C | CT | 5 | a0001c0001t0023 a0001c0001t0039 a0001c0001t0045 others(2): Show |
6 | HG00423.hp2 HG02145.hp1 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2744dupA | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2744 | chr12 | 56203702 | ||||||
| chr12:56203702 | C | CTA | 6 | a0001c0001t0004 a0001c0001t0017 a0001c0001t0028 others(3): Show |
14 | HG00323.hp1 HG00741.hp1 HG01175.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2744_*2745insTA | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2744 | chr12 | 56203702 | ||||||
| chr12:56203702 | CT | C | 2 | a0001c0001t0007 a0001c0001t0054 |
6 | HG02559.hp1 HG02572.hp1 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2744delA | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2744 | chr12 | 56203702 | ||||||
| chr12:56203703 | T | TA | 24 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(21): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
3_prime_UTR_variant | MODIFIER | c.*2743_*2744insT | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2743 | chr12 | 56203703 | ||||||
| chr12:56203704 | T | A | 2 | a0001c0001t0011 a0001c0001t0021 |
5 | HG02040.hp1 HG02040.hp2 HG03130.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2743A>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2743 | chr12 | 56203704 | ||||||
| chr12:56203736 | T | C | 48 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(45): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
3_prime_UTR_variant | MODIFIER | c.*2711A>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2711 | chr12 | 56203736 | ||||||
| chr12:56203799 | G | A | 31 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(28): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
3_prime_UTR_variant | MODIFIER | c.*2648C>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2648 | chr12 | 56203799 | ||||||
| chr12:56203807 | G | A | 2 | a0001c0001t0016 a0001c0001t0052 |
4 | HG02615.hp2 HG02895.hp2 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2640C>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2640 | chr12 | 56203807 | ||||||
| chr12:56204020 | A | G | 6 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0017 others(3): Show |
30 | HG00323.hp1 HG00558.hp1 HG00621.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2427T>C | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2427 | chr12 | 56204020 | ||||||
| chr12:56204181 | C | G | 1 | a0001c0001t0038 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2266G>C | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2266 | chr12 | 56204181 | ||||||
| chr12:56204184 | C | G | 1 | a0001c0001t0038 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2263G>C | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2263 | chr12 | 56204184 | ||||||
| chr12:56204186 | G | T | 1 | a0001c0001t0038 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2261C>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2261 | chr12 | 56204186 | ||||||
| chr12:56204187 | T | G | 1 | a0001c0001t0038 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2260A>C | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2260 | chr12 | 56204187 | ||||||
| chr12:56204189 | G | A | 1 | a0001c0001t0042 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2258C>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2258 | chr12 | 56204189 | ||||||
| chr12:56204192 | A | T | 1 | a0001c0001t0038 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2255T>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2255 | chr12 | 56204192 | ||||||
| chr12:56204193 | T | C | 1 | a0001c0001t0038 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2254A>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2254 | chr12 | 56204193 | ||||||
| chr12:56204195 | A | C | 1 | a0001c0001t0038 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2252T>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2252 | chr12 | 56204195 | ||||||
| chr12:56204198 | C | T | 1 | a0001c0001t0038 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2249G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2249 | chr12 | 56204198 | ||||||
| chr12:56204200 | A | T | 1 | a0001c0001t0038 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2247T>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2247 | chr12 | 56204200 | ||||||
| chr12:56204201 | A | T | 1 | a0001c0001t0038 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2246T>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2246 | chr12 | 56204201 | ||||||
| chr12:56204202 | A | T | 1 | a0001c0001t0038 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2245T>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2245 | chr12 | 56204202 | ||||||
| chr12:56204203 | A | T | 1 | a0001c0001t0038 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2244T>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2244 | chr12 | 56204203 | ||||||
| chr12:56204204 | A | C | 1 | a0001c0001t0038 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2243T>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2243 | chr12 | 56204204 | ||||||
| chr12:56204213 | C | T | 1 | a0001c0001t0038 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2234G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2234 | chr12 | 56204213 | ||||||
| chr12:56204214 | A | C | 1 | a0001c0001t0038 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2233T>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2233 | chr12 | 56204214 | ||||||
| chr12:56204218 | A | C | 1 | a0001c0001t0038 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2229T>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2229 | chr12 | 56204218 | ||||||
| chr12:56204220 | G | T | 1 | a0001c0001t0038 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2227C>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2227 | chr12 | 56204220 | ||||||
| chr12:56204222 | A | T | 1 | a0001c0001t0038 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2225T>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2225 | chr12 | 56204222 | ||||||
| chr12:56204223 | A | T | 1 | a0001c0001t0038 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2224T>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2224 | chr12 | 56204223 | ||||||
| chr12:56204226 | C | G | 1 | a0001c0001t0038 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2221G>C | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2221 | chr12 | 56204226 | ||||||
| chr12:56204228 | T | A | 1 | a0001c0001t0038 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2219A>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2219 | chr12 | 56204228 | ||||||
| chr12:56204260 | C | T | 32 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(29): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
3_prime_UTR_variant | MODIFIER | c.*2187G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2187 | chr12 | 56204260 | ||||||
| chr12:56204313 | G | C | 1 | a0001c0001t0042 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2134C>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 2134 | chr12 | 56204313 | ||||||
| chr12:56204583 | A | G | 1 | a0001c0001t0027 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1864T>C | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 1864 | chr12 | 56204583 | ||||||
| chr12:56204890 | T | C | 1 | a0001c0001t0021 | 2 | HG03130.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1557A>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 1557 | chr12 | 56204890 | ||||||
| chr12:56205001 | C | T | 1 | a0001c0001t0026 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1446G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 1446 | chr12 | 56205001 | ||||||
| chr12:56205044 | C | T | 12 | a0001c0001t0006 a0001c0001t0014 a0001c0001t0015 others(9): Show |
23 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1403G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 1403 | chr12 | 56205044 | ||||||
| chr12:56205322 | C | A | 1 | a0001c0001t0043 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1125G>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 1125 | chr12 | 56205322 | ||||||
| chr12:56205485 | TA | T | 52 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(49): Show |
328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
3_prime_UTR_variant | MODIFIER | c.*961delT | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 961 | chr12 | 56205485 | ||||||
| chr12:56205567 | A | AG | 5 | a0001c0001t0006 a0001c0001t0014 a0001c0001t0049 others(2): Show |
11 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*879dupC | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 879 | chr12 | 56205567 | ||||||
| chr12:56205568 | GA | G | 3 | a0001c0001t0025 a0002c0002t0024 a0002c0002t0050 |
3 | HG03139.hp2 HG03579.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*878delT | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 878 | chr12 | 56205568 | ||||||
| chr12:56205569 | A | AG | 18 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(15): Show |
43 | HG00423.hp2 HG00741.hp1 HG01109.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*877dupC | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 877 | chr12 | 56205569 | ||||||
| chr12:56205569 | A | G | 9 | a0001c0001t0006 a0001c0001t0014 a0001c0001t0015 others(6): Show |
20 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*878T>C | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 878 | chr12 | 56205569 | ||||||
| chr12:56205971 | G | A | 1 | a0001c0001t0047 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*476C>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 7/7 | 476 | chr12 | 56205971 | ||||||
| chr12:56221791 | C | G | 1 | a0001c0001t0049 | 1 | HG01891.hp2 | 5_prime_UTR_variant | MODIFIER | c.-240G>C | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/7 | 7744 | chr12 | 56221791 | ||||||
| chr12:56221831 | G | T | 9 | a0001c0001t0014 a0001c0001t0015 a0001c0001t0016 others(6): Show |
16 | HG01891.hp2 HG02145.hp1 HG02615.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-280C>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/7 | 7784 | chr12 | 56221831 | ||||||
| chr12:56221840 | C | A | 1 | a0001c0001t0048 | 1 | HG03486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-289G>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/7 | 7793 | chr12 | 56221840 | ||||||
| chr12:56221866 | G | A | 1 | a0001c0001t0022 | 2 | HG02895.hp1 HG02897.hp2 |
5_prime_UTR_variant | MODIFIER | c.-315C>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/7 | 7819 | chr12 | 56221866 | ||||||
| chr12:56221869 | G | A | 9 | a0001c0001t0014 a0001c0001t0015 a0001c0001t0016 others(6): Show |
16 | HG01891.hp2 HG02145.hp1 HG02615.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-318C>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/7 | 7822 | chr12 | 56221869 | ||||||
| chr12:56221878 | G | A | 1 | a0001c0001t0054 | 1 | HG03130.hp2 | 5_prime_UTR_variant | MODIFIER | c.-327C>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/7 | 7831 | chr12 | 56221878 | ||||||
| chr12:56221911 | G | A | 1 | a0001c0001t0009 | 4 | NA18964.hp1 NA18998.hp2 NA19080.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-360C>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/7 | 7864 | chr12 | 56221911 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:56206976 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.603-178G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 6/6 | chr12 | 56206976 | |||||||
| chr12:56207171 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.603-373A>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 6/6 | chr12 | 56207171 | |||||||
| chr12:56207405 | C | T | 1 | a0001c0001t0027g0120 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.602+241G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 6/6 | chr12 | 56207405 | |||||||
| chr12:56207453 | A | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(136): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.602+193T>C | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 6/6 | chr12 | 56207453 | |||||||
| chr12:56207787 | C | T | 2 | a0001c0001t0014g0177 a0001c0001t0015g0167 |
2 | HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.499-38G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 5/6 | chr12 | 56207787 | |||||||
| chr12:56207850 | A | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0057 a0001c0001t0001g0062 others(3): Show |
10 | HG02145.hp2 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.499-101T>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 5/6 | chr12 | 56207850 | |||||||
| chr12:56207955 | G | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(147): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.499-206C>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 5/6 | chr12 | 56207955 | |||||||
| chr12:56208543 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.363-245A>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 4/6 | chr12 | 56208543 | |||||||
| chr12:56208549 | T | C | 15 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0056 others(12): Show |
20 | HG00280.hp1 HG01081.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.363-251A>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 4/6 | chr12 | 56208549 | |||||||
| chr12:56208608 | AAACTGGA others(13): Show |
A | 1 | a0001c0001t0001g0092 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.363-330_363-311del others(20): Show |
RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 4/6 | chr12 | 56208608 | |||||||
| chr12:56208689 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.363-391G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 4/6 | chr12 | 56208689 | |||||||
| chr12:56208725 | C | T | 25 | a0001c0001t0006g0024 a0001c0001t0006g0043 a0001c0001t0006g0044 others(22): Show |
30 | HG00423.hp2 HG01884.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.363-427G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 4/6 | chr12 | 56208725 | |||||||
| chr12:56208817 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.363-519G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 4/6 | chr12 | 56208817 | |||||||
| chr12:56208865 | CT | C | 7 | a0001c0001t0001g0061 a0001c0001t0001g0089 a0001c0001t0001g0118 others(4): Show |
7 | HG02055.hp1 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.363-568delA | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 4/6 | chr12 | 56208865 | |||||||
| chr12:56208890 | G | C | 1 | a0001c0001t0030g0136 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.363-592C>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 4/6 | chr12 | 56208890 | |||||||
| chr12:56209027 | G | T | 1 | a0001c0001t0001g0030 | 2 | NA18947.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.363-729C>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 4/6 | chr12 | 56209027 | |||||||
| chr12:56209112 | G | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(136): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.363-814C>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 4/6 | chr12 | 56209112 | |||||||
| chr12:56209145 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.363-847C>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 4/6 | chr12 | 56209145 | |||||||
| chr12:56209154 | C | T | 1 | a0001c0001t0001g0035 | 2 | NA18974.hp1 NA19059.hp1 |
intron_variant | MODIFIER | c.363-856G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 4/6 | chr12 | 56209154 | |||||||
| chr12:56209235 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.363-937C>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 4/6 | chr12 | 56209235 | |||||||
| chr12:56209282 | C | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(120): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.363-984G>C | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 4/6 | chr12 | 56209282 | |||||||
| chr12:56209437 | A | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.362+860T>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 4/6 | chr12 | 56209437 | |||||||
| chr12:56209457 | A | AT | 18 | a0001c0001t0001g0078 a0001c0001t0001g0132 a0001c0001t0001g0149 others(15): Show |
20 | HG02145.hp1 HG02615.hp2 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.362+839dupA | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 4/6 | chr12 | 56209457 | |||||||
| chr12:56209602 | T | A | 13 | a0001c0001t0014g0171 a0001c0001t0014g0176 a0001c0001t0014g0177 others(10): Show |
15 | HG02145.hp1 HG02615.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.362+695A>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 4/6 | chr12 | 56209602 | |||||||
| chr12:56209657 | A | G | 8 | a0001c0001t0001g0010 a0001c0001t0001g0056 a0001c0001t0001g0057 others(5): Show |
12 | HG02145.hp2 HG02280.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.362+640T>C | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 4/6 | chr12 | 56209657 | |||||||
| chr12:56209692 | C | T | 21 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0033 others(18): Show |
33 | HG00423.hp1 HG00558.hp2 HG02027.hp2 others(30): Show |
intron_variant | MODIFIER | c.362+605G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 4/6 | chr12 | 56209692 | |||||||
| chr12:56209697 | T | C | 1 | a0001c0001t0001g0012 | 4 | HG01109.hp1 HG01192.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.362+600A>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 4/6 | chr12 | 56209697 | |||||||
| chr12:56209884 | G | C | 1 | a0001c0001t0041g0071 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.362+413C>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 4/6 | chr12 | 56209884 | |||||||
| chr12:56209952 | T | C | 1 | a0001c0001t0006g0043 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.362+345A>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 4/6 | chr12 | 56209952 | |||||||
| chr12:56209981 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.362+316G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 4/6 | chr12 | 56209981 | |||||||
| chr12:56210050 | G | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.362+247C>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 4/6 | chr12 | 56210050 | |||||||
| chr12:56210597 | G | A | 1 | a0001c0001t0021g0037 | 2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.91-29C>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 3/6 | chr12 | 56210597 | |||||||
| chr12:56210620 | G | A | 1 | a0001c0001t0023g0178 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.91-52C>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 3/6 | chr12 | 56210620 | |||||||
| chr12:56210632 | GAT | G | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.91-66_91-65delAT | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 3/6 | chr12 | 56210632 | |||||||
| chr12:56210636 | T | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.91-68A>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 3/6 | chr12 | 56210636 | |||||||
| chr12:56210689 | C | T | 12 | a0001c0001t0007g0013 a0001c0001t0007g0046 a0001c0001t0007g0048 others(9): Show |
18 | HG00423.hp2 HG02055.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.91-121G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 3/6 | chr12 | 56210689 | |||||||
| chr12:56210705 | T | C | 12 | a0001c0001t0007g0013 a0001c0001t0007g0046 a0001c0001t0007g0048 others(9): Show |
18 | HG00423.hp2 HG02055.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.91-137A>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 3/6 | chr12 | 56210705 | |||||||
| chr12:56210912 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.91-344G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 3/6 | chr12 | 56210912 | |||||||
| chr12:56211174 | GA | G | 6 | a0001c0001t0007g0013 a0001c0001t0007g0046 a0001c0001t0007g0048 others(3): Show |
9 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.91-607delT | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 3/6 | chr12 | 56211174 | |||||||
| chr12:56211201 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.91-633G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 3/6 | chr12 | 56211201 | |||||||
| chr12:56211270 | G | A | 1 | a0001c0001t0004g0087 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.91-702C>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 3/6 | chr12 | 56211270 | |||||||
| chr12:56211436 | A | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.91-868T>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 3/6 | chr12 | 56211436 | |||||||
| chr12:56211436 | A | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0155 a0001c0001t0004g0098 others(2): Show |
7 | HG01109.hp2 HG02559.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.91-868T>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 3/6 | chr12 | 56211436 | |||||||
| chr12:56211517 | CAAT | C | 6 | a0001c0001t0007g0013 a0001c0001t0007g0046 a0001c0001t0007g0048 others(3): Show |
9 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.91-952_91-950delAT others(1): Show |
RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 3/6 | chr12 | 56211517 | |||||||
| chr12:56211535 | T | C | 2 | a0001c0001t0003g0011 a0001c0001t0003g0051 |
5 | HG01884.hp2 HG02615.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.91-967A>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 3/6 | chr12 | 56211535 | |||||||
| chr12:56211621 | A | G | 1 | a0001c0001t0018g0100 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.91-1053T>C | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 3/6 | chr12 | 56211621 | |||||||
| chr12:56212159 | A | T | 2 | a0001c0001t0016g0022 a0001c0001t0052g0168 |
4 | HG02615.hp2 HG02895.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-1591T>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 3/6 | chr12 | 56212159 | |||||||
| chr12:56212438 | T | C | 6 | a0001c0001t0007g0013 a0001c0001t0007g0046 a0001c0001t0007g0048 others(3): Show |
9 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.90+1520A>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 3/6 | chr12 | 56212438 | |||||||
| chr12:56212560 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.90+1398T>C | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 3/6 | chr12 | 56212560 | |||||||
| chr12:56212701 | T | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG00408.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.90+1257A>C | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 3/6 | chr12 | 56212701 | |||||||
| chr12:56212779 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.90+1179A>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 3/6 | chr12 | 56212779 | |||||||
| chr12:56212978 | C | T | 2 | a0001c0001t0006g0024 a0001c0001t0006g0044 |
3 | HG01884.hp1 HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.90+980G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 3/6 | chr12 | 56212978 | |||||||
| chr12:56213175 | C | T | 5 | a0001c0001t0013g0016 a0001c0001t0039g0111 a0001c0001t0040g0069 others(2): Show |
7 | HG00423.hp2 NA18945.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.90+783G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 3/6 | chr12 | 56213175 | |||||||
| chr12:56213233 | C | T | 10 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0077 others(7): Show |
13 | HG01109.hp2 HG02040.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.90+725G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 3/6 | chr12 | 56213233 | |||||||
| chr12:56213263 | C | A | 1 | a0001c0001t0001g0081 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.90+695G>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 3/6 | chr12 | 56213263 | |||||||
| chr12:56213538 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.90+420G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 3/6 | chr12 | 56213538 | |||||||
| chr12:56213855 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.90+103T>C | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 3/6 | chr12 | 56213855 | |||||||
| chr12:56213881 | C | T | 1 | a0001c0001t0043g0160 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.90+77G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 3/6 | chr12 | 56213881 | |||||||
| chr12:56214143 | C | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.-23-73G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 2/6 | chr12 | 56214143 | |||||||
| chr12:56214520 | TA | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.-23-451delT | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 2/6 | chr12 | 56214520 | |||||||
| chr12:56214520 | TAA | T | 16 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0056 others(13): Show |
21 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.-23-452_-23-451del others(2): Show |
RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 2/6 | chr12 | 56214520 | |||||||
| chr12:56214689 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-23-619G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 2/6 | chr12 | 56214689 | |||||||
| chr12:56214923 | G | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.-23-853C>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 2/6 | chr12 | 56214923 | |||||||
| chr12:56215041 | T | A | 1 | a0001c0001t0001g0119 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-23-971A>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 2/6 | chr12 | 56215041 | |||||||
| chr12:56215163 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-23-1093G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 2/6 | chr12 | 56215163 | |||||||
| chr12:56215289 | T | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG01243.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-24+1140A>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 2/6 | chr12 | 56215289 | |||||||
| chr12:56215420 | G | C | 2 | a0001c0001t0014g0177 a0001c0001t0015g0167 |
2 | HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-24+1009C>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 2/6 | chr12 | 56215420 | |||||||
| chr12:56215442 | C | A | 1 | a0001c0001t0001g0113 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-24+987G>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 2/6 | chr12 | 56215442 | |||||||
| chr12:56215530 | C | T | 1 | a0001c0001t0021g0037 | 2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-24+899G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 2/6 | chr12 | 56215530 | |||||||
| chr12:56215543 | A | C | 1 | a0001c0001t0001g0092 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-24+886T>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 2/6 | chr12 | 56215543 | |||||||
| chr12:56215548 | G | A | 19 | a0001c0001t0006g0024 a0001c0001t0006g0043 a0001c0001t0006g0044 others(16): Show |
22 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.-24+881C>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 2/6 | chr12 | 56215548 | |||||||
| chr12:56215582 | G | C | 1 | a0001c0001t0001g0036 | 2 | HG02129.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.-24+847C>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 2/6 | chr12 | 56215582 | |||||||
| chr12:56215717 | C | CA | 9 | a0001c0001t0001g0010 a0001c0001t0001g0056 a0001c0001t0001g0057 others(6): Show |
13 | HG01891.hp1 HG01891.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-24+711dupT | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 2/6 | chr12 | 56215717 | |||||||
| chr12:56215717 | CA | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(111): Show |
223 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.-24+711delT | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 2/6 | chr12 | 56215717 | |||||||
| chr12:56215724 | A | G | 5 | a0001c0001t0001g0068 a0001c0001t0013g0016 a0001c0001t0040g0069 others(2): Show |
7 | NA18945.hp2 NA18946.hp1 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.-24+705T>C | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 2/6 | chr12 | 56215724 | |||||||
| chr12:56215737 | A | G | 1 | a0001c0001t0003g0049 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-24+692T>C | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 2/6 | chr12 | 56215737 | |||||||
| chr12:56215896 | T | A | 1 | a0001c0001t0001g0092 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-24+533A>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 2/6 | chr12 | 56215896 | |||||||
| chr12:56216069 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-24+360G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 2/6 | chr12 | 56216069 | |||||||
| chr12:56216101 | G | A | 27 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(24): Show |
76 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.-24+328C>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 2/6 | chr12 | 56216101 | |||||||
| chr12:56216141 | C | A | 2 | a0001c0001t0014g0176 a0001c0001t0051g0175 |
2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-24+288G>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 2/6 | chr12 | 56216141 | |||||||
| chr12:56216868 | T | C | 2 | a0001c0001t0001g0084 a0001c0001t0027g0120 |
2 | HG03942.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-208-255A>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56216868 | |||||||
| chr12:56216885 | A | T | 1 | a0001c0001t0001g0092 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-208-272T>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56216885 | |||||||
| chr12:56217139 | TA | T | 7 | a0001c0001t0001g0059 a0001c0001t0001g0092 a0001c0001t0001g0122 others(4): Show |
7 | HG01169.hp1 HG02897.hp1 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.-208-527delT | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56217139 | |||||||
| chr12:56217231 | A | T | 1 | a0001c0001t0001g0092 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-208-618T>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56217231 | |||||||
| chr12:56217266 | C | A | 1 | a0001c0001t0002g0121 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-208-653G>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56217266 | |||||||
| chr12:56217275 | G | A | 13 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0056 others(10): Show |
18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-208-662C>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56217275 | |||||||
| chr12:56217285 | G | A | 1 | a0001c0001t0014g0177 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-208-672C>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56217285 | |||||||
| chr12:56217362 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-208-749G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56217362 | |||||||
| chr12:56217470 | C | G | 5 | a0001c0001t0001g0068 a0001c0001t0013g0016 a0001c0001t0040g0069 others(2): Show |
7 | NA18945.hp2 NA18946.hp1 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.-208-857G>C | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56217470 | |||||||
| chr12:56217657 | C | G | 1 | a0001c0001t0003g0051 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-208-1044G>C | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56217657 | |||||||
| chr12:56217789 | C | T | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | NA19009.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-208-1176G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56217789 | |||||||
| chr12:56217882 | A | C | 1 | a0001c0001t0001g0092 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-208-1269T>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56217882 | |||||||
| chr12:56217954 | AATTATT | A | 15 | a0001c0001t0014g0171 a0001c0001t0014g0176 a0001c0001t0014g0177 others(12): Show |
17 | HG01891.hp2 HG02145.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.-208-1347_-208-134 others(10): Show |
RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56217954 | |||||||
| chr12:56217965 | T | C | 1 | a0001c0003t0012g0025 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-208-1352A>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56217965 | |||||||
| chr12:56218245 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0015g0167 |
3 | HG02717.hp1 HG03041.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-208-1632G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56218245 | |||||||
| chr12:56218262 | T | A | 1 | a0001c0001t0001g0092 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-208-1649A>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56218262 | |||||||
| chr12:56218264 | A | T | 1 | a0001c0001t0001g0092 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-208-1651T>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56218264 | |||||||
| chr12:56218265 | T | A | 1 | a0001c0001t0001g0092 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-208-1652A>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56218265 | |||||||
| chr12:56218344 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-208-1731G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56218344 | |||||||
| chr12:56218373 | C | T | 5 | a0001c0001t0001g0068 a0001c0001t0013g0016 a0001c0001t0040g0069 others(2): Show |
7 | NA18945.hp2 NA18946.hp1 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.-208-1760G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56218373 | |||||||
| chr12:56218527 | G | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.-208-1914C>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56218527 | |||||||
| chr12:56218564 | C | A | 1 | a0001c0001t0001g0091 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-208-1951G>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56218564 | |||||||
| chr12:56218714 | T | C | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | NA18948.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.-208-2101A>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56218714 | |||||||
| chr12:56218909 | G | A | 12 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0040 others(9): Show |
45 | HG00408.hp2 HG00544.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.-208-2296C>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56218909 | |||||||
| chr12:56218980 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-208-2367C>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56218980 | |||||||
| chr12:56219009 | C | CT | 7 | a0001c0001t0001g0092 a0001c0001t0004g0154 a0001c0001t0006g0024 others(4): Show |
8 | HG01884.hp1 HG01891.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-208-2397dupA | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56219009 | |||||||
| chr12:56219195 | A | AT | 3 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0004g0080 |
3 | HG00741.hp1 NA18955.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-209+2564dupA | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56219195 | |||||||
| chr12:56219195 | A | T | 8 | a0001c0001t0001g0034 a0001c0001t0001g0161 a0001c0001t0002g0020 others(5): Show |
9 | HG00558.hp1 HG02055.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-209+2565T>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56219195 | |||||||
| chr12:56219198 | TA | T | 6 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(3): Show |
6 | HG02602.hp1 HG02602.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-209+2561delT | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56219198 | |||||||
| chr12:56219199 | A | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(124): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.-209+2561T>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56219199 | |||||||
| chr12:56219203 | T | A | 1 | a0001c0001t0001g0066 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-209+2557A>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56219203 | |||||||
| chr12:56219213 | A | G | 1 | a0001c0001t0003g0050 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-209+2547T>C | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56219213 | |||||||
| chr12:56219447 | G | A | 1 | a0001c0001t0023g0178 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-209+2313C>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56219447 | |||||||
| chr12:56219651 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-209+2109C>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56219651 | |||||||
| chr12:56219660 | T | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.-209+2100A>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56219660 | |||||||
| chr12:56219662 | T | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.-209+2098A>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56219662 | |||||||
| chr12:56219663 | G | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.-209+2097C>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56219663 | |||||||
| chr12:56219665 | G | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.-209+2095C>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56219665 | |||||||
| chr12:56219668 | T | TACACACA others(1): Show |
7 | a0001c0001t0001g0068 a0001c0001t0001g0086 a0001c0001t0004g0087 others(4): Show |
9 | HG00323.hp2 HG01175.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.-209+2091_-209+209 others(12): Show |
RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56219668 | |||||||
| chr12:56219668 | T | TACACACA others(5): Show |
142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(139): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.-209+2091_-209+209 others(16): Show |
RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56219668 | |||||||
| chr12:56219668 | T | TACACACA others(7): Show |
3 | a0001c0001t0001g0124 a0001c0001t0001g0153 a0001c0001t0009g0180 |
3 | NA18989.hp2 NA18998.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-209+2091_-209+209 others(18): Show |
RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56219668 | |||||||
| chr12:56219670 | T | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.-209+2090A>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56219670 | |||||||
| chr12:56219673 | A | ACACACAC others(5): Show |
1 | a0001c0001t0001g0085 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-209+2086_-209+208 others(16): Show |
RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56219673 | |||||||
| chr12:56219756 | C | T | 1 | a0001c0001t0007g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-209+2004G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56219756 | |||||||
| chr12:56219757 | G | A | 19 | a0001c0001t0001g0003 a0001c0001t0001g0073 a0001c0001t0001g0125 others(16): Show |
35 | HG00621.hp1 HG01175.hp1 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.-209+2003C>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56219757 | |||||||
| chr12:56219992 | G | C | 1 | a0001c0001t0001g0126 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-209+1768C>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56219992 | |||||||
| chr12:56220018 | A | AAAAT | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(84): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.-209+1738_-209+174 others(8): Show |
RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56220018 | |||||||
| chr12:56220018 | A | AAAATAAA others(1): Show |
9 | a0001c0001t0001g0027 a0001c0001t0001g0077 a0001c0001t0001g0078 others(6): Show |
10 | HG00280.hp1 HG00741.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-209+1734_-209+174 others(12): Show |
RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56220018 | |||||||
| chr12:56220018 | AAAAT | A | 40 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0038 others(37): Show |
53 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.-209+1738_-209+174 others(8): Show |
RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56220018 | |||||||
| chr12:56220056 | A | C | 2 | a0001c0001t0003g0009 a0001c0001t0003g0049 |
6 | HG01243.hp2 HG02451.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-209+1704T>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56220056 | |||||||
| chr12:56220060 | T | A | 1 | a0001c0001t0002g0020 | 3 | HG00558.hp1 NA18994.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-209+1700A>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56220060 | |||||||
| chr12:56220157 | G | A | 15 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0056 others(12): Show |
22 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.-209+1603C>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56220157 | |||||||
| chr12:56220497 | G | A | 12 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0040 others(9): Show |
45 | HG00408.hp2 HG00544.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.-209+1263C>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56220497 | |||||||
| chr12:56220512 | C | T | 1 | a0001c0001t0049g0166 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-209+1248G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56220512 | |||||||
| chr12:56220730 | C | CA | 7 | a0001c0001t0001g0021 a0001c0001t0001g0155 a0001c0001t0001g0156 others(4): Show |
9 | HG01175.hp1 HG02056.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.-209+1029dupT | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56220730 | |||||||
| chr12:56220730 | CA | C | 6 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0003g0049 others(3): Show |
6 | HG02451.hp2 HG02895.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.-209+1029delT | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56220730 | |||||||
| chr12:56220859 | A | G | 5 | a0001c0001t0001g0068 a0001c0001t0013g0016 a0001c0001t0040g0069 others(2): Show |
7 | NA18945.hp2 NA18946.hp1 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.-209+901T>C | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56220859 | |||||||
| chr12:56220903 | T | C | 4 | a0001c0001t0001g0041 a0001c0001t0001g0161 a0001c0001t0001g0162 others(1): Show |
5 | NA18950.hp2 NA18953.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-209+857A>G | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56220903 | |||||||
| chr12:56221037 | T | A | 1 | a0001c0001t0001g0067 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-209+723A>T | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56221037 | |||||||
| chr12:56221479 | T | G | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.-209+281A>C | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56221479 | |||||||
| chr12:56221571 | C | T | 10 | a0001c0001t0006g0024 a0001c0001t0006g0043 a0001c0001t0006g0044 others(7): Show |
14 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-209+189G>A | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56221571 | |||||||
| chr12:56221740 | C | G | 1 | a0001c0001t0001g0042 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-209+20G>C | RNF41 | ENSG00000181852.18 | transcript | ENST00000345093.9 | protein_coding | 1/6 | chr12 | 56221740 |