Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9921 |
| ensemblid | ENSG00000022840.17 |
| hgncid | 10055 |
| symbol | RNF10 |
| name | ring finger protein 10 |
| refseq_nuc | NM_014868.5 |
| refseq_prot | NP_055683.3 |
| ensembl_nuc | ENST00000325954.9 |
| ensembl_prot | ENSP00000322242.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 120534356 |
| end | 120577588 |
| strand | + |
| ver | v1.2 |
| region | chr12:120534356-120577588 |
| region5000 | chr12:120529356-120582588 |
| regionname0 | RNF10_chr12_120534356_120577588 |
| regionname5000 | RNF10_chr12_120529356_120582588 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 811 | 365 | 87 | 72 | 156 | 14 | 34 | 116 | RNF10_chr12_120529356_120582588 | RNF10 | MPLSS others(806): Show |
chr12 | 120529356 | 120582588 |
| a0002 | 0/0 | 811 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | MPLSS others(806): Show |
chr12 | 120529356 | 120582588 |
| a0003 | 0/0 | 811 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | MPLSS others(806): Show |
chr12 | 120529356 | 120582588 |
| a0004 | 0/0 | 811 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | MPLSS others(806): Show |
chr12 | 120529356 | 120582588 |
| a0005 | 0/0 | 811 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | MPLSS others(806): Show |
chr12 | 120529356 | 120582588 |
| a0006 | 0/0 | 811 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | MPLSS others(806): Show |
chr12 | 120529356 | 120582588 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2433 | 357 | 87 | 67 | 153 | 14 | 34 | RNF10_chr12_120529356_120582588 | RNF10 | ATGCC others(2428): Show |
chr12 | 120529356 | 120582588 | ||
| a0001c0003 | 0/0 | 2433 | 3 | 0 | 3 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | ATGCC others(2428): Show |
chr12 | 120529356 | 120582588 | ||
| a0001c0004 | 0/0 | 2433 | 2 | 0 | 0 | 2 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | ATGCC others(2428): Show |
chr12 | 120529356 | 120582588 | ||
| a0001c0005 | 0/0 | 2433 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | ATGCC others(2428): Show |
chr12 | 120529356 | 120582588 | ||
| a0001c0010 | 0/0 | 2433 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | ATGCC others(2428): Show |
chr12 | 120529356 | 120582588 | ||
| a0001c0011 | 0/0 | 2433 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | ATGCC others(2428): Show |
chr12 | 120529356 | 120582588 | ||
| a0002c0002 | 0/0 | 2433 | 3 | 3 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | ATGCC others(2428): Show |
chr12 | 120529356 | 120582588 | ||
| a0003c0006 | 0/0 | 2433 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | ATGCC others(2428): Show |
chr12 | 120529356 | 120582588 | ||
| a0004c0009 | 0/0 | 2433 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | ATGCC others(2428): Show |
chr12 | 120529356 | 120582588 | ||
| a0005c0007 | 0/0 | 2433 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | ATGCC others(2428): Show |
chr12 | 120529356 | 120582588 | ||
| a0006c0008 | 0/0 | 2433 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | ATGCC others(2428): Show |
chr12 | 120529356 | 120582588 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3814 | 249 | 73 | 47 | 101 | 7 | 20 | RNF10_chr12_120529356_120582588 | RNF10 | GCTGT others(3809): Show |
chr12 | 120529356 | 120582588 |
| a0001c0001t0002 | 0/1 | 3814 | 91 | 4 | 17 | 50 | 7 | 12 | RNF10_chr12_120529356_120582588 | RNF10 | GCTGT others(3809): Show |
chr12 | 120529356 | 120582588 |
| a0001c0001t0003 | 0/0 | 3811 | 12 | 9 | 3 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | GCTGT others(3806): Show |
chr12 | 120529356 | 120582588 |
| a0001c0001t0004 | 0/0 | 3814 | 2 | 0 | 0 | 0 | 0 | 2 | RNF10_chr12_120529356_120582588 | RNF10 | GCTGT others(3809): Show |
chr12 | 120529356 | 120582588 |
| a0001c0001t0006 | 0/0 | 3814 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | GCTGT others(3809): Show |
chr12 | 120529356 | 120582588 |
| a0001c0001t0007 | 0/0 | 3814 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | GCTGT others(3809): Show |
chr12 | 120529356 | 120582588 |
| a0001c0001t0008 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | GCTGT others(3809): Show |
chr12 | 120529356 | 120582588 |
| a0001c0003t0002 | 0/0 | 3814 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | GCTGT others(3809): Show |
chr12 | 120529356 | 120582588 |
| a0001c0003t0005 | 0/0 | 3814 | 2 | 0 | 2 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | GCTGT others(3809): Show |
chr12 | 120529356 | 120582588 |
| a0001c0004t0001 | 0/0 | 3814 | 2 | 0 | 0 | 2 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | GCTGT others(3809): Show |
chr12 | 120529356 | 120582588 |
| a0001c0005t0002 | 0/0 | 3814 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | GCTGT others(3809): Show |
chr12 | 120529356 | 120582588 |
| a0001c0010t0001 | 0/0 | 3814 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | GCTGT others(3809): Show |
chr12 | 120529356 | 120582588 |
| a0001c0011t0001 | 0/0 | 3814 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | GCTGT others(3809): Show |
chr12 | 120529356 | 120582588 |
| a0002c0002t0001 | 0/0 | 3814 | 3 | 3 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | GCTGT others(3809): Show |
chr12 | 120529356 | 120582588 |
| a0003c0006t0001 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | GCTGT others(3809): Show |
chr12 | 120529356 | 120582588 |
| a0004c0009t0001 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | GCTGT others(3809): Show |
chr12 | 120529356 | 120582588 |
| a0005c0007t0001 | 0/0 | 3814 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | GCTGT others(3809): Show |
chr12 | 120529356 | 120582588 |
| a0006c0008t0001 | 0/0 | 3814 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | GCTGT others(3809): Show |
chr12 | 120529356 | 120582588 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0004 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0257 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0199 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0003g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0003g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0003g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0003g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0003g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0007g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0001t0008g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0003t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0003t0005g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0003t0005g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0004t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0004t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0005t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0010t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0001c0011t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0002c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0002c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0002c0002t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0003c0006t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0004c0009t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0005c0007t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| a0006c0008t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0193 | EUR | GBR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0316 | EUR | GBR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | GBR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0164 | EUR | GBR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0224 | EUR | FIN | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0135 | EUR | FIN | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0146 | EUR | FIN | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0043 | EUR | FIN | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | CHS | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | CHS | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | CHS | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | CHS | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | CHS | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | CHS | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | CHS | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | CHS | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01081 | hp2 | a0001 | c0003 | t0002 | g0165 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0331 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0330 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01256 | hp2 | a0001 | c0003 | t0005 | g0180 | AMR | CLM | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01258 | hp1 | a0001 | c0003 | t0005 | g0154 | AMR | CLM | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | CLM | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0341 | AMR | CLM | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0153 | AMR | CLM | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0139 | AMR | CLM | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | CLM | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0171 | EUR | IBS | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0342 | EUR | IBS | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0013 | EUR | IBS | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0340 | EUR | IBS | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01884 | hp2 | a0003 | c0006 | t0001 | g0062 | AFR | ACB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PEL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PEL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01943 | hp2 | a0001 | c0005 | t0002 | g0130 | AMR | PEL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PEL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | KHV | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | KHV | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | KHV | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | KHV | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | KHV | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | KHV | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | ACB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | CDX | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CDX | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | ACB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PEL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02273 | hp2 | a0001 | c0010 | t0001 | g0077 | AMR | PEL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0136 | SAS | PJL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0332 | AFR | GWD | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0328 | AFR | GWD | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | GWD | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0283 | AFR | GWD | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | PJL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0281 | AFR | GWD | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0145 | SAS | PJL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0206 | SAS | PJL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0282 | AFR | GWD | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0333 | AFR | GWD | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ESN | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ESN | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | MSL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0329 | AFR | ESN | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ESN | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0327 | AFR | MSL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | MSL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0205 | SAS | PJL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0343 | SAS | PJL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | MSL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0326 | AFR | MSL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0061 | AFR | MSL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0334 | AFR | MSL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0314 | SAS | PJL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0325 | AFR | MSL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | MSL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0064 | SAS | PJL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | STU | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | STU | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0176 | SAS | PJL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0066 | SAS | PJL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | BEB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0157 | SAS | BEB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0344 | SAS | BEB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | BEB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | STU | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | STU | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0338 | SAS | STU | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0175 | SAS | STU | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0195 | SAS | STU | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | STU | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | CHB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | CHB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18944 | hp1 | a0005 | c0007 | t0001 | g0241 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18950 | hp1 | a0001 | c0004 | t0001 | g0231 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18985 | hp1 | a0001 | c0001 | t0006 | g0138 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18989 | hp2 | a0006 | c0008 | t0001 | g0056 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19003 | hp2 | a0001 | c0011 | t0001 | g0094 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | LWK | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | LWK | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | LWK | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | LWK | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19067 | hp1 | a0001 | c0004 | t0001 | g0215 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19088 | hp1 | a0001 | c0001 | t0007 | g0089 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ASW | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ASW | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0160 | EUR | TSI | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0291 | EUR | TSI | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | CLM | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | CLM | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02486 | hp2 | a0004 | c0009 | t0001 | g0248 | AFR | ACB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | MSL | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | USA | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | USA | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | USA | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | LWK | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | LWK | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0199 | REF | REF | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0257 | REF | REF | RNF10_chr12_120529356_120582588 | RNF10 | chr12 | 120529356 | 120582588 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:120560741 | A | C | 1 | a0004 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.983A>C | p.Gln328Pro | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 7/17 | 1439/3814 | 983/2436 | 328/811 | chr12 | 120560741 | |||
| chr12:120562975 | G | A | 1 | a0002 | 3 | HG02630.hp2 HG02717.hp1 HG02818.hp1 |
missense_variant | MODERATE | c.1159G>A | p.Gly387Arg | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 8/17 | 1615/3814 | 1159/2436 | 387/811 | chr12 | 120562975 | |||
| chr12:120565094 | A | C | 1 | a0006 | 1 | NA18989.hp2 | missense_variant | MODERATE | c.1688A>C | p.Tyr563Ser | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 11/17 | 2144/3814 | 1688/2436 | 563/811 | chr12 | 120565094 | |||
| chr12:120566897 | A | C | 1 | a0005 | 1 | NA18944.hp1 | missense_variant | MODERATE | c.1958A>C | p.Asp653Ala | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/17 | 2414/3814 | 1958/2436 | 653/811 | chr12 | 120566897 | |||
| chr12:120575896 | A | C | 1 | a0003 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.2305A>C | p.Ile769Leu | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 16/17 | 2761/3814 | 2305/2436 | 769/811 | chr12 | 120575896 | |||
| chr12:120577587 | C | T | 1 | a0001 | 2 | HG01256.hp2 HG01258.hp1 |
splice_region_variant | LOW | c.*921C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 17/17 | chr12 | 120577587 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:120534904 | C | T | 1 | a0001c0011 | 1 | NA19003.hp2 | synonymous_variant | LOW | c.93C>T | p.Ser31Ser | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/17 | 549/3814 | 93/2436 | 31/811 | chr12 | 120534904 | |||
| chr12:120546499 | C | T | 1 | a0001c0010 | 1 | HG02273.hp2 | synonymous_variant | LOW | c.252C>T | p.Ser84Ser | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/17 | 708/3814 | 252/2436 | 84/811 | chr12 | 120546499 | |||
| chr12:120563043 | G | A | 1 | a0001c0003 | 3 | HG01081.hp2 HG01256.hp2 HG01258.hp1 |
synonymous_variant | LOW | c.1227G>A | p.Ala409Ala | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 8/17 | 1683/3814 | 1227/2436 | 409/811 | chr12 | 120563043 | |||
| chr12:120563361 | T | C | 1 | a0001c0005 | 1 | HG01943.hp2 | synonymous_variant | LOW | c.1269T>C | p.Tyr423Tyr | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 9/17 | 1725/3814 | 1269/2436 | 423/811 | chr12 | 120563361 | |||
| chr12:120565174 | C | T | 1 | a0001c0004 | 2 | NA18950.hp1 NA19067.hp1 |
synonymous_variant | LOW | c.1768C>T | p.Leu590Leu | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 11/17 | 2224/3814 | 1768/2436 | 590/811 | chr12 | 120565174 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:120534592 | GCCT | G | 1 | a0001c0001t0003 | 12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-215_-213delCTC | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/17 | 213 | INFO_REALIGN_3_PRIME | chr12 | 120534592 | |||||
| chr12:120534593 | C | T | 2 | a0001c0001t0001 a0006c0008t0001 |
64 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(61): Show |
5_prime_UTR_variant | MODIFIER | c.-219C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/17 | 219 | chr12 | 120534593 | ||||||
| chr12:120576904 | G | A | 1 | a0001c0001t0004 | 2 | HG03669.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*238G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 17/17 | 238 | chr12 | 120576904 | ||||||
| chr12:120576914 | C | A | 1 | a0001c0001t0006 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*248C>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 17/17 | 248 | chr12 | 120576914 | ||||||
| chr12:120577001 | C | T | 1 | a0001c0001t0008 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*335C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 17/17 | 335 | chr12 | 120577001 | ||||||
| chr12:120577038 | G | C | 5 | a0001c0001t0002 a0001c0001t0006 a0001c0003t0002 others(2): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*372G>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 17/17 | 372 | chr12 | 120577038 | ||||||
| chr12:120577365 | A | G | 1 | a0001c0001t0003 | 12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*699A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 17/17 | 699 | chr12 | 120577365 | ||||||
| chr12:120577431 | C | T | 1 | a0001c0001t0007 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*765C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 17/17 | 765 | chr12 | 120577431 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:120535036 | A | T | 5 | a0001c0001t0001g0340 a0001c0001t0001g0341 a0001c0001t0001g0342 others(2): Show |
5 | HG01261.hp2 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.157+68A>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120535036 | |||||||
| chr12:120535191 | G | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0339 |
3 | NA18945.hp1 NA18971.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.157+223G>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120535191 | |||||||
| chr12:120535302 | C | T | 1 | a0001c0001t0001g0338 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.157+334C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120535302 | |||||||
| chr12:120535436 | C | T | 1 | a0001c0001t0001g0337 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.157+468C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120535436 | |||||||
| chr12:120535448 | G | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(4): Show |
9 | HG01109.hp2 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.157+480G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120535448 | |||||||
| chr12:120535472 | C | A | 1 | a0001c0001t0001g0029 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.157+504C>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120535472 | |||||||
| chr12:120535606 | A | C | 5 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0026 others(2): Show |
6 | HG01109.hp2 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.157+638A>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120535606 | |||||||
| chr12:120535747 | C | G | 1 | a0001c0001t0002g0336 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.157+779C>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120535747 | |||||||
| chr12:120535825 | A | C | 1 | a0001c0001t0001g0335 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.157+857A>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120535825 | |||||||
| chr12:120535867 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.157+899T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120535867 | |||||||
| chr12:120535929 | T | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(30): Show |
39 | HG00323.hp2 HG00408.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.157+961T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120535929 | |||||||
| chr12:120535966 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.157+998T>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120535966 | |||||||
| chr12:120536088 | T | C | 2 | a0001c0001t0008g0061 a0003c0006t0001g0062 |
2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.157+1120T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120536088 | |||||||
| chr12:120536169 | C | G | 1 | a0001c0001t0002g0334 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.157+1201C>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120536169 | |||||||
| chr12:120536372 | C | G | 10 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0326 others(7): Show |
12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.157+1404C>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120536372 | |||||||
| chr12:120536417 | C | T | 1 | a0001c0001t0002g0325 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.157+1449C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120536417 | |||||||
| chr12:120536464 | C | CA | 11 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0001c0001t0001g0067 others(8): Show |
11 | HG01106.hp1 HG01169.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.157+1504dupA | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 120536464 | ||||||
| chr12:120536532 | G | C | 1 | a0001c0001t0002g0325 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.157+1564G>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120536532 | |||||||
| chr12:120536586 | G | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(4): Show |
9 | HG01109.hp2 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.157+1618G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120536586 | |||||||
| chr12:120536614 | C | G | 2 | a0001c0001t0001g0323 a0001c0001t0001g0324 |
2 | HG02040.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.157+1646C>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120536614 | |||||||
| chr12:120536647 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.157+1679A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120536647 | |||||||
| chr12:120536683 | G | C | 1 | a0001c0001t0001g0060 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.157+1715G>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120536683 | |||||||
| chr12:120536707 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(51): Show |
64 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.157+1739C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120536707 | |||||||
| chr12:120536794 | A | G | 1 | a0001c0001t0002g0309 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.157+1826A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120536794 | |||||||
| chr12:120537162 | C | T | 1 | a0001c0001t0001g0308 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.157+2194C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120537162 | |||||||
| chr12:120537340 | A | T | 1 | a0001c0001t0001g0307 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.157+2372A>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120537340 | |||||||
| chr12:120537347 | C | T | 55 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(52): Show |
60 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.157+2379C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120537347 | |||||||
| chr12:120537640 | T | A | 15 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0260 others(12): Show |
16 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.157+2672T>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120537640 | |||||||
| chr12:120537944 | C | A | 12 | a0001c0001t0001g0016 a0001c0001t0001g0273 a0001c0001t0001g0274 others(9): Show |
13 | HG02145.hp1 HG02559.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.157+2976C>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120537944 | |||||||
| chr12:120538441 | C | T | 10 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0326 others(7): Show |
12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.157+3473C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120538441 | |||||||
| chr12:120538453 | C | T | 10 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0326 others(7): Show |
12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.157+3485C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120538453 | |||||||
| chr12:120538568 | T | C | 19 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(16): Show |
22 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(19): Show |
intron_variant | MODIFIER | c.157+3600T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120538568 | |||||||
| chr12:120538731 | C | G | 1 | a0001c0001t0001g0059 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.157+3763C>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120538731 | |||||||
| chr12:120538788 | T | A | 1 | a0001c0001t0001g0069 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.157+3820T>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120538788 | |||||||
| chr12:120538805 | G | C | 1 | a0001c0001t0001g0070 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.157+3837G>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120538805 | |||||||
| chr12:120538822 | G | A | 65 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(62): Show |
67 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.157+3854G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120538822 | |||||||
| chr12:120538936 | G | A | 1 | a0001c0001t0002g0128 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.157+3968G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120538936 | |||||||
| chr12:120538993 | G | T | 15 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0260 others(12): Show |
16 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.157+4025G>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120538993 | |||||||
| chr12:120539111 | C | T | 2 | a0001c0001t0001g0297 a0001c0001t0001g0298 |
2 | HG00558.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.157+4143C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120539111 | |||||||
| chr12:120539375 | A | G | 1 | a0001c0001t0001g0344 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.157+4407A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120539375 | |||||||
| chr12:120539426 | T | C | 1 | a0001c0001t0003g0326 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.157+4458T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120539426 | |||||||
| chr12:120539543 | G | A | 1 | a0001c0001t0001g0307 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.157+4575G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120539543 | |||||||
| chr12:120539578 | T | C | 87 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(84): Show |
93 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.157+4610T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120539578 | |||||||
| chr12:120539627 | G | T | 2 | a0001c0001t0008g0061 a0003c0006t0001g0062 |
2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.157+4659G>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120539627 | |||||||
| chr12:120539801 | G | T | 10 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0326 others(7): Show |
12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.157+4833G>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120539801 | |||||||
| chr12:120539890 | C | G | 1 | a0001c0001t0002g0208 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.157+4922C>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120539890 | |||||||
| chr12:120539995 | G | A | 89 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(86): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.157+5027G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120539995 | |||||||
| chr12:120540015 | A | G | 89 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(86): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.157+5047A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120540015 | |||||||
| chr12:120540078 | T | TA | 13 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(10): Show |
16 | HG01070.hp1 HG01071.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.157+5124dupA | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 120540078 | ||||||
| chr12:120540078 | TA | T | 96 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0340 others(93): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.157+5124delA | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 120540078 | ||||||
| chr12:120540078 | TAAAAA | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(51): Show |
64 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.157+5120_157+5124d others(7): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 120540078 | ||||||
| chr12:120540078 | TAAAAAAA | T | 26 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(23): Show |
29 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.157+5118_157+5124d others(9): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 120540078 | ||||||
| chr12:120540130 | C | CT | 5 | a0001c0001t0001g0014 a0001c0001t0001g0259 a0001c0001t0002g0207 others(2): Show |
6 | HG00609.hp1 HG02738.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.157+5174dupT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 120540130 | ||||||
| chr12:120540130 | CT | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(220): Show |
244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.157+5174delT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 120540130 | ||||||
| chr12:120540207 | C | A | 1 | a0001c0001t0003g0327 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.157+5239C>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120540207 | |||||||
| chr12:120540350 | G | A | 10 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0326 others(7): Show |
12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.157+5382G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120540350 | |||||||
| chr12:120540650 | G | C | 1 | a0001c0001t0001g0031 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.157+5682G>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120540650 | |||||||
| chr12:120540686 | A | G | 26 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(23): Show |
29 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.157+5718A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120540686 | |||||||
| chr12:120540824 | C | T | 2 | a0001c0001t0002g0205 a0001c0001t0002g0206 |
2 | HG02738.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.158-5581C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120540824 | |||||||
| chr12:120540854 | CT | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(145): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.158-5534delT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 120540854 | ||||||
| chr12:120540854 | CTT | C | 76 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0015 others(73): Show |
84 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.158-5535_158-5534d others(4): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 120540854 | ||||||
| chr12:120540854 | CTTT | C | 103 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(100): Show |
105 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.158-5536_158-5534d others(5): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 120540854 | ||||||
| chr12:120540864 | T | G | 1 | a0001c0001t0001g0209 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.158-5541T>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120540864 | |||||||
| chr12:120540898 | A | G | 89 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(86): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.158-5507A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120540898 | |||||||
| chr12:120540936 | A | G | 89 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(86): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.158-5469A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120540936 | |||||||
| chr12:120540946 | C | G | 2 | a0001c0001t0001g0279 a0001c0001t0001g0280 |
2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.158-5459C>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120540946 | |||||||
| chr12:120541046 | G | A | 4 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(1): Show |
4 | HG02015.hp2 HG02129.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-5359G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120541046 | |||||||
| chr12:120541085 | G | A | 15 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0260 others(12): Show |
16 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.158-5320G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120541085 | |||||||
| chr12:120541133 | A | G | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.158-5272A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120541133 | |||||||
| chr12:120541146 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.158-5259C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120541146 | |||||||
| chr12:120541209 | C | A | 1 | a0001c0001t0008g0061 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.158-5196C>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120541209 | |||||||
| chr12:120541437 | C | CT | 86 | a0001c0001t0001g0081 a0001c0001t0002g0003 a0001c0001t0002g0010 others(83): Show |
93 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.158-4953dupT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 120541437 | ||||||
| chr12:120541437 | C | CTT | 98 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(95): Show |
100 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.158-4954_158-4953d others(4): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 120541437 | ||||||
| chr12:120541520 | C | A | 26 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(23): Show |
29 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.158-4885C>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120541520 | |||||||
| chr12:120541521 | G | A | 1 | a0001c0001t0001g0299 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.158-4884G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120541521 | |||||||
| chr12:120541591 | A | C | 192 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(189): Show |
200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.158-4814A>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120541591 | |||||||
| chr12:120541651 | G | A | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.158-4754G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120541651 | |||||||
| chr12:120541795 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.158-4610A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120541795 | |||||||
| chr12:120541927 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0339 |
3 | NA18945.hp1 NA18971.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.158-4478T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120541927 | |||||||
| chr12:120541965 | C | A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0031 others(26): Show |
33 | HG00323.hp2 HG00408.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.158-4440C>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120541965 | |||||||
| chr12:120542024 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.158-4381G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120542024 | |||||||
| chr12:120542155 | C | T | 4 | a0001c0001t0001g0052 a0001c0001t0003g0330 a0001c0001t0003g0331 others(1): Show |
4 | HG01168.hp1 HG01169.hp1 HG02015.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-4250C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120542155 | |||||||
| chr12:120542260 | C | G | 1 | a0001c0001t0001g0068 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.158-4145C>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120542260 | |||||||
| chr12:120542279 | T | C | 1 | a0001c0001t0002g0204 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.158-4126T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120542279 | |||||||
| chr12:120542380 | G | A | 2 | a0001c0001t0002g0135 a0001c0001t0002g0136 |
2 | HG00280.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.158-4025G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120542380 | |||||||
| chr12:120542453 | G | A | 15 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0260 others(12): Show |
16 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.158-3952G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120542453 | |||||||
| chr12:120542486 | T | C | 9 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0340 others(6): Show |
9 | HG01106.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.158-3919T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120542486 | |||||||
| chr12:120542696 | G | A | 26 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(23): Show |
29 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.158-3709G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120542696 | |||||||
| chr12:120542828 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.158-3577C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120542828 | |||||||
| chr12:120543000 | GTTTGGAG others(11): Show |
G | 87 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(84): Show |
93 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.158-3403_158-3386d others(20): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 120543000 | ||||||
| chr12:120543015 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.158-3390C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120543015 | |||||||
| chr12:120543393 | C | T | 1 | a0001c0001t0001g0306 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.158-3012C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120543393 | |||||||
| chr12:120543399 | A | G | 103 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(100): Show |
105 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.158-3006A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120543399 | |||||||
| chr12:120543493 | C | T | 1 | a0001c0001t0001g0306 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.158-2912C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120543493 | |||||||
| chr12:120543581 | C | T | 15 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0260 others(12): Show |
16 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.158-2824C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120543581 | |||||||
| chr12:120543607 | A | G | 96 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(93): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.158-2798A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120543607 | |||||||
| chr12:120543668 | T | C | 96 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(93): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.158-2737T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120543668 | |||||||
| chr12:120543669 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.158-2736A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120543669 | |||||||
| chr12:120543748 | C | T | 9 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0340 others(6): Show |
9 | HG01106.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.158-2657C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120543748 | |||||||
| chr12:120543823 | G | A | 1 | a0001c0001t0002g0137 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.158-2582G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120543823 | |||||||
| chr12:120543827 | G | T | 100 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(97): Show |
102 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.158-2578G>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120543827 | |||||||
| chr12:120543957 | G | T | 57 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(54): Show |
62 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.158-2448G>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120543957 | |||||||
| chr12:120543993 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.158-2412C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120543993 | |||||||
| chr12:120544056 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.158-2349C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120544056 | |||||||
| chr12:120544151 | C | T | 1 | a0001c0001t0002g0198 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.158-2254C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120544151 | |||||||
| chr12:120544182 | G | A | 1 | a0001c0001t0002g0325 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.158-2223G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120544182 | |||||||
| chr12:120544198 | G | C | 2 | a0001c0001t0008g0061 a0003c0006t0001g0062 |
2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.158-2207G>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120544198 | |||||||
| chr12:120544260 | T | A | 1 | a0001c0001t0001g0034 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.158-2145T>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120544260 | |||||||
| chr12:120544273 | A | G | 2 | a0001c0001t0002g0013 a0001c0001t0002g0197 |
3 | HG00738.hp1 HG01517.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.158-2132A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120544273 | |||||||
| chr12:120544356 | C | CA | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(163): Show |
179 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.158-2032dupA | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 120544356 | ||||||
| chr12:120544356 | C | CAA | 12 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0035 others(9): Show |
13 | HG01070.hp1 HG01071.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.158-2033_158-2032d others(4): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 120544356 | ||||||
| chr12:120544568 | G | T | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.158-1837G>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120544568 | |||||||
| chr12:120544595 | T | C | 3 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 |
3 | HG01884.hp1 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.158-1810T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120544595 | |||||||
| chr12:120544633 | G | C | 1 | a0001c0001t0001g0217 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.158-1772G>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120544633 | |||||||
| chr12:120544646 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.158-1759A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120544646 | |||||||
| chr12:120544814 | C | T | 96 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(93): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.158-1591C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120544814 | |||||||
| chr12:120544897 | G | A | 86 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(83): Show |
92 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.158-1508G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120544897 | |||||||
| chr12:120544930 | G | A | 96 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(93): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.158-1475G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120544930 | |||||||
| chr12:120544958 | G | A | 4 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(1): Show |
4 | HG02004.hp1 HG02148.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-1447G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120544958 | |||||||
| chr12:120544977 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.158-1428T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120544977 | |||||||
| chr12:120545174 | GA | G | 3 | a0001c0001t0001g0065 a0001c0001t0004g0064 a0001c0001t0004g0066 |
3 | HG01106.hp1 HG03669.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.158-1228delA | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 120545174 | ||||||
| chr12:120545211 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.158-1194C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120545211 | |||||||
| chr12:120545273 | T | C | 199 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(196): Show |
209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.158-1132T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120545273 | |||||||
| chr12:120545282 | C | T | 9 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0340 others(6): Show |
9 | HG01106.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.158-1123C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120545282 | |||||||
| chr12:120545342 | C | T | 10 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0326 others(7): Show |
12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.158-1063C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120545342 | |||||||
| chr12:120545348 | A | AT | 111 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(108): Show |
115 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.158-1040dupT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 120545348 | ||||||
| chr12:120545383 | A | G | 26 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(23): Show |
29 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.158-1022A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120545383 | |||||||
| chr12:120545436 | C | T | 55 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(52): Show |
60 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.158-969C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120545436 | |||||||
| chr12:120545472 | A | G | 1 | a0001c0001t0002g0195 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.158-933A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120545472 | |||||||
| chr12:120545667 | A | T | 1 | a0001c0001t0002g0137 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.158-738A>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120545667 | |||||||
| chr12:120545705 | T | C | 5 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0026 others(2): Show |
6 | HG01109.hp2 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.158-700T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120545705 | |||||||
| chr12:120545778 | A | G | 3 | a0001c0001t0002g0013 a0001c0001t0002g0197 a0001c0001t0002g0208 |
4 | HG00639.hp2 HG00738.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-627A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120545778 | |||||||
| chr12:120545847 | G | A | 1 | a0001c0001t0004g0064 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.158-558G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120545847 | |||||||
| chr12:120546068 | G | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0026 others(2): Show |
6 | HG01109.hp2 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.158-337G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120546068 | |||||||
| chr12:120546234 | ACT | A | 15 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0260 others(12): Show |
16 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.158-168_158-167del others(2): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 120546234 | ||||||
| chr12:120546267 | A | T | 2 | a0001c0001t0008g0061 a0003c0006t0001g0062 |
2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.158-138A>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 1/16 | chr12 | 120546267 | |||||||
| chr12:120546829 | A | C | 26 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(23): Show |
29 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.354+228A>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120546829 | |||||||
| chr12:120546972 | C | T | 9 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0340 others(6): Show |
9 | HG01106.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.354+371C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120546972 | |||||||
| chr12:120546979 | T | G | 3 | a0002c0002t0001g0281 a0002c0002t0001g0282 a0002c0002t0001g0283 |
3 | HG02630.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.354+378T>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120546979 | |||||||
| chr12:120547031 | G | A | 3 | a0002c0002t0001g0281 a0002c0002t0001g0282 a0002c0002t0001g0283 |
3 | HG02630.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.354+430G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120547031 | |||||||
| chr12:120547065 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.354+464G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120547065 | |||||||
| chr12:120547220 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.354+619G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120547220 | |||||||
| chr12:120547474 | T | A | 1 | a0001c0001t0002g0140 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.354+873T>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120547474 | |||||||
| chr12:120547533 | A | G | 9 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0340 others(6): Show |
9 | HG01106.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.354+932A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120547533 | |||||||
| chr12:120547574 | A | G | 328 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(325): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.354+973A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120547574 | |||||||
| chr12:120547686 | A | G | 1 | a0001c0001t0002g0194 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.354+1085A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120547686 | |||||||
| chr12:120547762 | T | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0284 a0001c0001t0001g0285 |
4 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.354+1161T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120547762 | |||||||
| chr12:120547766 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.354+1165G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120547766 | |||||||
| chr12:120547959 | G | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0312 |
2 | HG01123.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.354+1358G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120547959 | |||||||
| chr12:120547975 | T | C | 3 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 |
3 | HG01884.hp1 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.354+1374T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120547975 | |||||||
| chr12:120548015 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.354+1414G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120548015 | |||||||
| chr12:120548153 | C | A | 1 | a0001c0001t0001g0299 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.354+1552C>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120548153 | |||||||
| chr12:120548165 | G | T | 1 | a0001c0001t0003g0332 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.354+1564G>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120548165 | |||||||
| chr12:120548345 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.354+1744G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120548345 | |||||||
| chr12:120548363 | G | GA | 15 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0260 others(12): Show |
16 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.354+1764dupA | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr12 | 120548363 | ||||||
| chr12:120548378 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.354+1777G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120548378 | |||||||
| chr12:120548388 | C | G | 87 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(84): Show |
93 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.354+1787C>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120548388 | |||||||
| chr12:120548407 | C | G | 2 | a0001c0001t0001g0005 a0001c0001t0001g0024 |
3 | HG02280.hp2 HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.354+1806C>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120548407 | |||||||
| chr12:120548412 | C | T | 65 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(62): Show |
67 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.354+1811C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120548412 | |||||||
| chr12:120548504 | C | T | 2 | a0001c0001t0001g0260 a0001c0001t0001g0270 |
2 | HG01891.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.354+1903C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120548504 | |||||||
| chr12:120548598 | G | A | 1 | a0001c0001t0001g0299 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.354+1997G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120548598 | |||||||
| chr12:120548648 | T | C | 1 | a0001c0001t0001g0286 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.354+2047T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120548648 | |||||||
| chr12:120548660 | C | CT | 94 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0026 others(91): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.354+2075dupT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr12 | 120548660 | ||||||
| chr12:120548742 | C | A | 1 | a0001c0001t0001g0052 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.354+2141C>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120548742 | |||||||
| chr12:120548891 | C | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0312 |
2 | HG01123.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.354+2290C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120548891 | |||||||
| chr12:120548939 | G | A | 89 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(86): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.354+2338G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120548939 | |||||||
| chr12:120548950 | A | G | 329 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(326): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.354+2349A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120548950 | |||||||
| chr12:120548965 | C | T | 1 | a0001c0001t0003g0333 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.354+2364C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120548965 | |||||||
| chr12:120548998 | A | G | 275 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(272): Show |
292 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.354+2397A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120548998 | |||||||
| chr12:120549040 | G | C | 1 | a0001c0001t0001g0286 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.354+2439G>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120549040 | |||||||
| chr12:120549183 | G | A | 9 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0340 others(6): Show |
9 | HG01106.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.354+2582G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120549183 | |||||||
| chr12:120549229 | A | G | 2 | a0001c0001t0008g0061 a0003c0006t0001g0062 |
2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.354+2628A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120549229 | |||||||
| chr12:120549394 | G | C | 1 | a0001c0001t0001g0286 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.354+2793G>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120549394 | |||||||
| chr12:120549506 | C | T | 1 | a0001c0001t0003g0333 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.354+2905C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120549506 | |||||||
| chr12:120549529 | A | T | 2 | a0001c0001t0008g0061 a0003c0006t0001g0062 |
2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.354+2928A>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120549529 | |||||||
| chr12:120549588 | G | A | 100 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(97): Show |
102 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.355-2911G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120549588 | |||||||
| chr12:120549818 | A | C | 96 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(93): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.355-2681A>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120549818 | |||||||
| chr12:120549840 | C | T | 100 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(97): Show |
102 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.355-2659C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120549840 | |||||||
| chr12:120549855 | T | G | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(4): Show |
9 | HG01109.hp2 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.355-2644T>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120549855 | |||||||
| chr12:120550081 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.355-2418C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120550081 | |||||||
| chr12:120550246 | T | C | 10 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0326 others(7): Show |
12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.355-2253T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120550246 | |||||||
| chr12:120550323 | C | T | 3 | a0001c0001t0003g0330 a0001c0001t0003g0331 a0001c0001t0003g0332 |
3 | HG01168.hp1 HG01169.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.355-2176C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120550323 | |||||||
| chr12:120550428 | T | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0076 a0001c0001t0001g0079 |
4 | NA18940.hp2 NA18969.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.355-2071T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120550428 | |||||||
| chr12:120550435 | A | G | 103 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(100): Show |
105 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.355-2064A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120550435 | |||||||
| chr12:120550462 | T | A | 10 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0326 others(7): Show |
12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.355-2037T>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120550462 | |||||||
| chr12:120550543 | T | G | 2 | a0001c0001t0008g0061 a0003c0006t0001g0062 |
2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.355-1956T>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120550543 | |||||||
| chr12:120550568 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.355-1931T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120550568 | |||||||
| chr12:120550583 | G | A | 15 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0260 others(12): Show |
16 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.355-1916G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120550583 | |||||||
| chr12:120550583 | G | GT | 6 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0259 others(3): Show |
6 | HG02738.hp2 NA18943.hp2 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.355-1909dupT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr12 | 120550583 | ||||||
| chr12:120550609 | T | C | 3 | a0001c0001t0001g0065 a0001c0001t0004g0064 a0001c0001t0004g0066 |
3 | HG01106.hp1 HG03669.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.355-1890T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120550609 | |||||||
| chr12:120550657 | C | T | 89 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(86): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.355-1842C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120550657 | |||||||
| chr12:120550665 | C | T | 2 | a0001c0001t0002g0135 a0001c0001t0002g0136 |
2 | HG00280.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.355-1834C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120550665 | |||||||
| chr12:120550757 | C | T | 5 | a0001c0001t0001g0340 a0001c0001t0001g0341 a0001c0001t0001g0342 others(2): Show |
5 | HG01261.hp2 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.355-1742C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120550757 | |||||||
| chr12:120550895 | C | G | 16 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0232 others(13): Show |
16 | HG00597.hp2 HG00621.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.355-1604C>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120550895 | |||||||
| chr12:120550940 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.355-1559G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120550940 | |||||||
| chr12:120551073 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(4): Show |
9 | HG01109.hp2 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.355-1426C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120551073 | |||||||
| chr12:120551100 | C | T | 55 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(52): Show |
60 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.355-1399C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120551100 | |||||||
| chr12:120551277 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.355-1222C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120551277 | |||||||
| chr12:120551290 | G | GT | 108 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0028 others(105): Show |
110 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.355-1187dupT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr12 | 120551290 | ||||||
| chr12:120551290 | G | GTT | 90 | a0001c0001t0001g0063 a0001c0001t0001g0068 a0001c0001t0001g0079 others(87): Show |
96 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.355-1188_355-1187d others(4): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr12 | 120551290 | ||||||
| chr12:120551290 | G | GTTT | 24 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0260 others(21): Show |
25 | HG00099.hp1 HG01123.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.355-1189_355-1187d others(5): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr12 | 120551290 | ||||||
| chr12:120551292 | T | TTTTG | 8 | a0001c0001t0001g0016 a0001c0001t0001g0273 a0001c0001t0001g0274 others(5): Show |
9 | HG02559.hp2 HG02723.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.355-1204_355-1203i others(6): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr12 | 120551292 | ||||||
| chr12:120551380 | T | C | 199 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(196): Show |
209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.355-1119T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120551380 | |||||||
| chr12:120551537 | GA | G | 9 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0340 others(6): Show |
9 | HG01106.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.355-961delA | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120551537 | |||||||
| chr12:120551541 | C | T | 9 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0340 others(6): Show |
9 | HG01106.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.355-958C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120551541 | |||||||
| chr12:120551777 | G | A | 1 | a0001c0001t0002g0132 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.355-722G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120551777 | |||||||
| chr12:120551823 | C | G | 199 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(196): Show |
209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.355-676C>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120551823 | |||||||
| chr12:120551973 | C | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0319 a0001c0001t0001g0320 |
4 | HG02145.hp2 HG02258.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.355-526C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120551973 | |||||||
| chr12:120551987 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.355-512G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120551987 | |||||||
| chr12:120551993 | A | G | 26 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(23): Show |
29 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.355-506A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120551993 | |||||||
| chr12:120551997 | G | C | 15 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0260 others(12): Show |
16 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.355-502G>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120551997 | |||||||
| chr12:120552013 | C | CT | 7 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0311 others(4): Show |
10 | HG01943.hp1 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.355-472dupT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr12 | 120552013 | ||||||
| chr12:120552083 | C | CA | 104 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0024 others(101): Show |
106 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.355-398dupA | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr12 | 120552083 | ||||||
| chr12:120552215 | C | T | 15 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0260 others(12): Show |
16 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.355-284C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120552215 | |||||||
| chr12:120552273 | G | T | 7 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(4): Show |
7 | HG00673.hp1 HG02004.hp1 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.355-226G>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120552273 | |||||||
| chr12:120552333 | G | C | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.355-166G>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120552333 | |||||||
| chr12:120552399 | C | T | 1 | a0001c0001t0001g0258 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.355-100C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | chr12 | 120552399 | |||||||
| chr12:120552426 | G | GT | 6 | a0001c0001t0001g0050 a0001c0001t0001g0114 a0001c0001t0001g0126 others(3): Show |
6 | HG00544.hp2 HG02738.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.355-65dupT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr12 | 120552426 | ||||||
| chr12:120552776 | T | C | 1 | a0001c0004t0001g0231 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.554+78T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120552776 | |||||||
| chr12:120552779 | A | C | 99 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(96): Show |
101 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.554+81A>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120552779 | |||||||
| chr12:120552985 | A | G | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(4): Show |
9 | HG01109.hp2 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.554+287A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120552985 | |||||||
| chr12:120553032 | G | A | 2 | a0001c0001t0003g0326 a0001c0001t0003g0327 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.554+334G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120553032 | |||||||
| chr12:120553038 | GTTTTTTT others(3): Show |
G | 3 | a0001c0001t0001g0247 a0001c0001t0001g0253 a0001c0001t0001g0285 |
3 | HG02922.hp1 HG03130.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.554+394_554+403del others(10): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553038 | ||||||
| chr12:120553038 | GTTTTTTT others(7): Show |
G | 2 | a0001c0001t0001g0211 a0001c0001t0001g0303 |
2 | HG01884.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.554+390_554+403del others(14): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553038 | ||||||
| chr12:120553038 | GTTTTTTT others(8): Show |
G | 2 | a0001c0001t0001g0302 a0001c0001t0001g0306 |
2 | HG02273.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.554+389_554+403del others(15): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553038 | ||||||
| chr12:120553038 | GTTTTTTT others(10): Show |
G | 1 | a0001c0001t0001g0301 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.554+387_554+403del others(17): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553038 | ||||||
| chr12:120553038 | GTTTTTTT others(12): Show |
G | 2 | a0001c0001t0001g0293 a0001c0001t0003g0333 |
2 | HG00609.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.554+385_554+403del others(19): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553038 | ||||||
| chr12:120553038 | GTTTTTTT others(13): Show |
G | 10 | a0001c0001t0001g0292 a0001c0001t0003g0021 a0001c0001t0003g0022 others(7): Show |
12 | HG01168.hp1 HG01169.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.554+384_554+403del others(20): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553038 | ||||||
| chr12:120553038 | GTTTTTTT others(14): Show |
G | 1 | a0001c0001t0001g0019 | 2 | HG00140.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.554+383_554+403del others(21): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553038 | ||||||
| chr12:120553038 | GTTTTTTT others(15): Show |
G | 11 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0209 others(8): Show |
12 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.554+382_554+403del others(22): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553038 | ||||||
| chr12:120553038 | GTTTTTTT others(16): Show |
G | 2 | a0001c0001t0001g0289 a0001c0001t0001g0297 |
2 | NA18961.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.554+381_554+403del others(23): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553038 | ||||||
| chr12:120553038 | GTTTTTTT others(17): Show |
G | 1 | a0001c0001t0001g0269 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.554+380_554+403del others(24): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553038 | ||||||
| chr12:120553038 | GTTTTTTT others(18): Show |
G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0300 |
3 | HG02004.hp1 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.554+379_554+403del others(25): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553038 | ||||||
| chr12:120553038 | GTTTTTTT others(19): Show |
G | 1 | a0001c0001t0001g0252 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.554+378_554+403del others(26): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553038 | ||||||
| chr12:120553038 | GTTTTTTT others(20): Show |
G | 1 | a0001c0001t0001g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.554+377_554+403del others(27): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553038 | ||||||
| chr12:120553038 | GTTTTTTT others(22): Show |
G | 1 | a0001c0001t0001g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.554+375_554+403del others(29): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553038 | ||||||
| chr12:120553038 | GTTTTTTT others(23): Show |
G | 3 | a0001c0001t0001g0270 a0001c0001t0001g0280 a0004c0009t0001g0248 |
3 | HG01891.hp2 HG02486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.554+374_554+403del others(30): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553038 | ||||||
| chr12:120553038 | GTTTTTTT others(24): Show |
G | 12 | a0001c0001t0001g0097 a0001c0001t0001g0245 a0001c0001t0001g0246 others(9): Show |
12 | HG02055.hp1 HG02145.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.554+373_554+403del others(31): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553038 | ||||||
| chr12:120553038 | GTTTTTTT others(25): Show |
G | 16 | a0001c0001t0001g0016 a0001c0001t0001g0083 a0001c0001t0001g0096 others(13): Show |
17 | HG00621.hp1 HG00673.hp1 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.554+372_554+403del others(32): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553038 | ||||||
| chr12:120553038 | GTTTTTTT others(26): Show |
G | 40 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0076 others(37): Show |
42 | HG00597.hp2 HG00642.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.554+371_554+403del others(33): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553038 | ||||||
| chr12:120553038 | GTTTTTTT others(28): Show |
G | 7 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0210 others(4): Show |
7 | HG00099.hp1 HG03471.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.554+369_554+403del others(35): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553038 | ||||||
| chr12:120553038 | GTTTTTTT others(29): Show |
G | 27 | a0001c0001t0002g0012 a0001c0001t0002g0128 a0001c0001t0002g0134 others(24): Show |
28 | HG00323.hp1 HG00544.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.554+368_554+403del others(36): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553038 | ||||||
| chr12:120553038 | GTTTTTTT others(30): Show |
G | 56 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0002g0010 others(53): Show |
59 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.554+367_554+403del others(37): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553038 | ||||||
| chr12:120553038 | GTTTTTTT others(31): Show |
G | 8 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(5): Show |
12 | HG01891.hp1 HG02109.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.554+366_554+403del others(38): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553038 | ||||||
| chr12:120553038 | GTTTTTTT others(32): Show |
G | 1 | a0001c0001t0001g0299 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.554+365_554+403del others(39): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553038 | ||||||
| chr12:120553038 | GTTTTTTT others(33): Show |
G | 1 | a0001c0001t0001g0335 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.554+364_554+403del others(40): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553038 | ||||||
| chr12:120553038 | GTTTTTTT others(34): Show |
G | 8 | a0001c0001t0001g0023 a0001c0001t0001g0047 a0001c0001t0001g0048 others(5): Show |
9 | HG00408.hp2 HG01993.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.554+363_554+403del others(41): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553038 | ||||||
| chr12:120553038 | GTTTTTTT others(35): Show |
G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(42): Show |
54 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.554+362_554+403del others(42): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553038 | ||||||
| chr12:120553038 | GTTTTTTT others(36): Show |
G | 9 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0340 others(6): Show |
9 | HG01106.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.554+361_554+403del others(43): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553038 | ||||||
| chr12:120553038 | GTTTTTTT others(38): Show |
G | 2 | a0001c0001t0008g0061 a0003c0006t0001g0062 |
2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.554+359_554+403del others(45): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553038 | ||||||
| chr12:120553065 | T | G | 1 | a0001c0001t0001g0287 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.554+367T>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120553065 | |||||||
| chr12:120553068 | T | G | 1 | a0001c0001t0003g0333 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.554+370T>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120553068 | |||||||
| chr12:120553069 | T | G | 9 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0326 others(6): Show |
11 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.554+371T>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120553069 | |||||||
| chr12:120553072 | T | G | 1 | a0001c0001t0003g0333 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.554+374T>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120553072 | |||||||
| chr12:120553073 | T | G | 9 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0326 others(6): Show |
11 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.554+375T>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120553073 | |||||||
| chr12:120553076 | T | G | 1 | a0001c0001t0003g0333 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.554+378T>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120553076 | |||||||
| chr12:120553077 | T | G | 9 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0326 others(6): Show |
11 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.554+379T>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120553077 | |||||||
| chr12:120553132 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.554+434A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120553132 | |||||||
| chr12:120553138 | C | T | 3 | a0001c0001t0003g0330 a0001c0001t0003g0331 a0001c0001t0003g0332 |
3 | HG01168.hp1 HG01169.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.554+440C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120553138 | |||||||
| chr12:120553244 | C | T | 6 | a0001c0001t0001g0068 a0001c0001t0001g0340 a0001c0001t0001g0341 others(3): Show |
6 | HG01261.hp2 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.554+546C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120553244 | |||||||
| chr12:120553250 | AT | A | 96 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(93): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.554+559delT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553250 | ||||||
| chr12:120553324 | G | C | 10 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0326 others(7): Show |
12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.554+626G>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120553324 | |||||||
| chr12:120553401 | C | CT | 35 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0016 others(32): Show |
39 | HG00544.hp2 HG00621.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.554+722dupT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553401 | ||||||
| chr12:120553401 | CT | C | 10 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(7): Show |
12 | HG01169.hp1 HG02965.hp2 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.554+722delT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553401 | ||||||
| chr12:120553437 | C | T | 100 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(97): Show |
102 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.554+739C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120553437 | |||||||
| chr12:120553495 | C | T | 3 | a0001c0001t0001g0286 a0001c0001t0001g0290 a0001c0001t0001g0296 |
3 | NA18998.hp1 NA19070.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.554+797C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120553495 | |||||||
| chr12:120553653 | T | G | 196 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(193): Show |
206 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.554+955T>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120553653 | |||||||
| chr12:120553684 | T | G | 15 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0260 others(12): Show |
16 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.554+986T>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120553684 | |||||||
| chr12:120553905 | G | GT | 38 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0029 others(35): Show |
40 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.555-797dupT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553905 | ||||||
| chr12:120553905 | GT | G | 94 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(91): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.555-797delT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 120553905 | ||||||
| chr12:120554027 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.555-691C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120554027 | |||||||
| chr12:120554035 | G | A | 7 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(4): Show |
7 | HG00673.hp1 HG02004.hp1 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.555-683G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120554035 | |||||||
| chr12:120554050 | G | A | 1 | a0001c0001t0003g0333 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.555-668G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120554050 | |||||||
| chr12:120554122 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.555-596G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120554122 | |||||||
| chr12:120554157 | G | A | 2 | a0001c0001t0001g0247 a0004c0009t0001g0248 |
2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.555-561G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120554157 | |||||||
| chr12:120554210 | T | C | 96 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(93): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.555-508T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120554210 | |||||||
| chr12:120554222 | G | A | 2 | a0001c0001t0001g0005 a0001c0001t0001g0024 |
3 | HG02280.hp2 HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.555-496G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120554222 | |||||||
| chr12:120554319 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.555-399G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120554319 | |||||||
| chr12:120554416 | T | G | 4 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(1): Show |
4 | HG02004.hp1 HG02148.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.555-302T>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120554416 | |||||||
| chr12:120554459 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.555-259A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120554459 | |||||||
| chr12:120554598 | C | T | 100 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(97): Show |
102 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.555-120C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120554598 | |||||||
| chr12:120554600 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.555-118T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120554600 | |||||||
| chr12:120554670 | T | C | 1 | a0001c0001t0001g0098 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.555-48T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 3/16 | chr12 | 120554670 | |||||||
| chr12:120555118 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.645+310G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120555118 | |||||||
| chr12:120555262 | A | G | 89 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(86): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.645+454A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120555262 | |||||||
| chr12:120555490 | C | CT | 13 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0209 others(10): Show |
13 | HG01106.hp1 HG01261.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.645+696dupT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr12 | 120555490 | ||||||
| chr12:120555511 | G | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.645+703G>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120555511 | |||||||
| chr12:120555542 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0339 |
3 | NA18945.hp1 NA18971.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.645+734C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120555542 | |||||||
| chr12:120555582 | G | A | 10 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0326 others(7): Show |
12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.645+774G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120555582 | |||||||
| chr12:120555797 | C | G | 9 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0340 others(6): Show |
9 | HG01106.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.645+989C>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120555797 | |||||||
| chr12:120555836 | T | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(4): Show |
9 | HG01109.hp2 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.645+1028T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120555836 | |||||||
| chr12:120555988 | C | T | 1 | a0001c0001t0002g0144 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.645+1180C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120555988 | |||||||
| chr12:120556014 | C | T | 100 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(97): Show |
102 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.645+1206C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120556014 | |||||||
| chr12:120556069 | G | A | 6 | a0001c0001t0001g0014 a0001c0001t0001g0250 a0001c0001t0001g0251 others(3): Show |
7 | HG02451.hp1 HG02818.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.646-1213G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120556069 | |||||||
| chr12:120556231 | T | G | 1 | a0001c0001t0001g0036 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.646-1051T>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120556231 | |||||||
| chr12:120556263 | G | A | 9 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0340 others(6): Show |
9 | HG01106.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.646-1019G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120556263 | |||||||
| chr12:120556361 | C | T | 13 | a0001c0001t0001g0016 a0001c0001t0001g0273 a0001c0001t0001g0274 others(10): Show |
14 | HG02145.hp1 HG02559.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.646-921C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120556361 | |||||||
| chr12:120556414 | A | C | 274 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(271): Show |
291 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.646-868A>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120556414 | |||||||
| chr12:120556414 | A | T | 1 | a0001c0001t0001g0230 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.646-868A>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120556414 | |||||||
| chr12:120556448 | G | A | 10 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0326 others(7): Show |
12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.646-834G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120556448 | |||||||
| chr12:120556479 | C | G | 1 | a0001c0001t0002g0194 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.646-803C>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120556479 | |||||||
| chr12:120556526 | G | A | 5 | a0001c0001t0002g0131 a0001c0001t0002g0177 a0001c0001t0002g0184 others(2): Show |
5 | NA18942.hp1 NA18966.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.646-756G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120556526 | |||||||
| chr12:120556530 | C | CA | 136 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(133): Show |
143 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.646-725dupA | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr12 | 120556530 | ||||||
| chr12:120556530 | C | CAA | 30 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0076 others(27): Show |
30 | HG00280.hp1 HG00597.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.646-726_646-725dup others(2): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr12 | 120556530 | ||||||
| chr12:120556530 | C | CAAAAAAA others(4): Show |
1 | a0003c0006t0001g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.646-735_646-725dup others(11): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr12 | 120556530 | ||||||
| chr12:120556530 | CA | C | 46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(43): Show |
53 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.646-725delA | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr12 | 120556530 | ||||||
| chr12:120556553 | A | AC | 3 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0028 |
4 | HG01891.hp1 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.646-729_646-728ins others(1): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120556553 | |||||||
| chr12:120556558 | G | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0026 others(2): Show |
6 | HG01109.hp2 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.646-724G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120556558 | |||||||
| chr12:120556591 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.646-691A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120556591 | |||||||
| chr12:120556596 | C | T | 3 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 |
3 | HG01884.hp1 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.646-686C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120556596 | |||||||
| chr12:120556685 | T | A | 100 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(97): Show |
102 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.646-597T>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120556685 | |||||||
| chr12:120556865 | A | G | 10 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0326 others(7): Show |
12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.646-417A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120556865 | |||||||
| chr12:120556880 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0098 |
2 | HG02027.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.646-402C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120556880 | |||||||
| chr12:120556910 | T | C | 2 | a0001c0001t0002g0160 a0001c0005t0002g0130 |
2 | HG01943.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.646-372T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120556910 | |||||||
| chr12:120556989 | A | G | 1 | a0001c0001t0001g0312 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.646-293A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120556989 | |||||||
| chr12:120557016 | C | T | 89 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(86): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.646-266C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120557016 | |||||||
| chr12:120557038 | A | G | 189 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(186): Show |
197 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.646-244A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120557038 | |||||||
| chr12:120557069 | A | G | 272 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(269): Show |
289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.646-213A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120557069 | |||||||
| chr12:120557081 | G | A | 67 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(64): Show |
74 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.646-201G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120557081 | |||||||
| chr12:120557085 | C | CA | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(136): Show |
151 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.646-181dupA | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr12 | 120557085 | ||||||
| chr12:120557085 | CA | C | 18 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(15): Show |
22 | HG01109.hp2 HG01168.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.646-181delA | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr12 | 120557085 | ||||||
| chr12:120557085 | CAAA | C | 9 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0340 others(6): Show |
9 | HG01106.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.646-183_646-181del others(3): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr12 | 120557085 | ||||||
| chr12:120557097 | A | AG | 11 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0233 others(8): Show |
11 | HG00597.hp2 HG00621.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.646-185_646-184ins others(1): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120557097 | |||||||
| chr12:120557129 | G | A | 272 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(269): Show |
289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.646-153G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120557129 | |||||||
| chr12:120557169 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.646-113G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120557169 | |||||||
| chr12:120557254 | T | C | 5 | a0001c0001t0001g0340 a0001c0001t0001g0341 a0001c0001t0001g0342 others(2): Show |
5 | HG01261.hp2 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.646-28T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 4/16 | chr12 | 120557254 | |||||||
| chr12:120557529 | G | A | 188 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(185): Show |
196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.831-17G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 5/16 | chr12 | 120557529 | |||||||
| chr12:120557883 | C | T | 3 | a0001c0001t0002g0013 a0001c0001t0002g0197 a0001c0001t0002g0208 |
4 | HG00639.hp2 HG00738.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.967+201C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120557883 | |||||||
| chr12:120558150 | A | G | 9 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0340 others(6): Show |
9 | HG01106.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.967+468A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120558150 | |||||||
| chr12:120558454 | TAAAA | T | 10 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0326 others(7): Show |
12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.967+778_967+781del others(4): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr12 | 120558454 | ||||||
| chr12:120558455 | A | T | 1 | a0001c0001t0001g0052 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.967+773A>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120558455 | |||||||
| chr12:120558567 | G | GTA | 87 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(84): Show |
89 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.967+895_967+896dup others(2): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr12 | 120558567 | ||||||
| chr12:120558577 | A | AT | 13 | a0001c0001t0001g0030 a0001c0001t0001g0260 a0001c0001t0001g0262 others(10): Show |
13 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.967+904dupT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr12 | 120558577 | ||||||
| chr12:120558577 | A | ATT | 11 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0233 others(8): Show |
11 | HG00597.hp2 HG00621.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.967+903_967+904dup others(2): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr12 | 120558577 | ||||||
| chr12:120558578 | T | TA | 6 | a0001c0001t0001g0015 a0001c0001t0001g0209 a0001c0001t0001g0210 others(3): Show |
7 | HG01884.hp1 HG01884.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.967+896_967+897ins others(1): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120558578 | |||||||
| chr12:120558579 | T | A | 11 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(8): Show |
13 | HG01099.hp2 HG01109.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.967+897T>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120558579 | |||||||
| chr12:120558580 | T | A | 1 | a0003c0006t0001g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.967+898T>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120558580 | |||||||
| chr12:120558581 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.967+899T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120558581 | |||||||
| chr12:120558790 | C | T | 56 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(53): Show |
61 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.967+1108C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120558790 | |||||||
| chr12:120558798 | C | T | 2 | a0001c0001t0002g0142 a0001c0001t0002g0200 |
2 | NA18967.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.967+1116C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120558798 | |||||||
| chr12:120558865 | C | T | 87 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(84): Show |
93 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.967+1183C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120558865 | |||||||
| chr12:120558994 | TTTAA | T | 6 | a0001c0001t0001g0068 a0001c0001t0001g0340 a0001c0001t0001g0341 others(3): Show |
6 | HG01261.hp2 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.967+1321_967+1324d others(6): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr12 | 120558994 | ||||||
| chr12:120559009 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.967+1327T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120559009 | |||||||
| chr12:120559059 | T | A | 275 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(272): Show |
292 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.967+1377T>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120559059 | |||||||
| chr12:120559060 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.967+1378A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120559060 | |||||||
| chr12:120559066 | T | TA | 275 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(272): Show |
292 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.967+1384_967+1385i others(3): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120559066 | |||||||
| chr12:120559095 | A | G | 3 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 |
3 | HG01884.hp1 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.967+1413A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120559095 | |||||||
| chr12:120559156 | TA | T | 100 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(97): Show |
102 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.967+1475delA | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120559156 | |||||||
| chr12:120559176 | C | CT | 141 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(138): Show |
150 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.967+1517dupT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr12 | 120559176 | ||||||
| chr12:120559176 | C | CTT | 21 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0024 others(18): Show |
23 | HG01928.hp1 HG02145.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.967+1516_967+1517d others(4): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr12 | 120559176 | ||||||
| chr12:120559176 | CT | C | 51 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(48): Show |
61 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.967+1517delT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr12 | 120559176 | ||||||
| chr12:120559176 | CTTTTTTT others(8): Show |
C | 89 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(86): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.967+1503_967+1517d others(17): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr12 | 120559176 | ||||||
| chr12:120559216 | G | C | 275 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(272): Show |
292 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.968-1510G>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120559216 | |||||||
| chr12:120559465 | A | C | 1 | a0001c0001t0001g0068 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.968-1261A>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120559465 | |||||||
| chr12:120559505 | G | A | 1 | a0003c0006t0001g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.968-1221G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120559505 | |||||||
| chr12:120559552 | T | G | 9 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0340 others(6): Show |
9 | HG01106.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.968-1174T>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120559552 | |||||||
| chr12:120559799 | G | A | 89 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(86): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.968-927G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120559799 | |||||||
| chr12:120559822 | A | C | 9 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0340 others(6): Show |
9 | HG01106.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.968-904A>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120559822 | |||||||
| chr12:120559852 | C | T | 1 | a0001c0001t0002g0170 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.968-874C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120559852 | |||||||
| chr12:120559891 | A | G | 329 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(326): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.968-835A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120559891 | |||||||
| chr12:120559934 | T | C | 199 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(196): Show |
209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.968-792T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120559934 | |||||||
| chr12:120560072 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.968-654G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120560072 | |||||||
| chr12:120560096 | T | G | 1 | a0001c0001t0008g0061 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.968-630T>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120560096 | |||||||
| chr12:120560134 | T | C | 9 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0340 others(6): Show |
9 | HG01106.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.968-592T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120560134 | |||||||
| chr12:120560145 | GT | G | 46 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(43): Show |
50 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.968-573delT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr12 | 120560145 | ||||||
| chr12:120560153 | T | G | 20 | a0001c0001t0001g0264 a0001c0001t0001g0266 a0001c0001t0001g0273 others(17): Show |
22 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.968-573T>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120560153 | |||||||
| chr12:120560154 | G | GT | 113 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(110): Show |
116 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.968-558dupT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr12 | 120560154 | ||||||
| chr12:120560154 | G | GTT | 11 | a0001c0001t0001g0069 a0001c0001t0001g0083 a0001c0001t0001g0085 others(8): Show |
11 | HG00544.hp1 HG00621.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.968-559_968-558dup others(2): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr12 | 120560154 | ||||||
| chr12:120560154 | G | T | 24 | a0001c0001t0001g0016 a0001c0001t0001g0023 a0001c0001t0001g0025 others(21): Show |
28 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.968-572G>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120560154 | |||||||
| chr12:120560196 | A | G | 89 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(86): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.968-530A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120560196 | |||||||
| chr12:120560212 | C | T | 1 | a0001c0001t0008g0061 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.968-514C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120560212 | |||||||
| chr12:120560343 | G | A | 4 | a0001c0001t0001g0078 a0001c0001t0001g0090 a0001c0001t0001g0101 others(1): Show |
4 | NA18994.hp2 NA19003.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.968-383G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120560343 | |||||||
| chr12:120560374 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.968-352G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120560374 | |||||||
| chr12:120560472 | A | G | 3 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 |
3 | HG01884.hp1 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.968-254A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120560472 | |||||||
| chr12:120560500 | C | T | 2 | a0001c0001t0002g0325 a0001c0001t0002g0334 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.968-226C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120560500 | |||||||
| chr12:120560530 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.968-196T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120560530 | |||||||
| chr12:120560640 | A | G | 103 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(100): Show |
105 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.968-86A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120560640 | |||||||
| chr12:120560678 | G | A | 329 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(326): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.968-48G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 6/16 | chr12 | 120560678 | |||||||
| chr12:120560925 | T | C | 27 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0031 others(24): Show |
31 | HG00323.hp2 HG00408.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.1128+39T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 7/16 | chr12 | 120560925 | |||||||
| chr12:120561051 | A | G | 4 | a0001c0001t0001g0078 a0001c0001t0001g0090 a0001c0001t0001g0101 others(1): Show |
4 | NA18994.hp2 NA19003.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128+165A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 7/16 | chr12 | 120561051 | |||||||
| chr12:120561098 | T | TAACCTAG others(323): Show |
2 | a0001c0001t0002g0182 a0001c0001t0002g0207 |
2 | HG00609.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.1128+226_1128+227i others(332): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 120561098 | ||||||
| chr12:120561098 | T | TAACCTAG others(336): Show |
1 | a0001c0001t0002g0169 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1128+226_1128+227i others(345): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 120561098 | ||||||
| chr12:120561150 | G | T | 1 | a0001c0001t0002g0168 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1128+264G>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 7/16 | chr12 | 120561150 | |||||||
| chr12:120561324 | G | A | 65 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(62): Show |
67 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.1128+438G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 7/16 | chr12 | 120561324 | |||||||
| chr12:120561553 | G | C | 10 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0326 others(7): Show |
12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1128+667G>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 7/16 | chr12 | 120561553 | |||||||
| chr12:120561800 | C | T | 1 | a0001c0001t0002g0167 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1128+914C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 7/16 | chr12 | 120561800 | |||||||
| chr12:120561942 | T | C | 2 | a0001c0001t0001g0074 a0001c0010t0001g0077 |
2 | HG02273.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1129-1003T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 7/16 | chr12 | 120561942 | |||||||
| chr12:120562028 | G | A | 1 | a0001c0001t0002g0162 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1129-917G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 7/16 | chr12 | 120562028 | |||||||
| chr12:120562029 | G | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0127 |
2 | HG00323.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.1129-916G>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 7/16 | chr12 | 120562029 | |||||||
| chr12:120562267 | C | CT | 15 | a0001c0001t0001g0078 a0001c0001t0001g0115 a0001c0001t0001g0118 others(12): Show |
15 | HG00323.hp1 HG01109.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.1129-675dupT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 120562267 | ||||||
| chr12:120562267 | C | CTT | 75 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(72): Show |
81 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.1129-676_1129-675d others(4): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 120562267 | ||||||
| chr12:120562267 | C | CTTT | 5 | a0001c0001t0002g0139 a0001c0001t0002g0159 a0001c0001t0002g0177 others(2): Show |
5 | HG00621.hp2 HG01358.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.1129-677_1129-675d others(5): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 120562267 | ||||||
| chr12:120562267 | CTTTCTTT | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(4): Show |
9 | HG01109.hp2 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1129-674_1129-668d others(9): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 120562267 | ||||||
| chr12:120562270 | TC | T | 5 | a0001c0001t0001g0093 a0001c0001t0001g0109 a0001c0001t0001g0124 others(2): Show |
5 | HG01256.hp1 HG01993.hp2 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.1129-674delC | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 7/16 | chr12 | 120562270 | |||||||
| chr12:120562271 | C | CT | 26 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(23): Show |
28 | HG01123.hp2 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1129-654dupT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 120562271 | ||||||
| chr12:120562271 | C | CTT | 29 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(26): Show |
32 | HG00140.hp1 HG00558.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.1129-655_1129-654d others(4): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 120562271 | ||||||
| chr12:120562271 | C | T | 183 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(180): Show |
191 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.1129-674C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 7/16 | chr12 | 120562271 | |||||||
| chr12:120562271 | CT | C | 20 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0040 others(17): Show |
21 | HG01168.hp2 HG01261.hp2 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.1129-654delT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 120562271 | ||||||
| chr12:120562274 | T | TC | 8 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(5): Show |
8 | HG02145.hp1 HG02723.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1129-671_1129-670i others(3): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 7/16 | chr12 | 120562274 | |||||||
| chr12:120562275 | T | C | 1 | a0003c0006t0001g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1129-670T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 7/16 | chr12 | 120562275 | |||||||
| chr12:120562330 | A | G | 100 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(97): Show |
102 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1129-615A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 7/16 | chr12 | 120562330 | |||||||
| chr12:120562466 | G | A | 4 | a0001c0001t0001g0065 a0001c0001t0001g0117 a0001c0001t0004g0064 others(1): Show |
4 | HG01106.hp1 HG03669.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1129-479G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 7/16 | chr12 | 120562466 | |||||||
| chr12:120564022 | G | A | 6 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(3): Show |
6 | NA18939.hp1 NA18943.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.1665+79G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 10/16 | chr12 | 120564022 | |||||||
| chr12:120564153 | C | G | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(4): Show |
9 | HG01109.hp2 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1665+210C>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 10/16 | chr12 | 120564153 | |||||||
| chr12:120564303 | T | C | 2 | a0001c0001t0001g0260 a0001c0001t0001g0270 |
2 | HG01891.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1665+360T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 10/16 | chr12 | 120564303 | |||||||
| chr12:120564473 | A | C | 1 | a0001c0001t0001g0299 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1665+530A>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 10/16 | chr12 | 120564473 | |||||||
| chr12:120564582 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1666-490C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 10/16 | chr12 | 120564582 | |||||||
| chr12:120564916 | C | G | 1 | a0001c0001t0002g0334 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1666-156C>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 10/16 | chr12 | 120564916 | |||||||
| chr12:120564967 | A | G | 2 | a0001c0001t0002g0157 a0001c0001t0002g0158 |
2 | HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1666-105A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 10/16 | chr12 | 120564967 | |||||||
| chr12:120565002 | C | T | 5 | a0001c0001t0001g0340 a0001c0001t0001g0341 a0001c0001t0001g0342 others(2): Show |
5 | HG01261.hp2 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1666-70C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 10/16 | chr12 | 120565002 | |||||||
| chr12:120565329 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0024 |
3 | HG02280.hp2 HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1784-99C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 11/16 | chr12 | 120565329 | |||||||
| chr12:120565411 | A | C | 1 | a0001c0001t0001g0318 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1784-17A>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 11/16 | chr12 | 120565411 | |||||||
| chr12:120565600 | C | G | 1 | a0001c0001t0001g0288 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1885+71C>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 12/16 | chr12 | 120565600 | |||||||
| chr12:120565770 | A | G | 3 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0047 |
3 | HG01975.hp1 HG01993.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1885+241A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 12/16 | chr12 | 120565770 | |||||||
| chr12:120566020 | G | C | 1 | a0001c0001t0001g0269 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1885+491G>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 12/16 | chr12 | 120566020 | |||||||
| chr12:120566052 | A | G | 4 | a0001c0001t0001g0307 a0002c0002t0001g0281 a0002c0002t0001g0282 others(1): Show |
4 | HG02630.hp2 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1885+523A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 12/16 | chr12 | 120566052 | |||||||
| chr12:120566265 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1886-560T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 12/16 | chr12 | 120566265 | |||||||
| chr12:120566269 | A | G | 17 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(14): Show |
21 | HG01109.hp2 HG01168.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.1886-556A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 12/16 | chr12 | 120566269 | |||||||
| chr12:120566433 | A | C | 9 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0340 others(6): Show |
9 | HG01106.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.1886-392A>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 12/16 | chr12 | 120566433 | |||||||
| chr12:120566451 | C | T | 10 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0326 others(7): Show |
12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1886-374C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 12/16 | chr12 | 120566451 | |||||||
| chr12:120566573 | A | G | 272 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(269): Show |
289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.1886-252A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 12/16 | chr12 | 120566573 | |||||||
| chr12:120566657 | G | A | 2 | a0001c0001t0001g0220 a0001c0001t0001g0226 |
2 | HG01934.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1886-168G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 12/16 | chr12 | 120566657 | |||||||
| chr12:120566716 | C | G | 1 | a0001c0001t0001g0269 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1886-109C>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 12/16 | chr12 | 120566716 | |||||||
| chr12:120566761 | C | CA | 6 | a0001c0001t0001g0014 a0001c0001t0001g0250 a0001c0001t0001g0251 others(3): Show |
7 | HG02451.hp1 HG02818.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1886-46dupA | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr12 | 120566761 | ||||||
| chr12:120566761 | CA | C | 153 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0015 others(150): Show |
166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1886-46delA | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr12 | 120566761 | ||||||
| chr12:120566761 | CAA | C | 107 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(104): Show |
110 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.1886-47_1886-46del others(2): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr12 | 120566761 | ||||||
| chr12:120566787 | C | A | 100 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(97): Show |
102 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1886-38C>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 12/16 | chr12 | 120566787 | |||||||
| chr12:120566815 | T | G | 2 | a0001c0001t0001g0070 a0001c0001t0001g0122 |
2 | NA18983.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1886-10T>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 12/16 | chr12 | 120566815 | |||||||
| chr12:120567335 | C | CA | 146 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(143): Show |
156 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.2041+367dupA | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 120567335 | ||||||
| chr12:120567335 | C | CAA | 85 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0002g0003 others(82): Show |
92 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.2041+366_2041+367d others(4): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 120567335 | ||||||
| chr12:120567429 | G | A | 3 | a0001c0001t0003g0330 a0001c0001t0003g0331 a0001c0001t0003g0332 |
3 | HG01168.hp1 HG01169.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.2041+449G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120567429 | |||||||
| chr12:120567496 | T | A | 3 | a0001c0001t0001g0065 a0001c0001t0004g0064 a0001c0001t0004g0066 |
3 | HG01106.hp1 HG03669.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2041+516T>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120567496 | |||||||
| chr12:120567631 | G | A | 10 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0326 others(7): Show |
12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.2041+651G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120567631 | |||||||
| chr12:120567658 | G | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(4): Show |
9 | HG01109.hp2 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2041+678G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120567658 | |||||||
| chr12:120567700 | CA | C | 66 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(63): Show |
72 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.2041+738delA | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 120567700 | ||||||
| chr12:120567700 | CAA | C | 110 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(107): Show |
114 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.2041+737_2041+738d others(4): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 120567700 | ||||||
| chr12:120567745 | A | G | 339 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(336): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.2041+765A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120567745 | |||||||
| chr12:120567858 | T | TGG | 23 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(20): Show |
26 | HG01070.hp1 HG01071.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.2041+880_2041+881d others(4): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 120567858 | ||||||
| chr12:120567860 | G | GGGGT | 9 | a0001c0001t0001g0111 a0001c0001t0001g0273 a0001c0001t0001g0274 others(6): Show |
9 | HG01069.hp2 HG02145.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2041+881_2041+882i others(6): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 120567860 | ||||||
| chr12:120567860 | GGTGT | G | 89 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(86): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.2041+899_2041+902d others(6): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 120567860 | ||||||
| chr12:120567862 | T | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(204): Show |
225 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.2041+882T>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120567862 | |||||||
| chr12:120567864 | T | G | 2 | a0001c0001t0001g0059 a0001c0001t0001g0100 |
2 | HG02602.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.2041+884T>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120567864 | |||||||
| chr12:120567866 | T | G | 89 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(86): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.2041+886T>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120567866 | |||||||
| chr12:120567883 | A | G | 3 | a0001c0001t0001g0039 a0001c0001t0001g0049 a0001c0001t0001g0050 |
3 | HG02129.hp2 NA19000.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.2041+903A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120567883 | |||||||
| chr12:120567967 | AGAATT | A | 56 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(53): Show |
61 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.2041+991_2041+995d others(7): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 120567967 | ||||||
| chr12:120568155 | A | G | 198 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(195): Show |
206 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.2041+1175A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120568155 | |||||||
| chr12:120568213 | C | G | 1 | a0001c0001t0001g0127 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2041+1233C>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120568213 | |||||||
| chr12:120568470 | TATTA | T | 10 | a0001c0001t0001g0080 a0001c0001t0001g0085 a0001c0001t0001g0091 others(7): Show |
10 | HG00544.hp1 HG02027.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.2041+1494_2041+149 others(8): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 120568470 | ||||||
| chr12:120568479 | C | CT | 86 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(83): Show |
92 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.2041+1513dupT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 120568479 | ||||||
| chr12:120568479 | CT | C | 25 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(22): Show |
28 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.2041+1513delT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 120568479 | ||||||
| chr12:120568498 | T | C | 100 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(97): Show |
102 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.2041+1518T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120568498 | |||||||
| chr12:120568560 | C | G | 1 | a0001c0001t0001g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2041+1580C>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120568560 | |||||||
| chr12:120568568 | C | T | 1 | a0001c0001t0001g0306 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2041+1588C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120568568 | |||||||
| chr12:120568695 | C | T | 17 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(14): Show |
21 | HG01109.hp2 HG01168.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.2041+1715C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120568695 | |||||||
| chr12:120568696 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2041+1716G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120568696 | |||||||
| chr12:120568745 | G | C | 1 | a0001c0001t0001g0299 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2041+1765G>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120568745 | |||||||
| chr12:120568824 | T | G | 56 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(53): Show |
61 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.2041+1844T>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120568824 | |||||||
| chr12:120568899 | G | A | 3 | a0001c0001t0002g0163 a0001c0001t0002g0166 a0001c0001t0002g0174 |
3 | NA18959.hp2 NA19063.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.2041+1919G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120568899 | |||||||
| chr12:120568926 | A | G | 189 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(186): Show |
197 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.2041+1946A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120568926 | |||||||
| chr12:120568946 | C | T | 1 | a0001c0001t0002g0168 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2041+1966C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120568946 | |||||||
| chr12:120569027 | A | G | 15 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0260 others(12): Show |
16 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.2041+2047A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120569027 | |||||||
| chr12:120569035 | A | G | 1 | a0001c0001t0001g0286 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2041+2055A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120569035 | |||||||
| chr12:120569340 | TGTG | T | 17 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(14): Show |
21 | HG01109.hp2 HG01168.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.2042-1847_2042-184 others(7): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 120569340 | ||||||
| chr12:120569538 | C | CTTTTTTT others(4): Show |
9 | a0001c0001t0001g0016 a0001c0001t0001g0299 a0001c0001t0001g0300 others(6): Show |
10 | HG00673.hp1 HG02004.hp1 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.2042-1652_2042-164 others(15): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 120569538 | ||||||
| chr12:120569538 | C | CTTTTTTT others(5): Show |
55 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0015 others(52): Show |
63 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.2042-1642_2042-164 others(16): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 120569538 | ||||||
| chr12:120569538 | C | CTTTTTTT others(6): Show |
16 | a0001c0001t0001g0028 a0001c0001t0001g0103 a0001c0001t0001g0124 others(13): Show |
16 | HG00323.hp1 HG01891.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.2042-1642_2042-164 others(17): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 120569538 | ||||||
| chr12:120569538 | C | CTTTTTTT others(7): Show |
168 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(165): Show |
176 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.2042-1642_2042-164 others(18): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 120569538 | ||||||
| chr12:120569538 | C | CTTTTTTT others(8): Show |
13 | a0001c0001t0001g0078 a0001c0001t0001g0091 a0001c0001t0001g0107 others(10): Show |
13 | HG00558.hp2 HG01109.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.2042-1642_2042-164 others(19): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 120569538 | ||||||
| chr12:120569554 | C | T | 26 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(23): Show |
29 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.2042-1637C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120569554 | |||||||
| chr12:120569636 | T | G | 1 | a0001c0001t0002g0134 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2042-1555T>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120569636 | |||||||
| chr12:120569693 | A | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0033 |
4 | HG02965.hp2 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2042-1498A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120569693 | |||||||
| chr12:120569713 | T | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(4): Show |
9 | HG01109.hp2 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2042-1478T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120569713 | |||||||
| chr12:120569781 | G | A | 9 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0340 others(6): Show |
9 | HG01106.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.2042-1410G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120569781 | |||||||
| chr12:120569856 | T | G | 6 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(3): Show |
6 | HG02145.hp1 HG02723.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2042-1335T>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120569856 | |||||||
| chr12:120569892 | T | A | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2042-1299T>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120569892 | |||||||
| chr12:120569946 | G | A | 1 | a0006c0008t0001g0056 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2042-1245G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120569946 | |||||||
| chr12:120570019 | A | T | 4 | a0001c0001t0001g0088 a0001c0001t0001g0106 a0001c0001t0001g0109 others(1): Show |
4 | HG01256.hp1 HG03491.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.2042-1172A>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120570019 | |||||||
| chr12:120570165 | G | A | 9 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0340 others(6): Show |
9 | HG01106.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.2042-1026G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120570165 | |||||||
| chr12:120570169 | G | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(4): Show |
9 | HG01109.hp2 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2042-1022G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120570169 | |||||||
| chr12:120570184 | C | CT | 110 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
119 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.2042-987dupT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 120570184 | ||||||
| chr12:120570335 | C | T | 1 | a0001c0001t0008g0061 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2042-856C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120570335 | |||||||
| chr12:120570553 | T | A | 9 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0340 others(6): Show |
9 | HG01106.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.2042-638T>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120570553 | |||||||
| chr12:120570668 | A | G | 5 | a0001c0001t0001g0340 a0001c0001t0001g0341 a0001c0001t0001g0342 others(2): Show |
5 | HG01261.hp2 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.2042-523A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120570668 | |||||||
| chr12:120570806 | A | C | 1 | a0001c0001t0002g0202 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2042-385A>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120570806 | |||||||
| chr12:120570888 | G | GA | 4 | a0001c0001t0001g0078 a0001c0001t0001g0090 a0001c0001t0001g0101 others(1): Show |
4 | NA18994.hp2 NA19003.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.2042-300dupA | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 120570888 | ||||||
| chr12:120570916 | T | C | 2 | a0001c0001t0002g0325 a0001c0001t0002g0334 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2042-275T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120570916 | |||||||
| chr12:120570943 | C | T | 1 | a0001c0001t0003g0329 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2042-248C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120570943 | |||||||
| chr12:120570980 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2042-211C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120570980 | |||||||
| chr12:120570991 | A | G | 1 | a0001c0001t0001g0016 | 2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2042-200A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120570991 | |||||||
| chr12:120571129 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2042-62C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120571129 | |||||||
| chr12:120571155 | G | A | 74 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0015 others(71): Show |
83 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.2042-36G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 13/16 | chr12 | 120571155 | |||||||
| chr12:120571320 | G | T | 1 | a0001c0001t0002g0191 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2142+29G>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120571320 | |||||||
| chr12:120571395 | C | T | 99 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(96): Show |
101 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.2142+104C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120571395 | |||||||
| chr12:120571525 | A | C | 10 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0326 others(7): Show |
12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.2142+234A>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120571525 | |||||||
| chr12:120571527 | C | T | 2 | a0001c0001t0002g0325 a0001c0001t0002g0334 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2142+236C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120571527 | |||||||
| chr12:120571678 | C | G | 1 | a0001c0001t0002g0168 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2142+387C>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120571678 | |||||||
| chr12:120571693 | G | A | 1 | a0003c0006t0001g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2142+402G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120571693 | |||||||
| chr12:120571774 | T | A | 89 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(86): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.2142+483T>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120571774 | |||||||
| chr12:120571793 | A | G | 1 | a0001c0001t0008g0061 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2142+502A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120571793 | |||||||
| chr12:120572061 | G | GT | 237 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(234): Show |
251 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.2142+785dupT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr12 | 120572061 | ||||||
| chr12:120572061 | G | GTT | 20 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0001g0091 others(17): Show |
20 | HG00597.hp2 HG01361.hp2 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.2142+784_2142+785d others(4): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr12 | 120572061 | ||||||
| chr12:120572123 | G | C | 1 | a0001c0001t0001g0240 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2142+832G>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120572123 | |||||||
| chr12:120572140 | T | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(51): Show |
64 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.2142+849T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120572140 | |||||||
| chr12:120572141 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(51): Show |
64 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.2142+850G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120572141 | |||||||
| chr12:120572145 | T | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(51): Show |
64 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.2142+854T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120572145 | |||||||
| chr12:120572151 | C | G | 4 | a0001c0001t0001g0216 a0001c0001t0001g0293 a0001c0001t0001g0297 others(1): Show |
4 | HG00558.hp1 HG00609.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.2142+860C>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120572151 | |||||||
| chr12:120572227 | C | T | 89 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(86): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.2142+936C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120572227 | |||||||
| chr12:120572257 | A | G | 2 | a0001c0001t0002g0325 a0001c0001t0002g0334 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2142+966A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120572257 | |||||||
| chr12:120572267 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2142+976C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120572267 | |||||||
| chr12:120572289 | A | G | 6 | a0001c0001t0001g0068 a0001c0001t0001g0340 a0001c0001t0001g0341 others(3): Show |
6 | HG01261.hp2 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.2142+998A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120572289 | |||||||
| chr12:120572434 | T | C | 89 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(86): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.2142+1143T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120572434 | |||||||
| chr12:120572491 | T | C | 14 | a0001c0001t0002g0010 a0001c0001t0002g0152 a0001c0001t0002g0155 others(11): Show |
15 | HG00544.hp2 HG01123.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.2142+1200T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120572491 | |||||||
| chr12:120572585 | CTTGTT | C | 3 | a0001c0001t0001g0295 a0001c0001t0001g0307 a0001c0001t0002g0177 |
3 | HG01975.hp2 HG02895.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.2142+1318_2142+132 others(9): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr12 | 120572585 | ||||||
| chr12:120572585 | CTTGTTTT others(3): Show |
C | 1 | a0001c0001t0001g0258 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2142+1313_2142+132 others(14): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr12 | 120572585 | ||||||
| chr12:120572652 | A | G | 1 | a0001c0001t0002g0177 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2142+1361A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120572652 | |||||||
| chr12:120572688 | C | T | 3 | a0001c0001t0002g0169 a0001c0001t0002g0182 a0001c0001t0002g0207 |
3 | HG00609.hp1 HG00621.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.2142+1397C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120572688 | |||||||
| chr12:120572820 | A | G | 1 | a0001c0001t0001g0312 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2142+1529A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120572820 | |||||||
| chr12:120572893 | G | A | 104 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(101): Show |
106 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.2142+1602G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120572893 | |||||||
| chr12:120572900 | C | CT | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(108): Show |
128 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.2142+1630dupT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr12 | 120572900 | ||||||
| chr12:120572900 | C | CTT | 51 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0052 others(48): Show |
54 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.2142+1629_2142+163 others(6): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr12 | 120572900 | ||||||
| chr12:120572900 | C | CTTT | 34 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(31): Show |
37 | HG00544.hp2 HG00597.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.2142+1628_2142+163 others(7): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr12 | 120572900 | ||||||
| chr12:120572900 | C | CTTTT | 9 | a0001c0001t0002g0147 a0001c0001t0002g0158 a0001c0001t0002g0179 others(6): Show |
9 | HG00558.hp2 HG01361.hp1 HG04199.hp2 others(6): Show |
intron_variant | MODIFIER | c.2142+1627_2142+163 others(8): Show |
RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr12 | 120572900 | ||||||
| chr12:120572900 | CT | C | 7 | a0001c0001t0001g0070 a0001c0001t0001g0092 a0001c0001t0001g0104 others(4): Show |
7 | HG01243.hp1 HG01256.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.2142+1630delT | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr12 | 120572900 | ||||||
| chr12:120573060 | T | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(4): Show |
9 | HG01109.hp2 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2142+1769T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120573060 | |||||||
| chr12:120573082 | G | A | 9 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0340 others(6): Show |
9 | HG01106.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.2142+1791G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120573082 | |||||||
| chr12:120573113 | C | T | 10 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0326 others(7): Show |
12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.2142+1822C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120573113 | |||||||
| chr12:120573203 | G | A | 329 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(326): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.2142+1912G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120573203 | |||||||
| chr12:120573250 | G | A | 10 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0326 others(7): Show |
12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.2142+1959G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120573250 | |||||||
| chr12:120573369 | C | T | 1 | a0001c0003t0002g0165 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2142+2078C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120573369 | |||||||
| chr12:120573567 | C | T | 10 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0326 others(7): Show |
12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.2143-2064C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120573567 | |||||||
| chr12:120573585 | C | CA | 74 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0015 others(71): Show |
83 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.2143-2031dupA | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr12 | 120573585 | ||||||
| chr12:120573664 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2143-1967T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120573664 | |||||||
| chr12:120573811 | T | C | 1 | a0001c0001t0001g0291 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2143-1820T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120573811 | |||||||
| chr12:120573972 | C | G | 3 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 |
3 | HG01884.hp1 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2143-1659C>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120573972 | |||||||
| chr12:120573979 | A | G | 1 | a0001c0001t0002g0325 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2143-1652A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120573979 | |||||||
| chr12:120574004 | A | G | 24 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0030 others(21): Show |
26 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.2143-1627A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120574004 | |||||||
| chr12:120574045 | T | C | 189 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(186): Show |
197 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.2143-1586T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120574045 | |||||||
| chr12:120574117 | A | C | 1 | a0001c0001t0002g0208 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2143-1514A>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120574117 | |||||||
| chr12:120574312 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2143-1319T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120574312 | |||||||
| chr12:120574355 | A | G | 1 | a0001c0001t0001g0016 | 2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2143-1276A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120574355 | |||||||
| chr12:120574466 | A | C | 1 | a0001c0001t0002g0137 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2143-1165A>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120574466 | |||||||
| chr12:120574559 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2143-1072G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120574559 | |||||||
| chr12:120574653 | C | T | 67 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(64): Show |
74 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.2143-978C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120574653 | |||||||
| chr12:120574755 | G | A | 7 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0234 others(4): Show |
7 | HG00597.hp2 HG00621.hp1 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2143-876G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120574755 | |||||||
| chr12:120574757 | C | T | 2 | a0001c0001t0002g0141 a0001c0001t0002g0201 |
2 | NA18952.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.2143-874C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120574757 | |||||||
| chr12:120574782 | C | T | 10 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0326 others(7): Show |
12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.2143-849C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120574782 | |||||||
| chr12:120574876 | A | G | 1 | a0001c0001t0001g0312 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2143-755A>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120574876 | |||||||
| chr12:120574914 | C | T | 3 | a0001c0001t0001g0065 a0001c0001t0004g0064 a0001c0001t0004g0066 |
3 | HG01106.hp1 HG03669.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2143-717C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120574914 | |||||||
| chr12:120575076 | T | TA | 37 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(34): Show |
42 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.2143-542dupA | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr12 | 120575076 | ||||||
| chr12:120575076 | TA | T | 197 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(194): Show |
205 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.2143-542delA | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr12 | 120575076 | ||||||
| chr12:120575177 | A | C | 1 | a0001c0001t0001g0297 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2143-454A>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120575177 | |||||||
| chr12:120575273 | C | T | 1 | a0001c0001t0002g0309 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2143-358C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120575273 | |||||||
| chr12:120575282 | G | A | 1 | a0001c0001t0001g0008 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2143-349G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120575282 | |||||||
| chr12:120575345 | G | T | 88 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(85): Show |
94 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.2143-286G>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120575345 | |||||||
| chr12:120575609 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(4): Show |
9 | HG01109.hp2 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2143-22C>T | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 14/16 | chr12 | 120575609 | |||||||
| chr12:120575693 | G | C | 3 | a0001c0001t0001g0065 a0001c0001t0004g0064 a0001c0001t0004g0066 |
3 | HG01106.hp1 HG03669.hp2 HG03710.hp2 |
splice_region_variant&intron_variant | LOW | c.2200+5G>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 15/16 | chr12 | 120575693 | |||||||
| chr12:120575982 | T | C | 9 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0340 others(6): Show |
9 | HG01106.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.2359+32T>C | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 16/16 | chr12 | 120575982 | |||||||
| chr12:120576224 | G | A | 26 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(23): Show |
29 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.2359+274G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 16/16 | chr12 | 120576224 | |||||||
| chr12:120576264 | G | A | 12 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(9): Show |
14 | HG01109.hp2 HG01261.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.2359+314G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 16/16 | chr12 | 120576264 | |||||||
| chr12:120576357 | G | A | 56 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(53): Show |
61 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.2360-233G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 16/16 | chr12 | 120576357 | |||||||
| chr12:120576389 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2360-201G>A | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 16/16 | chr12 | 120576389 | |||||||
| chr12:120576570 | C | G | 10 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0326 others(7): Show |
12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.2360-20C>G | RNF10 | ENSG00000022840.17 | transcript | ENST00000325954.9 | protein_coding | 16/16 | chr12 | 120576570 |