Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 285498 |
| ensemblid | ENSG00000178222.14 |
| hgncid | 27729 |
| symbol | RNF212 |
| name | ring finger protein 212 |
| refseq_nuc | NM_001131034.4 |
| refseq_prot | NP_001124506.1 |
| ensembl_nuc | ENST00000433731.7 |
| ensembl_prot | ENSP00000389709.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 1071478 |
| end | 1113564 |
| strand | - |
| ver | v1.2 |
| region | chr4:1071478-1113564 |
| region5000 | chr4:1066478-1118564 |
| regionname0 | RNF212_chr4_1071478_1113564 |
| regionname5000 | RNF212_chr4_1066478_1118564 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 297 | 389 | 82 | 76 | 180 | 7 | 42 | 139 | RNF212_chr4_1066478_1118564 | RNF212 | MANWV others(292): Show |
chr4 | 1066478 | 1118564 |
| a0002 | 0/0 | 297 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | MASWV others(292): Show |
chr4 | 1066478 | 1118564 |
| a0003 | 0/0 | 297 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | RNF212_chr4_1066478_1118564 | RNF212 | MANWV others(292): Show |
chr4 | 1066478 | 1118564 |
| a0004 | 0/0 | 297 | 3 | 1 | 1 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | MANWV others(292): Show |
chr4 | 1066478 | 1118564 |
| a0005 | 0/0 | 297 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | MANWV others(292): Show |
chr4 | 1066478 | 1118564 |
| a0006 | 0/0 | 297 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | MANWV others(292): Show |
chr4 | 1066478 | 1118564 |
| a0007 | 0/0 | 297 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | MANWV others(292): Show |
chr4 | 1066478 | 1118564 |
| a0008 | 0/0 | 297 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | MANWV others(292): Show |
chr4 | 1066478 | 1118564 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 891 | 219 | 33 | 42 | 111 | 5 | 27 | RNF212_chr4_1066478_1118564 | RNF212 | ATGGC others(886): Show |
chr4 | 1066478 | 1118564 | ||
| a0001c0002 | 1/0 | 891 | 169 | 48 | 34 | 69 | 2 | 15 | RNF212_chr4_1066478_1118564 | RNF212 | ATGGC others(886): Show |
chr4 | 1066478 | 1118564 | ||
| a0001c0009 | 0/0 | 891 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | ATGGC others(886): Show |
chr4 | 1066478 | 1118564 | ||
| a0002c0003 | 0/0 | 891 | 5 | 5 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | ATGGC others(886): Show |
chr4 | 1066478 | 1118564 | ||
| a0003c0004 | 0/0 | 891 | 4 | 0 | 0 | 4 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | ATGGC others(886): Show |
chr4 | 1066478 | 1118564 | ||
| a0004c0005 | 0/0 | 891 | 3 | 1 | 1 | 0 | 1 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | ATGGC others(886): Show |
chr4 | 1066478 | 1118564 | ||
| a0005c0006 | 0/0 | 891 | 2 | 0 | 0 | 0 | 0 | 2 | RNF212_chr4_1066478_1118564 | RNF212 | ATGGC others(886): Show |
chr4 | 1066478 | 1118564 | ||
| a0006c0008 | 0/0 | 891 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | ATGGC others(886): Show |
chr4 | 1066478 | 1118564 | ||
| a0007c0007 | 0/0 | 891 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | ATGGC others(886): Show |
chr4 | 1066478 | 1118564 | ||
| a0008c0010 | 0/0 | 891 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | ATGGC others(886): Show |
chr4 | 1066478 | 1118564 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2389 | 206 | 30 | 41 | 106 | 5 | 23 | RNF212_chr4_1066478_1118564 | RNF212 | GCAGA others(2384): Show |
chr4 | 1066478 | 1118564 |
| a0001c0001t0005 | 0/0 | 2389 | 4 | 0 | 0 | 0 | 0 | 4 | RNF212_chr4_1066478_1118564 | RNF212 | GCAGA others(2384): Show |
chr4 | 1066478 | 1118564 |
| a0001c0001t0006 | 0/0 | 2389 | 3 | 2 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | GCAGA others(2384): Show |
chr4 | 1066478 | 1118564 |
| a0001c0001t0008 | 0/0 | 2389 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | GCAGA others(2384): Show |
chr4 | 1066478 | 1118564 |
| a0001c0001t0009 | 0/0 | 2380 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | CCCCC others(2375): Show |
chr4 | 1066478 | 1118564 |
| a0001c0001t0010 | 0/0 | 2389 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | GCAGA others(2384): Show |
chr4 | 1066478 | 1118564 |
| a0001c0001t0014 | 0/0 | 2389 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | GCAGA others(2384): Show |
chr4 | 1066478 | 1118564 |
| a0001c0001t0015 | 0/0 | 2389 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | GCAGA others(2384): Show |
chr4 | 1066478 | 1118564 |
| a0001c0002t0001 | 0/0 | 2389 | 22 | 21 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | GCAGA others(2384): Show |
chr4 | 1066478 | 1118564 |
| a0001c0002t0002 | 1/0 | 2390 | 109 | 3 | 25 | 68 | 2 | 10 | RNF212_chr4_1066478_1118564 | RNF212 | GCAGA others(2385): Show |
chr4 | 1066478 | 1118564 |
| a0001c0002t0003 | 0/0 | 2389 | 23 | 11 | 7 | 0 | 0 | 5 | RNF212_chr4_1066478_1118564 | RNF212 | GCAGA others(2384): Show |
chr4 | 1066478 | 1118564 |
| a0001c0002t0004 | 0/0 | 2390 | 7 | 7 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | GCAGA others(2385): Show |
chr4 | 1066478 | 1118564 |
| a0001c0002t0006 | 0/0 | 2389 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | GCAGA others(2384): Show |
chr4 | 1066478 | 1118564 |
| a0001c0002t0007 | 0/0 | 2417 | 3 | 3 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | GCAGA others(2412): Show |
chr4 | 1066478 | 1118564 |
| a0001c0002t0012 | 0/0 | 2390 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | GCAGA others(2385): Show |
chr4 | 1066478 | 1118564 |
| a0001c0002t0013 | 0/0 | 2389 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | GCAGA others(2384): Show |
chr4 | 1066478 | 1118564 |
| a0001c0002t0016 | 0/0 | 2389 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | GCAGA others(2384): Show |
chr4 | 1066478 | 1118564 |
| a0001c0002t0017 | 0/0 | 2390 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | GCAGA others(2385): Show |
chr4 | 1066478 | 1118564 |
| a0001c0009t0003 | 0/0 | 2389 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | GCAGA others(2384): Show |
chr4 | 1066478 | 1118564 |
| a0002c0003t0001 | 0/0 | 2389 | 5 | 5 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | GCAGA others(2384): Show |
chr4 | 1066478 | 1118564 |
| a0003c0004t0001 | 0/0 | 2389 | 4 | 0 | 0 | 4 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | GCAGA others(2384): Show |
chr4 | 1066478 | 1118564 |
| a0004c0005t0002 | 0/0 | 2390 | 3 | 1 | 1 | 0 | 1 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | GCAGA others(2385): Show |
chr4 | 1066478 | 1118564 |
| a0005c0006t0001 | 0/0 | 2389 | 2 | 0 | 0 | 0 | 0 | 2 | RNF212_chr4_1066478_1118564 | RNF212 | GCAGA others(2384): Show |
chr4 | 1066478 | 1118564 |
| a0006c0008t0011 | 0/0 | 2390 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | GCAGA others(2385): Show |
chr4 | 1066478 | 1118564 |
| a0007c0007t0002 | 0/0 | 2390 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | GCAGA others(2385): Show |
chr4 | 1066478 | 1118564 |
| a0008c0010t0001 | 0/0 | 2389 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | GCAGA others(2384): Show |
chr4 | 1066478 | 1118564 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0003 | 0/0 | 4 | 1 | 1 | 0 | 1 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0270 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0005g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0006g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0006g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0006g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0008g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0008g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0009g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0010g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0014g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0015g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0004 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0005 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0010 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0098 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0004g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0004g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0006g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0007g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0007g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0007g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0012g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0013g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0016g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0017g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0009t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0002c0003t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0002c0003t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0002c0003t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0003c0004t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0003c0004t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0003c0004t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0003c0004t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0004c0005t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0004c0005t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0004c0005t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0005c0006t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0005c0006t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0006c0008t0011g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0007c0007t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0008c0010t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0265 | EUR | GBR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00099 | hp2 | a0004 | c0005 | t0002 | g0245 | EUR | GBR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0188 | EUR | FIN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0191 | EUR | FIN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0158 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0217 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0231 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0246 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00597 | hp1 | a0003 | c0004 | t0001 | g0216 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0232 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00642 | hp2 | a0001 | c0002 | t0003 | g0345 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0257 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00735 | hp1 | a0001 | c0002 | t0003 | g0342 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0251 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01074 | hp2 | a0001 | c0002 | t0003 | g0339 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0058 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01167 | hp1 | a0001 | c0001 | t0006 | g0349 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0207 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0252 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0206 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0289 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0295 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01243 | hp2 | a0001 | c0002 | t0003 | g0325 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0299 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0010 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01261 | hp2 | a0004 | c0005 | t0002 | g0321 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0223 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01358 | hp2 | a0001 | c0002 | t0003 | g0346 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0306 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01433 | hp1 | a0001 | c0002 | t0016 | g0336 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0338 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0010 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01891 | hp1 | a0006 | c0008 | t0011 | g0040 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0233 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01934 | hp1 | a0001 | c0002 | t0003 | g0343 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0222 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01975 | hp2 | a0007 | c0007 | t0002 | g0224 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0228 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0057 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0227 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0159 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02071 | hp1 | a0001 | c0001 | t0008 | g0052 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0268 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0308 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0253 | EAS | CDX | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CDX | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0309 | EAS | CDX | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CDX | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0059 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02258 | hp1 | a0001 | c0002 | t0007 | g0353 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0302 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0234 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0241 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0096 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02451 | hp2 | a0001 | c0002 | t0003 | g0328 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0261 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02572 | hp1 | a0002 | c0003 | t0001 | g0011 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0319 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0149 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02622 | hp2 | a0001 | c0002 | t0003 | g0327 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02630 | hp1 | a0001 | c0002 | t0012 | g0102 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02630 | hp2 | a0001 | c0002 | t0003 | g0333 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02647 | hp2 | a0002 | c0003 | t0001 | g0323 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02683 | hp1 | a0005 | c0006 | t0001 | g0133 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0225 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02698 | hp2 | a0005 | c0006 | t0001 | g0128 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02717 | hp1 | a0001 | c0002 | t0004 | g0014 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02717 | hp2 | a0001 | c0002 | t0013 | g0101 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0296 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0350 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02886 | hp1 | a0001 | c0002 | t0003 | g0330 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02895 | hp1 | a0002 | c0003 | t0001 | g0324 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0235 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02922 | hp1 | a0001 | c0001 | t0010 | g0183 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02922 | hp2 | a0001 | c0002 | t0004 | g0013 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02965 | hp1 | a0001 | c0009 | t0003 | g0326 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02965 | hp2 | a0001 | c0002 | t0003 | g0329 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02970 | hp1 | a0001 | c0002 | t0003 | g0340 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0150 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02976 | hp1 | a0001 | c0002 | t0004 | g0048 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02976 | hp2 | a0001 | c0002 | t0003 | g0332 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0201 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0023 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0294 | AFR | MSL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0042 | AFR | MSL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03139 | hp1 | a0001 | c0002 | t0004 | g0014 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03139 | hp2 | a0001 | c0002 | t0004 | g0013 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0100 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03195 | hp2 | a0001 | c0002 | t0007 | g0354 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03209 | hp1 | a0001 | c0002 | t0007 | g0355 | AFR | MSL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0034 | AFR | MSL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0099 | AFR | MSL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | MSL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0023 | AFR | MSL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0030 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03491 | hp1 | a0001 | c0001 | t0005 | g0046 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0045 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0030 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03516 | hp2 | a0001 | c0002 | t0006 | g0351 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03540 | hp2 | a0001 | c0002 | t0003 | g0334 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | MSL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | MSL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03669 | hp1 | a0001 | c0002 | t0003 | g0341 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0264 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0310 | SAS | STU | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03688 | hp2 | a0001 | c0002 | t0003 | g0033 | SAS | STU | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0047 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03834 | hp1 | a0001 | c0002 | t0003 | g0344 | SAS | BEB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03927 | hp1 | a0001 | c0002 | t0003 | g0347 | SAS | BEB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | STU | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | STU | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0275 | SAS | BEB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | BEB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG04199 | hp1 | a0001 | c0002 | t0003 | g0033 | SAS | STU | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0036 | SAS | STU | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | STU | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0043 | SAS | STU | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0269 | SAS | STU | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18522 | hp1 | a0008 | c0010 | t0001 | g0091 | AFR | YRI | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | YRI | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0248 | EAS | CHB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | YRI | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | YRI | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0243 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0160 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18944 | hp1 | a0003 | c0004 | t0001 | g0139 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0273 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18948 | hp1 | a0001 | c0002 | t0002 | g0260 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0263 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0314 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0106 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0254 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0247 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0144 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0305 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18966 | hp2 | a0001 | c0001 | t0015 | g0196 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18967 | hp2 | a0001 | c0002 | t0002 | g0244 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0286 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18978 | hp1 | a0001 | c0002 | t0002 | g0291 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0218 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18981 | hp2 | a0001 | c0002 | t0002 | g0157 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0259 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0258 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18990 | hp2 | a0001 | c0001 | t0014 | g0087 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18992 | hp1 | a0001 | c0001 | t0009 | g0356 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18992 | hp2 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18994 | hp1 | a0001 | c0001 | t0008 | g0053 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18997 | hp2 | a0001 | c0002 | t0002 | g0312 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0303 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0255 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0229 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19005 | hp1 | a0003 | c0004 | t0001 | g0140 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0161 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19009 | hp2 | a0001 | c0002 | t0017 | g0352 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19010 | hp1 | a0001 | c0002 | t0002 | g0304 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0300 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0301 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19012 | hp2 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19030 | hp1 | a0001 | c0002 | t0004 | g0038 | AFR | LWK | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0298 | AFR | LWK | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | LWK | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0288 | AFR | LWK | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19056 | hp2 | a0001 | c0002 | t0002 | g0147 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0276 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0267 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0219 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19065 | hp2 | a0003 | c0004 | t0001 | g0141 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0162 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19067 | hp1 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19072 | hp2 | a0001 | c0002 | t0002 | g0315 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0287 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0274 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0230 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0307 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0266 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19240 | hp1 | a0002 | c0003 | t0001 | g0011 | AFR | YRI | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19240 | hp2 | a0001 | c0002 | t0003 | g0331 | AFR | YRI | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA20129 | hp1 | a0001 | c0002 | t0003 | g0337 | AFR | ASW | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ASW | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | TSI | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0236 | EUR | TSI | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0226 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0239 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0097 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0348 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02486 | hp1 | a0004 | c0005 | t0002 | g0238 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02486 | hp2 | a0002 | c0003 | t0001 | g0011 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0290 | AFR | USA | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG06807 | hp2 | a0001 | c0002 | t0004 | g0039 | AFR | USA | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0256 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | USA | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA20300 | hp2 | a0001 | c0002 | t0003 | g0335 | AFR | USA | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0270 | REF | REF | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0098 | REF | REF | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:1072981 | C | T | 1 | a0003 | 4 | HG00597.hp1 NA18944.hp1 NA19005.hp1 others(1): Show |
missense_variant | MODERATE | c.787G>A | p.Val263Ile | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 887/2390 | 787/894 | 263/297 | chr4 | 1072981 | |||
| chr4:1073170 | A | C | 1 | a0006 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.598T>G | p.Cys200Gly | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 698/2390 | 598/894 | 200/297 | chr4 | 1073170 | |||
| chr4:1081428 | G | C | 1 | a0005 | 2 | HG02683.hp1 HG02698.hp2 |
missense_variant | MODERATE | c.455C>G | p.Ala152Gly | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/10 | 555/2390 | 455/894 | 152/297 | chr4 | 1081428 | |||
| chr4:1081584 | A | G | 1 | a0008 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.398T>C | p.Ile133Thr | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 6/10 | 498/2390 | 398/894 | 133/297 | chr4 | 1081584 | |||
| chr4:1081619 | A | C | 1 | a0007 | 1 | HG01975.hp2 | missense_variant&splice_region_variant | MODERATE | c.363T>G | p.Ser121Arg | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 6/10 | 463/2390 | 363/894 | 121/297 | chr4 | 1081619 | |||
| chr4:1096836 | C | T | 1 | a0004 | 3 | HG00099.hp2 HG01261.hp2 HG02486.hp1 |
missense_variant | MODERATE | c.175G>A | p.Asp59Asn | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/10 | 275/2390 | 175/894 | 59/297 | chr4 | 1096836 | |||
| chr4:1113457 | T | C | 1 | a0002 | 5 | HG02486.hp2 HG02572.hp1 HG02647.hp2 others(2): Show |
missense_variant | MODERATE | c.8A>G | p.Asn3Ser | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/10 | 108/2390 | 8/894 | 3/297 | chr4 | 1113457 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:1072925 | A | G | 1 | a0001c0009 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.843T>C | p.Ala281Ala | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 943/2390 | 843/894 | 281/297 | chr4 | 1072925 | |||
| chr4:1096837 | G | A | 4 | a0001c0001 a0003c0004 a0005c0006 others(1): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
splice_region_variant&synonymous_variant | LOW | c.174C>T | p.Thr58Thr | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/10 | 274/2390 | 174/894 | 58/297 | chr4 | 1096837 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:1071587 | T | G | 1 | a0001c0001t0005 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1287A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 1287 | chr4 | 1071587 | ||||||
| chr4:1071698 | T | C | 3 | a0001c0002t0004 a0001c0002t0012 a0006c0008t0011 |
9 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1176A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 1176 | chr4 | 1071698 | ||||||
| chr4:1071922 | T | C | 1 | a0001c0002t0013 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*952A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 952 | chr4 | 1071922 | ||||||
| chr4:1071976 | T | C | 1 | a0001c0001t0014 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*898A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 898 | chr4 | 1071976 | ||||||
| chr4:1071994 | T | C | 1 | a0001c0002t0012 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*880A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 880 | chr4 | 1071994 | ||||||
| chr4:1072055 | A | C | 1 | a0001c0001t0008 | 2 | HG02071.hp1 NA18994.hp1 |
3_prime_UTR_variant | MODIFIER | c.*819T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 819 | chr4 | 1072055 | ||||||
| chr4:1072125 | C | T | 3 | a0001c0002t0004 a0001c0002t0012 a0006c0008t0011 |
9 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*749G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 749 | chr4 | 1072125 | ||||||
| chr4:1072154 | G | A | 1 | a0001c0001t0015 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*720C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 720 | chr4 | 1072154 | ||||||
| chr4:1072214 | C | T | 1 | a0006c0008t0011 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*660G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 660 | chr4 | 1072214 | ||||||
| chr4:1072284 | AT | A | 19 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(16): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
3_prime_UTR_variant | MODIFIER | c.*589delA | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 589 | chr4 | 1072284 | ||||||
| chr4:1072493 | G | T | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*381C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 381 | chr4 | 1072493 | ||||||
| chr4:1072602 | A | G | 1 | a0001c0002t0016 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*272T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 272 | chr4 | 1072602 | ||||||
| chr4:1113490 | G | A | 4 | a0001c0002t0003 a0001c0002t0007 a0001c0002t0016 others(1): Show |
28 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(25): Show |
5_prime_UTR_variant | MODIFIER | c.-26C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/10 | 26 | chr4 | 1113490 | ||||||
| chr4:1113528 | G | A | 2 | a0001c0001t0006 a0001c0002t0006 |
4 | HG01167.hp1 HG02109.hp2 HG02809.hp1 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-64C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/10 | chr4 | 1113528 | |||||||
| chr4:1113534 | C | A | 1 | a0001c0002t0017 | 1 | NA19009.hp2 | 5_prime_UTR_variant | MODIFIER | c.-70G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/10 | 70 | chr4 | 1113534 | ||||||
| chr4:1113549 | A | C | 1 | a0001c0001t0009 | 1 | NA18992.hp1 | 5_prime_UTR_variant | MODIFIER | c.-85T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/10 | 85 | chr4 | 1113549 | ||||||
| chr4:1113550 | G | A | 1 | a0001c0001t0009 | 1 | NA18992.hp1 | 5_prime_UTR_variant | MODIFIER | c.-86C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/10 | 86 | chr4 | 1113550 | ||||||
| chr4:1113552 | C | G | 1 | a0001c0001t0009 | 1 | NA18992.hp1 | 5_prime_UTR_variant | MODIFIER | c.-88G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/10 | 88 | chr4 | 1113552 | ||||||
| chr4:1113553 | G | GGGCAGCT others(21): Show |
1 | a0001c0002t0007 | 3 | HG02258.hp1 HG03195.hp2 HG03209.hp1 |
5_prime_UTR_variant | MODIFIER | c.-90_-89insGTCGACTT others(20): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/10 | 90 | chr4 | 1113553 | ||||||
| chr4:1113555 | GCAGCTCT others(8): Show |
G | 1 | a0001c0001t0009 | 1 | NA18992.hp1 | 5_prime_UTR_variant | MODIFIER | c.-106_-92delGCAGGCG others(8): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/10 | 92 | chr4 | 1113555 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:1073244 | G | A | 45 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(42): Show |
49 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.575-51C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 9/9 | chr4 | 1073244 | |||||||
| chr4:1073387 | T | G | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.575-194A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 9/9 | chr4 | 1073387 | |||||||
| chr4:1073451 | T | A | 14 | a0001c0002t0002g0106 a0001c0002t0002g0157 a0001c0002t0002g0217 others(11): Show |
14 | HG00423.hp1 HG00673.hp2 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.574+148A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 9/9 | chr4 | 1073451 | |||||||
| chr4:1073461 | T | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.574+138A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 9/9 | chr4 | 1073461 | |||||||
| chr4:1073479 | G | T | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.574+120C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 9/9 | chr4 | 1073479 | |||||||
| chr4:1073569 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.574+30G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 9/9 | chr4 | 1073569 | |||||||
| chr4:1073742 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.511-80T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1073742 | |||||||
| chr4:1073834 | C | G | 4 | a0001c0002t0001g0035 a0001c0002t0001g0099 a0001c0002t0001g0100 others(1): Show |
4 | HG03195.hp1 HG03225.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-172G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1073834 | |||||||
| chr4:1073850 | T | G | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
284 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.511-188A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1073850 | |||||||
| chr4:1073863 | TATTACCT others(1): Show |
T | 7 | a0001c0002t0004g0013 a0001c0002t0004g0014 a0001c0002t0004g0038 others(4): Show |
9 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.511-209_511-202del others(8): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1073863 | |||||||
| chr4:1073980 | G | A | 1 | a0001c0002t0002g0219 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.511-318C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1073980 | |||||||
| chr4:1074119 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.511-457A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1074119 | |||||||
| chr4:1074246 | CCT | C | 3 | a0001c0002t0002g0273 a0001c0002t0002g0274 a0001c0002t0002g0309 |
3 | HG02165.hp1 NA18944.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.511-586_511-585del others(2): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1074246 | |||||||
| chr4:1074338 | C | T | 1 | a0001c0002t0002g0159 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.511-676G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1074338 | |||||||
| chr4:1074390 | C | T | 1 | a0001c0002t0002g0300 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.511-728G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1074390 | |||||||
| chr4:1074447 | C | T | 1 | a0006c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.511-785G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1074447 | |||||||
| chr4:1074488 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.511-826G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1074488 | |||||||
| chr4:1074639 | G | A | 1 | a0006c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.511-977C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1074639 | |||||||
| chr4:1074660 | C | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0113 others(21): Show |
30 | HG00597.hp1 HG00621.hp2 HG02523.hp2 others(27): Show |
intron_variant | MODIFIER | c.511-998G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1074660 | |||||||
| chr4:1074777 | CAGG | C | 3 | a0001c0001t0006g0348 a0001c0001t0006g0349 a0001c0001t0006g0350 |
3 | HG01167.hp1 HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.511-1118_511-1116d others(5): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1074777 | |||||||
| chr4:1074916 | T | TC | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.511-1255dupG | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1074916 | |||||||
| chr4:1074937 | A | C | 2 | a0001c0001t0005g0045 a0001c0001t0005g0046 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.511-1275T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1074937 | |||||||
| chr4:1074989 | C | T | 2 | a0001c0002t0004g0014 a0001c0002t0004g0048 |
3 | HG02717.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.511-1327G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1074989 | |||||||
| chr4:1074990 | A | G | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.511-1328T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1074990 | |||||||
| chr4:1075031 | G | A | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(242): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.511-1369C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1075031 | |||||||
| chr4:1075190 | G | T | 1 | a0001c0002t0002g0308 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.511-1528C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1075190 | |||||||
| chr4:1075293 | G | A | 1 | a0001c0002t0002g0149 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.511-1631C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1075293 | |||||||
| chr4:1075306 | G | C | 1 | a0001c0001t0001g0015 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.511-1644C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1075306 | |||||||
| chr4:1075345 | A | G | 1 | a0001c0001t0010g0183 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.511-1683T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1075345 | |||||||
| chr4:1075397 | C | T | 1 | a0001c0002t0002g0057 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.511-1735G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1075397 | |||||||
| chr4:1075497 | G | C | 1 | a0001c0002t0002g0144 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.511-1835C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1075497 | |||||||
| chr4:1075507 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.511-1845C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1075507 | |||||||
| chr4:1075527 | G | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.511-1865C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1075527 | |||||||
| chr4:1075762 | A | G | 5 | a0001c0001t0001g0006 a0001c0001t0001g0065 a0001c0001t0001g0066 others(2): Show |
7 | HG01243.hp1 HG02257.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.511-2100T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1075762 | |||||||
| chr4:1076063 | A | G | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.511-2401T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1076063 | |||||||
| chr4:1076078 | A | G | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.511-2416T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1076078 | |||||||
| chr4:1076099 | C | T | 1 | a0006c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.511-2437G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1076099 | |||||||
| chr4:1076185 | C | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(242): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.511-2523G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1076185 | |||||||
| chr4:1076220 | T | A | 1 | a0006c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.511-2558A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1076220 | |||||||
| chr4:1076352 | G | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(242): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.511-2690C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1076352 | |||||||
| chr4:1076451 | C | A | 4 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02818.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-2789G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1076451 | |||||||
| chr4:1076547 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.511-2885G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1076547 | |||||||
| chr4:1076576 | C | A | 1 | a0001c0002t0002g0144 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.511-2914G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1076576 | |||||||
| chr4:1076675 | A | C | 3 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 |
4 | HG02922.hp2 HG03139.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+2968T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1076675 | |||||||
| chr4:1076703 | G | A | 7 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0104 others(4): Show |
7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+2940C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1076703 | |||||||
| chr4:1076781 | A | G | 1 | a0001c0002t0002g0106 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.510+2862T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1076781 | |||||||
| chr4:1076841 | A | G | 7 | a0001c0002t0004g0013 a0001c0002t0004g0014 a0001c0002t0004g0038 others(4): Show |
9 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.510+2802T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1076841 | |||||||
| chr4:1076998 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.510+2645C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1076998 | |||||||
| chr4:1077038 | A | T | 1 | a0001c0001t0010g0183 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.510+2605T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077038 | |||||||
| chr4:1077064 | C | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(235): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.510+2579G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077064 | |||||||
| chr4:1077142 | T | C | 1 | a0001c0001t0001g0169 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.510+2501A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077142 | |||||||
| chr4:1077176 | C | T | 2 | a0001c0002t0004g0014 a0001c0002t0004g0048 |
3 | HG02717.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.510+2467G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077176 | |||||||
| chr4:1077177 | G | A | 41 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(38): Show |
45 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.510+2466C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077177 | |||||||
| chr4:1077279 | T | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
284 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.510+2364A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077279 | |||||||
| chr4:1077280 | G | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0070 |
2 | NA18948.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.510+2363C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077280 | |||||||
| chr4:1077289 | T | C | 1 | a0001c0002t0002g0226 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.510+2354A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077289 | |||||||
| chr4:1077537 | G | A | 1 | a0001c0002t0002g0289 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.510+2106C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077537 | |||||||
| chr4:1077657 | C | G | 1 | a0001c0002t0004g0014 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.510+1986G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077657 | |||||||
| chr4:1077661 | C | T | 3 | a0001c0002t0002g0247 a0001c0002t0002g0266 a0001c0002t0017g0352 |
3 | NA18961.hp1 NA19009.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.510+1982G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077661 | |||||||
| chr4:1077720 | G | T | 1 | a0001c0002t0002g0255 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.510+1923C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077720 | |||||||
| chr4:1077797 | C | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0176 a0001c0001t0001g0177 |
3 | HG00609.hp2 HG02083.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.510+1846G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077797 | |||||||
| chr4:1077888 | C | T | 1 | a0001c0002t0003g0342 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.510+1755G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077888 | |||||||
| chr4:1077901 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.510+1742G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077901 | |||||||
| chr4:1077902 | G | A | 1 | a0001c0002t0004g0048 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.510+1741C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077902 | |||||||
| chr4:1077948 | T | A | 2 | a0001c0002t0002g0265 a0001c0002t0002g0319 |
2 | HG00099.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.510+1695A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077948 | |||||||
| chr4:1078002 | C | T | 1 | a0001c0002t0012g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.510+1641G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078002 | |||||||
| chr4:1078057 | C | A | 7 | a0001c0002t0004g0013 a0001c0002t0004g0014 a0001c0002t0004g0038 others(4): Show |
9 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.510+1586G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078057 | |||||||
| chr4:1078119 | A | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(93): Show |
115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.510+1524T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078119 | |||||||
| chr4:1078237 | G | A | 1 | a0001c0002t0002g0302 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.510+1406C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078237 | |||||||
| chr4:1078247 | C | A | 1 | a0001c0001t0001g0137 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.510+1396G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078247 | |||||||
| chr4:1078403 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0010g0183 |
2 | HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.510+1240C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078403 | |||||||
| chr4:1078432 | C | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.510+1211G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078432 | |||||||
| chr4:1078485 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.510+1158C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078485 | |||||||
| chr4:1078543 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.510+1100G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078543 | |||||||
| chr4:1078561 | A | G | 9 | a0001c0002t0001g0034 a0001c0002t0001g0041 a0001c0002t0001g0042 others(6): Show |
11 | HG02486.hp2 HG02572.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.510+1082T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078561 | |||||||
| chr4:1078697 | C | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.510+946G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078697 | |||||||
| chr4:1078729 | C | T | 7 | a0001c0001t0001g0032 a0001c0001t0001g0163 a0001c0001t0001g0164 others(4): Show |
8 | NA18977.hp2 NA18986.hp2 NA18988.hp2 others(5): Show |
intron_variant | MODIFIER | c.510+914G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078729 | |||||||
| chr4:1078749 | G | T | 1 | a0001c0002t0012g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.510+894C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078749 | |||||||
| chr4:1078801 | T | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | NA18941.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.510+842A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078801 | |||||||
| chr4:1078835 | GGGACCAA others(4): Show |
G | 1 | a0001c0002t0002g0305 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.510+797_510+807del others(11): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078835 | |||||||
| chr4:1078836 | G | A | 1 | a0001c0002t0012g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.510+807C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078836 | |||||||
| chr4:1078852 | A | G | 1 | a0001c0002t0001g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.510+791T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078852 | |||||||
| chr4:1078884 | C | T | 1 | a0001c0002t0002g0300 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.510+759G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078884 | |||||||
| chr4:1078923 | G | GGGACCAA others(4): Show |
7 | a0001c0002t0001g0059 a0001c0002t0001g0096 a0001c0002t0001g0298 others(4): Show |
7 | HG01255.hp1 HG01433.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.510+709_510+719dup others(11): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078923 | |||||||
| chr4:1078925 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0049 a0001c0001t0001g0050 |
4 | HG02559.hp1 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+718C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078925 | |||||||
| chr4:1078937 | G | A | 42 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(39): Show |
47 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.510+706C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078937 | |||||||
| chr4:1078938 | T | C | 42 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(39): Show |
47 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.510+705A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078938 | |||||||
| chr4:1078948 | A | G | 42 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(39): Show |
47 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.510+695T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078948 | |||||||
| chr4:1078949 | C | T | 42 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(39): Show |
47 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.510+694G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078949 | |||||||
| chr4:1078956 | A | G | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(201): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.510+687T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078956 | |||||||
| chr4:1078966 | T | C | 38 | a0001c0002t0001g0020 a0001c0002t0001g0023 a0001c0002t0001g0035 others(35): Show |
40 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.510+677A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078966 | |||||||
| chr4:1078977 | C | T | 36 | a0001c0002t0001g0020 a0001c0002t0001g0023 a0001c0002t0001g0035 others(33): Show |
38 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.510+666G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078977 | |||||||
| chr4:1078981 | G | A | 36 | a0001c0002t0001g0020 a0001c0002t0001g0023 a0001c0002t0001g0035 others(33): Show |
38 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.510+662C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078981 | |||||||
| chr4:1078982 | T | C | 36 | a0001c0002t0001g0020 a0001c0002t0001g0023 a0001c0002t0001g0035 others(33): Show |
38 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.510+661A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078982 | |||||||
| chr4:1078992 | A | G | 36 | a0001c0002t0001g0020 a0001c0002t0001g0023 a0001c0002t0001g0035 others(33): Show |
38 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.510+651T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078992 | |||||||
| chr4:1078993 | C | T | 37 | a0001c0001t0001g0054 a0001c0002t0001g0020 a0001c0002t0001g0023 others(34): Show |
39 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.510+650G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078993 | |||||||
| chr4:1078999 | T | C | 36 | a0001c0002t0001g0020 a0001c0002t0001g0023 a0001c0002t0001g0035 others(33): Show |
38 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.510+644A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078999 | |||||||
| chr4:1078999 | T | G | 4 | a0001c0001t0005g0043 a0001c0001t0005g0045 a0001c0001t0005g0046 others(1): Show |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+644A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078999 | |||||||
| chr4:1078999 | TAGGACCA others(4): Show |
T | 13 | a0001c0002t0001g0019 a0001c0002t0001g0059 a0001c0002t0001g0096 others(10): Show |
16 | HG01255.hp1 HG01433.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.510+633_510+643del others(11): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078999 | |||||||
| chr4:1079000 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(194): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.510+643T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079000 | |||||||
| chr4:1079010 | C | T | 36 | a0001c0002t0001g0020 a0001c0002t0001g0023 a0001c0002t0001g0035 others(33): Show |
38 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.510+633G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079010 | |||||||
| chr4:1079023 | G | A | 10 | a0001c0002t0001g0034 a0001c0002t0001g0037 a0001c0002t0001g0041 others(7): Show |
12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.510+620C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079023 | |||||||
| chr4:1079028 | AACATGGG others(39): Show |
A | 5 | a0001c0001t0001g0044 a0001c0001t0001g0104 a0001c0001t0005g0043 others(2): Show |
5 | HG02040.hp1 HG03491.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.510+569_510+614del others(46): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079028 | |||||||
| chr4:1079030 | CATGGGAC others(6): Show |
C | 2 | a0001c0001t0001g0061 a0001c0001t0005g0045 |
2 | HG03492.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.510+600_510+612del others(13): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079030 | |||||||
| chr4:1079032 | T | C | 1 | a0001c0002t0001g0059 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.510+611A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079032 | |||||||
| chr4:1079066 | G | GGGACCAA others(26): Show |
1 | a0006c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.510+544_510+576dup others(33): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079066 | |||||||
| chr4:1079066 | GGGACCAA others(26): Show |
G | 3 | a0001c0001t0001g0061 a0001c0001t0005g0045 a0001c0002t0006g0351 |
3 | HG03492.hp1 HG03516.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.510+544_510+576del others(33): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079066 | |||||||
| chr4:1079070 | CCAACACA others(4): Show |
C | 2 | a0001c0001t0001g0109 a0001c0001t0001g0214 |
2 | NA18970.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.510+562_510+572del others(11): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079070 | |||||||
| chr4:1079079 | G | A | 5 | a0001c0001t0001g0044 a0001c0001t0001g0104 a0001c0001t0005g0043 others(2): Show |
5 | HG02040.hp1 HG03491.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.510+564C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079079 | |||||||
| chr4:1079098 | T | C | 1 | a0001c0002t0002g0312 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.510+545A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079098 | |||||||
| chr4:1079099 | A | G | 5 | a0001c0001t0001g0044 a0001c0001t0001g0104 a0001c0001t0005g0043 others(2): Show |
5 | HG02040.hp1 HG03491.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.510+544T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079099 | |||||||
| chr4:1079133 | G | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0165 a0001c0001t0001g0166 |
4 | HG02155.hp2 NA18984.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+510C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079133 | |||||||
| chr4:1079208 | T | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(201): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.510+435A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079208 | |||||||
| chr4:1079211 | A | G | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(201): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.510+432T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079211 | |||||||
| chr4:1079219 | C | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(91): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.510+424G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079219 | |||||||
| chr4:1079251 | A | C | 7 | a0001c0001t0001g0032 a0001c0001t0001g0163 a0001c0001t0001g0164 others(4): Show |
8 | NA18977.hp2 NA18986.hp2 NA18988.hp2 others(5): Show |
intron_variant | MODIFIER | c.510+392T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079251 | |||||||
| chr4:1079331 | G | A | 1 | a0006c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.510+312C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079331 | |||||||
| chr4:1079369 | T | G | 1 | a0001c0002t0002g0144 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.510+274A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079369 | |||||||
| chr4:1079496 | T | A | 1 | a0001c0002t0001g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.510+147A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079496 | |||||||
| chr4:1079498 | A | C | 1 | a0001c0002t0001g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.510+145T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079498 | |||||||
| chr4:1079514 | C | T | 7 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0104 others(4): Show |
7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+129G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079514 | |||||||
| chr4:1079523 | G | A | 1 | a0006c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.510+120C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079523 | |||||||
| chr4:1079602 | G | A | 1 | a0001c0002t0002g0260 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.510+41C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079602 | |||||||
| chr4:1079743 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.465-55G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1079743 | |||||||
| chr4:1079749 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0010g0183 |
2 | HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.465-61A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1079749 | |||||||
| chr4:1079972 | C | T | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(201): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.465-284G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1079972 | |||||||
| chr4:1080047 | G | A | 1 | a0001c0002t0001g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.465-359C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080047 | |||||||
| chr4:1080058 | G | A | 4 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02818.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.465-370C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080058 | |||||||
| chr4:1080131 | C | G | 1 | a0001c0002t0001g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.465-443G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080131 | |||||||
| chr4:1080134 | G | T | 1 | a0001c0002t0001g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.465-446C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080134 | |||||||
| chr4:1080135 | T | C | 1 | a0001c0002t0001g0288 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.465-447A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080135 | |||||||
| chr4:1080221 | C | T | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(201): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.465-533G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080221 | |||||||
| chr4:1080444 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.465-756G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080444 | |||||||
| chr4:1080445 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.465-757C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080445 | |||||||
| chr4:1080578 | C | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.464+841G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080578 | |||||||
| chr4:1080611 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0108 |
5 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.464+808G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080611 | |||||||
| chr4:1080624 | T | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.464+795A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080624 | |||||||
| chr4:1080648 | G | A | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.464+771C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080648 | |||||||
| chr4:1080686 | CT | C | 14 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(11): Show |
16 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.464+732delA | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080686 | |||||||
| chr4:1080733 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.464+686C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080733 | |||||||
| chr4:1080777 | G | A | 4 | a0001c0002t0001g0019 a0001c0002t0001g0096 a0001c0002t0001g0298 others(1): Show |
5 | HG01255.hp1 HG02451.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.464+642C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080777 | |||||||
| chr4:1080902 | C | A | 2 | a0001c0002t0002g0265 a0001c0002t0002g0319 |
2 | HG00099.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.464+517G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080902 | |||||||
| chr4:1080950 | G | A | 3 | a0001c0002t0001g0023 a0001c0002t0001g0150 a0001c0002t0003g0330 |
4 | HG02886.hp1 HG02970.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.464+469C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080950 | |||||||
| chr4:1081069 | C | A | 3 | a0001c0001t0001g0095 a0001c0001t0001g0175 a0001c0001t0001g0292 |
3 | HG02258.hp2 HG03710.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.464+350G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1081069 | |||||||
| chr4:1081193 | C | T | 7 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0104 others(4): Show |
7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.464+226G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1081193 | |||||||
| chr4:1081221 | C | T | 1 | a0001c0002t0002g0149 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.464+198G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1081221 | |||||||
| chr4:1081312 | T | A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0063 others(9): Show |
15 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.464+107A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1081312 | |||||||
| chr4:1081374 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.464+45C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1081374 | |||||||
| chr4:1081483 | C | T | 77 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(74): Show |
88 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.416-16G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 6/9 | chr4 | 1081483 | |||||||
| chr4:1081552 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.415+15G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 6/9 | chr4 | 1081552 | |||||||
| chr4:1081627 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA19087.hp2 | splice_region_variant&intron_variant | LOW | c.363-8C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1081627 | |||||||
| chr4:1081893 | T | C | 7 | a0001c0002t0004g0013 a0001c0002t0004g0014 a0001c0002t0004g0038 others(4): Show |
9 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.363-274A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1081893 | |||||||
| chr4:1081896 | G | A | 7 | a0001c0002t0004g0013 a0001c0002t0004g0014 a0001c0002t0004g0038 others(4): Show |
9 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.363-277C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1081896 | |||||||
| chr4:1081907 | G | T | 1 | a0001c0002t0012g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.363-288C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1081907 | |||||||
| chr4:1081942 | C | T | 1 | a0001c0002t0001g0100 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.363-323G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1081942 | |||||||
| chr4:1081983 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.363-364G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1081983 | |||||||
| chr4:1081997 | T | A | 4 | a0001c0002t0003g0033 a0001c0002t0003g0342 a0001c0002t0003g0345 others(1): Show |
5 | HG00642.hp2 HG00735.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.363-378A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1081997 | |||||||
| chr4:1082029 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.363-410A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082029 | |||||||
| chr4:1082090 | C | G | 3 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 |
4 | HG02922.hp2 HG03139.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.363-471G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082090 | |||||||
| chr4:1082145 | A | G | 1 | a0001c0001t0001g0194 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.363-526T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082145 | |||||||
| chr4:1082152 | A | G | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.363-533T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082152 | |||||||
| chr4:1082392 | T | C | 1 | a0001c0001t0001g0165 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.363-773A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082392 | |||||||
| chr4:1082536 | T | C | 1 | a0001c0002t0002g0149 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.363-917A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082536 | |||||||
| chr4:1082564 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.363-945C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082564 | |||||||
| chr4:1082629 | G | C | 1 | a0001c0002t0001g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.363-1010C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082629 | |||||||
| chr4:1082667 | T | C | 1 | a0006c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.363-1048A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082667 | |||||||
| chr4:1082672 | G | C | 8 | a0001c0001t0001g0095 a0001c0002t0004g0013 a0001c0002t0004g0014 others(5): Show |
10 | HG01891.hp1 HG02258.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.363-1053C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082672 | |||||||
| chr4:1082709 | C | G | 7 | a0001c0001t0001g0024 a0001c0001t0001g0151 a0001c0001t0001g0154 others(4): Show |
8 | HG01192.hp1 HG01255.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.363-1090G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082709 | |||||||
| chr4:1082721 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.363-1102G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082721 | |||||||
| chr4:1082809 | G | A | 1 | a0006c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.363-1190C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082809 | |||||||
| chr4:1082891 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.363-1272A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082891 | |||||||
| chr4:1082905 | A | C | 7 | a0001c0002t0004g0013 a0001c0002t0004g0014 a0001c0002t0004g0038 others(4): Show |
9 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.363-1286T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082905 | |||||||
| chr4:1083001 | C | T | 7 | a0001c0002t0004g0013 a0001c0002t0004g0014 a0001c0002t0004g0038 others(4): Show |
9 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.363-1382G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083001 | |||||||
| chr4:1083097 | C | G | 41 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(38): Show |
45 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.363-1478G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083097 | |||||||
| chr4:1083157 | C | T | 1 | a0001c0002t0002g0239 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.363-1538G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083157 | |||||||
| chr4:1083219 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.363-1600C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083219 | |||||||
| chr4:1083353 | T | G | 1 | a0001c0001t0001g0056 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.363-1734A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083353 | |||||||
| chr4:1083494 | T | C | 7 | a0001c0002t0004g0013 a0001c0002t0004g0014 a0001c0002t0004g0038 others(4): Show |
9 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.363-1875A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083494 | |||||||
| chr4:1083504 | G | A | 7 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0104 others(4): Show |
7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.363-1885C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083504 | |||||||
| chr4:1083511 | G | T | 6 | a0001c0002t0004g0013 a0001c0002t0004g0014 a0001c0002t0004g0038 others(3): Show |
8 | HG01891.hp1 HG02717.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.363-1892C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083511 | |||||||
| chr4:1083562 | C | T | 1 | a0001c0002t0001g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.363-1943G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083562 | |||||||
| chr4:1083592 | C | T | 5 | a0001c0001t0001g0024 a0001c0001t0001g0151 a0001c0001t0001g0154 others(2): Show |
6 | HG01884.hp1 HG01891.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.363-1973G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083592 | |||||||
| chr4:1083629 | C | T | 4 | a0001c0002t0001g0034 a0002c0003t0001g0011 a0002c0003t0001g0323 others(1): Show |
6 | HG02486.hp2 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.363-2010G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083629 | |||||||
| chr4:1083639 | A | AAAAC | 10 | a0001c0001t0001g0055 a0001c0001t0001g0085 a0001c0001t0001g0279 others(7): Show |
10 | HG00673.hp2 HG01952.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.363-2024_363-2021d others(6): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083639 | |||||||
| chr4:1083639 | A | AAAACAAA others(1): Show |
3 | a0001c0001t0001g0051 a0001c0001t0001g0090 a0001c0001t0001g0145 |
3 | HG01175.hp2 HG03654.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.363-2028_363-2021d others(10): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083639 | |||||||
| chr4:1083639 | AAAAC | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(132): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.363-2024_363-2021d others(6): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083639 | |||||||
| chr4:1083639 | AAAACAAA others(1): Show |
A | 12 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0111 others(9): Show |
15 | HG00408.hp2 HG00621.hp1 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.363-2028_363-2021d others(10): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083639 | |||||||
| chr4:1083639 | AAAACAAA others(5): Show |
A | 1 | a0001c0001t0001g0163 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.363-2032_363-2021d others(14): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083639 | |||||||
| chr4:1083639 | AAAACAAA others(9): Show |
A | 1 | a0001c0002t0012g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.363-2036_363-2021d others(18): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083639 | |||||||
| chr4:1083646 | AC | A | 7 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0104 others(4): Show |
7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.363-2028delG | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083646 | |||||||
| chr4:1083672 | A | T | 1 | a0001c0001t0001g0185 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.363-2053T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083672 | |||||||
| chr4:1083688 | A | G | 1 | a0001c0002t0001g0042 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.363-2069T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083688 | |||||||
| chr4:1083754 | C | T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.363-2135G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083754 | |||||||
| chr4:1083787 | G | A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.362+2109C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083787 | |||||||
| chr4:1083868 | C | T | 2 | a0001c0002t0002g0236 a0001c0002t0002g0239 |
2 | HG01123.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.362+2028G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083868 | |||||||
| chr4:1083945 | A | AT | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
112 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.362+1950dupA | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083945 | |||||||
| chr4:1083945 | A | ATT | 14 | a0001c0001t0001g0107 a0001c0001t0001g0129 a0001c0001t0001g0136 others(11): Show |
16 | HG00438.hp2 HG01981.hp2 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.362+1949_362+1950d others(4): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083945 | |||||||
| chr4:1083945 | A | ATTT | 74 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(71): Show |
86 | HG00609.hp1 HG00609.hp2 HG00673.hp1 others(83): Show |
intron_variant | MODIFIER | c.362+1948_362+1950d others(5): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083945 | |||||||
| chr4:1083945 | A | ATTTT | 14 | a0001c0001t0001g0054 a0001c0001t0001g0072 a0001c0001t0001g0076 others(11): Show |
14 | HG00558.hp1 HG00558.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.362+1947_362+1950d others(6): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083945 | |||||||
| chr4:1083945 | A | T | 2 | a0001c0001t0001g0156 a0001c0002t0002g0149 |
2 | HG01891.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.362+1951T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083945 | |||||||
| chr4:1083945 | AT | A | 17 | a0001c0001t0001g0044 a0001c0001t0005g0046 a0001c0002t0001g0019 others(14): Show |
19 | HG00099.hp1 HG01255.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.362+1950delA | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083945 | |||||||
| chr4:1083945 | ATT | A | 30 | a0001c0002t0001g0023 a0001c0002t0001g0059 a0001c0002t0001g0150 others(27): Show |
32 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.362+1949_362+1950d others(4): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083945 | |||||||
| chr4:1083970 | C | T | 1 | a0001c0002t0003g0335 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.362+1926G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083970 | |||||||
| chr4:1083971 | G | A | 2 | a0001c0002t0012g0102 a0006c0008t0011g0040 |
2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.362+1925C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083971 | |||||||
| chr4:1084020 | C | T | 1 | a0001c0002t0003g0331 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.362+1876G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084020 | |||||||
| chr4:1084092 | G | A | 45 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(42): Show |
49 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.362+1804C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084092 | |||||||
| chr4:1084096 | G | C | 1 | a0001c0002t0002g0149 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.362+1800C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084096 | |||||||
| chr4:1084163 | T | C | 1 | a0001c0002t0012g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.362+1733A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084163 | |||||||
| chr4:1084205 | C | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0065 a0001c0001t0001g0066 others(2): Show |
7 | HG01243.hp1 HG02257.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.362+1691G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084205 | |||||||
| chr4:1084336 | G | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(91): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.362+1560C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084336 | |||||||
| chr4:1084363 | A | G | 1 | a0006c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.362+1533T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084363 | |||||||
| chr4:1084384 | G | A | 73 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0017 others(70): Show |
82 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.362+1512C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084384 | |||||||
| chr4:1084399 | G | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.362+1497C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084399 | |||||||
| chr4:1084451 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.362+1445G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084451 | |||||||
| chr4:1084596 | G | T | 7 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0104 others(4): Show |
7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.362+1300C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084596 | |||||||
| chr4:1084601 | G | A | 1 | a0001c0001t0010g0183 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.362+1295C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084601 | |||||||
| chr4:1084613 | C | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0318 |
2 | HG02615.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.362+1283G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084613 | |||||||
| chr4:1084726 | C | CA | 30 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0104 others(27): Show |
30 | HG00673.hp2 HG01261.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.362+1169dupT | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084726 | |||||||
| chr4:1084726 | CA | C | 60 | a0001c0001t0001g0050 a0001c0001t0001g0086 a0001c0001t0001g0122 others(57): Show |
64 | HG00609.hp1 HG00642.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.362+1169delT | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084726 | |||||||
| chr4:1084726 | CAA | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.362+1168_362+1169d others(4): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084726 | |||||||
| chr4:1084726 | CAAA | C | 13 | a0001c0001t0001g0070 a0001c0001t0001g0078 a0001c0001t0001g0105 others(10): Show |
15 | HG01168.hp2 HG01169.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.362+1167_362+1169d others(5): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084726 | |||||||
| chr4:1084738 | A | T | 1 | a0006c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.362+1158T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084738 | |||||||
| chr4:1084808 | C | T | 78 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(75): Show |
89 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.362+1088G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084808 | |||||||
| chr4:1084951 | T | C | 1 | a0001c0002t0012g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.362+945A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084951 | |||||||
| chr4:1084960 | C | A | 2 | a0001c0002t0001g0201 a0001c0002t0001g0294 |
2 | HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.362+936G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084960 | |||||||
| chr4:1084979 | C | T | 1 | a0001c0002t0002g0036 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.362+917G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084979 | |||||||
| chr4:1085139 | G | A | 1 | a0001c0002t0012g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.362+757C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1085139 | |||||||
| chr4:1085167 | G | A | 1 | a0001c0002t0004g0014 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.362+729C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1085167 | |||||||
| chr4:1085250 | C | A | 1 | a0001c0002t0012g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.362+646G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1085250 | |||||||
| chr4:1085295 | T | C | 1 | a0006c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.362+601A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1085295 | |||||||
| chr4:1085488 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.362+408A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1085488 | |||||||
| chr4:1085773 | T | C | 7 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0104 others(4): Show |
7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.362+123A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1085773 | |||||||
| chr4:1085835 | G | A | 1 | a0001c0002t0002g0260 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.362+61C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1085835 | |||||||
| chr4:1086105 | G | A | 2 | a0001c0001t0001g0123 a0001c0002t0002g0149 |
2 | HG02622.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.304-151C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086105 | |||||||
| chr4:1086295 | C | G | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.304-341G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086295 | |||||||
| chr4:1086370 | G | C | 1 | a0001c0002t0001g0288 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.304-416C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086370 | |||||||
| chr4:1086603 | G | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.304-649C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086603 | |||||||
| chr4:1086617 | A | G | 1 | a0001c0002t0002g0262 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.304-663T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086617 | |||||||
| chr4:1086631 | T | A | 1 | a0001c0002t0002g0262 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.304-677A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086631 | |||||||
| chr4:1086651 | T | A | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.304-697A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086651 | |||||||
| chr4:1086678 | G | C | 1 | a0001c0002t0002g0289 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.304-724C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086678 | |||||||
| chr4:1086680 | TGGGGTGG others(13): Show |
T | 1 | a0001c0002t0012g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.304-746_304-727del others(20): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086680 | |||||||
| chr4:1086685 | T | G | 1 | a0001c0002t0002g0262 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.304-731A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086685 | |||||||
| chr4:1086686 | G | T | 1 | a0001c0002t0002g0262 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.304-732C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086686 | |||||||
| chr4:1086727 | G | C | 3 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0171 |
3 | NA18955.hp1 NA18993.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.304-773C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086727 | |||||||
| chr4:1086745 | G | A | 3 | a0001c0002t0001g0041 a0001c0002t0001g0042 a0001c0002t0006g0351 |
3 | HG03098.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.304-791C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086745 | |||||||
| chr4:1086773 | G | A | 3 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 |
4 | HG02922.hp2 HG03139.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.304-819C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086773 | |||||||
| chr4:1086866 | A | G | 1 | a0001c0002t0001g0059 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.304-912T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086866 | |||||||
| chr4:1087048 | C | CGGTGGCA others(13): Show |
1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-1095_304-1094i others(22): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087048 | |||||||
| chr4:1087059 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-1105A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087059 | |||||||
| chr4:1087062 | C | G | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-1108G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087062 | |||||||
| chr4:1087063 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-1109T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087063 | |||||||
| chr4:1087072 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-1118C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087072 | |||||||
| chr4:1087073 | C | G | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-1119G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087073 | |||||||
| chr4:1087082 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-1128T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087082 | |||||||
| chr4:1087090 | T | A | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-1136A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087090 | |||||||
| chr4:1087106 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-1152T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087106 | |||||||
| chr4:1087109 | T | A | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-1155A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087109 | |||||||
| chr4:1087109 | T | TGAGAGGA others(31): Show |
4 | a0001c0002t0003g0033 a0001c0002t0003g0342 a0001c0002t0003g0345 others(1): Show |
5 | HG00642.hp2 HG00735.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.304-1156_304-1155i others(40): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087109 | |||||||
| chr4:1087118 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-1164C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087118 | |||||||
| chr4:1087118 | G | GGGGTGGG others(31): Show |
1 | a0001c0002t0001g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.304-1165_304-1164i others(40): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087118 | |||||||
| chr4:1087123 | G | GGGGGAGA others(31): Show |
1 | a0001c0001t0001g0123 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.304-1170_304-1169i others(40): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087123 | |||||||
| chr4:1087123 | G | GGGGGAGA others(31): Show |
192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(189): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.304-1170_304-1169i others(40): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087123 | |||||||
| chr4:1087123 | G | GGGGGAGA others(31): Show |
46 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0104 others(43): Show |
50 | HG01074.hp2 HG01255.hp1 HG01433.hp1 others(47): Show |
intron_variant | MODIFIER | c.304-1170_304-1169i others(40): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087123 | |||||||
| chr4:1087123 | G | GGGGGAGA others(29): Show |
1 | a0001c0001t0001g0070 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.304-1170_304-1169i others(38): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087123 | |||||||
| chr4:1087123 | G | GGGGGAGA others(31): Show |
2 | a0001c0002t0003g0325 a0001c0002t0003g0328 |
2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.304-1170_304-1169i others(40): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087123 | |||||||
| chr4:1087123 | G | GGGGGGAG others(32): Show |
1 | a0001c0001t0001g0105 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.304-1170_304-1169i others(41): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087123 | |||||||
| chr4:1087123 | G | T | 5 | a0001c0001t0001g0095 a0001c0002t0003g0033 a0001c0002t0003g0342 others(2): Show |
6 | HG00642.hp2 HG00735.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.304-1169C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087123 | |||||||
| chr4:1087123 | GGGGGAGA others(108): Show |
G | 3 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 |
4 | HG02922.hp2 HG03139.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.304-1284_304-1170d others(2): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087123 | |||||||
| chr4:1087142 | G | T | 1 | a0001c0002t0001g0097 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.304-1188C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087142 | |||||||
| chr4:1087160 | G | C | 1 | a0001c0001t0001g0177 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.304-1206C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087160 | |||||||
| chr4:1087163 | GGA | G | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(201): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.304-1211_304-1210d others(4): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087163 | |||||||
| chr4:1087205 | TGAGAGGA others(12): Show |
T | 2 | a0001c0002t0007g0353 a0001c0002t0007g0355 |
2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.304-1270_304-1252d others(21): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087205 | |||||||
| chr4:1087206 | G | C | 3 | a0001c0002t0001g0041 a0001c0002t0001g0042 a0001c0002t0006g0351 |
3 | HG03098.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.304-1252C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087206 | |||||||
| chr4:1087213 | TGGGGTAG others(12): Show |
T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.304-1278_304-1260d others(21): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087213 | |||||||
| chr4:1087257 | A | G | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.304-1303T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087257 | |||||||
| chr4:1087281 | T | A | 3 | a0001c0002t0001g0020 a0001c0002t0001g0097 a0001c0002t0013g0101 |
4 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.304-1327A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087281 | |||||||
| chr4:1087503 | TGGGGGGT others(14): Show |
T | 1 | a0001c0002t0004g0048 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.304-1570_304-1550d others(23): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087503 | |||||||
| chr4:1087523 | T | TG | 17 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0135 others(14): Show |
17 | HG01175.hp1 HG01361.hp2 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.304-1570dupC | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087523 | |||||||
| chr4:1087593 | T | C | 1 | a0006c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.304-1639A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087593 | |||||||
| chr4:1087631 | G | A | 17 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0158 others(14): Show |
22 | HG00408.hp1 HG01074.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.304-1677C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087631 | |||||||
| chr4:1087695 | T | C | 7 | a0001c0001t0001g0024 a0001c0001t0001g0151 a0001c0001t0001g0154 others(4): Show |
8 | HG01192.hp1 HG01255.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.304-1741A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087695 | |||||||
| chr4:1087791 | G | A | 2 | a0005c0006t0001g0128 a0005c0006t0001g0133 |
2 | HG02683.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.304-1837C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087791 | |||||||
| chr4:1087818 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.304-1864G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087818 | |||||||
| chr4:1087834 | C | A | 1 | a0001c0001t0001g0075 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.304-1880G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087834 | |||||||
| chr4:1087949 | C | T | 1 | a0001c0002t0012g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.304-1995G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087949 | |||||||
| chr4:1087967 | C | T | 18 | a0001c0002t0003g0033 a0001c0002t0003g0329 a0001c0002t0003g0331 others(15): Show |
19 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.304-2013G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087967 | |||||||
| chr4:1087993 | A | T | 1 | a0001c0002t0002g0262 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.304-2039T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087993 | |||||||
| chr4:1088096 | TG | T | 3 | a0001c0001t0005g0045 a0001c0001t0005g0046 a0001c0002t0002g0262 |
3 | HG03491.hp1 HG03492.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.304-2143delC | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1088096 | |||||||
| chr4:1088109 | A | G | 1 | a0001c0001t0001g0054 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.304-2155T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1088109 | |||||||
| chr4:1088121 | A | G | 7 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0104 others(4): Show |
7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.304-2167T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1088121 | |||||||
| chr4:1088273 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-2319G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1088273 | |||||||
| chr4:1088398 | C | T | 46 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(43): Show |
52 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.303+2384G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1088398 | |||||||
| chr4:1088584 | T | C | 3 | a0001c0001t0001g0051 a0001c0001t0001g0090 a0001c0001t0001g0145 |
3 | HG01175.hp2 HG03654.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.303+2198A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1088584 | |||||||
| chr4:1088792 | C | G | 1 | a0001c0002t0001g0059 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.303+1990G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1088792 | |||||||
| chr4:1088813 | T | C | 4 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02818.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.303+1969A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1088813 | |||||||
| chr4:1088825 | A | T | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.303+1957T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1088825 | |||||||
| chr4:1088919 | G | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.303+1863C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1088919 | |||||||
| chr4:1089041 | T | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.303+1741A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089041 | |||||||
| chr4:1089087 | C | A | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.303+1695G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089087 | |||||||
| chr4:1089099 | C | T | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(202): Show |
238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.303+1683G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089099 | |||||||
| chr4:1089201 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.303+1581C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089201 | |||||||
| chr4:1089211 | G | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.303+1571C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089211 | |||||||
| chr4:1089213 | T | C | 1 | a0001c0002t0002g0264 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.303+1569A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089213 | |||||||
| chr4:1089241 | C | G | 1 | a0001c0002t0002g0267 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.303+1541G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089241 | |||||||
| chr4:1089282 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.303+1500A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089282 | |||||||
| chr4:1089324 | C | T | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.303+1458G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089324 | |||||||
| chr4:1089443 | A | C | 3 | a0001c0001t0006g0348 a0001c0001t0006g0349 a0001c0001t0006g0350 |
3 | HG01167.hp1 HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.303+1339T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089443 | |||||||
| chr4:1089483 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.303+1299A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089483 | |||||||
| chr4:1089519 | G | A | 73 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0017 others(70): Show |
82 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.303+1263C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089519 | |||||||
| chr4:1089558 | T | C | 29 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0032 others(26): Show |
32 | HG00609.hp1 HG01109.hp2 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.303+1224A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089558 | |||||||
| chr4:1089596 | G | C | 1 | a0001c0002t0006g0351 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.303+1186C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089596 | |||||||
| chr4:1089604 | CA | C | 5 | a0001c0001t0001g0017 a0001c0001t0001g0064 a0001c0001t0001g0069 others(2): Show |
6 | NA18948.hp2 NA18956.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.303+1177delT | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089604 | |||||||
| chr4:1089636 | C | T | 7 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0104 others(4): Show |
7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.303+1146G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089636 | |||||||
| chr4:1089671 | T | C | 10 | a0001c0002t0001g0034 a0001c0002t0001g0037 a0001c0002t0001g0041 others(7): Show |
12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.303+1111A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089671 | |||||||
| chr4:1089689 | C | T | 6 | a0001c0002t0003g0329 a0001c0002t0003g0331 a0001c0002t0003g0332 others(3): Show |
6 | HG02630.hp2 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.303+1093G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089689 | |||||||
| chr4:1089706 | A | AT | 41 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(38): Show |
45 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.303+1075dupA | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089706 | |||||||
| chr4:1089797 | C | T | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.303+985G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089797 | |||||||
| chr4:1089886 | G | A | 1 | a0001c0002t0002g0243 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.303+896C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089886 | |||||||
| chr4:1089968 | G | A | 14 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(11): Show |
16 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.303+814C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089968 | |||||||
| chr4:1090079 | G | A | 1 | a0001c0002t0002g0261 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.303+703C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1090079 | |||||||
| chr4:1090110 | G | A | 6 | a0001c0002t0001g0034 a0001c0002t0001g0201 a0001c0002t0001g0294 others(3): Show |
8 | HG02486.hp2 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.303+672C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1090110 | |||||||
| chr4:1090273 | C | T | 78 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(75): Show |
89 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.303+509G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1090273 | |||||||
| chr4:1090349 | T | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.303+433A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1090349 | |||||||
| chr4:1090350 | G | A | 1 | a0001c0002t0004g0014 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.303+432C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1090350 | |||||||
| chr4:1090358 | G | A | 3 | a0004c0005t0002g0238 a0004c0005t0002g0245 a0004c0005t0002g0321 |
3 | HG00099.hp2 HG01261.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.303+424C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1090358 | |||||||
| chr4:1090513 | C | G | 2 | a0001c0002t0002g0286 a0001c0002t0002g0287 |
2 | NA18975.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.303+269G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1090513 | |||||||
| chr4:1090515 | A | G | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.303+267T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1090515 | |||||||
| chr4:1090543 | G | A | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.303+239C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1090543 | |||||||
| chr4:1090547 | G | C | 7 | a0001c0001t0001g0024 a0001c0001t0001g0151 a0001c0001t0001g0154 others(4): Show |
8 | HG01192.hp1 HG01255.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.303+235C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1090547 | |||||||
| chr4:1090674 | T | C | 3 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 |
4 | HG02922.hp2 HG03139.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.303+108A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1090674 | |||||||
| chr4:1090894 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.247-56T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1090894 | |||||||
| chr4:1090935 | G | C | 287 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(284): Show |
331 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.247-97C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1090935 | |||||||
| chr4:1090951 | T | A | 3 | a0001c0001t0006g0348 a0001c0001t0006g0349 a0001c0001t0006g0350 |
3 | HG01167.hp1 HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.247-113A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1090951 | |||||||
| chr4:1090977 | C | T | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-139G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1090977 | |||||||
| chr4:1091059 | G | A | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-221C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1091059 | |||||||
| chr4:1091096 | T | C | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-258A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1091096 | |||||||
| chr4:1091132 | T | C | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-294A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1091132 | |||||||
| chr4:1091183 | G | C | 47 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(44): Show |
53 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(50): Show |
intron_variant | MODIFIER | c.247-345C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1091183 | |||||||
| chr4:1091228 | C | T | 2 | a0001c0002t0002g0057 a0001c0002t0002g0058 |
2 | HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.247-390G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1091228 | |||||||
| chr4:1091377 | C | T | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-539G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1091377 | |||||||
| chr4:1091431 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.247-593G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1091431 | |||||||
| chr4:1091582 | G | A | 7 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0104 others(4): Show |
7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.247-744C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1091582 | |||||||
| chr4:1091953 | C | A | 7 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0104 others(4): Show |
7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.247-1115G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1091953 | |||||||
| chr4:1092010 | C | T | 3 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 |
4 | HG02922.hp2 HG03139.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-1172G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092010 | |||||||
| chr4:1092038 | A | G | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.247-1200T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092038 | |||||||
| chr4:1092103 | C | A | 1 | a0001c0001t0001g0117 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.247-1265G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092103 | |||||||
| chr4:1092146 | T | C | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-1308A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092146 | |||||||
| chr4:1092158 | A | G | 1 | a0001c0002t0002g0247 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.247-1320T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092158 | |||||||
| chr4:1092164 | G | A | 1 | a0001c0002t0002g0149 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.247-1326C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092164 | |||||||
| chr4:1092238 | C | T | 2 | a0001c0002t0002g0029 a0001c0002t0002g0307 |
3 | NA19012.hp2 NA19067.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.247-1400G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092238 | |||||||
| chr4:1092340 | G | C | 1 | a0001c0002t0002g0250 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.247-1502C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092340 | |||||||
| chr4:1092452 | G | C | 2 | a0001c0002t0002g0265 a0001c0002t0002g0319 |
2 | HG00099.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.247-1614C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092452 | |||||||
| chr4:1092453 | A | T | 2 | a0001c0002t0002g0265 a0001c0002t0002g0319 |
2 | HG00099.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.247-1615T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092453 | |||||||
| chr4:1092459 | T | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.247-1621A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092459 | |||||||
| chr4:1092499 | C | T | 49 | a0001c0001t0001g0130 a0001c0001t0001g0184 a0001c0002t0001g0019 others(46): Show |
55 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.247-1661G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092499 | |||||||
| chr4:1092517 | G | GA | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-1680_247-1679i others(3): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092517 | |||||||
| chr4:1092631 | A | T | 1 | a0001c0001t0001g0136 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.247-1793T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092631 | |||||||
| chr4:1092715 | C | T | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-1877G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092715 | |||||||
| chr4:1092725 | G | C | 7 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0104 others(4): Show |
7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.247-1887C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092725 | |||||||
| chr4:1092756 | C | G | 2 | a0001c0002t0004g0013 a0001c0002t0004g0039 |
3 | HG02922.hp2 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.247-1918G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092756 | |||||||
| chr4:1092756 | C | T | 2 | a0001c0001t0001g0104 a0006c0008t0011g0040 |
2 | HG01891.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.247-1918G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092756 | |||||||
| chr4:1092778 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0155 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.247-1940G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092778 | |||||||
| chr4:1092779 | G | A | 1 | a0001c0002t0002g0275 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.247-1941C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092779 | |||||||
| chr4:1092801 | G | A | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-1963C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092801 | |||||||
| chr4:1092802 | C | A | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-1964G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092802 | |||||||
| chr4:1092880 | G | A | 46 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(43): Show |
52 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.247-2042C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092880 | |||||||
| chr4:1092914 | G | A | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-2076C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092914 | |||||||
| chr4:1092926 | G | C | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-2088C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092926 | |||||||
| chr4:1092975 | A | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.247-2137T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092975 | |||||||
| chr4:1092976 | A | G | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.247-2138T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092976 | |||||||
| chr4:1092989 | CCAGGGTC others(43): Show |
C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.247-2201_247-2152d others(52): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092989 | |||||||
| chr4:1093041 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.247-2203C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093041 | |||||||
| chr4:1093075 | G | A | 1 | a0001c0002t0002g0036 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.247-2237C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093075 | |||||||
| chr4:1093083 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.247-2245A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093083 | |||||||
| chr4:1093278 | G | A | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-2440C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093278 | |||||||
| chr4:1093380 | A | AAT | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(240): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.247-2544_247-2543d others(4): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093380 | |||||||
| chr4:1093383 | G | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(240): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.247-2545C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093383 | |||||||
| chr4:1093451 | G | A | 4 | a0001c0001t0001g0178 a0001c0001t0001g0180 a0001c0001t0001g0181 others(1): Show |
4 | HG02015.hp2 HG02027.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-2613C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093451 | |||||||
| chr4:1093477 | T | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.247-2639A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093477 | |||||||
| chr4:1093525 | T | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0064 a0001c0001t0001g0069 others(3): Show |
7 | NA18948.hp2 NA18956.hp1 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.247-2687A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093525 | |||||||
| chr4:1093539 | G | GCTGCCCA others(14): Show |
249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(246): Show |
287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.247-2702_247-2701i others(23): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093539 | |||||||
| chr4:1093539 | G | GCTGCCCT others(14): Show |
3 | a0001c0002t0001g0019 a0001c0002t0001g0298 a0001c0002t0001g0299 |
4 | HG01255.hp1 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-2702_247-2701i others(23): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093539 | |||||||
| chr4:1093541 | C | T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.247-2703G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093541 | |||||||
| chr4:1093550 | C | T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.247-2712G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093550 | |||||||
| chr4:1093574 | C | T | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-2736G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093574 | |||||||
| chr4:1093581 | C | G | 10 | a0001c0002t0001g0034 a0001c0002t0001g0037 a0001c0002t0001g0041 others(7): Show |
12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.247-2743G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093581 | |||||||
| chr4:1093605 | G | T | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-2767C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093605 | |||||||
| chr4:1093613 | G | A | 5 | a0001c0001t0001g0031 a0001c0001t0001g0271 a0001c0001t0001g0272 others(2): Show |
6 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.247-2775C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093613 | |||||||
| chr4:1093699 | G | A | 10 | a0001c0001t0001g0016 a0001c0001t0001g0146 a0001c0001t0001g0152 others(7): Show |
11 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.247-2861C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093699 | |||||||
| chr4:1093726 | T | C | 4 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02818.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-2888A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093726 | |||||||
| chr4:1093743 | T | C | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-2905A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093743 | |||||||
| chr4:1093829 | C | A | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.246+2936G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093829 | |||||||
| chr4:1093878 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.246+2887G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093878 | |||||||
| chr4:1093938 | G | A | 1 | a0001c0002t0012g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.246+2827C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093938 | |||||||
| chr4:1093984 | G | A | 3 | a0001c0001t0006g0348 a0001c0001t0006g0349 a0001c0001t0006g0350 |
3 | HG01167.hp1 HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.246+2781C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093984 | |||||||
| chr4:1094050 | G | GCTTGCTG others(12): Show |
48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.246+2714_246+2715i others(21): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1094050 | |||||||
| chr4:1094113 | A | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(91): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.246+2652T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1094113 | |||||||
| chr4:1094141 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.246+2624G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1094141 | |||||||
| chr4:1094212 | G | A | 2 | a0001c0002t0003g0325 a0001c0002t0003g0328 |
2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.246+2553C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1094212 | |||||||
| chr4:1094232 | C | T | 4 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02818.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+2533G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1094232 | |||||||
| chr4:1094405 | G | A | 3 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0171 |
3 | NA18955.hp1 NA18993.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.246+2360C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1094405 | |||||||
| chr4:1094484 | C | T | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.246+2281G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1094484 | |||||||
| chr4:1094530 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.246+2235T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1094530 | |||||||
| chr4:1094630 | G | C | 2 | a0001c0002t0004g0014 a0001c0002t0004g0048 |
3 | HG02717.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.246+2135C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1094630 | |||||||
| chr4:1094631 | G | A | 4 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02818.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+2134C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1094631 | |||||||
| chr4:1094686 | G | C | 45 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(42): Show |
50 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.246+2079C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1094686 | |||||||
| chr4:1094817 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.246+1948C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1094817 | |||||||
| chr4:1094888 | A | T | 1 | a0007c0007t0002g0224 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.246+1877T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1094888 | |||||||
| chr4:1094903 | C | G | 1 | a0001c0002t0002g0240 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.246+1862G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1094903 | |||||||
| chr4:1095001 | T | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0142 a0001c0001t0001g0297 |
4 | HG03017.hp2 HG03831.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1764A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095001 | |||||||
| chr4:1095055 | G | C | 14 | a0001c0002t0002g0028 a0001c0002t0002g0060 a0001c0002t0002g0237 others(11): Show |
15 | HG00099.hp2 HG01261.hp2 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.246+1710C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095055 | |||||||
| chr4:1095083 | C | T | 21 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0025 others(18): Show |
25 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.246+1682G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095083 | |||||||
| chr4:1095084 | GGAACCAA others(465): Show |
G | 1 | a0001c0002t0002g0263 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.246+1209_246+1680d others(2): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095084 | |||||||
| chr4:1095123 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.246+1642A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095123 | |||||||
| chr4:1095127 | G | A | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.246+1638C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095127 | |||||||
| chr4:1095155 | G | A | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.246+1610C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095155 | |||||||
| chr4:1095155 | GCCCCCCA others(111): Show |
G | 80 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(77): Show |
92 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.246+1492_246+1609d others(2): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095155 | |||||||
| chr4:1095184 | G | C | 1 | a0001c0002t0002g0060 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.246+1581C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095184 | |||||||
| chr4:1095185 | C | T | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.246+1580G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095185 | |||||||
| chr4:1095202 | AGAACCAA others(1291): Show |
A | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.246+265_246+1562de others(1): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095202 | |||||||
| chr4:1095216 | T | C | 5 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0169 others(2): Show |
5 | NA18941.hp2 NA18989.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+1549A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095216 | |||||||
| chr4:1095217 | C | T | 5 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0169 others(2): Show |
5 | NA18941.hp2 NA18989.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+1548G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095217 | |||||||
| chr4:1095230 | TGGTCTCG others(996): Show |
T | 1 | a0001c0001t0001g0112 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.246+532_246+1534de others(1): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095230 | |||||||
| chr4:1095237 | G | A | 5 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0169 others(2): Show |
5 | NA18941.hp2 NA18989.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+1528C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095237 | |||||||
| chr4:1095239 | G | C | 5 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0169 others(2): Show |
5 | NA18941.hp2 NA18989.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+1526C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095239 | |||||||
| chr4:1095260 | C | T | 7 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0104 others(4): Show |
7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.246+1505G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095260 | |||||||
| chr4:1095277 | CCCACAGC others(110): Show |
C | 1 | a0001c0001t0001g0169 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.246+1371_246+1487d others(2): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095277 | |||||||
| chr4:1095289 | T | C | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(1): Show |
4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1476A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095289 | |||||||
| chr4:1095320 | A | G | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(1): Show |
4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1445T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095320 | |||||||
| chr4:1095335 | T | C | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(1): Show |
4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1430A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095335 | |||||||
| chr4:1095348 | T | C | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(1): Show |
4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1417A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095348 | |||||||
| chr4:1095355 | A | G | 1 | a0001c0002t0002g0218 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+1410T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095355 | |||||||
| chr4:1095357 | C | G | 5 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(2): Show |
5 | NA18941.hp2 NA18979.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+1408G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095357 | |||||||
| chr4:1095362 | C | T | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(1): Show |
4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1403G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095362 | |||||||
| chr4:1095379 | A | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.246+1386T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095379 | |||||||
| chr4:1095392 | A | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.246+1373T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095392 | |||||||
| chr4:1095394 | T | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.246+1371A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095394 | |||||||
| chr4:1095407 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(174): Show |
208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.246+1358A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095407 | |||||||
| chr4:1095407 | TGGTCTCG others(52): Show |
T | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.246+1299_246+1357d others(61): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095407 | |||||||
| chr4:1095414 | G | A | 1 | a0001c0002t0002g0218 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+1351C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095414 | |||||||
| chr4:1095416 | G | C | 1 | a0001c0002t0002g0218 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+1349C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095416 | |||||||
| chr4:1095421 | C | T | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(1): Show |
4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1344G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095421 | |||||||
| chr4:1095438 | A | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(174): Show |
208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.246+1327T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095438 | |||||||
| chr4:1095451 | A | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(177): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.246+1314T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095451 | |||||||
| chr4:1095453 | T | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.246+1312A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095453 | |||||||
| chr4:1095453 | T | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0278 |
3 | HG02074.hp1 NA18945.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.246+1312A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095453 | |||||||
| chr4:1095466 | C | T | 5 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(2): Show |
5 | NA18941.hp2 NA18979.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+1299G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095466 | |||||||
| chr4:1095473 | G | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.246+1292C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095473 | |||||||
| chr4:1095475 | G | C | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(1): Show |
4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1290C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095475 | |||||||
| chr4:1095480 | C | T | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.246+1285G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095480 | |||||||
| chr4:1095510 | A | C | 5 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(2): Show |
5 | NA18941.hp2 NA18979.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+1255T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095510 | |||||||
| chr4:1095512 | T | C | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(1): Show |
4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1253A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095512 | |||||||
| chr4:1095532 | G | A | 1 | a0001c0002t0002g0218 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+1233C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095532 | |||||||
| chr4:1095534 | G | C | 1 | a0001c0002t0002g0218 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+1231C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095534 | |||||||
| chr4:1095539 | T | C | 5 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(2): Show |
5 | NA18941.hp2 NA18979.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+1226A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095539 | |||||||
| chr4:1095569 | C | A | 5 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(2): Show |
5 | NA18941.hp2 NA18979.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+1196G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095569 | |||||||
| chr4:1095571 | T | C | 1 | a0001c0002t0002g0263 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.246+1194A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095571 | |||||||
| chr4:1095591 | A | G | 5 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(2): Show |
5 | NA18941.hp2 NA18979.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+1174T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095591 | |||||||
| chr4:1095593 | C | G | 5 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(2): Show |
5 | NA18941.hp2 NA18979.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+1172G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095593 | |||||||
| chr4:1095598 | C | T | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(1): Show |
4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1167G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095598 | |||||||
| chr4:1095628 | C | A | 1 | a0001c0002t0002g0218 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+1137G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095628 | |||||||
| chr4:1095630 | C | T | 5 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(2): Show |
5 | NA18941.hp2 NA18979.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+1135G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095630 | |||||||
| chr4:1095643 | T | C | 1 | a0001c0002t0002g0218 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+1122A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095643 | |||||||
| chr4:1095650 | G | A | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(1): Show |
4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1115C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095650 | |||||||
| chr4:1095650 | G | C | 4 | a0001c0001t0001g0125 a0001c0001t0001g0282 a0001c0001t0001g0283 others(1): Show |
4 | HG00438.hp2 HG02080.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1115C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095650 | |||||||
| chr4:1095652 | G | C | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(1): Show |
4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1113C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095652 | |||||||
| chr4:1095674 | A | G | 6 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0093 others(3): Show |
6 | HG01975.hp1 HG02280.hp1 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.246+1091T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095674 | |||||||
| chr4:1095687 | C | A | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(197): Show |
233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.246+1078G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095687 | |||||||
| chr4:1095689 | T | C | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(1): Show |
4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1076A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095689 | |||||||
| chr4:1095716 | C | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.246+1049G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095716 | |||||||
| chr4:1095741 | G | C | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(1): Show |
4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1024C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095741 | |||||||
| chr4:1095748 | T | C | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(1): Show |
4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1017A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095748 | |||||||
| chr4:1095774 | G | A | 1 | a0001c0002t0002g0300 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.246+991C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095774 | |||||||
| chr4:1095792 | G | A | 5 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(2): Show |
5 | NA18941.hp2 NA18979.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+973C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095792 | |||||||
| chr4:1095807 | C | T | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(1): Show |
4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+958G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095807 | |||||||
| chr4:1095829 | GATAGCGC others(52): Show |
G | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(1): Show |
4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+877_246+935del others(59): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095829 | |||||||
| chr4:1095859 | C | G | 1 | a0001c0002t0002g0218 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+906G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095859 | |||||||
| chr4:1095866 | C | T | 1 | a0001c0002t0002g0218 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+899G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095866 | |||||||
| chr4:1095886 | A | G | 2 | a0001c0002t0002g0036 a0001c0002t0002g0218 |
2 | HG04199.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.246+879T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095886 | |||||||
| chr4:1095888 | C | G | 1 | a0001c0002t0002g0218 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+877G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095888 | |||||||
| chr4:1095893 | C | T | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(1): Show |
4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+872G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095893 | |||||||
| chr4:1095923 | C | A | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(1): Show |
4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+842G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095923 | |||||||
| chr4:1095923 | CCTCCCAC others(52): Show |
C | 1 | a0001c0001t0001g0080 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.246+783_246+841del others(59): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095923 | |||||||
| chr4:1095925 | T | TCCCACAG others(111): Show |
1 | a0001c0002t0002g0218 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+839_246+840ins others(118): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095925 | |||||||
| chr4:1095945 | G | A | 1 | a0001c0002t0002g0218 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+820C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095945 | |||||||
| chr4:1095947 | G | C | 1 | a0001c0002t0002g0218 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+818C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095947 | |||||||
| chr4:1095952 | C | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(183): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.246+813G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095952 | |||||||
| chr4:1095969 | A | G | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(1): Show |
4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+796T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095969 | |||||||
| chr4:1095982 | A | C | 5 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(2): Show |
5 | NA18941.hp2 NA18979.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+783T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095982 | |||||||
| chr4:1095984 | T | C | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0180 others(1): Show |
4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+781A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095984 | |||||||
| chr4:1095984 | T | TCCCACAG others(52): Show |
12 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0109 others(9): Show |
15 | HG00408.hp2 HG00621.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.246+722_246+780dup others(59): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095984 | |||||||
| chr4:1095984 | T | TCCCACAG others(170): Show |
2 | a0001c0001t0001g0197 a0001c0001t0001g0199 |
2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.246+780_246+781ins others(177): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095984 | |||||||
| chr4:1095984 | T | TCCCACAG others(229): Show |
2 | a0001c0001t0001g0198 a0001c0001t0001g0200 |
2 | HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.246+780_246+781ins others(236): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095984 | |||||||
| chr4:1096002 | T | C | 7 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0104 others(4): Show |
7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.246+763A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096002 | |||||||
| chr4:1096011 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.246+754G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096011 | |||||||
| chr4:1096028 | G | A | 1 | a0001c0002t0002g0218 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+737C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096028 | |||||||
| chr4:1096041 | C | A | 1 | a0001c0002t0002g0218 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+724G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096041 | |||||||
| chr4:1096041 | C | CCCCCCAC others(52): Show |
1 | a0001c0001t0001g0135 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.246+723_246+724ins others(59): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096041 | |||||||
| chr4:1096043 | C | T | 1 | a0001c0002t0002g0218 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+722G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096043 | |||||||
| chr4:1096056 | T | C | 10 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0166 others(7): Show |
10 | HG00099.hp1 HG01123.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.246+709A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096056 | |||||||
| chr4:1096056 | TGGTCTCG others(52): Show |
T | 1 | a0001c0001t0001g0118 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.246+650_246+708del others(59): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096056 | |||||||
| chr4:1096086 | C | T | 6 | a0001c0001t0001g0025 a0001c0001t0001g0068 a0001c0001t0001g0078 others(3): Show |
7 | HG00558.hp1 HG02155.hp2 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.246+679G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096086 | |||||||
| chr4:1096115 | C | T | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.246+650G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096115 | |||||||
| chr4:1096116 | G | T | 1 | a0001c0001t0001g0119 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.246+649C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096116 | |||||||
| chr4:1096128 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.246+637C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096128 | |||||||
| chr4:1096154 | G | C | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.246+611C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096154 | |||||||
| chr4:1096154 | G | GCACACCC others(229): Show |
1 | a0001c0002t0002g0144 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.246+610_246+611ins others(236): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096154 | |||||||
| chr4:1096154 | GCACACCC others(170): Show |
G | 10 | a0001c0002t0001g0034 a0001c0002t0001g0037 a0001c0002t0001g0041 others(7): Show |
12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.246+434_246+610del | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096154 | |||||||
| chr4:1096174 | C | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.246+591G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096174 | |||||||
| chr4:1096213 | GCACACCC others(111): Show |
G | 1 | a0001c0002t0002g0149 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.246+434_246+551del | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096213 | |||||||
| chr4:1096233 | C | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(72): Show |
90 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.246+532G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096233 | |||||||
| chr4:1096241 | G | A | 1 | a0001c0002t0002g0263 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.246+524C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096241 | |||||||
| chr4:1096263 | C | T | 4 | a0001c0002t0002g0206 a0001c0002t0002g0207 a0001c0002t0002g0295 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+502G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096263 | |||||||
| chr4:1096272 | GCACACCC others(52): Show |
G | 7 | a0001c0001t0001g0095 a0001c0001t0005g0043 a0001c0001t0005g0047 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.246+434_246+492del others(59): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096272 | |||||||
| chr4:1096278 | C | T | 5 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0104 others(2): Show |
5 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.246+487G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096278 | |||||||
| chr4:1096289 | C | T | 1 | a0001c0001t0006g0350 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.246+476G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096289 | |||||||
| chr4:1096292 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.246+473G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096292 | |||||||
| chr4:1096298 | C | T | 1 | a0001c0001t0001g0006 | 2 | HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.246+467G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096298 | |||||||
| chr4:1096307 | G | A | 1 | a0001c0002t0002g0251 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.246+458C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096307 | |||||||
| chr4:1096321 | A | G | 3 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0156 |
3 | HG01891.hp2 HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.246+444T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096321 | |||||||
| chr4:1096331 | C | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(177): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.246+434G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096331 | |||||||
| chr4:1096331 | CCACACCC others(52): Show |
C | 86 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0118 others(83): Show |
97 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.246+375_246+433del others(59): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096331 | |||||||
| chr4:1096351 | C | T | 10 | a0001c0002t0001g0034 a0001c0002t0001g0037 a0001c0002t0001g0041 others(7): Show |
12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.246+414G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096351 | |||||||
| chr4:1096384 | A | T | 1 | a0001c0001t0001g0126 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.246+381T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096384 | |||||||
| chr4:1096390 | G | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.246+375C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096390 | |||||||
| chr4:1096390 | G | GCACACCC others(52): Show |
3 | a0001c0001t0001g0115 a0001c0001t0001g0198 a0001c0001t0001g0200 |
3 | HG02818.hp2 HG03471.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.246+374_246+375ins others(59): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096390 | |||||||
| chr4:1096390 | G | GCACACCC others(111): Show |
2 | a0001c0001t0001g0197 a0001c0001t0001g0199 |
2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.246+374_246+375ins others(118): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096390 | |||||||
| chr4:1096410 | C | T | 10 | a0001c0002t0001g0034 a0001c0002t0001g0037 a0001c0002t0001g0041 others(7): Show |
12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.246+355G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096410 | |||||||
| chr4:1096440 | C | CGGAACCA others(52): Show |
1 | a0001c0001t0001g0117 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.246+324_246+325ins others(59): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096440 | |||||||
| chr4:1096449 | G | C | 3 | a0001c0001t0001g0178 a0001c0001t0005g0043 a0001c0001t0005g0047 |
3 | HG02015.hp2 HG03710.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.246+316C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096449 | |||||||
| chr4:1096469 | C | T | 10 | a0001c0002t0001g0034 a0001c0002t0001g0037 a0001c0002t0001g0041 others(7): Show |
12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.246+296G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096469 | |||||||
| chr4:1096475 | C | G | 1 | a0001c0001t0001g0142 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.246+290G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096475 | |||||||
| chr4:1096476 | GGGATAGC others(52): Show |
G | 12 | a0001c0001t0001g0095 a0001c0001t0001g0172 a0001c0002t0002g0057 others(9): Show |
12 | HG01109.hp1 HG01123.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.246+230_246+288del others(59): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096476 | |||||||
| chr4:1096500 | G | A | 11 | a0001c0002t0001g0034 a0001c0002t0001g0037 a0001c0002t0001g0041 others(8): Show |
13 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.246+265C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096500 | |||||||
| chr4:1096513 | C | A | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.246+252G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096513 | |||||||
| chr4:1096515 | C | T | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.246+250G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096515 | |||||||
| chr4:1096535 | A | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0044 others(75): Show |
86 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.246+230T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096535 | |||||||
| chr4:1096559 | A | G | 32 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0095 others(29): Show |
38 | HG00280.hp2 HG00597.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.246+206T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096559 | |||||||
| chr4:1096618 | A | G | 5 | a0001c0001t0001g0095 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG02258.hp2 NA19056.hp1 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.246+147T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096618 | |||||||
| chr4:1096633 | C | T | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.246+132G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096633 | |||||||
| chr4:1096635 | T | C | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.246+130A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096635 | |||||||
| chr4:1096697 | T | C | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.246+68A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096697 | |||||||
| chr4:1096714 | G | A | 47 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(44): Show |
53 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(50): Show |
intron_variant | MODIFIER | c.246+51C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096714 | |||||||
| chr4:1096974 | A | C | 45 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(42): Show |
50 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.172-135T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1096974 | |||||||
| chr4:1096974 | A | T | 3 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 |
4 | HG02922.hp2 HG03139.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-135T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1096974 | |||||||
| chr4:1096997 | C | T | 1 | a0006c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.172-158G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1096997 | |||||||
| chr4:1096998 | G | A | 46 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(43): Show |
52 | HG00642.hp2 HG00735.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.172-159C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1096998 | |||||||
| chr4:1097037 | G | A | 1 | a0001c0002t0002g0269 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.172-198C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097037 | |||||||
| chr4:1097163 | C | T | 1 | a0001c0002t0002g0220 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.172-324G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097163 | |||||||
| chr4:1097274 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(239): Show |
279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.172-435T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097274 | |||||||
| chr4:1097319 | C | T | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.172-480G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097319 | |||||||
| chr4:1097327 | G | A | 1 | a0001c0002t0001g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.172-488C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097327 | |||||||
| chr4:1097375 | C | T | 52 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(49): Show |
58 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.172-536G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097375 | |||||||
| chr4:1097473 | C | T | 7 | a0001c0001t0001g0024 a0001c0001t0001g0151 a0001c0001t0001g0154 others(4): Show |
8 | HG01192.hp1 HG01255.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.172-634G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097473 | |||||||
| chr4:1097474 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.172-635C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097474 | |||||||
| chr4:1097663 | T | A | 7 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0104 others(4): Show |
7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-824A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097663 | |||||||
| chr4:1097676 | C | A | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-837G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097676 | |||||||
| chr4:1097677 | C | G | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-838G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097677 | |||||||
| chr4:1097678 | T | C | 1 | a0001c0002t0002g0149 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.172-839A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097678 | |||||||
| chr4:1097678 | T | G | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-839A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097678 | |||||||
| chr4:1097680 | T | A | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-841A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097680 | |||||||
| chr4:1097683 | C | G | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-844G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097683 | |||||||
| chr4:1097685 | T | A | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-846A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097685 | |||||||
| chr4:1097689 | C | G | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-850G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097689 | |||||||
| chr4:1097690 | T | G | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-851A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097690 | |||||||
| chr4:1097695 | T | TGTGAAGG others(12): Show |
1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-857_172-856ins others(19): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097695 | |||||||
| chr4:1097698 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-859G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097698 | |||||||
| chr4:1097699 | C | G | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-860G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097699 | |||||||
| chr4:1097702 | G | C | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.172-863C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097702 | |||||||
| chr4:1097708 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-869T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097708 | |||||||
| chr4:1097713 | A | G | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.172-874T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097713 | |||||||
| chr4:1097716 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-877T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097716 | |||||||
| chr4:1097717 | G | T | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-878C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097717 | |||||||
| chr4:1097718 | C | A | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-879G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097718 | |||||||
| chr4:1097721 | A | C | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-882T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097721 | |||||||
| chr4:1097726 | A | T | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-887T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097726 | |||||||
| chr4:1097727 | C | G | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-888G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097727 | |||||||
| chr4:1097728 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-889A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097728 | |||||||
| chr4:1097729 | A | T | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-890T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097729 | |||||||
| chr4:1097731 | G | T | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-892C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097731 | |||||||
| chr4:1097733 | G | T | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-894C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097733 | |||||||
| chr4:1097734 | A | T | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-895T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097734 | |||||||
| chr4:1097736 | A | T | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-897T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097736 | |||||||
| chr4:1097737 | G | T | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-898C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097737 | |||||||
| chr4:1097740 | G | T | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-901C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097740 | |||||||
| chr4:1097741 | T | G | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-902A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097741 | |||||||
| chr4:1097744 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-905A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097744 | |||||||
| chr4:1097749 | A | C | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-910T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097749 | |||||||
| chr4:1097750 | T | C | 1 | a0006c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.172-911A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097750 | |||||||
| chr4:1097759 | C | A | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-920G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097759 | |||||||
| chr4:1097766 | T | G | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-927A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097766 | |||||||
| chr4:1097767 | A | T | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-928T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097767 | |||||||
| chr4:1097768 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-929C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097768 | |||||||
| chr4:1097772 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0202 |
3 | HG01081.hp2 HG01257.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.172-933G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097772 | |||||||
| chr4:1097773 | G | T | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-934C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097773 | |||||||
| chr4:1097775 | T | G | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-936A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097775 | |||||||
| chr4:1097776 | T | A | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-937A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097776 | |||||||
| chr4:1097778 | A | C | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-939T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097778 | |||||||
| chr4:1097779 | G | T | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-940C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097779 | |||||||
| chr4:1097782 | G | C | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-943C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097782 | |||||||
| chr4:1097784 | C | G | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-945G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097784 | |||||||
| chr4:1097801 | A | C | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-962T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097801 | |||||||
| chr4:1097803 | G | T | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-964C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097803 | |||||||
| chr4:1097812 | C | G | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-973G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097812 | |||||||
| chr4:1097815 | AGCACTTT others(19): Show |
A | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-1002_172-977de others(27): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097815 | |||||||
| chr4:1097842 | A | T | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-1003T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097842 | |||||||
| chr4:1097845 | G | T | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-1006C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097845 | |||||||
| chr4:1097847 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-1008A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097847 | |||||||
| chr4:1097852 | G | C | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-1013C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097852 | |||||||
| chr4:1097855 | A | C | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-1016T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097855 | |||||||
| chr4:1097856 | G | T | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-1017C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097856 | |||||||
| chr4:1097872 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-1033G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097872 | |||||||
| chr4:1097873 | T | G | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-1034A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097873 | |||||||
| chr4:1097878 | A | T | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-1039T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097878 | |||||||
| chr4:1098009 | G | T | 26 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0032 others(23): Show |
29 | HG00609.hp1 HG01109.hp2 HG02015.hp2 others(26): Show |
intron_variant | MODIFIER | c.172-1170C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098009 | |||||||
| chr4:1098041 | G | C | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.172-1202C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098041 | |||||||
| chr4:1098137 | G | A | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.172-1298C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098137 | |||||||
| chr4:1098165 | T | C | 1 | a0001c0001t0015g0196 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.172-1326A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098165 | |||||||
| chr4:1098186 | T | TAG | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.172-1349_172-1348d others(4): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098186 | |||||||
| chr4:1098198 | A | G | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.172-1359T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098198 | |||||||
| chr4:1098231 | G | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.172-1392C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098231 | |||||||
| chr4:1098370 | T | C | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.172-1531A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098370 | |||||||
| chr4:1098429 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.172-1590G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098429 | |||||||
| chr4:1098542 | C | T | 3 | a0001c0002t0001g0041 a0001c0002t0001g0042 a0001c0002t0006g0351 |
3 | HG03098.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.172-1703G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098542 | |||||||
| chr4:1098576 | T | C | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.172-1737A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098576 | |||||||
| chr4:1098610 | G | A | 1 | a0001c0001t0014g0087 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.172-1771C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098610 | |||||||
| chr4:1098617 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(239): Show |
279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.172-1778T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098617 | |||||||
| chr4:1098690 | C | T | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.172-1851G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098690 | |||||||
| chr4:1098720 | T | C | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.172-1881A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098720 | |||||||
| chr4:1098731 | CAG | C | 2 | a0001c0002t0004g0014 a0001c0002t0004g0048 |
3 | HG02717.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.172-1894_172-1893d others(4): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098731 | |||||||
| chr4:1098760 | C | T | 3 | a0001c0001t0006g0348 a0001c0001t0006g0349 a0001c0001t0006g0350 |
3 | HG01167.hp1 HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.172-1921G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098760 | |||||||
| chr4:1098813 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.172-1974G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098813 | |||||||
| chr4:1098839 | C | T | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.172-2000G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098839 | |||||||
| chr4:1099117 | C | T | 10 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0110 others(7): Show |
13 | HG00408.hp2 HG02071.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.172-2278G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099117 | |||||||
| chr4:1099149 | G | A | 1 | a0001c0002t0002g0291 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.172-2310C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099149 | |||||||
| chr4:1099171 | G | A | 48 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(45): Show |
54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.172-2332C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099171 | |||||||
| chr4:1099189 | G | A | 2 | a0001c0002t0003g0338 a0001c0002t0003g0339 |
2 | HG01074.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.172-2350C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099189 | |||||||
| chr4:1099232 | T | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.172-2393A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099232 | |||||||
| chr4:1099312 | T | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.172-2473A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099312 | |||||||
| chr4:1099337 | T | C | 4 | a0001c0002t0002g0206 a0001c0002t0002g0207 a0001c0002t0002g0295 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-2498A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099337 | |||||||
| chr4:1099437 | A | G | 350 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(347): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.172-2598T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099437 | |||||||
| chr4:1099470 | C | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.172-2631G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099470 | |||||||
| chr4:1099575 | G | A | 4 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02818.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-2736C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099575 | |||||||
| chr4:1099616 | G | A | 1 | a0001c0001t0015g0196 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.172-2777C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099616 | |||||||
| chr4:1099766 | T | C | 10 | a0001c0001t0006g0348 a0001c0001t0006g0349 a0001c0001t0006g0350 others(7): Show |
12 | HG01167.hp1 HG01255.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.172-2927A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099766 | |||||||
| chr4:1099811 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0297 |
3 | HG03017.hp2 HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.172-2972G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099811 | |||||||
| chr4:1099821 | C | T | 7 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0104 others(4): Show |
7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-2982G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099821 | |||||||
| chr4:1099859 | C | G | 3 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 |
4 | HG02922.hp2 HG03139.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-3020G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099859 | |||||||
| chr4:1100043 | T | C | 2 | a0001c0001t0001g0178 a0001c0001t0001g0180 |
2 | HG02015.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.172-3204A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100043 | |||||||
| chr4:1100111 | T | C | 6 | a0001c0002t0001g0034 a0001c0002t0001g0201 a0001c0002t0001g0294 others(3): Show |
8 | HG02486.hp2 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.172-3272A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100111 | |||||||
| chr4:1100126 | A | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.172-3287T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100126 | |||||||
| chr4:1100196 | TTTCC | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0163 a0001c0001t0001g0164 |
4 | NA18977.hp2 NA19067.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-3361_172-3358d others(6): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100196 | |||||||
| chr4:1100201 | C | G | 3 | a0001c0001t0001g0032 a0001c0001t0001g0163 a0001c0001t0001g0164 |
4 | NA18977.hp2 NA19067.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-3362G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100201 | |||||||
| chr4:1100237 | C | T | 10 | a0001c0002t0001g0034 a0001c0002t0001g0037 a0001c0002t0001g0041 others(7): Show |
12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.172-3398G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100237 | |||||||
| chr4:1100335 | C | T | 10 | a0001c0002t0001g0034 a0001c0002t0001g0037 a0001c0002t0001g0041 others(7): Show |
12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.172-3496G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100335 | |||||||
| chr4:1100363 | G | A | 102 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0010 others(99): Show |
113 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.172-3524C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100363 | |||||||
| chr4:1100398 | AT | A | 25 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0023 others(22): Show |
29 | HG00642.hp2 HG00735.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.172-3560delA | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100398 | |||||||
| chr4:1100398 | ATTT | A | 8 | a0001c0001t0001g0075 a0001c0001t0001g0197 a0001c0001t0001g0198 others(5): Show |
10 | HG02083.hp2 HG02717.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.172-3562_172-3560d others(5): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100398 | |||||||
| chr4:1100398 | ATTTT | A | 12 | a0001c0001t0001g0031 a0001c0001t0001g0050 a0001c0001t0001g0116 others(9): Show |
13 | HG00438.hp2 HG00639.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.172-3563_172-3560d others(6): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100398 | |||||||
| chr4:1100398 | ATTTTT | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.172-3564_172-3560d others(7): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100398 | |||||||
| chr4:1100398 | ATTTTTT | A | 84 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(81): Show |
95 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.172-3565_172-3560d others(8): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100398 | |||||||
| chr4:1100398 | ATTTTTTT | A | 94 | a0001c0001t0001g0056 a0001c0001t0001g0095 a0001c0001t0001g0179 others(91): Show |
105 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.172-3566_172-3560d others(9): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100398 | |||||||
| chr4:1100403 | T | A | 1 | a0001c0001t0001g0075 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.172-3564A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100403 | |||||||
| chr4:1100404 | T | A | 4 | a0001c0001t0001g0125 a0001c0001t0001g0282 a0001c0001t0001g0283 others(1): Show |
4 | HG00438.hp2 HG02080.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-3565A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100404 | |||||||
| chr4:1100428 | G | A | 4 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02818.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-3589C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100428 | |||||||
| chr4:1100526 | G | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.172-3687C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100526 | |||||||
| chr4:1100598 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.172-3759C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100598 | |||||||
| chr4:1100660 | C | T | 8 | a0001c0001t0001g0026 a0001c0001t0001g0167 a0001c0001t0001g0168 others(5): Show |
9 | HG01109.hp2 NA18747.hp1 NA18955.hp1 others(6): Show |
intron_variant | MODIFIER | c.172-3821G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100660 | |||||||
| chr4:1100720 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.172-3881T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100720 | |||||||
| chr4:1100766 | T | G | 2 | a0001c0001t0001g0190 a0001c0001t0001g0284 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.172-3927A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100766 | |||||||
| chr4:1100882 | T | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(201): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.172-4043A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100882 | |||||||
| chr4:1100957 | C | T | 4 | a0001c0001t0001g0113 a0001c0002t0002g0236 a0001c0002t0002g0239 others(1): Show |
4 | HG01123.hp2 HG01168.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-4118G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100957 | |||||||
| chr4:1100973 | T | C | 1 | a0001c0002t0012g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.172-4134A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100973 | |||||||
| chr4:1101049 | T | A | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.172-4210A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1101049 | |||||||
| chr4:1101178 | C | T | 8 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0095 others(5): Show |
8 | HG02040.hp1 HG02258.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.172-4339G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1101178 | |||||||
| chr4:1101199 | A | G | 4 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02818.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-4360T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1101199 | |||||||
| chr4:1101213 | G | A | 7 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0104 others(4): Show |
7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-4374C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1101213 | |||||||
| chr4:1101291 | A | G | 102 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0010 others(99): Show |
113 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.172-4452T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1101291 | |||||||
| chr4:1101402 | A | G | 1 | a0001c0002t0002g0223 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.172-4563T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1101402 | |||||||
| chr4:1101493 | A | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.172-4654T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1101493 | |||||||
| chr4:1101532 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.172-4693G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1101532 | |||||||
| chr4:1101587 | A | C | 7 | a0001c0001t0001g0024 a0001c0001t0001g0151 a0001c0001t0001g0154 others(4): Show |
8 | HG01192.hp1 HG01255.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.172-4748T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1101587 | |||||||
| chr4:1101621 | C | T | 6 | a0001c0002t0002g0246 a0001c0002t0002g0247 a0001c0002t0002g0248 others(3): Show |
6 | HG00438.hp1 HG02071.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-4782G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1101621 | |||||||
| chr4:1101622 | G | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.172-4783C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1101622 | |||||||
| chr4:1101634 | G | A | 18 | a0001c0002t0003g0033 a0001c0002t0003g0329 a0001c0002t0003g0331 others(15): Show |
19 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.172-4795C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1101634 | |||||||
| chr4:1102053 | T | C | 1 | a0005c0006t0001g0128 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.172-5214A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102053 | |||||||
| chr4:1102132 | C | A | 101 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0010 others(98): Show |
112 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.172-5293G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102132 | |||||||
| chr4:1102352 | G | T | 3 | a0001c0001t0006g0348 a0001c0001t0006g0349 a0001c0001t0006g0350 |
3 | HG01167.hp1 HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.172-5513C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102352 | |||||||
| chr4:1102448 | A | G | 10 | a0001c0002t0001g0034 a0001c0002t0001g0037 a0001c0002t0001g0041 others(7): Show |
12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.172-5609T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102448 | |||||||
| chr4:1102458 | G | A | 10 | a0001c0002t0001g0034 a0001c0002t0001g0037 a0001c0002t0001g0041 others(7): Show |
12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.172-5619C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102458 | |||||||
| chr4:1102476 | C | T | 3 | a0001c0002t0001g0041 a0001c0002t0001g0042 a0001c0002t0006g0351 |
3 | HG03098.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.172-5637G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102476 | |||||||
| chr4:1102477 | C | T | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.172-5638G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102477 | |||||||
| chr4:1102579 | A | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.172-5740T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102579 | |||||||
| chr4:1102583 | A | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.172-5744T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102583 | |||||||
| chr4:1102594 | CA | C | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(291): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.171+5748delT | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102594 | |||||||
| chr4:1102604 | A | C | 3 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 |
4 | HG02922.hp2 HG03139.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+5739T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102604 | |||||||
| chr4:1102628 | A | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.171+5715T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102628 | |||||||
| chr4:1102635 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | NA18941.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.171+5708C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102635 | |||||||
| chr4:1102712 | C | T | 1 | a0001c0002t0002g0144 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.171+5631G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102712 | |||||||
| chr4:1102738 | G | A | 1 | a0001c0002t0012g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.171+5605C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102738 | |||||||
| chr4:1102777 | G | A | 1 | a0001c0002t0001g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.171+5566C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102777 | |||||||
| chr4:1102808 | C | T | 1 | a0001c0002t0012g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.171+5535G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102808 | |||||||
| chr4:1102833 | C | A | 7 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0104 others(4): Show |
7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+5510G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102833 | |||||||
| chr4:1102899 | T | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.171+5444A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102899 | |||||||
| chr4:1102988 | CA | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.171+5354delT | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102988 | |||||||
| chr4:1102988 | CAA | C | 101 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(98): Show |
113 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.171+5353_171+5354d others(4): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102988 | |||||||
| chr4:1103020 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.171+5323T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1103020 | |||||||
| chr4:1103066 | A | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.171+5277T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1103066 | |||||||
| chr4:1103327 | T | C | 1 | a0001c0002t0001g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.171+5016A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1103327 | |||||||
| chr4:1103432 | A | G | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.171+4911T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1103432 | |||||||
| chr4:1103545 | A | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.171+4798T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1103545 | |||||||
| chr4:1103621 | TAACAA | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.171+4717_171+4721d others(7): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1103621 | |||||||
| chr4:1103827 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.171+4516T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1103827 | |||||||
| chr4:1103888 | G | A | 101 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0010 others(98): Show |
112 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.171+4455C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1103888 | |||||||
| chr4:1104127 | G | A | 350 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(347): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.171+4216C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104127 | |||||||
| chr4:1104381 | T | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.171+3962A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104381 | |||||||
| chr4:1104407 | G | A | 6 | a0001c0001t0001g0024 a0001c0001t0001g0151 a0001c0001t0001g0154 others(3): Show |
7 | HG01884.hp1 HG01891.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.171+3936C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104407 | |||||||
| chr4:1104434 | A | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.171+3909T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104434 | |||||||
| chr4:1104701 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.171+3642G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104701 | |||||||
| chr4:1104758 | C | T | 1 | a0001c0002t0002g0251 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.171+3585G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104758 | |||||||
| chr4:1104759 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.171+3584C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104759 | |||||||
| chr4:1104765 | C | T | 10 | a0001c0002t0001g0034 a0001c0002t0001g0037 a0001c0002t0001g0041 others(7): Show |
12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.171+3578G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104765 | |||||||
| chr4:1104778 | A | C | 4 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02818.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+3565T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104778 | |||||||
| chr4:1104818 | C | T | 9 | a0001c0002t0001g0034 a0001c0002t0001g0037 a0001c0002t0001g0041 others(6): Show |
11 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.171+3525G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104818 | |||||||
| chr4:1104879 | C | T | 8 | a0001c0002t0002g0246 a0001c0002t0002g0247 a0001c0002t0002g0248 others(5): Show |
8 | HG00438.hp1 HG02071.hp2 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.171+3464G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104879 | |||||||
| chr4:1104909 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.171+3434G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104909 | |||||||
| chr4:1104934 | G | T | 2 | a0001c0002t0007g0353 a0001c0002t0007g0355 |
2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.171+3409C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104934 | |||||||
| chr4:1104935 | C | A | 1 | a0001c0001t0001g0088 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.171+3408G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104935 | |||||||
| chr4:1104987 | T | C | 2 | a0001c0002t0002g0265 a0001c0002t0002g0319 |
2 | HG00099.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.171+3356A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104987 | |||||||
| chr4:1105009 | G | C | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(301): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.171+3334C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105009 | |||||||
| chr4:1105085 | G | C | 1 | a0001c0001t0001g0191 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.171+3258C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105085 | |||||||
| chr4:1105162 | C | T | 1 | a0006c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.171+3181G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105162 | |||||||
| chr4:1105198 | C | G | 1 | a0001c0001t0001g0114 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.171+3145G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105198 | |||||||
| chr4:1105300 | GT | G | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
346 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(343): Show |
intron_variant | MODIFIER | c.171+3042delA | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105300 | |||||||
| chr4:1105314 | C | A | 4 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02818.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+3029G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105314 | |||||||
| chr4:1105314 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.171+3029G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105314 | |||||||
| chr4:1105326 | C | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(87): Show |
109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.171+3017G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105326 | |||||||
| chr4:1105407 | C | T | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(306): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.171+2936G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105407 | |||||||
| chr4:1105413 | G | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(189): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.171+2930C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105413 | |||||||
| chr4:1105512 | AACACAGC others(3): Show |
A | 1 | a0001c0002t0002g0314 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.171+2821_171+2830d others(12): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105512 | |||||||
| chr4:1105575 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0165 a0001c0001t0001g0166 |
4 | HG02155.hp2 NA18984.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.171+2768G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105575 | |||||||
| chr4:1105579 | T | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.171+2764A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105579 | |||||||
| chr4:1105647 | C | T | 10 | a0001c0002t0001g0034 a0001c0002t0001g0037 a0001c0002t0001g0041 others(7): Show |
12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.171+2696G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105647 | |||||||
| chr4:1105682 | C | T | 1 | a0006c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.171+2661G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105682 | |||||||
| chr4:1105745 | C | CT | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(309): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.171+2597dupA | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105745 | |||||||
| chr4:1105749 | C | T | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(309): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.171+2594G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105749 | |||||||
| chr4:1105752 | C | G | 1 | a0006c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.171+2591G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105752 | |||||||
| chr4:1105757 | G | A | 1 | a0001c0002t0003g0344 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.171+2586C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105757 | |||||||
| chr4:1105818 | G | A | 1 | a0006c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.171+2525C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105818 | |||||||
| chr4:1105852 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.171+2491G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105852 | |||||||
| chr4:1105961 | C | A | 1 | a0001c0002t0003g0347 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.171+2382G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105961 | |||||||
| chr4:1106009 | T | A | 1 | a0001c0002t0002g0289 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.171+2334A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106009 | |||||||
| chr4:1106026 | A | T | 1 | a0001c0001t0001g0297 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.171+2317T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106026 | |||||||
| chr4:1106094 | A | G | 1 | a0001c0002t0002g0244 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.171+2249T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106094 | |||||||
| chr4:1106121 | G | C | 1 | a0001c0002t0003g0344 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.171+2222C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106121 | |||||||
| chr4:1106178 | A | G | 1 | a0001c0002t0002g0057 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.171+2165T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106178 | |||||||
| chr4:1106249 | T | TAC | 24 | a0001c0001t0001g0061 a0001c0001t0001g0197 a0001c0001t0001g0198 others(21): Show |
27 | HG01074.hp1 HG01123.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.171+2092_171+2093d others(4): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106249 | |||||||
| chr4:1106249 | T | TACAC | 21 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0297 others(18): Show |
23 | HG00423.hp2 HG00597.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.171+2090_171+2093d others(6): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106249 | |||||||
| chr4:1106249 | T | TACACAC | 7 | a0001c0001t0005g0045 a0001c0001t0005g0046 a0001c0002t0002g0233 others(4): Show |
7 | HG01361.hp2 HG01928.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+2088_171+2093d others(8): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106249 | |||||||
| chr4:1106249 | TAC | T | 35 | a0001c0001t0001g0024 a0001c0001t0001g0129 a0001c0001t0001g0138 others(32): Show |
39 | HG00642.hp1 HG00642.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.171+2092_171+2093d others(4): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106249 | |||||||
| chr4:1106249 | TACAC | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(74): Show |
93 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.171+2090_171+2093d others(6): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106249 | |||||||
| chr4:1106249 | TACACAC | T | 11 | a0001c0001t0001g0109 a0001c0001t0001g0113 a0001c0001t0001g0148 others(8): Show |
13 | HG01255.hp1 HG02109.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.171+2088_171+2093d others(8): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106249 | |||||||
| chr4:1106249 | TACACACA others(3): Show |
T | 1 | a0001c0002t0012g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.171+2084_171+2093d others(12): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106249 | |||||||
| chr4:1106249 | TACACACA others(7): Show |
T | 12 | a0001c0001t0001g0088 a0001c0001t0001g0182 a0001c0002t0001g0034 others(9): Show |
14 | HG01884.hp2 HG02148.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.171+2080_171+2093d others(16): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106249 | |||||||
| chr4:1106249 | TACACACA others(9): Show |
T | 76 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(73): Show |
87 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.171+2078_171+2093d others(18): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106249 | |||||||
| chr4:1106249 | TACACACA others(11): Show |
T | 6 | a0001c0001t0001g0031 a0001c0001t0001g0271 a0001c0001t0001g0272 others(3): Show |
8 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.171+2076_171+2093d others(20): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106249 | |||||||
| chr4:1106249 | TACACACA others(15): Show |
T | 1 | a0001c0001t0001g0112 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.171+2072_171+2093d others(24): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106249 | |||||||
| chr4:1106249 | TACACACA others(17): Show |
T | 1 | a0001c0009t0003g0326 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.171+2070_171+2093d others(26): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106249 | |||||||
| chr4:1106431 | G | A | 1 | a0005c0006t0001g0133 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.171+1912C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106431 | |||||||
| chr4:1106564 | C | T | 10 | a0001c0002t0001g0034 a0001c0002t0001g0037 a0001c0002t0001g0041 others(7): Show |
12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.171+1779G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106564 | |||||||
| chr4:1106661 | C | T | 8 | a0001c0001t0001g0017 a0001c0001t0001g0064 a0001c0001t0001g0069 others(5): Show |
9 | NA18941.hp2 NA18948.hp2 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.171+1682G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106661 | |||||||
| chr4:1106750 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.171+1593C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106750 | |||||||
| chr4:1106802 | G | C | 4 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02818.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+1541C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106802 | |||||||
| chr4:1106886 | A | G | 1 | a0001c0002t0002g0236 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.171+1457T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106886 | |||||||
| chr4:1106949 | A | G | 1 | a0001c0002t0002g0301 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.171+1394T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106949 | |||||||
| chr4:1107021 | T | C | 1 | a0001c0002t0012g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.171+1322A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107021 | |||||||
| chr4:1107054 | C | G | 1 | a0001c0001t0001g0068 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.171+1289G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107054 | |||||||
| chr4:1107078 | G | A | 1 | a0001c0002t0013g0101 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.171+1265C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107078 | |||||||
| chr4:1107082 | T | G | 1 | a0001c0002t0012g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.171+1261A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107082 | |||||||
| chr4:1107088 | G | C | 1 | a0001c0001t0001g0134 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.171+1255C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107088 | |||||||
| chr4:1107091 | G | A | 6 | a0001c0001t0001g0109 a0001c0001t0001g0135 a0001c0001t0001g0136 others(3): Show |
6 | HG02074.hp2 HG02293.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.171+1252C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107091 | |||||||
| chr4:1107121 | A | G | 307 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(304): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.171+1222T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107121 | |||||||
| chr4:1107180 | T | C | 112 | a0001c0002t0001g0034 a0001c0002t0001g0037 a0001c0002t0001g0041 others(109): Show |
125 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.171+1163A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107180 | |||||||
| chr4:1107294 | G | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.171+1049C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107294 | |||||||
| chr4:1107306 | C | T | 1 | a0001c0002t0002g0149 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.171+1037G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107306 | |||||||
| chr4:1107360 | C | A | 9 | a0001c0002t0003g0033 a0001c0002t0003g0341 a0001c0002t0003g0342 others(6): Show |
10 | HG00642.hp2 HG00735.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.171+983G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107360 | |||||||
| chr4:1107378 | A | G | 1 | a0001c0002t0002g0219 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.171+965T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107378 | |||||||
| chr4:1107428 | T | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.171+915A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107428 | |||||||
| chr4:1107458 | C | CT | 19 | a0001c0001t0001g0006 a0001c0001t0001g0062 a0001c0001t0001g0064 others(16): Show |
21 | HG01167.hp1 HG01175.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.171+884dupA | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107458 | |||||||
| chr4:1107508 | T | C | 7 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0104 others(4): Show |
7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+835A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107508 | |||||||
| chr4:1107544 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.171+799C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107544 | |||||||
| chr4:1107650 | C | A | 1 | a0001c0001t0001g0311 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.171+693G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107650 | |||||||
| chr4:1107693 | G | A | 2 | a0001c0002t0002g0273 a0001c0002t0002g0274 |
2 | NA18944.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.171+650C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107693 | |||||||
| chr4:1107824 | C | A | 2 | a0001c0001t0001g0143 a0001c0002t0002g0058 |
2 | HG01109.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.171+519G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107824 | |||||||
| chr4:1107824 | C | G | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(306): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.171+519G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107824 | |||||||
| chr4:1107862 | T | C | 7 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0104 others(4): Show |
7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+481A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107862 | |||||||
| chr4:1107877 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.171+466A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107877 | |||||||
| chr4:1107969 | G | T | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.171+374C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107969 | |||||||
| chr4:1108079 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.171+264T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1108079 | |||||||
| chr4:1108121 | G | A | 1 | a0001c0002t0002g0275 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.171+222C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1108121 | |||||||
| chr4:1108212 | C | G | 2 | a0001c0001t0001g0061 a0001c0001t0001g0104 |
2 | NA18984.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.171+131G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1108212 | |||||||
| chr4:1108217 | A | G | 2 | a0001c0001t0001g0316 a0001c0001t0001g0320 |
2 | HG01192.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.171+126T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1108217 | |||||||
| chr4:1108262 | C | T | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.171+81G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1108262 | |||||||
| chr4:1108407 | A | G | 34 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0158 others(31): Show |
39 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(36): Show |
splice_region_variant&intron_variant | LOW | c.110-3T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1108407 | |||||||
| chr4:1108552 | A | G | 1 | a0001c0001t0001g0012 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.110-148T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1108552 | |||||||
| chr4:1108577 | G | C | 10 | a0001c0002t0001g0034 a0001c0002t0001g0037 a0001c0002t0001g0041 others(7): Show |
12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.110-173C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1108577 | |||||||
| chr4:1108602 | T | C | 1 | a0006c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.110-198A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1108602 | |||||||
| chr4:1108691 | A | T | 1 | a0001c0002t0002g0312 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.110-287T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1108691 | |||||||
| chr4:1108730 | T | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.110-326A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1108730 | |||||||
| chr4:1108764 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.110-360A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1108764 | |||||||
| chr4:1108787 | A | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.110-383T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1108787 | |||||||
| chr4:1108851 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.110-447G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1108851 | |||||||
| chr4:1108893 | G | T | 3 | a0001c0002t0002g0157 a0001c0002t0002g0217 a0001c0002t0002g0300 |
3 | HG00423.hp1 NA18981.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.110-489C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1108893 | |||||||
| chr4:1108997 | G | T | 1 | a0001c0002t0002g0312 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.110-593C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1108997 | |||||||
| chr4:1109010 | C | CT | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(174): Show |
206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.110-607dupA | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109010 | |||||||
| chr4:1109010 | C | CTT | 8 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0105 others(5): Show |
8 | HG00738.hp2 HG00741.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.110-608_110-607dup others(2): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109010 | |||||||
| chr4:1109010 | C | CTTT | 105 | a0001c0001t0001g0031 a0001c0001t0001g0107 a0001c0001t0001g0271 others(102): Show |
117 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.110-609_110-607dup others(3): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109010 | |||||||
| chr4:1109070 | C | T | 1 | a0001c0002t0012g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.110-666G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109070 | |||||||
| chr4:1109177 | T | G | 1 | a0001c0002t0002g0312 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.110-773A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109177 | |||||||
| chr4:1109199 | G | A | 1 | a0001c0002t0002g0275 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.110-795C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109199 | |||||||
| chr4:1109256 | C | G | 1 | a0001c0002t0001g0035 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.110-852G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109256 | |||||||
| chr4:1109260 | G | A | 1 | a0001c0002t0012g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.110-856C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109260 | |||||||
| chr4:1109573 | C | T | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.110-1169G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109573 | |||||||
| chr4:1109625 | T | C | 1 | a0006c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.110-1221A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109625 | |||||||
| chr4:1109686 | C | A | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.110-1282G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109686 | |||||||
| chr4:1109711 | A | G | 5 | a0001c0001t0001g0024 a0001c0001t0001g0151 a0001c0001t0001g0154 others(2): Show |
6 | HG01884.hp1 HG01891.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.110-1307T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109711 | |||||||
| chr4:1109749 | AC | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.110-1346delG | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109749 | |||||||
| chr4:1109852 | C | T | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG01496.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.110-1448G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109852 | |||||||
| chr4:1109900 | C | T | 1 | a0001c0002t0004g0048 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.110-1496G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109900 | |||||||
| chr4:1109989 | C | T | 4 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02818.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.110-1585G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109989 | |||||||
| chr4:1110090 | T | C | 4 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02818.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.110-1686A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1110090 | |||||||
| chr4:1110159 | G | A | 5 | a0001c0001t0001g0138 a0003c0004t0001g0139 a0003c0004t0001g0140 others(2): Show |
5 | HG00597.hp1 NA18944.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-1755C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1110159 | |||||||
| chr4:1110215 | G | A | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.110-1811C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1110215 | |||||||
| chr4:1110255 | T | C | 3 | a0001c0002t0002g0286 a0001c0002t0002g0287 a0001c0002t0002g0314 |
3 | NA18956.hp2 NA18975.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.110-1851A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1110255 | |||||||
| chr4:1110416 | A | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.110-2012T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1110416 | |||||||
| chr4:1110731 | C | T | 2 | a0001c0002t0001g0201 a0001c0002t0001g0294 |
2 | HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.110-2327G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1110731 | |||||||
| chr4:1110797 | C | A | 1 | a0001c0002t0012g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.110-2393G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1110797 | |||||||
| chr4:1110809 | C | T | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.110-2405G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1110809 | |||||||
| chr4:1110889 | G | A | 1 | a0006c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.109+2467C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1110889 | |||||||
| chr4:1111128 | T | C | 10 | a0001c0002t0001g0034 a0001c0002t0001g0037 a0001c0002t0001g0041 others(7): Show |
12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.109+2228A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1111128 | |||||||
| chr4:1111534 | G | T | 5 | a0001c0001t0001g0044 a0001c0001t0005g0043 a0001c0001t0005g0045 others(2): Show |
5 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.109+1822C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1111534 | |||||||
| chr4:1111604 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.109+1752G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1111604 | |||||||
| chr4:1111676 | C | G | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.109+1680G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1111676 | |||||||
| chr4:1111892 | C | T | 41 | a0001c0002t0001g0023 a0001c0002t0001g0034 a0001c0002t0001g0037 others(38): Show |
46 | HG00642.hp2 HG00735.hp1 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.109+1464G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1111892 | |||||||
| chr4:1111917 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.109+1439T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1111917 | |||||||
| chr4:1111968 | G | A | 2 | a0001c0002t0002g0057 a0001c0002t0002g0058 |
2 | HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.109+1388C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1111968 | |||||||
| chr4:1111975 | C | G | 1 | a0001c0002t0002g0149 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.109+1381G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1111975 | |||||||
| chr4:1111985 | G | C | 6 | a0001c0002t0001g0034 a0001c0002t0001g0201 a0001c0002t0001g0294 others(3): Show |
8 | HG02486.hp2 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.109+1371C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1111985 | |||||||
| chr4:1112032 | C | A | 1 | a0001c0002t0012g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.109+1324G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1112032 | |||||||
| chr4:1112184 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0142 a0001c0001t0001g0297 |
4 | HG03017.hp2 HG03831.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+1172C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1112184 | |||||||
| chr4:1112544 | C | G | 3 | a0001c0001t0001g0095 a0001c0001t0001g0148 a0001c0002t0001g0041 |
3 | HG02258.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.109+812G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1112544 | |||||||
| chr4:1112557 | G | T | 1 | a0001c0002t0002g0147 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.109+799C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1112557 | |||||||
| chr4:1112680 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.109+676G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1112680 | |||||||
| chr4:1112765 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.109+591G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1112765 | |||||||
| chr4:1112816 | T | TC | 19 | a0001c0001t0001g0050 a0001c0001t0001g0090 a0001c0001t0001g0095 others(16): Show |
19 | HG00597.hp1 HG00621.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.109+539dupG | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1112816 | |||||||
| chr4:1112824 | A | C | 346 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(343): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.109+532T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1112824 | |||||||
| chr4:1112827 | C | T | 17 | a0001c0001t0001g0016 a0001c0001t0001g0051 a0001c0001t0001g0054 others(14): Show |
19 | HG01109.hp1 HG01175.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.109+529G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1112827 | |||||||
| chr4:1112837 | C | T | 17 | a0001c0001t0001g0016 a0001c0001t0001g0051 a0001c0001t0001g0054 others(14): Show |
19 | HG01109.hp1 HG01175.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.109+519G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1112837 | |||||||
| chr4:1112903 | G | A | 5 | a0001c0001t0001g0044 a0001c0001t0005g0043 a0001c0001t0005g0045 others(2): Show |
5 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.109+453C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1112903 | |||||||
| chr4:1112906 | G | A | 1 | a0001c0002t0012g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.109+450C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1112906 | |||||||
| chr4:1112936 | C | T | 1 | a0001c0002t0004g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.109+420G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1112936 | |||||||
| chr4:1112987 | C | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
122 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.109+369G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1112987 | |||||||
| chr4:1113024 | T | A | 5 | a0001c0001t0001g0044 a0001c0001t0005g0043 a0001c0001t0005g0045 others(2): Show |
5 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.109+332A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1113024 | |||||||
| chr4:1113063 | A | AC | 60 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(57): Show |
72 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.109+292dupG | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1113063 | |||||||
| chr4:1113073 | G | GC | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(129): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.109+282dupG | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1113073 | |||||||
| chr4:1113073 | G | GCC | 122 | a0001c0001t0001g0031 a0001c0001t0001g0204 a0001c0001t0001g0205 others(119): Show |
135 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.109+281_109+282dup others(2): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1113073 | |||||||
| chr4:1113073 | G | GCCC | 25 | a0001c0001t0001g0297 a0001c0001t0001g0310 a0001c0001t0001g0311 others(22): Show |
25 | HG00639.hp1 HG01192.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.109+280_109+282dup others(3): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1113073 | |||||||
| chr4:1113081 | C | G | 7 | a0001c0001t0001g0044 a0001c0001t0005g0043 a0001c0001t0005g0045 others(4): Show |
7 | HG02040.hp1 HG03098.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.109+275G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1113081 | |||||||
| chr4:1113106 | C | T | 14 | a0001c0002t0001g0037 a0001c0002t0003g0325 a0001c0002t0003g0327 others(11): Show |
14 | HG01243.hp2 HG01433.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.109+250G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1113106 | |||||||
| chr4:1113119 | G | GC | 8 | a0001c0001t0001g0032 a0001c0001t0001g0317 a0001c0001t0001g0318 others(5): Show |
9 | HG01255.hp2 HG01261.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.109+236dupG | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1113119 | |||||||
| chr4:1113149 | C | A | 1 | a0001c0001t0001g0322 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.109+207G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1113149 | |||||||
| chr4:1113206 | G | T | 21 | a0001c0002t0001g0037 a0001c0002t0003g0325 a0001c0002t0003g0327 others(18): Show |
22 | HG01074.hp2 HG01243.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.109+150C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1113206 | |||||||
| chr4:1113251 | C | T | 1 | a0001c0002t0002g0036 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.109+105G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1113251 | |||||||
| chr4:1113268 | C | G | 1 | a0001c0002t0001g0035 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.109+88G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1113268 | |||||||
| chr4:1113288 | C | G | 2 | a0001c0001t0001g0012 a0001c0002t0001g0034 |
3 | HG01069.hp2 HG01071.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.109+68G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1113288 |